Summary

IMPPAT Phytochemical identifier: IMPHY013893

Phytochemical name: Brisbagenin

Synonymous chemical names:
brisbagenin

External chemical identifiers:
CID:167596

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Chemical structure information

SMILES:
C[C@@H]1CCC2(OC1)O[C@@H]1[C@H]([C@@H]2C)[C@@]2([C@@H](C1)[C@@H]1CC[C@@H]3[C@]([C@H]1CC2)(C)[C@H](O)C[C@@H](C3)O)C

InChI:
InChI=1S/C27H44O4/c1-15-7-10-27(30-14-15)16(2)24-22(31-27)13-21-19-6-5-17-11-18(28)12-23(29)26(17,4)20(19)8-9-25(21,24)3/h15-24,28-29H,5-14H2,1-4H3/t15-,16+,17+,18-,19-,20+,21+,22+,23-,24+,25+,26+,27?/m1/s1

InChIKey:
NCLLSOCDVMFDSK-CNJRTTOXSA-N

DeepSMILES:
C[C@@H]CCCOC6))O[C@@H][C@H][C@@H]5C))[C@@][C@@H]C5)[C@@H]CC[C@@H][C@][C@H]6CC%10)))C)[C@H]O)C[C@@H]C6)O))))))))))C

Functional groups:
CO, COC(C)(C)OC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1CCC2(CC3C(CC4C3CCC3C5CCCCC5CCC34)O2)OC1

Scaffold Graph/Node level:
C1CCC2(CC3C(CC4C3CCC3C5CCCCC5CCC34)O2)OC1

Scaffold Graph level:
C1CCC2(CC1)CC1CC3C(CCC4C5CCCCC5CCC43)C1C2

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lipids and lipid-like molecules

ClassyFire Class: Prenol lipids

ClassyFire Subclass: Triterpenoids

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Steroids

NP Classifier Class: Spirostane steroids

NP-Likeness score: 3.375

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Chemical structure download