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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:31:23 UTC

Update Date

2022-03-07 02:54:32 UTC

HMDB ID

HMDB0035513

Secondary Accession Numbers

HMDB35513

Metabolite Identification

Common Name

Schleicherastatin 6

Description

Schleicherastatin 6 belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups. Schleicherastatin 6 is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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


  Mrv0541 02241210102D          

 31 34  0  0  0  0            999 V2000
   -3.6042   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607   -2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350    0.0784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473    0.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    0.0784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7458   -0.9972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2267   -0.3319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7458    0.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350    0.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7458    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350   -2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -0.3319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205   -2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1758    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6056    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3205    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609    2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907    2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6056    0.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0310    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2 22  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  2  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 21  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 20  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 12 18  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 19  1  0  0  0  0
 19 23  1  0  0  0  0
 19 31  1  0  0  0  0
 23 24  1  0  0  0  0
 23 28  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 29  1  0  0  0  0
 26 27  1  0  0  0  0
 26 30  1  0  0  0  0
M  END

HMDB0035513
     RDKit          3D
Schleicherastatin 6
 77 80  0  0  0  0  0  0  0  0999 V2000
   -6.6317   -1.5694   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6394   -0.9902    0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7862   -0.0463    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2845   -0.2683    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2891    0.2868    1.9844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2178   -1.1321    0.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7957   -0.7511    0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2704   -0.4777    1.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3780    0.2277   -0.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6211   -0.3063   -2.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1132    0.9267   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8873    1.8043    0.4308 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348    2.3519    0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0946    1.4660   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5287    1.1858   -0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2899    2.3640   -0.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    3.4985   -0.3989 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6143    2.1421    0.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    0.9142    0.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4854    0.7311    0.8909 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5928   -0.3960    1.8686 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.0804    3.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4051   -1.3129    1.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8898   -1.5250    0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3765   -0.2543   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749   -0.3322   -1.6860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9373    0.0274    0.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0343   -1.1384    0.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.6424    0.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1937    0.2122   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548   -0.4194   -2.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1750   -2.5740   -1.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041   -0.8519   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7007   -1.7244   -1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7716   -1.7929    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6164   -0.4983   -0.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2264    0.0454    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6014    0.9428    0.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3733    0.6090   -0.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3726    0.5119    2.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    1.3325    2.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778   -0.3794    2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4413   -1.5049   -0.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2863   -2.1030    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461   -1.7093   -0.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8392    0.1344    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688    1.0475   -0.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2094   -1.2899   -2.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2888    0.4834   -2.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7201   -0.3765   -2.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0465    1.6703   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5649    2.6816    0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8611    1.3274    1.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1456    2.2909    1.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    3.4230   -0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8692    1.9706   -1.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9056    1.0054   -1.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1508    3.0129    0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1956    0.6157    0.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8021    1.6761    1.4104 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4946   -0.9879    1.5975 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4828   -0.4117    3.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6103   -1.0359    2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7724   -2.3251    2.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656   -1.9071   -0.1620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1636   -2.3355    0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6442   -0.9035   -1.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8972    0.6700   -2.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9296   -0.9049   -2.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8880    0.4151    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176   -1.7600   -0.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0446   -1.5564    0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.4445   -2.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1650   -1.4949   -2.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0837    0.1666   -3.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
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 30 14  1  0
 27 15  1  0
 25 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
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 11 51  1  0
 12 52  1  0
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 23 63  1  0
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 26 67  1  0
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 26 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 31 75  1  0
 31 76  1  0
 31 77  1  0
M  END


  Mrv0541 02241210102D          

 31 34  0  0  0  0            999 V2000
   -3.6042   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607   -2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -1.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350   -0.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0350    0.0784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0350   -2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1757   -0.3319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205   -2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1758    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6056    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3205    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609    2.3954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8907    2.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6056    0.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0310    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
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  2 22  1  0  0  0  0
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  4  5  1  0  0  0  0
  4  7  2  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 21  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 20  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
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 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 19  1  0  0  0  0
 19 23  1  0  0  0  0
 19 31  1  0  0  0  0
 23 24  1  0  0  0  0
 23 28  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 29  1  0  0  0  0
 26 27  1  0  0  0  0
 26 30  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035513

