Reaction Details |
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Target | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] |
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Ligand | BDBM50378618 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_610636 (CHEMBL1069650) |
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IC50 | 274±n/a nM |
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Citation | Wu, Y; Tai, HH; Cho, H Synthesis and SAR of thiazolidinedione derivatives as 15-PGDH inhibitors. Bioorg Med Chem18:1428-33 (2010) [PubMed] Article |
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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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BDBM50378618 |
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n/a |
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Name | BDBM50378618 |
Synonyms: | CHEMBL599407 | US8637558, 5 |
Type | Small organic molecule |
Emp. Form. | C16H18N2O5S2 |
Mol. Mass. | 382.455 |
SMILES | OC1=NC(=O)C(S1)=Cc1ccc(OCCN2CCS(=O)(=O)CC2)cc1 |w:7.8,t:1| |
Structure |
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