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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:53:07 UTC

Update Date

2022-03-07 02:55:49 UTC

HMDB ID

HMDB0038561

Secondary Accession Numbers

HMDB38561

Metabolite Identification

Common Name

8-Isobutanoylneosolaniol

Description

8-Isobutanoylneosolaniol belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain. Based on a literature review a small amount of articles have been published on 8-Isobutanoylneosolaniol.

Structure

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

  Mrv0541 01251307562D          

 34 37  0  0  0  0            999 V2000
   -1.1579   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -3.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -4.4736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1579   -4.8861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -4.4736    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4434   -3.6486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2710   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -4.8861    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9855   -4.4736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9855   -3.6486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5868   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5868   -4.8861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -5.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8105   -4.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3980   -5.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1115   -6.2159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9964   -4.8075    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7971   -4.6086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690   -7.0257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158   -4.8861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7302   -4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -3.6486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1579   -6.5361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -6.9486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1579   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -6.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690   -7.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -8.2632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -8.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -2.8236    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801   -2.8556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10  7  1  0  0  0  0
  2 11  1  0  0  0  0
  3 12  1  6  0  0  0
  5 13  1  6  0  0  0
  8 14  1  1  0  0  0
  9 16  1  1  0  0  0
 16 15  1  0  0  0  0
  8 17  1  0  0  0  0
 10 18  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 17 20  1  1  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  2  0  0  0  0
 13 27  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 29 20  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  9 15  1  6  0  0  0
 22 32  1  0  0  0  0
  6 33  1  6  0  0  0
 10 34  1  1  0  0  0
M  END

HMDB0038561
     RDKit          3D
8-Isobutanoylneosolaniol
 64 67  0  0  0  0  0  0  0  0999 V2000
   -0.4887    4.0266    1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1174    3.0338    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    3.4437   -1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3631    1.6931    0.1966 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0039    0.8045   -0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3396   -0.6522   -0.4529 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4288   -0.9370    0.8066 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9057   -1.0753    0.6283 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5885    0.1617    0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5278    0.5302    1.5477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -0.2932    2.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2299    1.8516    1.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9857    1.9203    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1838    1.9435    2.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2578   -1.9127   -0.5411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955   -2.5726   -0.5958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -2.0755   -1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0468   -1.4915   -1.6151 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7579   -2.5332   -1.9404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0587   -2.4884   -1.5677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7419   -1.2938   -2.2313 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0832   -0.8539   -3.3518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7288   -0.2569   -1.1464 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0348   -0.2702   -0.5528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8397    0.8298   -0.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1899    0.7555    0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4049    1.9146   -0.9697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7869   -0.7475   -0.0870 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2207    1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1474   -2.2389   -0.1066 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1289   -3.1022    0.9471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4181   -2.5821    0.4475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5440    3.8818    1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1425    3.8877    1.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3321    5.0460    0.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5158    1.0162   -1.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0742    0.9312   -1.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504   -1.8951    1.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2659   -0.0726    1.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894   -1.6076    1.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5043    2.6823    1.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612    2.7800   -0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8152    1.0186   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0445    2.1055    0.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9714    1.1673    2.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5820    1.7706    3.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6241    2.9531    2.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -2.0070   -1.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4512   -3.6306   -0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0467   -2.6747    0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7204   -2.7033   -2.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1098   -0.8517   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5666   -3.4043   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7814   -1.5542   -2.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0710    0.1423   -3.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5251    0.7522   -1.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1798    0.2492    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5720    1.7840    0.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9122    0.2195   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2310   -0.5721    1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992   -0.6215    2.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2169    0.8689    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0379   -2.7769    2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0173   -4.1959    0.8337 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  6
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  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  2  0
 23 28  1  0
 28 29  1  1
 28 30  1  0
 30 31  1  0
 31 32  1  0
 18  6  1  0
 30 20  1  0
 28  6  1  0
 30 32  1  6
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  0
  5 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  1
 12 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  6
 20 53  1  1
 21 54  1  6
 22 55  1  0
 23 56  1  6
 26 57  1  0
 26 58  1  0
 26 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 31 63  1  0
 31 64  1  0
M  END

  Mrv0541 01251307562D          

 34 37  0  0  0  0            999 V2000
   -1.1579   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -3.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -4.4736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1579   -4.8861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -4.4736    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4434   -3.6486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2710   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -4.8861    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9855   -4.4736    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9855   -3.6486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5868   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5868   -4.8861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -5.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8105   -4.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3980   -5.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1115   -6.2159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9964   -4.8075    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7971   -4.6086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690   -7.0257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158   -4.8861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7302   -4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -3.6486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1579   -6.5361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8724   -6.9486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1579   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -6.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690   -7.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -8.2632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -8.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0158   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434   -2.8236    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801   -2.8556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10  7  1  0  0  0  0
  2 11  1  0  0  0  0
  3 12  1  6  0  0  0
  5 13  1  6  0  0  0
  8 14  1  1  0  0  0
  9 16  1  1  0  0  0
 16 15  1  0  0  0  0
  8 17  1  0  0  0  0
 10 18  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 17 20  1  1  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  2  0  0  0  0
 13 27  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 29 20  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  9 15  1  6  0  0  0
 22 32  1  0  0  0  0
  6 33  1  6  0  0  0
 10 34  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0038561

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12O[C@]3([H])C=C(C)[C@H](C[C@]3(COC(C)=O)[C@@](C)([C@H](OC(C)=O)[C@H]1O)[C@]21CO1)OC(=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O9/c1-11(2)20(27)31-15-8-22(9-28-13(4)24)16(7-12(15)3)32-19-17(26)18(30-14(5)25)21(22,6)23(19)10-29-23/h7,11,15-19,26H,8-10H2,1-6H3/t15-,16+,17+,18+,19+,21+,22+,23-/m0/s1

> <INCHI_KEY>
CZZOBJORBLRBLT-DSCHAYMESA-N

> <FORMULA>
C23H32O9

> <MOLECULAR_WEIGHT>
452.4948

> <EXACT_MASS>
452.204632622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
46.26777896208313

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2S,2'R,4'S,7'R,9'R,10'R,11'S)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 2-methylpropanoate

> <ALOGPS_LOGP>
1.56

> <JCHEM_LOGP>
0.8308360740000008

> <ALOGPS_LOGS>
-2.84

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.072305054496198

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6419737691633625

> <JCHEM_POLAR_SURFACE_AREA>
120.89000000000001

> <JCHEM_REFRACTIVITY>
108.96809999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.48e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,2'R,4'S,7'R,9'R,10'R,11'S)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038561
     RDKit          3D
8-Isobutanoylneosolaniol
 64 67  0  0  0  0  0  0  0  0999 V2000
   -0.4887    4.0266    1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1174    3.0338    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    3.4437   -1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3631    1.6931    0.1966 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0039    0.8045   -0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3396   -0.6522   -0.4529 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4288   -0.9370    0.8066 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9057   -1.0753    0.6283 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5885    0.1617    0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5278    0.5302    1.5477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -0.2932    2.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2299    1.8516    1.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9857    1.9203    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1838    1.9435    2.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2578   -1.9127   -0.5411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955   -2.5726   -0.5958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -2.0755   -1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0468   -1.4915   -1.6151 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7579   -2.5332   -1.9404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0587   -2.4884   -1.5677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7419   -1.2938   -2.2313 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0832   -0.8539   -3.3518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7288   -0.2569   -1.1464 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0348   -0.2702   -0.5528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8397    0.8298   -0.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1899    0.7555    0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4049    1.9146   -0.9697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7869   -0.7475   -0.0870 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2207    1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1474   -2.2389   -0.1066 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1289   -3.1022    0.9471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4181   -2.5821    0.4475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5440    3.8818    1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1425    3.8877    1.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3321    5.0460    0.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5158    1.0162   -1.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0742    0.9312   -1.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504   -1.8951    1.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2659   -0.0726    1.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894   -1.6076    1.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5043    2.6823    1.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612    2.7800   -0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8152    1.0186   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0445    2.1055    0.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9714    1.1673    2.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5820    1.7706    3.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6241    2.9531    2.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -2.0070   -1.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4512   -3.6306   -0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0467   -2.6747    0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7204   -2.7033   -2.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1098   -0.8517   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5666   -3.4043   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7814   -1.5542   -2.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0710    0.1423   -3.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5251    0.7522   -1.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1798    0.2492    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5720    1.7840    0.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9122    0.2195   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2310   -0.5721    1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992   -0.6215    2.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2169    0.8689    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0379   -2.7769    2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0173   -4.1959    0.8337 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  6
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  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  2  0
 23 28  1  0
 28 29  1  1
 28 30  1  0
 30 31  1  0
 31 32  1  0
 18  6  1  0
 30 20  1  0
 28  6  1  0
 30 32  1  6
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  0
  5 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  1
 12 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  6
 20 53  1  1
 21 54  1  6
 22 55  1  0
 23 56  1  6
 26 57  1  0
 26 58  1  0
 26 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 31 63  1  0
 31 64  1  0
M  END

