Reaction Details |
![](/images/Email.png) | Report a problem with these data |
Target | Cytochrome P450 4A11 |
---|
Ligand | BDBM50527963 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1904212 (CHEMBL4406434) |
---|
IC50 | 179000±n/a nM |
---|
Citation | Kowalski, JP; McDonald, MG; Pelletier, RD; Hanenberg, H; Wiek, C; Rettie, AE Design and Characterization of the First Selective and Potent Mechanism-Based Inhibitor of Cytochrome P450 4Z1. J Med Chem63:4824-4836 (2020) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Cytochrome P450 4A11 |
---|
Name: | Cytochrome P450 4A11 |
Synonyms: | 1.14.14.1 | 1.14.14.80 | 20-HETE synthase | 20-hydroxyeicosatetraenoic acid synthase | CP4AB_HUMAN | CYP4A11 | CYP4A2 | CYP4AII | CYPIVA11 | Cytochrome P-450HK-omega | Cytochrome P450 4A11 | Cytochrome P450HL-omega | Fatty acid omega-hydroxylase | Lauric acid omega-hydroxylase | Long-chain fatty acid omega-monooxygenase | Synonyms=CYP4A2 |
Type: | PROTEIN |
Mol. Mass.: | 59367.30 |
Organism: | Homo sapiens |
Description: | ChEMBL_119703 |
Residue: | 519 |
Sequence: | MSVSVLSPSRLLGDVSGILQAASLLILLLLLIKAVQLYLHRQWLLKALQQFPCPPSHWLF
GHIQELQQDQELQRIQKWVETFPSACPHWLWGGKVRVQLYDPDYMKVILGRSDPKSHGSY
RFLAPWIGYGLLLLNGQTWFQHRRMLTPAFHYDILKPYVGLMADSVRVMLDKWEELLGQD
SPLEVFQHVSLMTLDTIMKCAFSHQGSIQVDRNSQSYIQAISDLNNLVFSRVRNAFHQND
TIYSLTSAGRWTHRACQLAHQHTDQVIQLRKAQLQKEGELEKIKRKRHLDFLDILLLAKM
ENGSILSDKDLRAEVDTFMFEGHDTTASGISWILYALATHPKHQERCREEIHSLLGDGAS
ITWNHLDQMPYTTMCIKEALRLYPPVPGIGRELSTPVTFPDGRSLPKGIMVLLSIYGLHH
NPKVWPNPEVFDPFRFAPGSAQHSHAFLPFSGGSRNCIGKQFAMNELKVATALTLLRFEL
LPDPTRIPIPIARLVLKSKNGIHLRLRRLPNPCEDKDQL
|
|
|
BDBM50527963 |
---|
n/a |
---|
Name | BDBM50527963 |
Synonyms: | CHEMBL4557940 |
Type | Small organic molecule |
Emp. Form. | C14H20N4O2 |
Mol. Mass. | 276.3342 |
SMILES | OC(=O)CCCCCCCNn1nnc2ccccc12 |
Structure |
|