| Weight | 152.237 g/mol |
|---|---|
| Formula | C10H16O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Perilla alcohol (536-59-4)
perillyl alcohol · (-)-p-mentha-1,8-dien-7-ol · dihydrocuminyl alcohol
Score:
#1460 in Biochemistry
,
#4311 in Chemistry
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- Induction of apoptosis in liver tumors by the monoterpene perillyl alcohol (Cancer Research, 1995)
- Chemoprevention of colon carcinogenesis by dietary perillyl alcohol. (Cancer Research, 1997)
- Mammary carcinoma regression induced by perillyl alcohol, a hydroxylated analog of limonene (Cancer Chemotherapy and Pharmacology, 1994)
- Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production (Metabolic Engineering, 2013)
- Inhibitory effects of perillyl alcohol on UVB-induced murine skin cancer and AP-1 transactivation (Cancer Research, 1998)
- The inhibition of protein prenyltransferases by oxygenated metabolites of limonene and perillyl alcohol (Cancer Letters, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - perillyl alcohol
- (-)-p-mentha-1,8-dien-7-ol
- dihydrocuminyl alcohol
- NSC 641066
- perilla alcohol, (R)-isomer
- 1-cyclohexene-1-methanol, 4-(1-methylethenyl)-, (4S)-
- 4-isopropenyl-cyclohex-1-ene-1-methanol
- cyclohex-1-ene-1-methanol, 4(1-methylethenyl)
- (S)-perillyl alcohol
- perilla alcohol, (S)-isomer
- p-mentha-1,8-dien-7-ol
-
SMILESCC(=C)C1CCC(=CC1)CO
-
InChIKeyNDTYTMIUWGWIMO-UHFFFAOYSA-N
- Pubchem - Perilla alcohol
- Wikipedia - perillyl alcohol
Perillyl alcohol (IUPAC name: [4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol) and its precursor limonene are naturally occurring monocyclic terpenes derived from the mevalonate pathway in plants. Perillyl alcohol can be found in the essential oils of various plants, such as lavender, lemongrass, sage, and peppermint. It has a number of manufacturing, household, and medical applications.
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