Reaction Details |
| Report a problem with these data |
Target | Cytochrome P450 2E1 |
---|
Ligand | BDBM31656 |
---|
Substrate/Competitor | BDBM31678 |
---|
Meas. Tech. | Measurement of CYP2E1 Enzymatic Activity |
---|
pH | 7.4±n/a |
---|
Temperature | 310.15±n/a K |
---|
IC50 | >100000±n/a nM |
---|
Citation | Vlahakis, JZ; Hum, M; Rahman, MN; Jia, Z; Nakatsu, K; Szarek, WA Synthesis and evaluation of imidazole-dioxolane compounds as selective heme oxygenase inhibitors: effect of substituents at the 4-position of the dioxolane ring. Bioorg Med Chem17:2461-75 (2009) [PubMed] Article |
---|
More Info.: | Get all data from this article, Inhibition_Run data, Solution Info, Assay Method |
---|
|
Cytochrome P450 2E1 |
---|
Name: | Cytochrome P450 2E1 |
Synonyms: | 4-nitrophenol 2-hydroxylase | CP2E1_RAT | CYPIIE1 | Cyp2e | Cyp2e-1 | Cyp2e1 |
Type: | Enzyme |
Mol. Mass.: | 56637.32 |
Organism: | Rattus norvegicus (rat) |
Description: | CYP2E1 prepared from rat liver microsomes was used in enzyme assays. |
Residue: | 493 |
Sequence: | MAVLGITIALLVWVATLLVISIWKQIYNSWNLPPGPFPLPILGNIFQLDLKDIPKSFTKL
AKRFGPVFTLHLGSRRIVVLHGYKAVKEVLLNHKNEFSGRGDIPVFQEYKNKGIIFNNGP
TWKDVRRFSLSILRDWGMGKQGNEARIQREAQFLVEELKKTKGQPFDPTFLIGCAPCNVI
ADILFNKRFDYNDKKCLRLMSLFNENFYLLSTPWIQLYNNFADYLRYLPGSHRKIMKNVS
EIKQYTLEKAKEHLQSLDINCARDVTDCLLIEMEKEKHSQEPMYTMENVSVTLADLFFAG
TETTSTTLRYGLLILMKYPEIEEKLHEEIDRVIGPSRVPAVRDRLDMPYMDAVVHEIQRF
INLVPSNLPHEATRDTVFQGYVIPKGTVVIPTLDSLLYDSHEFPDPEKFKPEHFLNENGK
FKYSDYFKAFSAGKRVCVGEGLARMELFLLLSAILQHFNLKSLVDPKDIDLSPVTVGFGS
IPPQFKLCVIPRS
|
|
|
BDBM31656 |
---|
BDBM31678 |
---|
Name | BDBM31656 |
Synonyms: | imidazole-dioxolane, 8 |
Type | Small organic molecule |
Emp. Form. | C21H22ClN3O2S |
Mol. Mass. | 415.936 |
SMILES | Clc1ccc(CC[C@@]2(Cn3ccnc3)OC[C@@H](CSc3ccncc3)O2)cc1 |r| |
Structure |
|