| Weight | 196.249 g/mol |
|---|---|
| Formula | C14H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Stilbene oxide (17619-97-5, 1439-07-2)
stilbene oxide, (trans)-isomer · stilbene oxide, trans- · stilbene oxide, (cis)-isomer
Score:
#2942 in Biochemistry
,
#7202 in Chemistry
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- Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Effects of stilbene constituents from rhubarb on nitric oxide production in lipopolysaccharide-activated macrophages (Bioorganic & Medicinal Chemistry Letters, 2000)
- The hereditary transmission of high glutathione transferase activity towards trans-stilbene oxide in human mononuclear leukocytes (Human Genetics, 1985)
- Correlation between trans-stilbene oxide-glutathione conjugation activity and the deletion mutation in the glutathione S-transferase class Mu gene detected by polymerase chain reaction (Biochemical Pharmacology, 1992)
- Interindividual and interspecies variation in hepatic microsomal epoxide hydrolase activity: studies with cis-stilbene oxide, carbamazepine 10, 11-epoxide and naphthalene. (Journal of Pharmacology and Experimental Therapeutics, 1996)
- Hereditary interindividual differences in the glutathione transferase activity towards trans -stilbene oxide in resting human mononuclear leukocytes are due to a particular isozyme(s) (Carcinogenesis, 1985)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - stilbene oxide, (trans)-isomer
- stilbene oxide, trans-
- stilbene oxide, (cis)-isomer
- stilbene oxide, trans-(+-)-isomer
- stilbene oxide, (2S-trans)-isomer
- trans-stilbene oxide
- stilbene oxide, (2R-trans)-isomer
-
SMILESC1=CC=C(C=C1)C2C(O2)C3=CC=CC=C3
-
InChIKeyARCJQKUWGAZPFX-UHFFFAOYSA-N
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