Reaction Details |
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Target | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] |
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Ligand | BDBM50438423 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibition Assay |
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pH | 7.5±n/a |
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IC50 | 84.1±n/a nM |
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Comments | extracted |
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Citation | Cho, H; Wu, Y; Choi, C Thiazolidinedione derivative and use thereof US Patent US8637558 Publication Date 1/28/2014 |
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More Info.: | Get all data from this article, Assay Method |
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15-hydroxyprostaglandin dehydrogenase [NAD(+)] |
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Name: | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] |
Synonyms: | 15-PGDH | 15-hydroxyprostaglandin dehydrogenase [NAD+] | HPGD | PGDH1 | PGDH_HUMAN | Prostaglandin dehydrogenase 1 (15-PGDH) | SDR36C1 |
Type: | Enzyme |
Mol. Mass.: | 28974.46 |
Organism: | Homo sapiens (Human) |
Description: | P15428 |
Residue: | 266 |
Sequence: | MHVNGKVALVTGAAQGIGRAFAEALLLKGAKVALVDWNLEAGVQCKAALDEQFEPQKTLF
IQCDVADQQQLRDTFRKVVDHFGRLDILVNNAGVNNEKNWEKTLQINLVSVISGTYLGLD
YMSKQNGGEGGIIINMSSLAGLMPVAQQPVYCASKHGIVGFTRSAALAANLMNSGVRLNA
ICPGFVNTAILESIEKEENMGQYIEYKDHIKDMIKYYGILDPPLIANGLITLIEDDALNG
AIMKITTSKGIHFQDYDTTPFQAKTQ
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BDBM50438423 |
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n/a |
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Name | BDBM50438423 |
Synonyms: | CHEMBL2414140 | US8637558, 101 |
Type | Small organic molecule |
Emp. Form. | C16H12ClNO3S2 |
Mol. Mass. | 365.854 |
SMILES | OC1=NC(=O)C(S1)=Cc1ccc(OCCc2cccs2)c(Cl)c1 |w:7.8,t:1| |
Structure |
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