Reaction Details |
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Target | Prostaglandin E synthase |
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Ligand | BDBM50460533 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1769747 (CHEMBL4221859) |
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IC50 | 4.9±n/a nM |
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Citation | Muthukaman, N; Deshmukh, S; Tambe, M; Pisal, D; Tondlekar, S; Shaikh, M; Sarode, N; Kattige, VG; Sawant, P; Pisat, M; Karande, V; Honnegowda, S; Kulkarni, A; Behera, D; Jadhav, SB; Sangana, RR; Gudi, GS; Khairatkar-Joshi, N; Gharat, LA Alleviating CYP and hERG liabilities by structure optimization of dihydrofuran-fused tricyclic benzo[d]imidazole series - Potent, selective and orally efficacious microsomal prostaglandin E synthase-1 (mPGES-1) inhibitors: Part-2. Bioorg Med Chem Lett28:1211-1218 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin E synthase |
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Name: | Prostaglandin E synthase |
Synonyms: | MGST1L1 | MPGES1 | PGES | PIG12 | PTGES | PTGES_HUMAN | Prostaglandin E synthase (PGES-1) | Prostaglandin E synthase 1 (mPGES-1) | Prostaglandin E synthase-1 (PGES-1) | Prostaglandin E synthase/G/H synthase 2 | Prostaglandin E2 synthase-1 ( mPGES-1) |
Type: | Protein |
Mol. Mass.: | 17112.22 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 152 |
Sequence: | MPAHSLVMSSPALPAFLLCSTLLVIKMYVVAIITGQVRLRKKAFANPEDALRHGGPQYCR
SDPDVERCLRAHRNDMETIYPFLFLGFVYSFLGPNPFVAWMHFLVFLVGRVAHTVAYLGK
LRAPIRSVTYTLAQLPCASMALQILWEAARHL
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BDBM50460533 |
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n/a |
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Name | BDBM50460533 |
Synonyms: | CHEMBL4225008 |
Type | Small organic molecule |
Emp. Form. | C25H19Cl2F3N4O2 |
Mol. Mass. | 535.345 |
SMILES | CC1(C)Cc2c(O1)c(cc1nc(Nc3c(Cl)cccc3Cl)[nH]c21)C(=O)Nc1ccccc1C(F)(F)F |
Structure |
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