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Target
Thromboxane-A synthase
Ligand
BDBM50028718
Substrate
n/a
Meas. Tech.
ChEBML_210443
IC50
42±n/a nM
Citation
 Iizuka, K; Akahane, K; Momose, D; Nakazawa, M; Tanouchi, T; Kawamura, M; Ohyama, I; Kajiwara, I; Iguchi, Y; Okada, T; Taniguchi, K; Miyamoto, T; Hayashi, M Highly selective inhibitors of thromboxane synthetase. 1. Imidazole derivatives. J Med Chem 24:1139-48 (1982) [PubMed]  Article 
Target
Name:
Thromboxane-A synthase
Synonyms:
CYP5 | CYP5A1 | Cytochrome P450 5A1 | P450 TxA2 | TBXAS1 | THAS_HUMAN | TXA synthase | TXAS | TXS | Thromboxane A2 Synthase | Thromboxane A2 Synthase (P450 TxA2) | Thromboxane Alpha | Thromboxane prostanoid | Thromboxane synthase | Thromboxane-A synthase
Type:
Enzyme
Mol. Mass.:
60524.67
Organism:
Homo sapiens (Human)
Description:
P24557
Residue:
533
Sequence:
MEALGFLKLEVNGPMVTVALSVALLALLKWYSTSAFSRLEKLGLRHPKPSPFIGNLTFFRQGFWESQMELRKLYGPLCGYYLGRRMFIVISEPDMIKQVLVENFSNFTNRMASGLEFKSVADSVLFLRDKRWEEVRGALMSAFSPEKLNEMVPLISQACDLLLAHLKRYAESGDAFDIQRCYCNYTTDVVASVAFGTPVDSWQAPEDPFVKHCKRFFEFCIPRPILVLLLSFPSIMVPLARILPNKNRDELNGFFNKLIRNVIALRDQQAAEERRRDFLQMVLDARHSASPMGVQDFDIVRDVFSSTGCKPNPSRQHQPSPMARPLTVDEIVGQAFIFLIAGYEIITNTLSFATYLLATNPDCQEKLLREVDVFKEKHMAPEFCSLEEGLPYLDMVIAETLRMYPPAFRFTREAAQDCEVLGQRIPAGAVLEMAVGALHHDPEHWPSPETFNPERFTAEARQQHRPFTYLPFGAGPRSCLGVRLGLLEVKLTLLHVLHKFRFQACPETQVPLQLESKSALGPKNGVYIKIVSR
  
Inhibitor
Name:
BDBM50028718
Synonyms:
8-Imidazol-1-yl-octa-6,7-dienoic acid; hydrochloride | CHEMBL542547
Type:
Small organic molecule
Emp. Form.:
C11H14N2O2
Mol. Mass.:
206.2411
SMILES:
OC(=O)CCCCC=C=Cn1ccnc1 |(18.93,-1.35,;17.59,-.58,;17.59,.97,;16.27,-1.37,;14.91,-.6,;13.59,-1.37,;12.25,-.63,;10.91,-1.4,;9.57,-.63,;8.25,.15,;6.92,.92,;5.41,.53,;4.59,1.83,;5.57,3.03,;7.01,2.47,)|
Structure:
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