CARVEOL, CIS-(±)-

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 Search

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

Title	Date	PubMed
Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols.	1995 Oct 1	7574722
Degradation of pinene by Bacillus pallidus BR425.	1998	10192895
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	15618705
Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice.	2002 Dec 19	12493079
Metabolism of (+)- and (-)-limonenes to respective carveols and perillyl alcohols by CYP2C9 and CYP2C19 in human liver microsomes.	2002 May	11950794
Monoterpene regulation of Ras and Ras-related protein expression.	2003 Jun	12671036
Monoterpene biosynthesis pathway construction in Escherichia coli.	2003 Sep	12943759
Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system.	2005 Dec	15841371
Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes.	2005 May	15856218
Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time.	2006 May 30	16436284
Monoterpenoid agonists of TRPV3.	2007 Jun	17420775
Inhibitory effects of substrate and product on the carvone biotransformation activity of Rhodococcus erythropolis.	2008 Jul	18327538
Distinct effects of carvone analogues on the isolated nerve of rats.	2010 Oct 25	20670618

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