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C(C)CC(O)C(C)C1CCC2C3C(CCC12C)C1(C)CCC(O)CC1=CC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H46O3/c1-16(2)17(3)13-24(30)18(4)21-7-8-22-26-23(10-12-28(21,22)6)27(5)11-9-20(29)14-19(27)15-25(26)31/h15-18,20-24,26,29-30H,7-14H2,1-6H3

> <INCHI_KEY>
PKESXWKAOMUZDM-UHFFFAOYSA-N

> <FORMULA>
C28H46O3

> <MOLECULAR_WEIGHT>
430.663

> <EXACT_MASS>
430.344695338

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
52.63062865412412

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-9-one

> <ALOGPS_LOGP>
4.51

> <JCHEM_LOGP>
5.527637933000001

> <ALOGPS_LOGS>
-4.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.270745923091404

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.38833010645442

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6020449288788842

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
127.40159999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.99e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035513
     RDKit          3D
Schleicherastatin 6
 77 80  0  0  0  0  0  0  0  0999 V2000
   -6.6317   -1.5694   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6394   -0.9902    0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7862   -0.0463    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2845   -0.2683    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2891    0.2868    1.9844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2178   -1.1321    0.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7957   -0.7511    0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2704   -0.4777    1.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3780    0.2277   -0.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6211   -0.3063   -2.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1132    0.9267   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8873    1.8043    0.4308 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348    2.3519    0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0946    1.4660   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5287    1.1858   -0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2899    2.3640   -0.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    3.4985   -0.3989 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6143    2.1421    0.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    0.9142    0.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4854    0.7311    0.8909 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5928   -0.3960    1.8686 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.0804    3.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4051   -1.3129    1.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8898   -1.5250    0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3765   -0.2543   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749   -0.3322   -1.6860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9373    0.0274    0.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0343   -1.1384    0.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.6424    0.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1937    0.2122   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548   -0.4194   -2.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1750   -2.5740   -1.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041   -0.8519   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7007   -1.7244   -1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7716   -1.7929    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6164   -0.4983   -0.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2264    0.0454    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6014    0.9428    0.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3733    0.6090   -0.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3726    0.5119    2.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    1.3325    2.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778   -0.3794    2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4413   -1.5049   -0.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2863   -2.1030    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461   -1.7093   -0.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8392    0.1344    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688    1.0475   -0.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2094   -1.2899   -2.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2888    0.4834   -2.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7201   -0.3765   -2.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0465    1.6703   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5649    2.6816    0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8611    1.3274    1.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1456    2.2909    1.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    3.4230   -0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8692    1.9706   -1.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9056    1.0054   -1.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1508    3.0129    0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1956    0.6157    0.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8021    1.6761    1.4104 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4946   -0.9879    1.5975 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4828   -0.4117    3.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6103   -1.0359    2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7724   -2.3251    2.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656   -1.9071   -0.1620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1636   -2.3355    0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6442   -0.9035   -1.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8972    0.6700   -2.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9296   -0.9049   -2.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8880    0.4151    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176   -1.7600   -0.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2263   -1.7953    0.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6631   -0.0224    1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0446   -1.5564    0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.4445   -2.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1650   -1.4949   -2.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0837    0.1666   -3.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 11  1  0
 30 14  1  0
 27 15  1  0
 25 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 14 56  1  0
 15 57  1  0
 18 58  1  0
 20 59  1  0
 20 60  1  0
 21 61  1  0
 22 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 26 67  1  0
 26 68  1  0
 26 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 31 75  1  0
 31 76  1  0
 31 77  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -6.728  -2.157   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.728  -3.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.393  -4.471   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.061  -3.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.061  -2.157   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.393  -1.388   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.727  -4.471   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.395  -3.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.395  -2.157   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.727  -1.388   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.065  -1.388   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.065   0.146   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.395   0.913   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.727   0.146   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.392  -1.861   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.290  -0.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.392   0.617   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.065   1.689   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.392   2.160   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.065  -4.471   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.061  -0.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -8.065  -4.471   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.727   2.929   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.061   2.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.396   2.929   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.730   2.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.065   2.929   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.727   4.471   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.396   4.471   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.730   0.617   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.058   2.929   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6   10   21                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    5    9   14                                                  
CONECT   11    9   12   15                                                  
CONECT   12   11   13   17   18                                             
CONECT   13   12   14                                                       
CONECT   14   10   13                                                       
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   12   16   19                                                  
CONECT   18   12                                                            
CONECT   19   17   23   31                                                  
CONECT   20    8                                                            
CONECT   21    5                                                            
CONECT   22    2                                                            
CONECT   23   19   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27   30                                                  
CONECT   27   26                                                            
CONECT   28   23                                                            
CONECT   29   25                                                            
CONECT   30   26                                                            
CONECT   31   19                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0035513
HETATM    1  C1  UNL     1      -6.632  -1.569  -0.983  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.639  -0.990   0.438  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.786  -0.046   0.517  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.285  -0.268   0.624  1.00  0.00           C  
HETATM    5  C5  UNL     1      -5.289   0.287   1.984  1.00  0.00           C  
HETATM    6  C6  UNL     1      -4.218  -1.132   0.151  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.796  -0.751   0.173  1.00  0.00           C  
HETATM    8  O1  UNL     1      -2.270  -0.478   1.425  1.00  0.00           O  
HETATM    9  C8  UNL     1      -2.378   0.228  -0.888  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.621  -0.306  -2.283  1.00  0.00           C  
HETATM   11  C10 UNL     1      -1.113   0.927  -0.761  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.887   1.804   0.431  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.535   2.352   0.230  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.095   1.466  -0.828  1.00  0.00           C  
HETATM   15  C14 UNL     1       2.529   1.186  -0.779  1.00  0.00           C  
HETATM   16  C15 UNL     1       3.290   2.364  -0.307  1.00  0.00           C  
HETATM   17  O2  UNL     1       2.788   3.499  -0.399  1.00  0.00           O  
HETATM   18  C16 UNL     1       4.614   2.142   0.253  1.00  0.00           C  
HETATM   19  C17 UNL     1       5.146   0.914   0.319  1.00  0.00           C  
HETATM   20  C18 UNL     1       6.485   0.731   0.891  1.00  0.00           C  
HETATM   21  C19 UNL     1       6.593  -0.396   1.869  1.00  0.00           C  
HETATM   22  O3  UNL     1       6.742   0.080   3.160  1.00  0.00           O  
HETATM   23  C20 UNL     1       5.405  -1.313   1.837  1.00  0.00           C  
HETATM   24  C21 UNL     1       4.890  -1.525   0.422  1.00  0.00           C  
HETATM   25  C22 UNL     1       4.377  -0.254  -0.187  1.00  0.00           C  
HETATM   26  C23 UNL     1       4.675  -0.332  -1.686  1.00  0.00           C  
HETATM   27  C24 UNL     1       2.937   0.027   0.096  1.00  0.00           C  
HETATM   28  C25 UNL     1       2.034  -1.138   0.008  1.00  0.00           C  
HETATM   29  C26 UNL     1       0.601  -0.642   0.252  1.00  0.00           C  
HETATM   30  C27 UNL     1       0.194   0.212  -0.868  1.00  0.00           C  
HETATM   31  C28 UNL     1       0.455  -0.419  -2.203  1.00  0.00           C  
HETATM   32  H1  UNL     1      -6.175  -2.574  -1.008  1.00  0.00           H  
HETATM   33  H2  UNL     1      -6.204  -0.852  -1.688  1.00  0.00           H  
HETATM   34  H3  UNL     1      -7.701  -1.724  -1.313  1.00  0.00           H  
HETATM   35  H4  UNL     1      -6.772  -1.793   1.167  1.00  0.00           H  
HETATM   36  H5  UNL     1      -8.616  -0.498  -0.104  1.00  0.00           H  
HETATM   37  H6  UNL     1      -8.226   0.045   1.536  1.00  0.00           H  
HETATM   38  H7  UNL     1      -7.601   0.943   0.046  1.00  0.00           H  
HETATM   39  H8  UNL     1      -5.373   0.609  -0.089  1.00  0.00           H  
HETATM   40  H9  UNL     1      -6.373   0.512   2.256  1.00  0.00           H  
HETATM   41  H10 UNL     1      -4.863   1.332   2.075  1.00  0.00           H  
HETATM   42  H11 UNL     1      -4.978  -0.379   2.802  1.00  0.00           H  
HETATM   43  H12 UNL     1      -4.441  -1.505  -0.894  1.00  0.00           H  
HETATM   44  H13 UNL     1      -4.286  -2.103   0.742  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.246  -1.709  -0.124  1.00  0.00           H  
HETATM   46  H15 UNL     1      -2.839   0.134   1.917  1.00  0.00           H  
HETATM   47  H16 UNL     1      -3.169   1.047  -0.786  1.00  0.00           H  
HETATM   48  H17 UNL     1      -2.209  -1.290  -2.468  1.00  0.00           H  
HETATM   49  H18 UNL     1      -2.289   0.483  -2.991  1.00  0.00           H  
HETATM   50  H19 UNL     1      -3.720  -0.376  -2.420  1.00  0.00           H  
HETATM   51  H20 UNL     1      -1.046   1.670  -1.638  1.00  0.00           H  
HETATM   52  H21 UNL     1      -1.565   2.682   0.456  1.00  0.00           H  
HETATM   53  H22 UNL     1      -0.861   1.327   1.402  1.00  0.00           H  
HETATM   54  H23 UNL     1       1.146   2.291   1.135  1.00  0.00           H  
HETATM   55  H24 UNL     1       0.489   3.423  -0.071  1.00  0.00           H  
HETATM   56  H25 UNL     1       0.869   1.971  -1.815  1.00  0.00           H  
HETATM   57  H26 UNL     1       2.906   1.005  -1.831  1.00  0.00           H  
HETATM   58  H27 UNL     1       5.151   3.013   0.614  1.00  0.00           H  
HETATM   59  H28 UNL     1       7.196   0.616   0.036  1.00  0.00           H  
HETATM   60  H29 UNL     1       6.802   1.676   1.410  1.00  0.00           H  
HETATM   61  H30 UNL     1       7.495  -0.988   1.598  1.00  0.00           H  
HETATM   62  H31 UNL     1       7.483  -0.412   3.614  1.00  0.00           H  
HETATM   63  H32 UNL     1       4.610  -1.036   2.540  1.00  0.00           H  
HETATM   64  H33 UNL     1       5.772  -2.325   2.171  1.00  0.00           H  
HETATM   65  H34 UNL     1       5.766  -1.907  -0.162  1.00  0.00           H  
HETATM   66  H35 UNL     1       4.164  -2.336   0.464  1.00  0.00           H  
HETATM   67  H36 UNL     1       5.644  -0.903  -1.791  1.00  0.00           H  
HETATM   68  H37 UNL     1       4.897   0.670  -2.109  1.00  0.00           H  
HETATM   69  H38 UNL     1       3.930  -0.905  -2.235  1.00  0.00           H  
HETATM   70  H39 UNL     1       2.888   0.415   1.156  1.00  0.00           H  
HETATM   71  H40 UNL     1       2.118  -1.760  -0.881  1.00  0.00           H  
HETATM   72  H41 UNL     1       2.226  -1.795   0.909  1.00  0.00           H  
HETATM   73  H42 UNL     1       0.663  -0.022   1.181  1.00  0.00           H  
HETATM   74  H43 UNL     1       0.045  -1.556   0.445  1.00  0.00           H  
HETATM   75  H44 UNL     1       1.578  -0.445  -2.338  1.00  0.00           H  
HETATM   76  H45 UNL     1       0.165  -1.495  -2.237  1.00  0.00           H  
HETATM   77  H46 UNL     1       0.084   0.167  -3.053  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    4   35
CONECT    3   36   37   38
CONECT    4    5    6   39
CONECT    5   40   41   42
CONECT    6    7   43   44
CONECT    7    8    9   45
CONECT    8   46
CONECT    9   10   11   47
CONECT   10   48   49   50
CONECT   11   12   30   51
CONECT   12   13   52   53
CONECT   13   14   54   55
CONECT   14   15   30   56
CONECT   15   16   27   57
CONECT   16   17   17   18
CONECT   18   19   19   58
CONECT   19   20   25
CONECT   20   21   59   60
CONECT   21   22   23   61
CONECT   22   62
CONECT   23   24   63   64
CONECT   24   25   65   66
CONECT   25   26   27
CONECT   26   67   68   69
CONECT   27   28   70
CONECT   28   29   71   72
CONECT   29   30   73   74
CONECT   30   31
CONECT   31   75   76   77
END

HMDB0035513
     RDKit          3D
Schleicherastatin 6
 77 80  0  0  0  0  0  0  0  0999 V2000
   -6.6317   -1.5694   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6394   -0.9902    0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7862   -0.0463    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2845   -0.2683    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2891    0.2868    1.9844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2178   -1.1321    0.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7957   -0.7511    0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2704   -0.4777    1.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3780    0.2277   -0.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6211   -0.3063   -2.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1132    0.9267   -0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8873    1.8043    0.4308 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348    2.3519    0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0946    1.4660   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5287    1.1858   -0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2899    2.3640   -0.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    3.4985   -0.3989 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6143    2.1421    0.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    0.9142    0.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4854    0.7311    0.8909 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5928   -0.3960    1.8686 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.0804    3.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4051   -1.3129    1.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8898   -1.5250    0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3765   -0.2543   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6749   -0.3322   -1.6860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9373    0.0274    0.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0343   -1.1384    0.0082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.6424    0.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1937    0.2122   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548   -0.4194   -2.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1750   -2.5740   -1.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041   -0.8519   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7007   -1.7244   -1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7716   -1.7929    1.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6164   -0.4983   -0.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2264    0.0454    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6014    0.9428    0.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3733    0.6090   -0.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3726    0.5119    2.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    1.3325    2.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778   -0.3794    2.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4413   -1.5049   -0.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2863   -2.1030    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461   -1.7093   -0.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8392    0.1344    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1688    1.0475   -0.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2094   -1.2899   -2.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2888    0.4834   -2.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7201   -0.3765   -2.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0465    1.6703   -1.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5649    2.6816    0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8611    1.3274    1.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1456    2.2909    1.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    3.4230   -0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8692    1.9706   -1.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9056    1.0054   -1.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1508    3.0129    0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1956    0.6157    0.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8021    1.6761    1.4104 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4946   -0.9879    1.5975 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4828   -0.4117    3.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6103   -1.0359    2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7724   -2.3251    2.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656   -1.9071   -0.1620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1636   -2.3355    0.4635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6442   -0.9035   -1.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8972    0.6700   -2.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9296   -0.9049   -2.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8880    0.4151    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176   -1.7600   -0.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2263   -1.7953    0.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6631   -0.0224    1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0446   -1.5564    0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.4445   -2.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1650   -1.4949   -2.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0837    0.1666   -3.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 11  1  0
 30 14  1  0
 27 15  1  0
 25 19  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 14 56  1  0
 15 57  1  0
 18 58  1  0
 20 59  1  0
 20 60  1  0
 21 61  1  0
 22 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 26 67  1  0
 26 68  1  0
 26 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 31 75  1  0
 31 76  1  0
 31 77  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3,22-Dihydroxy-24-methylcholest-5-en-7-one	HMDB
3,22-Dihydroxyergost-5-en-7-one	HMDB

Chemical Formula

C₂₈H₄₆O₃

Average Molecular Weight

430.663

Monoisotopic Molecular Weight

430.344695338

IUPAC Name

5-hydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-9-one

Traditional Name

5-hydroxy-14-(3-hydroxy-5,6-dimethylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-9-one

CAS Registry Number

256445-61-1

SMILES

CC(C)C(C)CC(O)C(C)C1CCC2C3C(CCC12C)C1(C)CCC(O)CC1=CC3=O

InChI Identifier

InChI=1S/C28H46O3/c1-16(2)17(3)13-24(30)18(4)21-7-8-22-26-23(10-12-28(21,22)6)27(5)11-9-20(29)14-19(27)15-25(26)31/h15-18,20-24,26,29-30H,7-14H2,1-6H3

InChI Key

PKESXWKAOMUZDM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Dihydroxy bile acids, alcohols and derivatives

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Fruits (FooDB: FOOD00871)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	209 - 212 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.005 g/L	ALOGPS
logP	4.51	ALOGPS
logP	5.53	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	17.39	ChemAxon
pKa (Strongest Basic)	-0.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	127.4 m³·mol⁻¹	ChemAxon
Polarizability	52.63 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	200.088	31661259
DarkChem	[M-H]-	196.778	31661259
DeepCCS	[M-2H]-	237.667	30932474
DeepCCS	[M+Na]+	212.895	30932474
AllCCS	[M+H]+	210.0	32859911
AllCCS	[M+H-H2O]+	208.0	32859911
AllCCS	[M+NH4]+	211.7	32859911
AllCCS	[M+Na]+	212.3	32859911
AllCCS	[M-H]-	208.0	32859911
AllCCS	[M+Na-2H]-	210.1	32859911
AllCCS	[M+HCOO]-	212.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Schleicherastatin 6	CC(C)C(C)CC(O)C(C)C1CCC2C3C(CCC12C)C1(C)CCC(O)CC1=CC3=O	3900.5	Standard polar	33892256
Schleicherastatin 6	CC(C)C(C)CC(O)C(C)C1CCC2C3C(CCC12C)C1(C)CCC(O)CC1=CC3=O	3344.1	Standard non polar	33892256
Schleicherastatin 6	CC(C)C(C)CC(O)C(C)C1CCC2C3C(CCC12C)C1(C)CCC(O)CC1=CC3=O	3658.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Schleicherastatin 6,1TMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3C(=O)C=C4CC(O)CCC4(C)C3CCC12C	3671.7	Semi standard non polar	33892256
Schleicherastatin 6,1TMS,isomer #2	CC(C)C(C)CC(O)C(C)C1CCC2C3C(=O)C=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3700.3	Semi standard non polar	33892256
Schleicherastatin 6,1TMS,isomer #3	CC(C)C(C)CC(O)C(C)C1CCC2C3=C(O[Si](C)(C)C)C=C4CC(O)CCC4(C)C3CCC21C	3625.2	Semi standard non polar	33892256
Schleicherastatin 6,2TMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3C(=O)C=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12C	3588.8	Semi standard non polar	33892256
Schleicherastatin 6,2TMS,isomer #2	CC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C)C=C4CC(O)CCC4(C)C3CCC21C	3559.1	Semi standard non polar	33892256
Schleicherastatin 6,2TMS,isomer #3	CC(C)C(C)CC(O)C(C)C1CCC2C3=C(O[Si](C)(C)C)C=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC21C	3647.6	Semi standard non polar	33892256
Schleicherastatin 6,3TMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C)C=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC21C	3493.6	Semi standard non polar	33892256
Schleicherastatin 6,3TMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C)C=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC21C	3584.2	Standard non polar	33892256
Schleicherastatin 6,1TBDMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3C(=O)C=C4CC(O)CCC4(C)C3CCC12C	3894.7	Semi standard non polar	33892256
Schleicherastatin 6,1TBDMS,isomer #2	CC(C)C(C)CC(O)C(C)C1CCC2C3C(=O)C=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	3914.7	Semi standard non polar	33892256
Schleicherastatin 6,1TBDMS,isomer #3	CC(C)C(C)CC(O)C(C)C1CCC2C3=C(O[Si](C)(C)C(C)(C)C)C=C4CC(O)CCC4(C)C3CCC21C	3863.6	Semi standard non polar	33892256
Schleicherastatin 6,2TBDMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3C(=O)C=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12C	4019.4	Semi standard non polar	33892256
Schleicherastatin 6,2TBDMS,isomer #2	CC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C(C)(C)C)C=C4CC(O)CCC4(C)C3CCC21C	4029.6	Semi standard non polar	33892256
Schleicherastatin 6,2TBDMS,isomer #3	CC(C)C(C)CC(O)C(C)C1CCC2C3=C(O[Si](C)(C)C(C)(C)C)C=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C	4098.6	Semi standard non polar	33892256
Schleicherastatin 6,3TBDMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C(C)(C)C)C=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C	4190.8	Semi standard non polar	33892256
Schleicherastatin 6,3TBDMS,isomer #1	CC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3=C(O[Si](C)(C)C(C)(C)C)C=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC21C	4305.6	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Schleicherastatin 6 GC-MS (Non-derivatized) - 70eV, Positive	splash10-00ri-4136900000-c2e3e5d14710ebd702a8	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Schleicherastatin 6 GC-MS (2 TMS) - 70eV, Positive	splash10-0bt9-4122490000-992e2dc5cb6303156ee9	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Schleicherastatin 6 GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 10V, Negative-QTOF	splash10-004i-0000900000-2e37cb7ca0cc68070f3d	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 20V, Negative-QTOF	splash10-01t9-1001900000-e106a1b940ad4504e268	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 40V, Negative-QTOF	splash10-02tj-9267300000-6cce7e274602ba3b7238	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 10V, Negative-QTOF	splash10-004i-0000900000-2f0d3b816683d4a35385	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 20V, Negative-QTOF	splash10-004i-1102900000-50a2e83094f7fc9817c1	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 40V, Negative-QTOF	splash10-004m-4129700000-8aac3a317ddc92317d75	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 10V, Positive-QTOF	splash10-03e9-0004900000-1c381152034bd044d75d	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 20V, Positive-QTOF	splash10-01r2-3119300000-f39c3de4266d15996bc3	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 40V, Positive-QTOF	splash10-014r-9525100000-41970032d9679413e868	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 10V, Positive-QTOF	splash10-001l-2017900000-c98587eb5d5346f72cda	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 20V, Positive-QTOF	splash10-002g-9146600000-9ef1d69268fd7784e7d9	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Schleicherastatin 6 40V, Positive-QTOF	splash10-000l-5492000000-ba8e69a215aa0ae8bb9d	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB014205

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

75048831

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Schleicherastatin 6 (HMDB0035513)

MOL for HMDB0035513 (Schleicherastatin 6)

3D MOL for HMDB0035513 (Schleicherastatin 6)

3D SDF for HMDB0035513 (Schleicherastatin 6)

3D-SDF for HMDB0035513 (Schleicherastatin 6)

PDB for HMDB0035513 (Schleicherastatin 6)

3D PDB for HMDB0035513 (Schleicherastatin 6)

SMILES for HMDB0035513 (Schleicherastatin 6)

INCHI for HMDB0035513 (Schleicherastatin 6)

Structure for HMDB0035513 (Schleicherastatin 6)

3D Structure for HMDB0035513 (Schleicherastatin 6)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra