Reaction Details |
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Target | Prostaglandin F2-alpha receptor |
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Ligand | BDBM50547366 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2017943 (CHEMBL4671521) |
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IC50 | <1.000000±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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BDBM50547366 |
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n/a |
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Name | BDBM50547366 |
Synonyms: | CHEMBL4761725 |
Type | Small organic molecule |
Emp. Form. | C27H25BrN2O2 |
Mol. Mass. | 489.404 |
SMILES | COc1ccccc1C(C)CNC(=O)c1c(C)c(nc2ccc(Br)cc12)-c1ccccc1 |
Structure |
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