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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:39:36 UTC

Update Date

2021-09-26 22:52:17 UTC

HMDB ID

HMDB0244505

Secondary Accession Numbers

None

Metabolite Identification

Common Name

13-Dihydrocarminomycin

Description

13-Dihydrocarminomycin, also known as carminomycinol, belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage. Based on a literature review a significant number of articles have been published on 13-Dihydrocarminomycin. This compound has been identified in human blood as reported by (PMID: 31557052 ). 13-dihydrocarminomycin is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 13-Dihydrocarminomycin is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv1652309102123392D          

 37 41  0  0  0  0            999 V2000
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5403   -0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9276   -0.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9774    0.6708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1530   -0.6996    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  2  0  0  0  0
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 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 18  1  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
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 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
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 23 26  1  0  0  0  0
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 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 14 31  1  0  0  0  0
 11 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 11 35  1  0  0  0  0
  4 36  1  0  0  0  0
  3 37  1  0  0  0  0
M  END

HMDB0257322
     RDKit          3D
Dihydrokarminomycin
 66 70  0  0  0  0  0  0  0  0999 V2000
   -3.2859   -3.3099   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5701   -1.8810   -1.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8695   -1.6549    0.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530   -0.3141    0.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7925    0.2872   -0.1058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7727    0.7226    0.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854    2.2701    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1769    2.8367    1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0584    3.6782    0.8683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5207    3.7098    2.6039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4441    4.4845    3.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4136    2.9759    3.3657 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0555    1.7968    2.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5472    0.9362    1.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    0.7076    0.9294 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7579    1.2889    1.8054 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2775   -0.0988   -0.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343   -0.6438   -0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9525   -0.4244   -0.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0663   -1.0066   -1.6811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6149    0.3771    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6874   -1.5044   -2.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8096   -1.9849   -2.8607 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0971   -1.7993   -2.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593   -2.6018   -3.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5789   -3.1693   -4.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8366   -2.8371   -3.6579 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7673   -2.2859   -2.8167 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3780   -1.4890   -1.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0248   -1.2410   -1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6671   -0.3814   -0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5651    0.0820    0.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1910    0.2691    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2815   -0.8124    0.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3442   -1.4358    1.6069 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0744   -1.8064   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6651   -1.3644   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2078   -3.8297   -1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -3.3343   -2.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8481   -3.8958   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692   -1.2194   -1.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7073   -0.3626    1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8730    0.5411    1.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6452    2.6470   -0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8111    2.5511    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349    3.7307   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0022    5.4812    3.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    3.9780    4.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9488    2.3536    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5506    1.2217    3.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7075    1.2527    1.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9006   -0.9147   -1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6360   -3.1910   -4.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1749   -3.4594   -4.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8424   -2.4412   -2.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0914   -1.0413   -1.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4934    1.0198    1.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3298    0.7567   -0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2367   -0.2856    0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5085   -2.7695   -0.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9590   -0.4131   -1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
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 10 12  1  0
  8 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 18 22  1  0
 22 23  2  0
 22 24  1  0
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 29 30  2  0
 30 31  1  0
 31 32  2  0
  4 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36  2  1  0
 21  6  1  0
 30 24  1  0
 21 14  1  0
 31 17  1  0
  1 38  1  0
  1 39  1  0
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  2 41  1  0
  4 42  1  0
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 33 60  1  0
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 36 65  1  0
 37 66  1  0
M  END

  Mrv1652309102123392D          

 37 41  0  0  0  0            999 V2000
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8592    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
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  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 29 30  1  0  0  0  0
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 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 11 35  1  0  0  0  0
  4 36  1  0  0  0  0
  3 37  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0244505

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)C1(O)CC(OC2CC(N)C(O)C(C)O2)C2=C(O)C3=C(C(O)=C2C1)C(=O)C1=C(C(O)=CC=C1)C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H29NO10/c1-9-21(30)13(27)6-16(36-9)37-15-8-26(35,10(2)28)7-12-18(15)25(34)20-19(23(12)32)22(31)11-4-3-5-14(29)17(11)24(20)33/h3-5,9-10,13,15-16,21,28-30,32,34-35H,6-8,27H2,1-2H3

> <INCHI_KEY>
YXBSCYMMPXQFDS-UHFFFAOYSA-N

> <FORMULA>
C26H29NO10

> <MOLECULAR_WEIGHT>
515.515

> <EXACT_MASS>
515.179146138

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
52.89383762136246

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-1,6,8,11-tetrahydroxy-8-(1-hydroxyethyl)-5,7,8,9,10,12-hexahydrotetracene-5,12-dione

> <ALOGPS_LOGP>
0.69

> <JCHEM_LOGP>
1.3412792711303776

> <ALOGPS_LOGS>
-2.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
8.501025426690836

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.890312102011861

> <JCHEM_PKA_STRONGEST_BASIC>
9.420957058658608

> <JCHEM_POLAR_SURFACE_AREA>
200.0

> <JCHEM_REFRACTIVITY>
129.33439999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-1,6,8,11-tetrahydroxy-8-(1-hydroxyethyl)-9,10-dihydro-7H-tetracene-5,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0257322
     RDKit          3D
Dihydrokarminomycin
 66 70  0  0  0  0  0  0  0  0999 V2000
   -3.2859   -3.3099   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5701   -1.8810   -1.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8695   -1.6549    0.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530   -0.3141    0.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7925    0.2872   -0.1058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7727    0.7226    0.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854    2.2701    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1769    2.8367    1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0584    3.6782    0.8683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5207    3.7098    2.6039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4441    4.4845    3.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4136    2.9759    3.3657 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0555    1.7968    2.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5472    0.9362    1.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    0.7076    0.9294 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7579    1.2889    1.8054 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2775   -0.0988   -0.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343   -0.6438   -0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9525   -0.4244   -0.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0663   -1.0066   -1.6811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6149    0.3771    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6874   -1.5044   -2.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8096   -1.9849   -2.8607 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0971   -1.7993   -2.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593   -2.6018   -3.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5789   -3.1693   -4.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8366   -2.8371   -3.6579 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7673   -2.2859   -2.8167 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3780   -1.4890   -1.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0248   -1.2410   -1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6671   -0.3814   -0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5651    0.0820    0.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1910    0.2691    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2815   -0.8124    0.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3442   -1.4358    1.6069 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0744   -1.8064   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6651   -1.3644   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2078   -3.8297   -1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -3.3343   -2.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8481   -3.8958   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692   -1.2194   -1.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7073   -0.3626    1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8730    0.5411    1.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6452    2.6470   -0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8111    2.5511    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349    3.7307   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1148    4.4546    2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3686    4.7202    2.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0022    5.4812    3.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    3.9780    4.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0527    3.5346    3.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9488    2.3536    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5506    1.2217    3.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7075    1.2527    1.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9006   -0.9147   -1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6360   -3.1910   -4.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1749   -3.4594   -4.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8424   -2.4412   -2.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0914   -1.0413   -1.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4934    1.0198    1.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3298    0.7567   -0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2367   -0.2856    0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2311   -2.4663    1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7453   -0.9950    2.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5085   -2.7695   -0.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9590   -0.4131   -1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
  8 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 18 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
  4 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36  2  1  0
 21  6  1  0
 30 24  1  0
 21 14  1  0
 31 17  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  2 41  1  0
  4 42  1  0
  6 43  1  0
  7 44  1  0
  7 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 16 54  1  0
 20 55  1  0
 26 56  1  0
 27 57  1  0
 28 58  1  0
 29 59  1  0
 33 60  1  0
 33 61  1  0
 34 62  1  0
 35 63  1  0
 35 64  1  0
 36 65  1  0
 37 66  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0      14.670   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.003   3.850   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      12.208  -0.054   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.931  -1.413   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      13.025   1.252   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      11.486  -1.306   0.000  0.00  0.00           O+0
HETATM   36  N   UNK     0      12.003   8.470   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0      14.670   6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4   37                                                  
CONECT    4    3    5   36                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   32   35                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   31                                                  
CONECT   15   14   16   24                                                  
CONECT   16   15   17   20                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17    9   13                                                  
CONECT   19   17                                                            
CONECT   20   16   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   29                                                  
CONECT   23   22   24   26                                                  
CONECT   24   23   15   25                                                  
CONECT   25   24                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29                                                            
CONECT   31   14                                                            
CONECT   32   11   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   11                                                            
CONECT   36    4                                                            
CONECT   37    3                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

COMPND    HMDB0257322
HETATM    1  C1  UNL     1      -3.286  -3.310  -1.485  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.570  -1.881  -1.047  1.00  0.00           C  
HETATM    3  O1  UNL     1      -2.869  -1.655   0.109  1.00  0.00           O  
HETATM    4  C3  UNL     1      -2.853  -0.314   0.501  1.00  0.00           C  
HETATM    5  O2  UNL     1      -1.793   0.287  -0.106  1.00  0.00           O  
HETATM    6  C4  UNL     1      -0.773   0.723   0.613  1.00  0.00           C  
HETATM    7  C5  UNL     1      -0.785   2.270   0.601  1.00  0.00           C  
HETATM    8  C6  UNL     1       0.177   2.837   1.586  1.00  0.00           C  
HETATM    9  O3  UNL     1       1.058   3.678   0.868  1.00  0.00           O  
HETATM   10  C7  UNL     1      -0.521   3.710   2.604  1.00  0.00           C  
HETATM   11  C8  UNL     1       0.444   4.484   3.447  1.00  0.00           C  
HETATM   12  O4  UNL     1      -1.414   2.976   3.366  1.00  0.00           O  
HETATM   13  C9  UNL     1       1.056   1.797   2.252  1.00  0.00           C  
HETATM   14  C10 UNL     1       1.547   0.936   1.119  1.00  0.00           C  
HETATM   15  C11 UNL     1       2.896   0.708   0.929  1.00  0.00           C  
HETATM   16  O5  UNL     1       3.758   1.289   1.805  1.00  0.00           O  
HETATM   17  C12 UNL     1       3.278  -0.099  -0.141  1.00  0.00           C  
HETATM   18  C13 UNL     1       2.334  -0.644  -0.974  1.00  0.00           C  
HETATM   19  C14 UNL     1       0.953  -0.424  -0.801  1.00  0.00           C  
HETATM   20  O6  UNL     1       0.066  -1.007  -1.681  1.00  0.00           O  
HETATM   21  C15 UNL     1       0.615   0.377   0.267  1.00  0.00           C  
HETATM   22  C16 UNL     1       2.687  -1.504  -2.121  1.00  0.00           C  
HETATM   23  O7  UNL     1       1.810  -1.985  -2.861  1.00  0.00           O  
HETATM   24  C17 UNL     1       4.097  -1.799  -2.396  1.00  0.00           C  
HETATM   25  C18 UNL     1       4.459  -2.602  -3.462  1.00  0.00           C  
HETATM   26  O8  UNL     1       3.579  -3.169  -4.321  1.00  0.00           O  
HETATM   27  C19 UNL     1       5.837  -2.837  -3.658  1.00  0.00           C  
HETATM   28  C20 UNL     1       6.767  -2.286  -2.817  1.00  0.00           C  
HETATM   29  C21 UNL     1       6.378  -1.489  -1.760  1.00  0.00           C  
HETATM   30  C22 UNL     1       5.025  -1.241  -1.545  1.00  0.00           C  
HETATM   31  C23 UNL     1       4.667  -0.381  -0.400  1.00  0.00           C  
HETATM   32  O9  UNL     1       5.565   0.082   0.318  1.00  0.00           O  
HETATM   33  C24 UNL     1      -4.191   0.269   0.262  1.00  0.00           C  
HETATM   34  C25 UNL     1      -5.281  -0.812   0.317  1.00  0.00           C  
HETATM   35  N1  UNL     1      -5.344  -1.436   1.607  1.00  0.00           N  
HETATM   36  C26 UNL     1      -5.074  -1.806  -0.801  1.00  0.00           C  
HETATM   37  O10 UNL     1      -5.665  -1.364  -1.987  1.00  0.00           O  
HETATM   38  H1  UNL     1      -4.208  -3.830  -1.808  1.00  0.00           H  
HETATM   39  H2  UNL     1      -2.604  -3.334  -2.375  1.00  0.00           H  
HETATM   40  H3  UNL     1      -2.848  -3.896  -0.651  1.00  0.00           H  
HETATM   41  H4  UNL     1      -3.269  -1.219  -1.885  1.00  0.00           H  
HETATM   42  H5  UNL     1      -2.707  -0.363   1.622  1.00  0.00           H  
HETATM   43  H6  UNL     1      -0.873   0.541   1.736  1.00  0.00           H  
HETATM   44  H7  UNL     1      -0.645   2.647  -0.434  1.00  0.00           H  
HETATM   45  H8  UNL     1      -1.811   2.551   0.918  1.00  0.00           H  
HETATM   46  H9  UNL     1       0.835   3.731  -0.075  1.00  0.00           H  
HETATM   47  H10 UNL     1      -1.115   4.455   2.017  1.00  0.00           H  
HETATM   48  H11 UNL     1       1.369   4.720   2.845  1.00  0.00           H  
HETATM   49  H12 UNL     1      -0.002   5.481   3.692  1.00  0.00           H  
HETATM   50  H13 UNL     1       0.751   3.978   4.373  1.00  0.00           H  
HETATM   51  H14 UNL     1      -2.053   3.535   3.840  1.00  0.00           H  
HETATM   52  H15 UNL     1       1.949   2.354   2.632  1.00  0.00           H  
HETATM   53  H16 UNL     1       0.551   1.222   3.027  1.00  0.00           H  
HETATM   54  H17 UNL     1       4.708   1.253   1.843  1.00  0.00           H  
HETATM   55  H18 UNL     1      -0.901  -0.915  -1.647  1.00  0.00           H  
HETATM   56  H19 UNL     1       2.636  -3.191  -4.438  1.00  0.00           H  
HETATM   57  H20 UNL     1       6.175  -3.459  -4.480  1.00  0.00           H  
HETATM   58  H21 UNL     1       7.842  -2.441  -2.931  1.00  0.00           H  
HETATM   59  H22 UNL     1       7.091  -1.041  -1.081  1.00  0.00           H  
HETATM   60  H23 UNL     1      -4.493   1.020   1.027  1.00  0.00           H  
HETATM   61  H24 UNL     1      -4.330   0.757  -0.718  1.00  0.00           H  
HETATM   62  H25 UNL     1      -6.237  -0.286   0.121  1.00  0.00           H  
HETATM   63  H26 UNL     1      -5.231  -2.466   1.534  1.00  0.00           H  
HETATM   64  H27 UNL     1      -4.745  -0.995   2.321  1.00  0.00           H  
HETATM   65  H28 UNL     1      -5.508  -2.770  -0.526  1.00  0.00           H  
HETATM   66  H29 UNL     1      -5.959  -0.413  -1.828  1.00  0.00           H  
CONECT    1    2   38   39   40
CONECT    2    3   36   41
CONECT    3    4
CONECT    4    5   33   42
CONECT    5    6
CONECT    6    7   21   43
CONECT    7    8   44   45
CONECT    8    9   10   13
CONECT    9   46
CONECT   10   11   12   47
CONECT   11   48   49   50
CONECT   12   51
CONECT   13   14   52   53
CONECT   14   15   15   21
CONECT   15   16   17
CONECT   16   54
CONECT   17   18   18   31
CONECT   18   19   22
CONECT   19   20   21   21
CONECT   20   55
CONECT   22   23   23   24
CONECT   24   25   25   30
CONECT   25   26   27
CONECT   26   56
CONECT   27   28   28   57
CONECT   28   29   58
CONECT   29   30   30   59
CONECT   30   31
CONECT   31   32   32
CONECT   33   34   60   61
CONECT   34   35   36   62
CONECT   35   63   64
CONECT   36   37   65
CONECT   37   66
END

HMDB0257322
     RDKit          3D
Dihydrokarminomycin
 66 70  0  0  0  0  0  0  0  0999 V2000
   -3.2859   -3.3099   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5701   -1.8810   -1.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8695   -1.6549    0.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530   -0.3141    0.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7925    0.2872   -0.1058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7727    0.7226    0.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854    2.2701    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1769    2.8367    1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0584    3.6782    0.8683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5207    3.7098    2.6039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4441    4.4845    3.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4136    2.9759    3.3657 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0555    1.7968    2.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5472    0.9362    1.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    0.7076    0.9294 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7579    1.2889    1.8054 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2775   -0.0988   -0.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343   -0.6438   -0.9744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9525   -0.4244   -0.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0663   -1.0066   -1.6811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6149    0.3771    0.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6874   -1.5044   -2.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8096   -1.9849   -2.8607 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0971   -1.7993   -2.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593   -2.6018   -3.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5789   -3.1693   -4.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8366   -2.8371   -3.6579 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7673   -2.2859   -2.8167 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3780   -1.4890   -1.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0248   -1.2410   -1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6671   -0.3814   -0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5651    0.0820    0.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1910    0.2691    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2815   -0.8124    0.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3442   -1.4358    1.6069 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0744   -1.8064   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6651   -1.3644   -1.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2078   -3.8297   -1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -3.3343   -2.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8481   -3.8958   -0.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692   -1.2194   -1.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7073   -0.3626    1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8730    0.5411    1.7362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6452    2.6470   -0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8111    2.5511    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349    3.7307   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1148    4.4546    2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3686    4.7202    2.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0022    5.4812    3.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7507    3.9780    4.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0527    3.5346    3.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9488    2.3536    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5506    1.2217    3.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7075    1.2527    1.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9006   -0.9147   -1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6360   -3.1910   -4.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1749   -3.4594   -4.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8424   -2.4412   -2.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0914   -1.0413   -1.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4934    1.0198    1.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3298    0.7567   -0.7180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2367   -0.2856    0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2311   -2.4663    1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7453   -0.9950    2.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5085   -2.7695   -0.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9590   -0.4131   -1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
  8 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 18 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
  4 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36  2  1  0
 21  6  1  0
 30 24  1  0
 21 14  1  0
 31 17  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  2 41  1  0
  4 42  1  0
  6 43  1  0
  7 44  1  0
  7 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 16 54  1  0
 20 55  1  0
 26 56  1  0
 27 57  1  0
 28 58  1  0
 29 59  1  0
 33 60  1  0
 33 61  1  0
 34 62  1  0
 35 63  1  0
 35 64  1  0
 36 65  1  0
 37 66  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Carminomycinol	HMDB

Chemical Formula

C₂₆H₂₉NO₁₀

Average Molecular Weight

515.515

Monoisotopic Molecular Weight

515.179146138

IUPAC Name

10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-1,6,8,11-tetrahydroxy-8-(1-hydroxyethyl)-5,7,8,9,10,12-hexahydrotetracene-5,12-dione

Traditional Name

10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-1,6,8,11-tetrahydroxy-8-(1-hydroxyethyl)-9,10-dihydro-7H-tetracene-5,12-dione

CAS Registry Number

Not Available

SMILES

CC(O)C1(O)CC(OC2CC(N)C(O)C(C)O2)C2=C(O)C3=C(C(O)=C2C1)C(=O)C1=C(C(O)=CC=C1)C3=O

InChI Identifier

InChI=1S/C26H29NO10/c1-9-21(30)13(27)6-16(36-9)37-15-8-26(35,10(2)28)7-12-18(15)25(34)20-19(23(12)32)22(31)11-4-3-5-14(29)17(11)24(20)33/h3-5,9-10,13,15-16,21,28-30,32,34-35H,6-8,27H2,1-2H3

InChI Key

YXBSCYMMPXQFDS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Anthracyclines

Sub Class

Not Available

Direct Parent

Anthracyclines

Alternative Parents

Substituents

Anthracycline
Anthracyclinone-skeleton
Aminoglycoside core
Tetracenequinone
9,10-anthraquinone
1,4-anthraquinone
Anthracene
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Tetralin
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Amino saccharide
Monosaccharide
Benzenoid
Oxane
Tertiary alcohol
Vinylogous acid
Secondary alcohol
1,2-aminoalcohol
Ketone
Polyol
Oxacycle
Acetal
Organoheterocyclic compound
Alcohol
Primary aliphatic amine
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Aldehyde
Primary amine
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.69	ALOGPS
logP	1.34	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	7.89	ChemAxon
pKa (Strongest Basic)	9.42	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	200 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	129.33 m³·mol⁻¹	ChemAxon
Polarizability	52.89 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	209.805	30932474
DeepCCS	[M-H]-	207.41	30932474
DeepCCS	[M-2H]-	240.366	30932474
DeepCCS	[M+Na]+	215.718	30932474
AllCCS	[M+H]+	215.9	32859911
AllCCS	[M+H-H2O]+	214.4	32859911
AllCCS	[M+NH4]+	217.2	32859911
AllCCS	[M+Na]+	217.6	32859911
AllCCS	[M-H]-	207.6	32859911
AllCCS	[M+Na-2H]-	208.6	32859911
AllCCS	[M+HCOO]-	209.9	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
13-Dihydrocarminomycin,1TMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4452.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4275.9	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6483.3	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4458.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4265.7	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6716.0	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4504.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4251.8	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	6391.8	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4534.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4247.2	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	6525.1	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4549.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4227.4	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6539.8	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4599.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4298.7	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6431.7	Standard polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4546.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4368.4	Standard non polar	33892256
13-Dihydrocarminomycin,1TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	6436.0	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4376.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4298.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6186.1	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4357.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4296.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	6105.5	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4371.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4400.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	6150.0	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4415.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4276.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5992.6	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4399.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4275.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5985.3	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4484.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4322.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5917.1	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4415.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4372.3	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5817.7	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4439.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4252.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	6103.9	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4509.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4294.2	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	6039.5	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4445.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4378.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	6000.7	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4505.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4299.3	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6044.8	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4386.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4291.2	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6029.8	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4454.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4371.2	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	6014.0	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4528.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4427.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5925.6	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4555.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4481.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	6101.2	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4374.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4287.8	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	6029.6	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4444.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4334.9	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5960.9	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4367.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4309.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5904.7	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4357.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4406.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5934.4	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4390.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4268.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6240.0	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4381.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4270.3	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	6219.0	Standard polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4432.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4320.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6160.5	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4255.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4304.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5803.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4335.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4321.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5660.0	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4249.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4322.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5594.7	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4246.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4401.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5582.9	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4317.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4359.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5540.9	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4305.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4440.3	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5537.9	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4224.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4408.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5408.8	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4377.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4502.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5672.8	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4262.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4271.3	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5854.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4329.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4308.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5818.6	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4254.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4309.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5759.0	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4246.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4300.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5798.7	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4264.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4393.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5767.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4320.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4300.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5800.8	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4244.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4304.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5739.5	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4260.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4391.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5742.5	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4299.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4341.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5695.1	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4306.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4431.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5709.5	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4224.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4398.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5578.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4370.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4483.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5846.9	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4305.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4282.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5677.0	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4368.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4323.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5630.1	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4318.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4332.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5754.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4293.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4379.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5490.7	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4366.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4311.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5626.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4290.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4377.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5481.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4352.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4414.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5443.2	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4483.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4467.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5602.8	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4368.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4290.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5741.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4323.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4364.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5653.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4397.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4405.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5610.2	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4410.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4462.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5750.2	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4395.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4408.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5618.2	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4251.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4335.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5692.8	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4440.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4467.3	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5756.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4489.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4510.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5703.4	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4246.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4410.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5677.9	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4263.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4290.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5703.0	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4341.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4333.3	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5657.1	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4261.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4331.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5592.3	Standard polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4255.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4404.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5585.9	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4149.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4294.5	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5486.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4085.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4404.9	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5177.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4254.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4498.6	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5453.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4211.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4308.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5409.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4150.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4313.5	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5345.2	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4159.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4379.2	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5305.9	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4218.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4349.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5308.2	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4208.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4418.1	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5286.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4116.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4404.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5145.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4270.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4495.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5399.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4217.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4338.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5311.2	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4222.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4316.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5461.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4205.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4411.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5284.7	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4114.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4394.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5143.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4252.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4486.6	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5401.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4156.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4419.2	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5123.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4299.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4521.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5372.8	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4276.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4492.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5255.5	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4205.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4305.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5525.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4142.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4303.8	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5457.0	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4164.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4372.6	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5419.7	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4209.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4333.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5431.8	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4146.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4330.1	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5394.7	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4218.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4409.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5414.8	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4126.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4392.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5268.6	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4270.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4476.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5541.0	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4205.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4332.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5414.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4215.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4405.6	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5393.6	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4128.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4387.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5245.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4254.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4469.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5522.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #37	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4169.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #37	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4410.8	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #37	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5237.6	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #38	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4296.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #38	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4505.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #38	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5504.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #39	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4275.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #39	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4476.1	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #39	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5382.5	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4141.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4400.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5343.9	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4255.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4304.5	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5392.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4202.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4358.6	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5212.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #42	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4252.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #42	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4395.9	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #42	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5197.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #43	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4356.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #43	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4458.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #43	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5332.5	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #44	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4253.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #44	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4386.1	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #44	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5190.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #45	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4344.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #45	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4450.8	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #45	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5327.0	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #46	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4385.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #46	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4485.4	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #46	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5303.2	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #47	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4272.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #47	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4381.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #47	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5352.7	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #48	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4291.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #48	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4447.1	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #48	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5469.1	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #49	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4341.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #49	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4477.3	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #49	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5444.0	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4221.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4322.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5458.3	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #50	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4359.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #50	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4488.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #50	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5449.0	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4138.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4332.5	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5390.7	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4136.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4397.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5339.6	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4210.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4348.0	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5361.4	Standard polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4187.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4416.7	Standard non polar	33892256
13-Dihydrocarminomycin,4TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5325.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4127.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	4317.6	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O	5243.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4027.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4398.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4913.4	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4188.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4484.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5177.5	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #12	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4074.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #12	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4406.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #12	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4908.5	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #13	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4236.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #13	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4499.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #13	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5170.7	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #14	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4208.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #14	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4479.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #14	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5036.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4116.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4321.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5143.4	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4129.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4384.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5074.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4041.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4369.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #17	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4925.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4180.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4464.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #18	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5165.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4099.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4402.2	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #19	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4910.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4065.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4317.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5178.6	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4243.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4498.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #20	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5152.0	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4219.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4477.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #21	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5026.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4093.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4396.2	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #22	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4912.1	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4226.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4491.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #23	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5154.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4205.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4467.5	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #24	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5029.1	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4246.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4490.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #25	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5008.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4115.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4325.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5225.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4133.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4387.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5154.3	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4048.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4368.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #28	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4997.5	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4185.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4455.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #29	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5253.7	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4075.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4371.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5074.7	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4106.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4399.4	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #30	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	5000.3	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4247.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4486.4	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #31	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5253.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4225.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4465.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #32	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5125.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4101.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4401.5	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #33	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4979.3	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4231.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4484.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #34	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5236.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4214.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4461.7	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #35	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5105.5	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4250.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4481.4	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #36	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5097.2	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4153.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4370.5	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4981.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4257.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4428.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5099.1	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4316.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4462.6	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5084.7	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4140.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	4342.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C	5158.0	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4300.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	4451.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O[Si](C)(C)C	5080.6	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4242.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4455.9	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5223.7	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4127.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	4401.0	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O	5074.8	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4029.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4396.1	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #6	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C)C1O[Si](C)(C)C	4913.9	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4198.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	4483.8	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O[Si](C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C)[Si](C)(C)C)C1O	5177.4	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4130.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	4350.5	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N)C1O[Si](C)(C)C	5156.4	Standard polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4120.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	4406.3	Standard non polar	33892256
13-Dihydrocarminomycin,5TMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C)(C(C)O[Si](C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C)=C32)CC(N[Si](C)(C)C)C1O	5073.7	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4687.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4513.8	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #1	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6412.6	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4681.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4489.6	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6572.2	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4741.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4494.2	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	6323.9	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4732.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4473.1	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	6453.7	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4741.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4460.0	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6456.9	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4790.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4538.9	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6373.7	Standard polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4798.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4582.8	Standard non polar	33892256
13-Dihydrocarminomycin,1TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	6333.3	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4807.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4713.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6044.3	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4794.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4712.9	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #10	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5980.4	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4805.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4797.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #11	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	6000.8	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4865.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4696.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5947.3	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4855.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4688.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5948.8	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4934.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4755.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5897.8	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4877.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4783.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5800.6	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4849.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4656.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	6057.8	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4933.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4705.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #17	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	6017.7	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4870.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4771.9	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #18	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5949.3	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4928.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4715.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #19	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6016.1	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4823.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4715.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #2	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5979.0	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4889.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4770.5	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #20	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5952.2	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4959.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4840.1	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #21	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5906.4	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4929.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4848.8	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #22	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	6004.7	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4813.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4706.8	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #3	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5987.1	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4887.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4769.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #4	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5939.9	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4817.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4748.8	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #5	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5868.2	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4822.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4823.6	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5884.5	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4808.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4668.7	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #7	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6099.9	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4797.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4673.2	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #8	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	6090.0	Standard polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4870.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4731.4	Standard non polar	33892256
13-Dihydrocarminomycin,2TBDMS,isomer #9	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	6051.2	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4915.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4866.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #1	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5726.0	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4969.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4906.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #10	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5686.6	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4897.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4901.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #11	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5607.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4874.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4969.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #12	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5619.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4999.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4959.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #13	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5572.2	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4969.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5024.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #14	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5595.7	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4868.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4993.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #15	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5478.0	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4992.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5048.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #16	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5667.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4843.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4817.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #17	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5793.2	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4960.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4863.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #18	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5770.7	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4895.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4865.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #19	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5688.1	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4890.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4870.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #2	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5731.8	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4870.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4943.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #20	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5702.5	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4944.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4867.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #21	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5762.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4868.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4866.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #22	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5679.2	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4851.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4949.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #23	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5689.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4974.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4916.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #24	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5654.3	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4943.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4996.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #25	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5677.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4840.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4962.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #26	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5556.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4973.7	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5016.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #27	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5755.3	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4903.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4835.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #28	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5681.1	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5014.0	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4895.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #29	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5647.3	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4996.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4911.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #3	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5706.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4927.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4942.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #30	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5544.5	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5004.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4880.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #31	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5650.0	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4916.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4932.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #32	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5543.2	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5016.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4990.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #33	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5523.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5050.5	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5012.5	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #34	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5616.7	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4956.6	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4842.0	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #35	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5760.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4906.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4913.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #36	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5677.6	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5010.2	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4968.7	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #37	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5660.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5029.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4983.4	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #38	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5736.0	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5018.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4972.8	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #39	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5661.9	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4942.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4914.1	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #4	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5623.8	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5047.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	4996.3	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #40	CC1OC(OC2CC(O)(C(C)O)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5733.8	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5109.4	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5047.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #41	CC1OC(OC2CC(O)(C(C)O)CC3=C(O)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1O	5711.3	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4896.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4976.6	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #5	CC1OC(OC2CC(O[Si](C)(C)C(C)(C)C)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5632.0	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4872.1	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	4861.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #6	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O[Si](C)(C)C(C)(C)C)=C32)CC(N)C1O	5709.7	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4983.3	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	4915.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #7	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O[Si](C)(C)C(C)(C)C)C=CC=C5C4=O)C(O)=C32)CC(N)C1O	5677.1	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4919.9	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	4915.2	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #8	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N)C1O[Si](C)(C)C(C)(C)C	5598.4	Standard polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4895.8	Semi standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	4977.9	Standard non polar	33892256
13-Dihydrocarminomycin,3TBDMS,isomer #9	CC1OC(OC2CC(O)(C(C)O[Si](C)(C)C(C)(C)C)CC3=C(O[Si](C)(C)C(C)(C)C)C4=C(C(=O)C5=C(O)C=CC=C5C4=O)C(O)=C32)CC(N[Si](C)(C)C(C)(C)C)C1O	5614.1	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 10V, Positive-QTOF	splash10-0fsj-0809810000-7867e1d0f8316546c0ae	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 20V, Positive-QTOF	splash10-0wn9-2509500000-8411ee38bea123f41827	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 40V, Positive-QTOF	splash10-03e9-5921100000-0c5f5fa933c0237a2e78	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 10V, Negative-QTOF	splash10-014i-0009000000-0d295bd4cf7dc3212f3a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 20V, Negative-QTOF	splash10-0gb9-0009000000-5b0d303eb3702f84cc97	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 13-Dihydrocarminomycin 40V, Negative-QTOF	splash10-0uxr-0009100000-66ebe70dad42d2f51c1c	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

13800134

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21829839

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 13-Dihydrocarminomycin (HMDB0244505)

MOL for HMDB0244505 (13-Dihydrocarminomycin)

3D MOL for HMDB0244505 (13-Dihydrocarminomycin)

3D SDF for HMDB0244505 (13-Dihydrocarminomycin)

3D-SDF for HMDB0244505 (13-Dihydrocarminomycin)

PDB for HMDB0244505 (13-Dihydrocarminomycin)

3D PDB for HMDB0244505 (13-Dihydrocarminomycin)

SMILES for HMDB0244505 (13-Dihydrocarminomycin)

INCHI for HMDB0244505 (13-Dihydrocarminomycin)

Structure for HMDB0244505 (13-Dihydrocarminomycin)

3D Structure for HMDB0244505 (13-Dihydrocarminomycin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

MS/MS Spectra