Summary

IMPPAT Phytochemical identifier: IMPHY011876

Phytochemical name: 24-Ethyl-5alpha-cholest-7-en-3beta-ol

Synonymous chemical names:
22 dihydrospinasterol, 22-dihydro-spinasterol, 22-dihydrospinasterol, dihydrospinasterol

External chemical identifiers:
CID:131751392

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Chemical structure information

SMILES:
CC[C@H](C(C)C)CC[C@H]([C@H]1CCC2[C@]1(C)CCC1C2=CC[C@@H]2[C@]1(C)CC[C@@H](C2)O)C

InChI:
InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h11,19-23,25-27,30H,7-10,12-18H2,1-6H3/t20-,21+,22+,23+,25-,26?,27?,28+,29-/m1/s1

InChIKey:
YSKVBPGQYRAUQO-BSTNUWHUSA-N

DeepSMILES:
CC[C@H]CC)C))CC[C@H][C@H]CCC[C@]5C)CCCC6=CC[C@@H][C@]6C)CC[C@@H]C6)O)))))))))))))))))C

Functional groups:
CC=C(C)C, CO

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=C2C3CCCC3CCC2C2CCCCC2C1

Scaffold Graph/Node level:
C1CCC2C(C1)CCC1C3CCCC3CCC21

Scaffold Graph level:
C1CCC2C(C1)CCC1C3CCCC3CCC21

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Lipids and lipid-like molecules

ClassyFire Class: Steroids and steroid derivatives

ClassyFire Subclass: Stigmastanes and derivatives

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Steroids

NP Classifier Class: Stigmastane steroids

NP-Likeness score: 2.729

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Chemical structure download