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TargetProstaglandin-H2 D-isomerase
LigandBDBM50060462
Substrate/Competitorn/a
Ki 1.6±n/a nM
CommentsPDSP_2287
Citation Arimura, AYasui, KKishino, JAsanuma, FHasegawa, HKakudo, SOhtani, MArita, H Prevention of allergic inflammation by a novel prostaglandin receptor antagonist, S-5751. J Pharmacol Exp Ther298:411-9 (2001) [PubMed]
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Prostaglandin-H2 D-isomerase
Name:Prostaglandin-H2 D-isomerase
Synonyms:PDS | PGD2 | PTGDS | PTGDS_HUMAN
Type:Enzyme Catalytic Domain
Mol. Mass.:21031.11
Organism:Homo sapiens (Human)
Description:PGD2 0 HUMAN::P41222
Residue:190
Sequence:
MATHHTLWMGLALLGVLGDLQAAPEAQVSVQPNFQQDKFLGRWFSAGLASNSSWLREKKA
ALSMCKSVVAPATDGGLNLTSTFLRKNQCETRTMLLQPAGSLGSYSYRSPHWGSTYSVSV
VETDYDQYALLYSQGSKGPGEDFRMATLYSRTQTPRAELKEKFTAFCKAQGFTEDTIVFL
PQTDKCMTEQ
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  Blast E-value cutoff:
BDBM50060462
n/a
NameBDBM50060462
Synonyms:(Z)-7-{(1R,2R,3S,5S)-2-[(5-Hydroxy-benzo[b]thiophene-3-carbonyl)-amino]-6,6-dimethyl-bicyclo[3.1.1]hept-3-yl}-hept-5-enoic acid | CHEMBL116837 | S-5751
TypeSmall organic molecule
Emp. Form.C25H31NO4S
Mol. Mass.441.583
SMILESCC1(C)[C@@H]2C[C@H]1[C@H](NC(=O)c1csc3ccc(O)cc13)[C@@H](C\C=C/CCCC(O)=O)C2
Structure
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