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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | ||
| Ligand | BDBM50378642 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_610636 (CHEMBL1069650) | ||
| IC50 | 620±n/a nM | ||
| 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 | ||
| More Info.: | Get all data from this article, Assay Method | ||
| 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | |||
| 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: |
| ||
| BDBM50378642 | |||
| n/a | |||
| Name | BDBM50378642 | ||
| Synonyms: | CHEMBL599220 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C19H21NO5S | ||
| Mol. Mass. | 375.439 | ||
| SMILES | COC(=O)C1CCC(COc2ccc(C=C3SC(O)=NC3=O)cc2)CC1 |w:14.13,c:18,(-4.58,.16,;-4.58,.98,;-3.87,1.4,;-3.87,2.22,;-3.15,.98,;-2.44,1.4,;-1.72,.98,;-1.72,.16,;-1.01,-.25,;-.3,.16,;.42,-.25,;1.13,.16,;1.85,-.25,;1.85,-1.08,;2.56,-1.49,;3.28,-1.08,;3.36,-.26,;4.17,-.09,;4.51,.67,;4.58,-.8,;4.03,-1.41,;4.2,-2.22,;1.13,-1.49,;.42,-1.08,;-2.44,-.25,;-3.15,.16,)| | ||
| Structure | 
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