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
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
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 |
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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 |
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Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice. | 2002 Dec 19 |
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Monoterpene regulation of Ras and Ras-related protein expression. | 2003 Jun |
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Monoterpene biosynthesis pathway construction in Escherichia coli. | 2003 Sep |
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Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system. | 2005 Dec |
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Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes. | 2005 May |
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Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time. | 2006 May 30 |
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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
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 14:13:20 GMT 2023
by
admin
on
Sat Dec 16 14:13:20 GMT 2023
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Record UNII |
DI8OD510EO
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Record Status |
Validated (UNII)
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Record Version |
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DI8OD510EO
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330573
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DTXSID60317646
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319644
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1197-06-4
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |