Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H22O |
| Molecular Weight | 218.3346 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C1=CC(=C)C=C(C1=O)C(C)(C)C
InChI
InChIKey=JJQCWPWUHZFKBN-UHFFFAOYSA-N
InChI=1S/C15H22O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9H,1H2,2-7H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inhibition of glutathione S-transferase P1-1 in mouse lung epithelial cells by the tumor promoter 2,6-di-tert-butyl-4-methylene-2,5-cyclohexadienone (BHT-quinone methide): protein adducts investigated by electrospray mass spectrometry. | 2004 Dec |
|
| Immunochemical and proteomic analysis of covalent adducts formed by quinone methide tumor promoters in mouse lung epithelial cell lines. | 2005 Oct |
|
| Carbonyl reductase inactivation may contribute to mouse lung tumor promotion by electrophilic metabolites of butylated hydroxytoluene: protein alkylation in vivo and in vitro. | 2008 Aug |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID70180707
Created by
admin on Fri Dec 15 18:18:25 GMT 2023 , Edited by admin on Fri Dec 15 18:18:25 GMT 2023
|
PRIMARY | |||
|
2607-52-5
Created by
admin on Fri Dec 15 18:18:25 GMT 2023 , Edited by admin on Fri Dec 15 18:18:25 GMT 2023
|
PRIMARY | |||
|
107736
Created by
admin on Fri Dec 15 18:18:25 GMT 2023 , Edited by admin on Fri Dec 15 18:18:25 GMT 2023
|
PRIMARY | |||
|
49860VI52B
Created by
admin on Fri Dec 15 18:18:25 GMT 2023 , Edited by admin on Fri Dec 15 18:18:25 GMT 2023
|
PRIMARY | |||
|
C024709
Created by
admin on Fri Dec 15 18:18:25 GMT 2023 , Edited by admin on Fri Dec 15 18:18:25 GMT 2023
|
PRIMARY |
PARENT (METABOLITE)
SUBSTANCE RECORD
