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TargetHematopoietic prostaglandin D synthase
LigandBDBM50526495
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1900120 (CHEMBL4402235)
IC50 9.7±n/a nM
Citation Deaton, DNDo, YHolt, JJeune, MRKramer, HFLarkin, ALOrband-Miller, LAPeckham, GEPoole, CPrice, DJSchaller, LTShen, YShewchuk, LMStewart, ELStuart, JDThomson, SAWard, PWilson, JWXu, TGuss, JHMusetti, CRendina, ARAffleck, KAnders, DHancock, APHobbs, HHodgson, STHutchinson, JLeveridge, MVNicholls, HSmith, IEDSomers, DOSneddon, HFUddin, SCleasby, AMortenson, PNRichardson, CSaxty, G The discovery of quinoline-3-carboxamides as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors. Bioorg Med Chem27:1456-1478 (2019) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Hematopoietic prostaglandin D synthase
Name:Hematopoietic prostaglandin D synthase
Synonyms:GSTS | Glutathione-dependent PGD synthetase | Glutathione-requiring prostaglandin D synthase | H-PGDS | HPGDS | HPGDS_HUMAN | Hematopoietic prostaglandin D synthase | Hematopoietic prostaglandin D synthase (H-PGDS) | Hematopoietic prostaglandin D synthase (HPGDS) | PGDS | PTGDS2 | Prostaglandin D | Prostaglandin D Synthase
Type:Enzyme
Mol. Mass.:23341.07
Organism:Homo sapiens (Human)
Description:The protein was expressed in E. coli strain BL21(DE3) with an N-terminal 6-His tag.
Residue:199
Sequence:
MPNYKLTYFNMRGRAEIIRYIFAYLDIQYEDHRIEQADWPEIKSTLPFGKIPILEVDGLT
LHQSLAIARYLTKNTDLAGNTEMEQCHVDAIVDTLDDFMSCFPWAEKKQDVKEQMFNELL
TYNAPHLMQDLDTYLGGREWLIGNSVTWADFYWEICSTTLLVFKPDLLDNHPRLVTLRKK
VQAIPAVANWIKRRPQTKL
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  Blast E-value cutoff:
BDBM50526495
n/a
NameBDBM50526495
Synonyms:CHEMBL4452633
TypeSmall organic molecule
Emp. Form.C19H20N4O2S
Mol. Mass.368.453
SMILESCOc1ccc2cc(cnc2c1)C(=O)NC1CCN(CC1)c1nccs1
Structure
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