| Reaction Details |
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 | Report a problem with these data |
| Target | Prostaglandin F2-alpha receptor |
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| Ligand | BDBM523442 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | In Vitro Test of Inhibition of Human FP Receptor Activity |
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| IC50 | 1.10±n/a nM |
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| Citation |  Beck, H; Kast, R; Meininghaus, M; Dietz, L; Fuerstner, C; Stellfeld, T; Anlauf, S; Von Buehler, C; Bairlein, M; Anlahr, J; Muenster, U; Terjung, C; Joerissen, H; Hauff, P; Mueller, J; Droebner, K; Nagel, J Substituted N-arylethyl-2-arylquinoline-4-carboxamides and use thereof US Patent US11136296 Publication Date 10/5/2021 |
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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 |
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| Synonyms: | PF2R_HUMAN | PGF receptor | PGF2 alpha receptor | PGF2-alpha receptor | PTGFR | Prostaglandin F | Prostanoid FP receptor |
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| Type: | Enzyme |
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| Mol. Mass.: | 40072.29 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P43088 |
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| Residue: | 359 |
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| Sequence: | MSMNNSKQLVSPAAALLSNTTCQTENRLSVFFSVIFMTVGILSNSLAIAILMKAYQRFRQ
KSKASFLLLASGLVITDFFGHLINGAIAVFVYASDKEWIRFDQSNVLCSIFGICMVFSGL
CPLLLGSVMAIERCIGVTKPIFHSTKITSKHVKMMLSGVCLFAVFIALLPILGHRDYKIQ
ASRTWCFYNTEDIKDWEDRFYLLLFSFLGLLALGVSLLCNAITGITLLRVKFKSQQHRQG
RSHHLEMVIQLLAIMCVSCICWSPFLVTMANIGINGNHSLETCETTLFALRMATWNQILD
PWVYILLRKAVLKNLYKLASQCCGVHVISLHIWELSSIKNSLKVAAISESPVAEKSAST
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| BDBM523442 |
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| n/a |
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| Name | BDBM523442 |
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| Synonyms: | US11136296, Example 173 | US11136296, Example 222 | US11136296, Example 250 |
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| Type | Small organic molecule |
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| Emp. Form. | C28H22BrClF2N2O3 |
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| Mol. Mass. | 587.84 |
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| SMILES | Cc1c(nc2ccc(Br)cc2c1C(=O)NC[C@H](CCC(O)=O)c1c(F)ccc(F)c1Cl)-c1ccccc1 |r| |
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| Structure | 
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