HEADER    PROTEIN                                 25-JAN-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-JAN-13         0                                  
HETATM    1  C   UNK     0      -2.161  -6.041   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.495  -6.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.495  -8.351   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.161  -9.121   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.828  -8.351   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.828  -6.811   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.506  -6.041   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.506  -9.121   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.840  -8.351   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.840  -6.811   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.829  -6.041   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.829  -9.121   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.828  -9.891   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.506 -10.661   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.380  -8.351   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.610  -9.684   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.941 -11.603   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.593  -8.974   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.088  -8.603   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.235 -13.115   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -6.162  -8.351   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -7.496  -9.121   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.830  -8.351   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -6.162  -6.811   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.161 -12.201   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.495 -12.971   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.161 -10.661   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.828 -12.971   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.235 -14.655   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.902 -15.425   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.569 -15.425   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -7.496 -10.661   0.000  0.00  0.00           C+0
HETATM   33  H   UNK     0      -0.828  -5.271   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.390  -5.330   0.000  0.00  0.00           H+0
CONECT    1    2    6                                                       
CONECT    2    1    3   11                                                  
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8   13                                             
CONECT    6    1    7    5   33                                             
CONECT    7    6   10                                                       
CONECT    8    5    9   14   17                                             
CONECT    9    8   10   16   15                                             
CONECT   10    9    7   18   34                                             
CONECT   11    2                                                            
CONECT   12    3   21                                                       
CONECT   13    5   27                                                       
CONECT   14    8                                                            
CONECT   15   16    9                                                       
CONECT   16    9   15                                                       
CONECT   17    8   18   20                                                  
CONECT   18   10   17   19                                                  
CONECT   19   18                                                            
CONECT   20   17   29                                                       
CONECT   21   12   22   24                                                  
CONECT   22   21   23   32                                                  
CONECT   23   22                                                            
CONECT   24   21                                                            
CONECT   25   26   27   28                                                  
CONECT   26   25                                                            
CONECT   27   13   25                                                       
CONECT   28   25                                                            
CONECT   29   20   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   22                                                            
CONECT   33    6                                                            
CONECT   34   10                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

COMPND    HMDB0038561
HETATM    1  C1  UNL     1      -0.489   4.027   1.059  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.117   3.034   0.020  1.00  0.00           C  
HETATM    3  O1  UNL     1       0.434   3.444  -1.043  1.00  0.00           O  
HETATM    4  O2  UNL     1      -0.363   1.693   0.197  1.00  0.00           O  
HETATM    5  C3  UNL     1       0.004   0.805  -0.807  1.00  0.00           C  
HETATM    6  C4  UNL     1      -0.340  -0.652  -0.453  1.00  0.00           C  
HETATM    7  C5  UNL     1       0.429  -0.937   0.807  1.00  0.00           C  
HETATM    8  C6  UNL     1       1.906  -1.075   0.628  1.00  0.00           C  
HETATM    9  O3  UNL     1       2.589   0.162   0.597  1.00  0.00           O  
HETATM   10  C7  UNL     1       3.528   0.530   1.548  1.00  0.00           C  
HETATM   11  O4  UNL     1       3.766  -0.293   2.472  1.00  0.00           O  
HETATM   12  C8  UNL     1       4.230   1.852   1.478  1.00  0.00           C  
HETATM   13  C9  UNL     1       4.986   1.920   0.173  1.00  0.00           C  
HETATM   14  C10 UNL     1       5.184   1.944   2.650  1.00  0.00           C  
HETATM   15  C11 UNL     1       2.258  -1.913  -0.541  1.00  0.00           C  
HETATM   16  C12 UNL     1       3.595  -2.573  -0.596  1.00  0.00           C  
HETATM   17  C13 UNL     1       1.422  -2.076  -1.508  1.00  0.00           C  
HETATM   18  C14 UNL     1       0.047  -1.492  -1.615  1.00  0.00           C  
HETATM   19  O5  UNL     1      -0.758  -2.533  -1.940  1.00  0.00           O  
HETATM   20  C15 UNL     1      -2.059  -2.488  -1.568  1.00  0.00           C  
HETATM   21  C16 UNL     1      -2.742  -1.294  -2.231  1.00  0.00           C  
HETATM   22  O6  UNL     1      -2.083  -0.854  -3.352  1.00  0.00           O  
HETATM   23  C17 UNL     1      -2.729  -0.257  -1.146  1.00  0.00           C  
HETATM   24  O7  UNL     1      -4.035  -0.270  -0.553  1.00  0.00           O  
HETATM   25  C18 UNL     1      -4.840   0.830  -0.483  1.00  0.00           C  
HETATM   26  C19 UNL     1      -6.190   0.755   0.147  1.00  0.00           C  
HETATM   27  O8  UNL     1      -4.405   1.915  -0.970  1.00  0.00           O  
HETATM   28  C20 UNL     1      -1.787  -0.748  -0.087  1.00  0.00           C  
HETATM   29  C21 UNL     1      -2.171  -0.221   1.232  1.00  0.00           C  
HETATM   30  C22 UNL     1      -2.147  -2.239  -0.107  1.00  0.00           C  
HETATM   31  C23 UNL     1      -2.129  -3.102   0.947  1.00  0.00           C  
HETATM   32  O9  UNL     1      -3.418  -2.582   0.448  1.00  0.00           O  
HETATM   33  H1  UNL     1      -1.544   3.882   1.344  1.00  0.00           H  
HETATM   34  H2  UNL     1       0.142   3.888   1.975  1.00  0.00           H  
HETATM   35  H3  UNL     1      -0.332   5.046   0.709  1.00  0.00           H  
HETATM   36  H4  UNL     1      -0.516   1.016  -1.786  1.00  0.00           H  
HETATM   37  H5  UNL     1       1.074   0.931  -1.007  1.00  0.00           H  
HETATM   38  H6  UNL     1       0.050  -1.895   1.218  1.00  0.00           H  
HETATM   39  H7  UNL     1       0.266  -0.073   1.493  1.00  0.00           H  
HETATM   40  H8  UNL     1       2.289  -1.608   1.526  1.00  0.00           H  
HETATM   41  H9  UNL     1       3.504   2.682   1.586  1.00  0.00           H  
HETATM   42  H10 UNL     1       4.561   2.780  -0.405  1.00  0.00           H  
HETATM   43  H11 UNL     1       4.815   1.019  -0.449  1.00  0.00           H  
HETATM   44  H12 UNL     1       6.045   2.105   0.383  1.00  0.00           H  
HETATM   45  H13 UNL     1       5.971   1.167   2.526  1.00  0.00           H  
HETATM   46  H14 UNL     1       4.582   1.771   3.566  1.00  0.00           H  
HETATM   47  H15 UNL     1       5.624   2.953   2.715  1.00  0.00           H  
HETATM   48  H16 UNL     1       4.274  -2.007  -1.247  1.00  0.00           H  
HETATM   49  H17 UNL     1       3.451  -3.631  -0.946  1.00  0.00           H  
HETATM   50  H18 UNL     1       4.047  -2.675   0.422  1.00  0.00           H  
HETATM   51  H19 UNL     1       1.720  -2.703  -2.357  1.00  0.00           H  
HETATM   52  H20 UNL     1       0.110  -0.852  -2.549  1.00  0.00           H  
HETATM   53  H21 UNL     1      -2.567  -3.404  -1.869  1.00  0.00           H  
HETATM   54  H22 UNL     1      -3.781  -1.554  -2.534  1.00  0.00           H  
HETATM   55  H23 UNL     1      -2.071   0.142  -3.421  1.00  0.00           H  
HETATM   56  H24 UNL     1      -2.525   0.752  -1.508  1.00  0.00           H  
HETATM   57  H25 UNL     1      -6.180   0.249   1.123  1.00  0.00           H  
HETATM   58  H26 UNL     1      -6.572   1.784   0.293  1.00  0.00           H  
HETATM   59  H27 UNL     1      -6.912   0.219  -0.509  1.00  0.00           H  
HETATM   60  H28 UNL     1      -3.231  -0.572   1.426  1.00  0.00           H  
HETATM   61  H29 UNL     1      -1.599  -0.622   2.090  1.00  0.00           H  
HETATM   62  H30 UNL     1      -2.217   0.869   1.343  1.00  0.00           H  
HETATM   63  H31 UNL     1      -2.038  -2.777   2.000  1.00  0.00           H  
HETATM   64  H32 UNL     1      -2.017  -4.196   0.834  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3    3    4
CONECT    4    5
CONECT    5    6   36   37
CONECT    6    7   18   28
CONECT    7    8   38   39
CONECT    8    9   15   40
CONECT    9   10
CONECT   10   11   11   12
CONECT   12   13   14   41
CONECT   13   42   43   44
CONECT   14   45   46   47
CONECT   15   16   17   17
CONECT   16   48   49   50
CONECT   17   18   51
CONECT   18   19   52
CONECT   19   20
CONECT   20   21   30   53
CONECT   21   22   23   54
CONECT   22   55
CONECT   23   24   28   56
CONECT   24   25
CONECT   25   26   27   27
CONECT   26   57   58   59
CONECT   28   29   30
CONECT   29   60   61   62
CONECT   30   31   32
CONECT   31   32   63   64
END

HMDB0038561
     RDKit          3D
8-Isobutanoylneosolaniol
 64 67  0  0  0  0  0  0  0  0999 V2000
   -0.4887    4.0266    1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1174    3.0338    0.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4343    3.4437   -1.0430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3631    1.6931    0.1966 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0039    0.8045   -0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3396   -0.6522   -0.4529 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4288   -0.9370    0.8066 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9057   -1.0753    0.6283 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5885    0.1617    0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5278    0.5302    1.5477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -0.2932    2.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2299    1.8516    1.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9857    1.9203    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1838    1.9435    2.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2578   -1.9127   -0.5411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5955   -2.5726   -0.5958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -2.0755   -1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0468   -1.4915   -1.6151 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7579   -2.5332   -1.9404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0587   -2.4884   -1.5677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7419   -1.2938   -2.2313 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0832   -0.8539   -3.3518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7288   -0.2569   -1.1464 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0348   -0.2702   -0.5528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8397    0.8298   -0.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1899    0.7555    0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4049    1.9146   -0.9697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7869   -0.7475   -0.0870 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2207    1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1474   -2.2389   -0.1066 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1289   -3.1022    0.9471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4181   -2.5821    0.4475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5440    3.8818    1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1425    3.8877    1.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3321    5.0460    0.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5158    1.0162   -1.7862 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0742    0.9312   -1.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504   -1.8951    1.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2659   -0.0726    1.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894   -1.6076    1.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5043    2.6823    1.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5612    2.7800   -0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8152    1.0186   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0445    2.1055    0.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9714    1.1673    2.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5820    1.7706    3.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6241    2.9531    2.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2742   -2.0070   -1.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4512   -3.6306   -0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0467   -2.6747    0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7204   -2.7033   -2.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1098   -0.8517   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5666   -3.4043   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7814   -1.5542   -2.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0710    0.1423   -3.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5251    0.7522   -1.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1798    0.2492    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5720    1.7840    0.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9122    0.2195   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2310   -0.5721    1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992   -0.6215    2.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2169    0.8689    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0379   -2.7769    2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0173   -4.1959    0.8337 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  6
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  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  2  0
 23 28  1  0
 28 29  1  1
 28 30  1  0
 30 31  1  0
 31 32  1  0
 18  6  1  0
 30 20  1  0
 28  6  1  0
 30 32  1  6
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  0
  5 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  1
 12 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  6
 20 53  1  1
 21 54  1  6
 22 55  1  0
 23 56  1  6
 26 57  1  0
 26 58  1  0
 26 59  1  0
 29 60  1  0
 29 61  1  0
 29 62  1  0
 31 63  1  0
 31 64  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(1's,2S,2'r,4's,7'r,9'r,10'r,11's)-11'-(Acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 2-methylpropanoic acid	HMDB

Chemical Formula

C₂₃H₃₂O₉

Average Molecular Weight

452.4948

Monoisotopic Molecular Weight

452.204632622

IUPAC Name

(1'S,2S,2'R,4'S,7'R,9'R,10'R,11'S)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 2-methylpropanoate

Traditional Name

(1'S,2S,2'R,4'S,7'R,9'R,10'R,11'S)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 2-methylpropanoate

CAS Registry Number

111112-48-2

SMILES

[H][C@@]12O[C@]3([H])C=C(C)[C@H](C[C@]3(COC(C)=O)[C@@](C)([C@H](OC(C)=O)[C@H]1O)[C@]21CO1)OC(=O)C(C)C

InChI Identifier

InChI=1S/C23H32O9/c1-11(2)20(27)31-15-8-22(9-28-13(4)24)16(7-12(15)3)32-19-17(26)18(30-14(5)25)21(22,6)23(19)10-29-23/h7,11,15-19,26H,8-10H2,1-6H3/t15-,16+,17+,18+,19+,21+,22+,23-/m0/s1

InChI Key

CZZOBJORBLRBLT-DSCHAYMESA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Trichothecenes

Alternative Parents

Substituents

Trichothecene skeleton
Tricarboxylic acid or derivatives
Oxepane
Oxane
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038561)

Source

Endogenous

Endogenous (HMDB: HMDB0038561)

Animal

Animal (HMDB: HMDB0038561)

Exogenous

Food

Food (HMDB: HMDB0038561)

Exogenous (HMDB: HMDB0038561)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0038561)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0038561)

Lipid metabolism pathway (HMDB: HMDB0038561)

Cellular process

Cell signaling (HMDB: HMDB0038561)

Biochemical process

Lipid transport (HMDB: HMDB0038561)

Role

Biological role

Energy source (HMDB: HMDB0038561)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.65 g/L	ALOGPS
logP	1.56	ALOGPS
logP	0.83	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.07	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	120.89 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	108.97 m³·mol⁻¹	ChemAxon
Polarizability	46.27 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	206.746	31661259
DarkChem	[M-H]-	199.004	31661259
DeepCCS	[M-2H]-	233.151	30932474
DeepCCS	[M+Na]+	207.532	30932474
AllCCS	[M+H]+	203.3	32859911
AllCCS	[M+H-H2O]+	201.4	32859911
AllCCS	[M+NH4]+	205.1	32859911
AllCCS	[M+Na]+	205.6	32859911
AllCCS	[M-H]-	206.1	32859911
AllCCS	[M+Na-2H]-	207.2	32859911
AllCCS	[M+HCOO]-	208.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8-Isobutanoylneosolaniol	[H][C@@]12O[C@]3([H])C=C(C)[C@H](C[C@]3(COC(C)=O)[C@@](C)([C@H](OC(C)=O)[C@H]1O)[C@]21CO1)OC(=O)C(C)C	3778.4	Standard polar	33892256
8-Isobutanoylneosolaniol	[H][C@@]12O[C@]3([H])C=C(C)[C@H](C[C@]3(COC(C)=O)[C@@](C)([C@H](OC(C)=O)[C@H]1O)[C@]21CO1)OC(=O)C(C)C	2662.6	Standard non polar	33892256
8-Isobutanoylneosolaniol	[H][C@@]12O[C@]3([H])C=C(C)[C@H](C[C@]3(COC(C)=O)[C@@](C)([C@H](OC(C)=O)[C@H]1O)[C@]21CO1)OC(=O)C(C)C	2763.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8-Isobutanoylneosolaniol,1TMS,isomer #1	CC(=O)OC[C@]12C[C@H](OC(=O)C(C)C)C(C)=C[C@H]1O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](OC(C)=O)[C@@]2(C)[C@]12CO2	2755.0	Semi standard non polar	33892256
8-Isobutanoylneosolaniol,1TBDMS,isomer #1	CC(=O)OC[C@]12C[C@H](OC(=O)C(C)C)C(C)=C[C@H]1O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](OC(C)=O)[C@@]2(C)[C@]12CO2	2986.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Isobutanoylneosolaniol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9137000000-f4b6a61f92447248536f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Isobutanoylneosolaniol GC-MS (1 TMS) - 70eV, Positive	splash10-0006-9032200000-73dcac0df85f66263970	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Isobutanoylneosolaniol 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 - 8-Isobutanoylneosolaniol 10V, Positive-QTOF	splash10-0h2f-4109700000-2c7d8a548d3792c8c9c0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 20V, Positive-QTOF	splash10-006x-8219200000-fbf9dd19750999b560ed	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 40V, Positive-QTOF	splash10-00dl-9104000000-eb9931ac44be22da18a5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 10V, Negative-QTOF	splash10-0zfu-3002900000-03bf13c4b16d4ac41438	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 20V, Negative-QTOF	splash10-0a4l-9205500000-cab559730c77590f6f97	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 40V, Negative-QTOF	splash10-0a4i-7900000000-468dd04a66b02f41e1f3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 10V, Negative-QTOF	splash10-000i-9003300000-500cad0662db7c6b09cf	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 20V, Negative-QTOF	splash10-059i-9000000000-a5b150773238092e6190	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 40V, Negative-QTOF	splash10-007c-9000000000-fbe339197d2633bca107	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 10V, Positive-QTOF	splash10-0a4i-0009100000-d730e3efab316ad6bf2a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 20V, Positive-QTOF	splash10-052f-3009100000-f722b1f86d5f4cc06800	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Isobutanoylneosolaniol 40V, Positive-QTOF	splash10-0006-9004000000-eb674cf5915538fdba35	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
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

FDB017948

KNApSAcK ID

Not Available

Chemspider ID

26504044

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91809166

PDB ID

Not Available

ChEBI ID

175609

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 8-Isobutanoylneosolaniol (HMDB0038561)

MOL for HMDB0038561 (8-Isobutanoylneosolaniol)

3D MOL for HMDB0038561 (8-Isobutanoylneosolaniol)

3D SDF for HMDB0038561 (8-Isobutanoylneosolaniol)

3D-SDF for HMDB0038561 (8-Isobutanoylneosolaniol)

PDB for HMDB0038561 (8-Isobutanoylneosolaniol)

3D PDB for HMDB0038561 (8-Isobutanoylneosolaniol)

SMILES for HMDB0038561 (8-Isobutanoylneosolaniol)

INCHI for HMDB0038561 (8-Isobutanoylneosolaniol)

Structure for HMDB0038561 (8-Isobutanoylneosolaniol)

3D Structure for HMDB0038561 (8-Isobutanoylneosolaniol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra