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Showing metabocard for Loquatoside (HMDB0041238)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 02:54:20 UTC
Update Date2022-03-07 02:56:56 UTC
HMDB IDHMDB0041238
Secondary Accession Numbers
  • HMDB41238
Metabolite Identification
Common NameLoquatoside
DescriptionLoquatoside belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Loquatoside has been detected, but not quantified in, fruits and loquats (Eriobotrya japonica). This could make loquatoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Loquatoside.
Structure
Data?1563863640
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0041238 (Loquatoside)


  Mrv0541 05061312302D          

 31 34  0  0  0  0            999 V2000
    3.5724   -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
    2.8579    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    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
   -0.7145   -0.4125    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   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
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  4  2  0  0  0  0
  8  5  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  9  2  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 13  5  2  0  0  0  0
 14 11  2  0  0  0  0
 14 13  1  0  0  0  0
 15 12  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18  7  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 15  1  0  0  0  0
 27 16  1  0  0  0  0
 28 17  1  0  0  0  0
 29  6  1  0  0  0  0
 29 20  1  0  0  0  0
 30 13  1  0  0  0  0
 30 18  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
M  END
Download

3D MOL for HMDB0041238 (Loquatoside)

HMDB0041238
     RDKit          3D
Loquatoside
 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.9306   -4.4524   -1.6996 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9003   -3.8645   -0.9987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0468   -4.6230   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0151   -4.0443    0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599   -4.7927    1.2339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8238   -2.6541    0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493   -1.8821   -0.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6777   -2.5108   -1.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4550   -0.5218   -0.3882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6035    0.1073    0.5440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4094    1.5260    0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4271    2.5249    1.1561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2597    3.8590    0.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0580    4.2343   -0.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8797    5.5722   -0.7708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0331    3.2498   -1.4179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8326    3.6335   -2.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059    1.9175   -1.1089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3519   -0.6616    0.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5610   -0.6010   -0.2425 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7871   -0.0555    0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6969   -1.0915    0.0545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9992   -0.7536    0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    0.6680    0.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0850    1.5064    1.0976 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5509    1.1602   -1.1503 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7745    0.4390   -2.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0897    1.0967   -0.7511 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2833   -0.0290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7034   -2.0733    1.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0617   -2.1797    2.5366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8606   -4.5971   -1.3277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810   -5.7126   -0.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2611   -5.7918    1.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3254   -1.8631   -1.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1564    0.1144    1.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5861    2.2301    2.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    4.6256    1.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9044    6.2517   -0.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021    4.6023   -2.9793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1778    1.1913   -1.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1595   -0.2163    1.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6987    0.2119    1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6314   -1.3894   -0.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2990   -1.0856    1.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4399    0.7105   -0.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    1.9807    1.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8095    2.2106   -1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1929   -0.4428   -2.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5147    1.1517   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084    3.0156   -0.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1805   -2.7472    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6558   -1.4665    3.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 10 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 19 30  1  0
 30 31  1  0
  8  2  1  0
 18 11  1  0
 28 21  1  0
 30  6  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  0
  8 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 15 39  1  0
 17 40  1  0
 18 41  1  0
 19 42  1  0
 21 43  1  0
 23 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
M  END
Download

3D SDF for HMDB0041238 (Loquatoside)


  Mrv0541 05061312302D          

 31 34  0  0  0  0            999 V2000
    3.5724   -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
    2.8579    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    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
   -0.7145   -0.4125    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   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
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  4  2  0  0  0  0
  8  5  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  9  2  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 13  5  2  0  0  0  0
 14 11  2  0  0  0  0
 14 13  1  0  0  0  0
 15 12  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18  7  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 15  1  0  0  0  0
 27 16  1  0  0  0  0
 28 17  1  0  0  0  0
 29  6  1  0  0  0  0
 29 20  1  0  0  0  0
 30 13  1  0  0  0  0
 30 18  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041238

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15-28H,6H2

> <INCHI_KEY>
YISJRMFABYGQSX-UHFFFAOYSA-N

> <FORMULA>
C20H22O11

> <MOLECULAR_WEIGHT>
438.3821

> <EXACT_MASS>
438.116211546

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
41.8853182987407

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-3,4-dihydro-2H-1-benzopyran-4,5,7-triol

> <ALOGPS_LOGP>
-0.07

> <JCHEM_LOGP>
-0.2643898353333335

> <ALOGPS_LOGS>
-1.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.546924467365715

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.950335417393838

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526580667211041

> <JCHEM_POLAR_SURFACE_AREA>
189.52999999999997

> <JCHEM_REFRACTIVITY>
101.658

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.50e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-3,4-dihydro-2H-1-benzopyran-4,5,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0041238 (Loquatoside)

HMDB0041238
     RDKit          3D
Loquatoside
 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.9306   -4.4524   -1.6996 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9003   -3.8645   -0.9987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0468   -4.6230   -0.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0151   -4.0443    0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599   -4.7927    1.2339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8238   -2.6541    0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493   -1.8821   -0.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6777   -2.5108   -1.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4550   -0.5218   -0.3882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6035    0.1073    0.5440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4094    1.5260    0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4271    2.5249    1.1561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2597    3.8590    0.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0580    4.2343   -0.4221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8797    5.5722   -0.7708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0331    3.2498   -1.4179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8326    3.6335   -2.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059    1.9175   -1.1089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3519   -0.6616    0.8018 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5610   -0.6010   -0.2425 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7871   -0.0555    0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6969   -1.0915    0.0545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9992   -0.7536    0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    0.6680    0.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0850    1.5064    1.0976 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5509    1.1602   -1.1503 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7745    0.4390   -2.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0897    1.0967   -0.7511 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    2.2833   -0.0290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7034   -2.0733    1.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0617   -2.1797    2.5366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8606   -4.5971   -1.3277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810   -5.7126   -0.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2611   -5.7918    1.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3254   -1.8631   -1.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1564    0.1144    1.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5861    2.2301    2.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    4.6256    1.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9044    6.2517   -0.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021    4.6023   -2.9793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1778    1.1913   -1.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1595   -0.2163    1.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6987    0.2119    1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6314   -1.3894   -0.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2990   -1.0856    1.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4399    0.7105   -0.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    1.9807    1.3260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8095    2.2106   -1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1929   -0.4428   -2.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5147    1.1517   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084    3.0156   -0.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1805   -2.7472    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6558   -1.4665    3.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 10 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 19 30  1  0
 30 31  1  0
  8  2  1  0
 18 11  1  0
 28 21  1  0
 30  6  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  0
  8 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 15 39  1  0
 17 40  1  0
 18 41  1  0
 19 42  1  0
 21 43  1  0
 23 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
M  END
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PDB for HMDB0041238 (Loquatoside)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    9                                                       
CONECT    3    7   10                                                       
CONECT    4    8   11                                                       
CONECT    5    8   13                                                       
CONECT    6   12   29                                                       
CONECT    7    1    3   18                                                  
CONECT    8    4    5   21                                                  
CONECT    9    2   10   22                                                  
CONECT   10    3    9   23                                                  
CONECT   11    4   14   24                                                  
CONECT   12    6   15   25                                                  
CONECT   13    5   14   30                                                  
CONECT   14   11   13   16                                                  
CONECT   15   12   17   26                                                  
CONECT   16   14   19   27                                                  
CONECT   17   15   20   28                                                  
CONECT   18    7   19   30                                                  
CONECT   19   16   18   31                                                  
CONECT   20   17   29   31                                                  
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   15                                                            
CONECT   27   16                                                            
CONECT   28   17                                                            
CONECT   29    6   20                                                       
CONECT   30   13   18                                                       
CONECT   31   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END
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3D PDB for HMDB0041238 (Loquatoside)

COMPND    HMDB0041238
HETATM    1  O1  UNL     1      -4.931  -4.452  -1.700  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.900  -3.864  -0.999  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.047  -4.623  -0.234  1.00  0.00           C  
HETATM    4  C3  UNL     1      -2.015  -4.044   0.469  1.00  0.00           C  
HETATM    5  O2  UNL     1      -1.160  -4.793   1.234  1.00  0.00           O  
HETATM    6  C4  UNL     1      -1.824  -2.654   0.410  1.00  0.00           C  
HETATM    7  C5  UNL     1      -2.649  -1.882  -0.335  1.00  0.00           C  
HETATM    8  C6  UNL     1      -3.678  -2.511  -1.029  1.00  0.00           C  
HETATM    9  O3  UNL     1      -2.455  -0.522  -0.388  1.00  0.00           O  
HETATM   10  C7  UNL     1      -1.603   0.107   0.544  1.00  0.00           C  
HETATM   11  C8  UNL     1      -1.409   1.526   0.206  1.00  0.00           C  
HETATM   12  C9  UNL     1      -1.427   2.525   1.156  1.00  0.00           C  
HETATM   13  C10 UNL     1      -1.260   3.859   0.892  1.00  0.00           C  
HETATM   14  C11 UNL     1      -1.058   4.234  -0.422  1.00  0.00           C  
HETATM   15  O4  UNL     1      -0.880   5.572  -0.771  1.00  0.00           O  
HETATM   16  C12 UNL     1      -1.033   3.250  -1.418  1.00  0.00           C  
HETATM   17  O5  UNL     1      -0.833   3.633  -2.716  1.00  0.00           O  
HETATM   18  C13 UNL     1      -1.206   1.917  -1.109  1.00  0.00           C  
HETATM   19  C14 UNL     1      -0.352  -0.662   0.802  1.00  0.00           C  
HETATM   20  O6  UNL     1       0.561  -0.601  -0.242  1.00  0.00           O  
HETATM   21  C15 UNL     1       1.787  -0.056   0.138  1.00  0.00           C  
HETATM   22  O7  UNL     1       2.697  -1.091   0.055  1.00  0.00           O  
HETATM   23  C16 UNL     1       3.999  -0.754   0.283  1.00  0.00           C  
HETATM   24  C17 UNL     1       4.350   0.668   0.020  1.00  0.00           C  
HETATM   25  O8  UNL     1       4.085   1.506   1.098  1.00  0.00           O  
HETATM   26  C18 UNL     1       3.551   1.160  -1.150  1.00  0.00           C  
HETATM   27  O9  UNL     1       3.774   0.439  -2.314  1.00  0.00           O  
HETATM   28  C19 UNL     1       2.090   1.097  -0.751  1.00  0.00           C  
HETATM   29  O10 UNL     1       1.826   2.283  -0.029  1.00  0.00           O  
HETATM   30  C20 UNL     1      -0.703  -2.073   1.184  1.00  0.00           C  
HETATM   31  O11 UNL     1      -1.062  -2.180   2.537  1.00  0.00           O  
HETATM   32  H1  UNL     1      -5.861  -4.597  -1.328  1.00  0.00           H  
HETATM   33  H2  UNL     1      -3.181  -5.713  -0.176  1.00  0.00           H  
HETATM   34  H3  UNL     1      -1.261  -5.792   1.304  1.00  0.00           H  
HETATM   35  H4  UNL     1      -4.325  -1.863  -1.620  1.00  0.00           H  
HETATM   36  H5  UNL     1      -2.156   0.114   1.538  1.00  0.00           H  
HETATM   37  H6  UNL     1      -1.586   2.230   2.193  1.00  0.00           H  
HETATM   38  H7  UNL     1      -1.279   4.626   1.665  1.00  0.00           H  
HETATM   39  H8  UNL     1      -0.904   6.252  -0.023  1.00  0.00           H  
HETATM   40  H9  UNL     1      -0.702   4.602  -2.979  1.00  0.00           H  
HETATM   41  H10 UNL     1      -1.178   1.191  -1.922  1.00  0.00           H  
HETATM   42  H11 UNL     1       0.159  -0.216   1.699  1.00  0.00           H  
HETATM   43  H12 UNL     1       1.699   0.212   1.229  1.00  0.00           H  
HETATM   44  H13 UNL     1       4.631  -1.389  -0.406  1.00  0.00           H  
HETATM   45  H14 UNL     1       4.299  -1.086   1.308  1.00  0.00           H  
HETATM   46  H15 UNL     1       5.440   0.711  -0.265  1.00  0.00           H  
HETATM   47  H16 UNL     1       4.919   1.981   1.326  1.00  0.00           H  
HETATM   48  H17 UNL     1       3.809   2.211  -1.363  1.00  0.00           H  
HETATM   49  H18 UNL     1       4.193  -0.443  -2.161  1.00  0.00           H  
HETATM   50  H19 UNL     1       1.515   1.152  -1.679  1.00  0.00           H  
HETATM   51  H20 UNL     1       2.008   3.016  -0.698  1.00  0.00           H  
HETATM   52  H21 UNL     1       0.180  -2.747   1.060  1.00  0.00           H  
HETATM   53  H22 UNL     1      -0.656  -1.467   3.078  1.00  0.00           H  
CONECT    1    2   32
CONECT    2    3    3    8
CONECT    3    4   33
CONECT    4    5    6    6
CONECT    5   34
CONECT    6    7   30
CONECT    7    8    8    9
CONECT    8   35
CONECT    9   10
CONECT   10   11   19   36
CONECT   11   12   12   18
CONECT   12   13   37
CONECT   13   14   14   38
CONECT   14   15   16
CONECT   15   39
CONECT   16   17   18   18
CONECT   17   40
CONECT   18   41
CONECT   19   20   30   42
CONECT   20   21
CONECT   21   22   28   43
CONECT   22   23
CONECT   23   24   44   45
CONECT   24   25   26   46
CONECT   25   47
CONECT   26   27   28   48
CONECT   27   49
CONECT   28   29   50
CONECT   29   51
CONECT   30   31   52
CONECT   31   53
END
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SMILES for HMDB0041238 (Loquatoside)

OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O
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INCHI for HMDB0041238 (Loquatoside)

InChI=1S/C20H22O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15-28H,6H2
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View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC20H22O11
Average Molecular Weight438.3821
Monoisotopic Molecular Weight438.116211546
IUPAC Name2-(3,4-dihydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-3,4-dihydro-2H-1-benzopyran-4,5,7-triol
Traditional Name2-(3,4-dihydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-3,4-dihydro-2H-1-benzopyran-4,5,7-triol
CAS Registry Number74046-15-4
SMILES
OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O
InChI Identifier
InChI=1S/C20H22O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15-28H,6H2
InChI KeyYISJRMFABYGQSX-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassO-methylated flavonoids
Direct Parent7-O-methylated flavonoids
Alternative Parents
Substituents
  • 4p-methoxyflavonoid-skeleton
  • 7-methoxyflavonoid-skeleton
  • Hydroxyflavonoid
  • Flavanone
  • 5-hydroxyflavonoid
  • Flavan
  • Chromone
  • Methoxyphenol
  • Chromane
  • 1-benzopyran
  • Benzopyran
  • Phenoxy compound
  • Methoxybenzene
  • Phenol ether
  • Anisole
  • Aryl ketone
  • Aryl alkyl ketone
  • Phenol
  • Alkyl aryl ether
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Ketone
  • Oxacycle
  • Organoheterocyclic compound
  • Ether
  • Organic oxide
  • Organic oxygen compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point208 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility16320 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility4.5 g/LALOGPS
logP-0.07ALOGPS
logP-0.26ChemAxon
logS-2ALOGPS
pKa (Strongest Acidic)8.95ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area189.53 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity101.66 m³·mol⁻¹ChemAxon
Polarizability41.89 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+199.26731661259
DarkChem[M-H]-190.83131661259
DeepCCS[M+H]+197.3830932474
DeepCCS[M-H]-195.02230932474
DeepCCS[M-2H]-228.70230932474
DeepCCS[M+Na]+203.83230932474
AllCCS[M+H]+201.932859911
AllCCS[M+H-H2O]+199.432859911
AllCCS[M+NH4]+204.132859911
AllCCS[M+Na]+204.832859911
AllCCS[M-H]-197.632859911
AllCCS[M+Na-2H]-198.032859911
AllCCS[M+HCOO]-198.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
LoquatosideOC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O5163.1Standard polar33892256
LoquatosideOC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O4239.8Standard non polar33892256
LoquatosideOC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC(O)=C(O)C=C2)C(O)C1O4277.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Loquatoside,1TMS,isomer #1C[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O4239.7Semi standard non polar33892256
Loquatoside,1TMS,isomer #2C[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O)C1O4188.7Semi standard non polar33892256
Loquatoside,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24255.6Semi standard non polar33892256
Loquatoside,1TMS,isomer #4C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O4282.9Semi standard non polar33892256
Loquatoside,1TMS,isomer #5C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)=CC=C1O4251.3Semi standard non polar33892256
Loquatoside,1TMS,isomer #6C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O4271.5Semi standard non polar33892256
Loquatoside,1TMS,isomer #7C[Si](C)(C)OC1C(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OCC(O)C1O4209.4Semi standard non polar33892256
Loquatoside,1TMS,isomer #8C[Si](C)(C)OC1C(O)COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O4222.1Semi standard non polar33892256
Loquatoside,2TMS,isomer #1C[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C)C(O)C1O4146.4Semi standard non polar33892256
Loquatoside,2TMS,isomer #10C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O4208.8Semi standard non polar33892256
Loquatoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)=CC=C1O4192.6Semi standard non polar33892256
Loquatoside,2TMS,isomer #12C[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O[Si](C)(C)C)C1O4149.4Semi standard non polar33892256
Loquatoside,2TMS,isomer #13C[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O)C1O[Si](C)(C)C4141.1Semi standard non polar33892256
Loquatoside,2TMS,isomer #14C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24195.3Semi standard non polar33892256
Loquatoside,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24178.3Semi standard non polar33892256
Loquatoside,2TMS,isomer #16C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24174.4Semi standard non polar33892256
Loquatoside,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O4229.4Semi standard non polar33892256
Loquatoside,2TMS,isomer #18C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)=CC=C1O4215.5Semi standard non polar33892256
Loquatoside,2TMS,isomer #19C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O4231.1Semi standard non polar33892256
Loquatoside,2TMS,isomer #2C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24188.0Semi standard non polar33892256
Loquatoside,2TMS,isomer #20C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O4217.3Semi standard non polar33892256
Loquatoside,2TMS,isomer #21C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O4199.6Semi standard non polar33892256
Loquatoside,2TMS,isomer #22C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O4195.6Semi standard non polar33892256
Loquatoside,2TMS,isomer #23C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)=CC=C1O4174.4Semi standard non polar33892256
Loquatoside,2TMS,isomer #24C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)=CC=C1O4180.9Semi standard non polar33892256
Loquatoside,2TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C4208.7Semi standard non polar33892256
Loquatoside,2TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O4195.3Semi standard non polar33892256
Loquatoside,2TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O4199.7Semi standard non polar33892256
Loquatoside,2TMS,isomer #28C[Si](C)(C)OC1C(O)COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O[Si](C)(C)C4136.1Semi standard non polar33892256
Loquatoside,2TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O4207.6Semi standard non polar33892256
Loquatoside,2TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O4208.3Semi standard non polar33892256
Loquatoside,2TMS,isomer #5C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)=CC=C1O4190.5Semi standard non polar33892256
Loquatoside,2TMS,isomer #6C[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C1O4139.2Semi standard non polar33892256
Loquatoside,2TMS,isomer #7C[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C4168.2Semi standard non polar33892256
Loquatoside,2TMS,isomer #8C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24199.0Semi standard non polar33892256
Loquatoside,2TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C4207.0Semi standard non polar33892256
Loquatoside,3TMS,isomer #1C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O4043.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #10C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O4049.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #11C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)=CC=C1O4034.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O4067.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O4051.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #14C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O4075.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #15C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O4066.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O4061.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O4061.4Semi standard non polar33892256
Loquatoside,3TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C4089.3Semi standard non polar33892256
Loquatoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O4039.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #2C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)=CC=C1O4029.0Semi standard non polar33892256
Loquatoside,3TMS,isomer #20C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O4040.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #21C[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C4079.4Semi standard non polar33892256
Loquatoside,3TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24057.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #23C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24048.4Semi standard non polar33892256
Loquatoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24050.6Semi standard non polar33892256
Loquatoside,3TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O4058.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #26C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)=CC=C1O4044.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C4064.0Semi standard non polar33892256
Loquatoside,3TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C4045.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C4044.5Semi standard non polar33892256
Loquatoside,3TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O[Si](C)(C)C4068.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C4048.3Semi standard non polar33892256
Loquatoside,3TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O4018.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O4031.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C4081.4Semi standard non polar33892256
Loquatoside,3TMS,isomer #34C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)=CC=C1O3994.5Semi standard non polar33892256
Loquatoside,3TMS,isomer #35C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)=CC=C1O4015.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #36C[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4032.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24012.5Semi standard non polar33892256
Loquatoside,3TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24031.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O24054.0Semi standard non polar33892256
Loquatoside,3TMS,isomer #4C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24065.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O24032.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #41C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24047.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #42C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O4005.5Semi standard non polar33892256
Loquatoside,3TMS,isomer #43C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)=CC=C1O3982.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #44C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O4037.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #45C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)=CC=C1O4021.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #46C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C4095.0Semi standard non polar33892256
Loquatoside,3TMS,isomer #47C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O4109.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #48C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O4022.8Semi standard non polar33892256
Loquatoside,3TMS,isomer #49C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O4050.1Semi standard non polar33892256
Loquatoside,3TMS,isomer #5C[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4046.3Semi standard non polar33892256
Loquatoside,3TMS,isomer #50C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O3998.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #51C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O4031.6Semi standard non polar33892256
Loquatoside,3TMS,isomer #52C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O4053.6Semi standard non polar33892256
Loquatoside,3TMS,isomer #53C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O4019.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #54C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C4057.7Semi standard non polar33892256
Loquatoside,3TMS,isomer #55C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4067.8Semi standard non polar33892256
Loquatoside,3TMS,isomer #56C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O4044.3Semi standard non polar33892256
Loquatoside,3TMS,isomer #6C[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4047.2Semi standard non polar33892256
Loquatoside,3TMS,isomer #7C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24056.9Semi standard non polar33892256
Loquatoside,3TMS,isomer #8C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24069.6Semi standard non polar33892256
Loquatoside,3TMS,isomer #9C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24059.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #1C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O[Si](C)(C)C3924.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #10C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O23941.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #11C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3962.5Semi standard non polar33892256
Loquatoside,4TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3963.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #13C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O23953.1Semi standard non polar33892256
Loquatoside,4TMS,isomer #14C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23958.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #15C[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3983.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #16C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O23930.4Semi standard non polar33892256
Loquatoside,4TMS,isomer #17C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23936.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #18C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23918.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #19C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23898.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #2C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O3909.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #20C[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23956.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O3887.4Semi standard non polar33892256
Loquatoside,4TMS,isomer #22C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O3872.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #23C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O3897.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #24C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O3879.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C3954.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #26C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O3979.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O3918.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O3926.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O3899.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #3C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O3918.5Semi standard non polar33892256
Loquatoside,4TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O3906.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3982.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3957.5Semi standard non polar33892256
Loquatoside,4TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3961.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3974.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #35C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3936.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O23884.1Semi standard non polar33892256
Loquatoside,4TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23918.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23920.5Semi standard non polar33892256
Loquatoside,4TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23896.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O3924.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #40C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23926.5Semi standard non polar33892256
Loquatoside,4TMS,isomer #41C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O3852.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #42C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)=CC=C1O3830.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #43C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O3881.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #44C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)=CC=C1O3869.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #45C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C3968.8Semi standard non polar33892256
Loquatoside,4TMS,isomer #46C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C3968.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #47C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3865.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #48C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3894.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #49C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3843.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #5C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C3961.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #50C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3879.4Semi standard non polar33892256
Loquatoside,4TMS,isomer #51C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3936.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #52C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3897.4Semi standard non polar33892256
Loquatoside,4TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3924.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #54C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3943.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #55C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3883.1Semi standard non polar33892256
Loquatoside,4TMS,isomer #56C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23905.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #57C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23855.6Semi standard non polar33892256
Loquatoside,4TMS,isomer #58C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23836.3Semi standard non polar33892256
Loquatoside,4TMS,isomer #59C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23879.8Semi standard non polar33892256
Loquatoside,4TMS,isomer #6C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O[Si](C)(C)C3908.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #60C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23858.2Semi standard non polar33892256
Loquatoside,4TMS,isomer #61C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23971.1Semi standard non polar33892256
Loquatoside,4TMS,isomer #62C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3864.8Semi standard non polar33892256
Loquatoside,4TMS,isomer #63C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3847.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #64C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3891.8Semi standard non polar33892256
Loquatoside,4TMS,isomer #65C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3935.1Semi standard non polar33892256
Loquatoside,4TMS,isomer #66C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O3912.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #67C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O3959.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #68C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3895.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #69C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3876.4Semi standard non polar33892256
Loquatoside,4TMS,isomer #7C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)=CC=C1O3896.0Semi standard non polar33892256
Loquatoside,4TMS,isomer #70C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3945.9Semi standard non polar33892256
Loquatoside,4TMS,isomer #8C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O3904.7Semi standard non polar33892256
Loquatoside,4TMS,isomer #9C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O3910.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #1C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23800.6Semi standard non polar33892256
Loquatoside,5TMS,isomer #10C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3852.3Semi standard non polar33892256
Loquatoside,5TMS,isomer #11C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23779.3Semi standard non polar33892256
Loquatoside,5TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3762.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3769.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #14C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O3737.5Semi standard non polar33892256
Loquatoside,5TMS,isomer #15C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O3747.2Semi standard non polar33892256
Loquatoside,5TMS,isomer #16C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3830.6Semi standard non polar33892256
Loquatoside,5TMS,isomer #17C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O23789.6Semi standard non polar33892256
Loquatoside,5TMS,isomer #18C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23805.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #19C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3880.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #2C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C2O[Si](C)(C)C3851.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #20C[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23868.2Semi standard non polar33892256
Loquatoside,5TMS,isomer #21C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23832.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23777.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23752.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23785.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23762.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23859.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3792.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #28C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3774.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3815.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3787.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3816.1Semi standard non polar33892256
Loquatoside,5TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O3847.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O3847.2Semi standard non polar33892256
Loquatoside,5TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3828.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3806.2Semi standard non polar33892256
Loquatoside,5TMS,isomer #35C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3874.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23784.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23753.5Semi standard non polar33892256
Loquatoside,5TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23725.1Semi standard non polar33892256
Loquatoside,5TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23758.5Semi standard non polar33892256
Loquatoside,5TMS,isomer #4C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3793.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23738.9Semi standard non polar33892256
Loquatoside,5TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23842.3Semi standard non polar33892256
Loquatoside,5TMS,isomer #42C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3755.9Semi standard non polar33892256
Loquatoside,5TMS,isomer #43C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3731.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #44C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3777.1Semi standard non polar33892256
Loquatoside,5TMS,isomer #45C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3808.5Semi standard non polar33892256
Loquatoside,5TMS,isomer #46C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3801.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #47C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3817.9Semi standard non polar33892256
Loquatoside,5TMS,isomer #48C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3778.3Semi standard non polar33892256
Loquatoside,5TMS,isomer #49C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3758.2Semi standard non polar33892256
Loquatoside,5TMS,isomer #5C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O3764.3Semi standard non polar33892256
Loquatoside,5TMS,isomer #50C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3835.5Semi standard non polar33892256
Loquatoside,5TMS,isomer #51C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23768.9Semi standard non polar33892256
Loquatoside,5TMS,isomer #52C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23745.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #53C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23813.8Semi standard non polar33892256
Loquatoside,5TMS,isomer #54C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23819.7Semi standard non polar33892256
Loquatoside,5TMS,isomer #55C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3803.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #56C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3833.0Semi standard non polar33892256
Loquatoside,5TMS,isomer #6C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O3772.4Semi standard non polar33892256
Loquatoside,5TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C3840.6Semi standard non polar33892256
Loquatoside,5TMS,isomer #8C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3840.1Semi standard non polar33892256
Loquatoside,5TMS,isomer #9C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3841.9Semi standard non polar33892256
Loquatoside,6TMS,isomer #1C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23680.1Semi standard non polar33892256
Loquatoside,6TMS,isomer #10C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3797.1Semi standard non polar33892256
Loquatoside,6TMS,isomer #11C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23657.8Semi standard non polar33892256
Loquatoside,6TMS,isomer #12C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23648.3Semi standard non polar33892256
Loquatoside,6TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3694.3Semi standard non polar33892256
Loquatoside,6TMS,isomer #14C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3667.6Semi standard non polar33892256
Loquatoside,6TMS,isomer #15C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O23718.8Semi standard non polar33892256
Loquatoside,6TMS,isomer #16C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23672.7Semi standard non polar33892256
Loquatoside,6TMS,isomer #17C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23653.7Semi standard non polar33892256
Loquatoside,6TMS,isomer #18C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23729.4Semi standard non polar33892256
Loquatoside,6TMS,isomer #19C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23728.3Semi standard non polar33892256
Loquatoside,6TMS,isomer #2C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23667.1Semi standard non polar33892256
Loquatoside,6TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3743.1Semi standard non polar33892256
Loquatoside,6TMS,isomer #21C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O3773.8Semi standard non polar33892256
Loquatoside,6TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O)=C1)O23662.5Semi standard non polar33892256
Loquatoside,6TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C)=C1)O23640.7Semi standard non polar33892256
Loquatoside,6TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23709.6Semi standard non polar33892256
Loquatoside,6TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23715.5Semi standard non polar33892256
Loquatoside,6TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3726.1Semi standard non polar33892256
Loquatoside,6TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3744.2Semi standard non polar33892256
Loquatoside,6TMS,isomer #28C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23716.5Semi standard non polar33892256
Loquatoside,6TMS,isomer #3C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O23758.8Semi standard non polar33892256
Loquatoside,6TMS,isomer #4C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C2O[Si](C)(C)C3747.0Semi standard non polar33892256
Loquatoside,6TMS,isomer #5C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C2O[Si](C)(C)C3751.0Semi standard non polar33892256
Loquatoside,6TMS,isomer #6C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C2O[Si](C)(C)C3719.8Semi standard non polar33892256
Loquatoside,6TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3691.5Semi standard non polar33892256
Loquatoside,6TMS,isomer #8C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3726.4Semi standard non polar33892256
Loquatoside,6TMS,isomer #9C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(O[Si](C)(C)C)C2OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3730.0Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O4506.4Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O)C1O4451.8Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24496.4Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O4511.8Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)=CC=C1O4516.9Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O4530.0Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1C(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OCC(O)C1O4484.7Semi standard non polar33892256
Loquatoside,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O4498.3Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C(C)(C)C)C(O)C1O4654.7Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O4679.9Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)=CC=C1O4655.6Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O4643.7Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C4628.6Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24651.9Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24645.3Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24635.8Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O4671.8Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)=CC=C1O4656.0Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O4698.3Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24665.4Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O4676.8Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4658.1Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4647.5Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4648.2Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4646.6Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4679.0Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4674.6Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4665.1Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O[Si](C)(C)C(C)(C)C4644.1Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O4681.0Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4689.4Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4669.8Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O4661.7Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C4689.6Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24666.5Semi standard non polar33892256
Loquatoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4662.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4731.6Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4742.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4720.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O4771.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O4746.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4723.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4722.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4730.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4726.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4775.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4708.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4707.9Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4703.8Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1COC(OC2C(O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4721.8Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24746.4Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24691.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24680.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O4761.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)=CC=C1O4734.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4776.8Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4748.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O[Si](C)(C)C(C)(C)C4694.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4740.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C4685.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4701.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4687.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4773.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4675.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4661.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1C2=C(O)C=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4658.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24694.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24686.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O24767.6Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24732.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)O24741.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24669.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4705.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4678.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4691.6Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4668.9Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4774.1Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O4798.7Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4738.0Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4725.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4697.5Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4707.4Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4698.4Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C2O4685.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4667.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O[Si](C)(C)C(C)(C)C4739.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4730.3Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O4692.4Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4702.8Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24744.6Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24710.2Semi standard non polar33892256
Loquatoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24708.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4798.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24787.6Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C2O[Si](C)(C)C(C)(C)C4758.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C4764.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24740.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24746.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1COC(OC2C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4756.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24749.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24751.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O24829.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)O24799.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4772.8Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24740.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4743.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4719.3Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4730.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4707.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4805.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O4840.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4790.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4778.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4765.3Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4732.8Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4754.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C2O4780.6Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O4761.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O[Si](C)(C)C(C)(C)C4777.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4777.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4736.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24715.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24742.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O24809.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)O24777.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4735.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(O[Si](C)(C)C(C)(C)C)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24709.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4735.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4705.3Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4719.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4696.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4813.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4833.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O[Si](C)(C)C(C)(C)C4761.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C4743.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O[Si](C)(C)C(C)(C)C4731.0Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4794.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C4718.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C4732.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O4712.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O[Si](C)(C)C(C)(C)C4739.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4745.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4686.3Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24717.6Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #57CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O24797.6Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #58CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)O24769.9Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #59CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O24777.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C2O[Si](C)(C)C(C)(C)C4774.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #60CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)O24748.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #61CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C(OC1OCC(O)C(O)C1O)C(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)O24838.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #62CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O4705.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #63CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4683.6Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #64CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O[Si](C)(C)C(C)(C)C4754.7Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #65CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O)C2OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4756.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #66CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C2O4792.2Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #67CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C2O4790.1Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #68CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C2O4755.5Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #69CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C2O4732.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4748.7Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #70CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(O)C2OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4743.4Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4708.3Semi standard non polar33892256
Loquatoside,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(O[Si](C)(C)C(C)(C)C)C2OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4709.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-00di-9224800000-7a1eae65661d412810792017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (3 TMS) - 70eV, Positivesplash10-007c-3710239000-9b8e6bd52bec06f6d9a92017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_2_8) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_4) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_22) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_23) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_24) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_25) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_3_26) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_2) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_7) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_10) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_13) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_14) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_36) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_37) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_38) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_39) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_40) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_41) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_42) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_43) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_44) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Loquatoside GC-MS (TBDMS_4_45) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 10V, Positive-QTOFsplash10-0a4r-0337900000-88404e302198f0b59f2a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 20V, Positive-QTOFsplash10-0a4r-0965100000-4fec0669b6dd99d466c52017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 40V, Positive-QTOFsplash10-059i-1910000000-020b2a6683989bc897e82017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 10V, Negative-QTOFsplash10-052r-1314900000-84dd432e725a2ae864b32017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 20V, Negative-QTOFsplash10-0a4r-1947400000-cad491cfd2918a46d7182017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 40V, Negative-QTOFsplash10-0a6u-4910000000-e16f2f66e34231fc7eff2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 10V, Positive-QTOFsplash10-0a4r-0079000000-02c5b73a27cc4378bdbf2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 20V, Positive-QTOFsplash10-0540-0923000000-50612094cacd3371b4072021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 40V, Positive-QTOFsplash10-05oa-2911000000-747f63dbf3f8576a0de52021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 10V, Negative-QTOFsplash10-000i-0014900000-33883ca4fa632e029a5f2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 20V, Negative-QTOFsplash10-066r-1019000000-4b05df8c34f606c9eee92021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Loquatoside 40V, Negative-QTOFsplash10-053m-1941000000-8fdfaf50baf0cde90f0a2021-09-24Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB021144
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound78178070
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1890761
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .