Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H24O3 |
| Molecular Weight | 252.3493 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C1=CC(C)(OO)C=C(C1=O)C(C)(C)C
InChI
InChIKey=FNLSGYWVCGOYGD-UHFFFAOYSA-N
InChI=1S/C15H24O3/c1-13(2,3)10-8-15(7,18-17)9-11(12(10)16)14(4,5)6/h8-9,17H,1-7H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Protective effect of Hibiscus anthocyanins against tert-butyl hydroperoxide-induced hepatic toxicity in rats. | 2000-05 |
|
| Mitogen-activated protein kinase (MAPK) activation by butylated hydroxytoluene hydroperoxide: implications for cellular survival and tumor promotion. | 1996-08-01 |
|
| Generation of reactive intermediates from the tumor promoter butylated hydroxytoluene hydroperoxide in isolated murine keratinocytes or by hematin. | 1989-07 |
|
| Nonheme iron in sickle erythrocyte membranes: association with phospholipids and potential role in lipid peroxidation. | 1988-10 |
|
| Tumor promotion by a hydroperoxide metabolite of butylated hydroxytoluene, 2,6-di-tert-butyl-4-hydroperoxy-4-methyl-2,5-cyclohexadienone, in mouse skin. | 1988-09 |
|
| Cytochrome P-450-catalyzed rearrangement of a peroxyquinol derived from butylated hydroxytoluene. Involvement of radical and cationic intermediates. | 1986-10-25 |
|
| Interaction of cytochrome P-450 with a hydroperoxide derived from butylated hydroxytoluene. Mechanism of isomerization. | 1985-09-05 |
|
| The acute toxicity of butylated hydroxytoluene and its metabolites in mice. | 1980-08 |
|
| Cyclic metabolic pathway of a butylated hydroxytoluene by rat liver microsomal fractions. | 1974-12 |
|
| Ring hydroxylation of di-t-butylhydroxytoluene by rat liver microsomal preparations. | 1972-08 |
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DTXSID20215139
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6485-57-0
Created by
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114687
Created by
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HK05U8X26D
Created by
admin on Mon Mar 31 19:31:49 GMT 2025 , Edited by admin on Mon Mar 31 19:31:49 GMT 2025
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