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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H24O2
Molecular Weight 236.3499
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPSIDIOL

SMILES

C[C@@H]1[C@H](O)C[C@@H](O)C2=CC[C@H](C[C@]12C)C(C)=C

InChI

InChIKey=BXXSHQYDJWZXPB-OKNSCYNVSA-N
InChI=1S/C15H24O2/c1-9(2)11-5-6-12-14(17)7-13(16)10(3)15(12,4)8-11/h6,10-11,13-14,16-17H,1,5,7-8H2,2-4H3/t10-,11-,13-,14-,15-/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Differential induction of sesquiterpene metabolism in tobacco cell suspension cultures by methyl jasmonate and fungal elicitor.
2000 Sep 15
Cloning, heterologous expression, and functional characterization of 5-epi-aristolochene-1,3-dihydroxylase from tobacco (Nicotiana tabacum).
2001 Sep 15
Probing sesquiterpene hydroxylase activities in a coupled assay with terpene synthases.
2003 Jan 15
Kinetic and molecular analysis of 5-epiaristolochene 1,3-dihydroxylase, a cytochrome P450 enzyme catalyzing successive hydroxylations of sesquiterpenes.
2005 Feb 4
Patents
Name Type Language
CAPSIDIOL
Common Name English
(1R,3R,4S,4AR,6R)-4,4A-DIMETHYL-6-PROP-1-EN-2-YL-2,3,4,5,6,7-HEXAHYDRO-1H-NAPHTHALENE-1,3-DIOL
Systematic Name English
Code System Code Type Description
FDA UNII
1O869T5P54
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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WIKIPEDIA
CAPSIDIOL
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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CAS
37208-05-2
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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EPA CompTox
DTXSID50190703
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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PUBCHEM
161937
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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CHEBI
28283
Created by admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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