Summary

IMPPAT Phytochemical identifier: IMPHY000814

Phytochemical name: Forskolin

Synonymous chemical names:
coleonol, forskolin, forskolin (coleonol)

External chemical identifiers:
CID:47936, ChEMBL:CHEMBL52606, ChEBI:42471, ZINC:ZINC000003977779, FDASRS:1F7A44V6OU, SureChEMBL:SCHEMBL4928, MolPort-002-493-717

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Chemical structure information

SMILES:
C=C[C@@]1(C)CC(=O)[C@]2([C@@](O1)(C)[C@@H](OC(=O)C)[C@H]([C@@H]1[C@]2(C)[C@@H](O)CCC1(C)C)O)O

InChI:
InChI=1S/C22H34O7/c1-8-19(5)11-14(25)22(27)20(6)13(24)9-10-18(3,4)16(20)15(26)17(28-12(2)23)21(22,7)29-19/h8,13,15-17,24,26-27H,1,9-11H2,2-7H3/t13-,15-,16-,17-,19-,20-,21+,22-/m0/s1

InChIKey:
OHCQJHSOBUTRHG-KGGHGJDLSA-N

DeepSMILES:
C=C[C@@]C)CC=O)[C@][C@@]O6)C)[C@@H]OC=O)C)))[C@H][C@@H][C@]6C)[C@@H]O)CCC6C)C)))))))O))))O

Functional groups:
C=CC, CC(=O)OC, CC(C)=O, CO, COC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1CCOC2CCC3CCCCC3C12

Scaffold Graph/Node level:
OC1CCOC2CCC3CCCCC3C12

Scaffold Graph level:
CC1CCCC2CCC3CCCCC3C12

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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: Diterpenoids

NP Classifier Class: Labdane diterpenoids

NP-Likeness score: 3.144

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Chemical structure download