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Details

Stereochemistry RACEMIC
Molecular Formula C10H16O
Molecular Weight 152.2334
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARVEOL, CIS-(±)-

SMILES

CC(=C)[C@@H]1CC=C(C)[C@H](O)C1

InChI

InChIKey=BAVONGHXFVOKBV-NXEZZACHSA-N
InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H16O
Molecular Weight 152.2334
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols.
1995 Oct 1
Species differences in the metabolism of (+)- and (-)-limonenes and their metabolites, carveols and carvones, by cytochrome P450 enzymes in liver microsomes of mice, rats, guinea pigs, rabbits, dogs, monkeys, and humans.
2002
Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice.
2002 Dec 19
Monoterpene regulation of Ras and Ras-related protein expression.
2003 Jun
Monoterpene biosynthesis pathway construction in Escherichia coli.
2003 Sep
Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system.
2005 Dec
Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes.
2005 May
Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time.
2006 May 30
Monoterpenoid agonists of TRPV3.
2007 Jun
Inhibitory effects of substrate and product on the carvone biotransformation activity of Rhodococcus erythropolis.
2008 Jul
Distinct effects of carvone analogues on the isolated nerve of rats.
2010 Oct 25
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 14:13:20 GMT 2023
Edited
by admin
on Sat Dec 16 14:13:20 GMT 2023
Record UNII
DI8OD510EO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARVEOL, CIS-(±)-
Common Name English
CARVEOL, CIS-
Common Name English
NSC-319644
Code English
CIS-2-METHYL-5-(1-METHYLVINYL)-2-CYCLOHEXENE-1-OL
Systematic Name English
CIS-MENTHA-1,8-DIEN-6-OL
Common Name English
2-CYCLOHEXEN-1-OL, 2-METHYL-5-(1-METHYLETHENYL)-, (1R,5R)-REL-
Systematic Name English
(±)-CIS-CARVEOL
Common Name English
Code System Code Type Description
FDA UNII
DI8OD510EO
Created by admin on Sat Dec 16 14:13:20 GMT 2023 , Edited by admin on Sat Dec 16 14:13:20 GMT 2023
PRIMARY
PUBCHEM
330573
Created by admin on Sat Dec 16 14:13:20 GMT 2023 , Edited by admin on Sat Dec 16 14:13:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID60317646
Created by admin on Sat Dec 16 14:13:20 GMT 2023 , Edited by admin on Sat Dec 16 14:13:20 GMT 2023
PRIMARY
NSC
319644
Created by admin on Sat Dec 16 14:13:20 GMT 2023 , Edited by admin on Sat Dec 16 14:13:20 GMT 2023
PRIMARY
CAS
1197-06-4
Created by admin on Sat Dec 16 14:13:20 GMT 2023 , Edited by admin on Sat Dec 16 14:13:20 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE