Reaction Details |
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Target | Prostaglandin F2-alpha receptor |
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Ligand | BDBM520770 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2017950 (CHEMBL4671528) |
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IC50 | 0.830±n/a nM |
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Citation | Beck, H; Thaler, T; Meibom, D; Meininghaus, M; Jörißen, H; Dietz, L; Terjung, C; Bairlein, M; von Bühler, CJ; Anlauf, S; Fürstner, C; Stellfeld, T; Schneider, D; Gericke, KM; Buyck, T; Lovis, K; Münster, U; Anlahr, J; Kersten, E; Levilain, G; Marossek, V; Kast, R Potent and Selective Human Prostaglandin F (FP) Receptor Antagonist (BAY-6672) for the Treatment of Idiopathic Pulmonary Fibrosis (IPF). J Med Chem63:11639-11662 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin F2-alpha receptor |
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Name: | Prostaglandin F2-alpha receptor |
Synonyms: | PF2R_HUMAN | PGF receptor | PGF2 alpha receptor | PGF2-alpha receptor | PTGFR | Prostaglandin F | Prostanoid FP receptor |
Type: | Enzyme |
Mol. Mass.: | 40072.29 |
Organism: | Homo sapiens (Human) |
Description: | P43088 |
Residue: | 359 |
Sequence: | MSMNNSKQLVSPAAALLSNTTCQTENRLSVFFSVIFMTVGILSNSLAIAILMKAYQRFRQ
KSKASFLLLASGLVITDFFGHLINGAIAVFVYASDKEWIRFDQSNVLCSIFGICMVFSGL
CPLLLGSVMAIERCIGVTKPIFHSTKITSKHVKMMLSGVCLFAVFIALLPILGHRDYKIQ
ASRTWCFYNTEDIKDWEDRFYLLLFSFLGLLALGVSLLCNAITGITLLRVKFKSQQHRQG
RSHHLEMVIQLLAIMCVSCICWSPFLVTMANIGINGNHSLETCETTLFALRMATWNQILD
PWVYILLRKAVLKNLYKLASQCCGVHVISLHIWELSSIKNSLKVAAISESPVAEKSAST
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BDBM520770 |
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n/a |
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Name | BDBM520770 |
Synonyms: | (+/−)-5-[({6-Bromo-2-[3-ethylpiperidin-1-yl]-3-methylquinolin-4-yl}carbonyl)amino]-4-(2-chlorophenyl)pentanoic acid (Diastereomer Mixture) | US11149018, Example 57 |
Type | Small organic molecule |
Emp. Form. | C29H33BrClN3O3 |
Mol. Mass. | 586.948 |
SMILES | CCC1CCCN(C1)c1nc2ccc(Br)cc2c(C(=O)NCC(CCC(O)=O)c2ccccc2Cl)c1C |
Structure |
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