Reaction Details |
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Target | Proteinase-activated receptor 1 |
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Ligand | BDBM230743 |
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Substrate/Competitor | n/a |
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Meas. Tech. | FLIPR Assay |
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IC50 | 1.5±n/a nM |
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Citation | Mandal, M; Blizzard, TA; Chen, H; Chobanian, H; Guo, Y; Pio, B; Wu, Z; Biftu, T; Greenlee, WJ; Zhu, JZ Preparation and use of bicyclic himbacine derivatives as PAR-1 receptor antagonists US Patent US9340530 Publication Date 5/17/2016 |
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More Info.: | Get all data from this article, Assay Method |
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Proteinase-activated receptor 1 |
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Name: | Proteinase-activated receptor 1 |
Synonyms: | CF2R | Coagulation factor II receptor | F2R | PAR-1 | PAR1 | PAR1_HUMAN | Proteinase activated receptor 1 | Proteinase-activated receptor 1 (PAR-1) | TR | Thrombin receptor | Thrombin receptor/ Proteinase-activated receptor 1(Par-1) |
Type: | Protein |
Mol. Mass.: | 47450.07 |
Organism: | Homo sapiens (Human) |
Description: | P25116 |
Residue: | 425 |
Sequence: | MGPRRLLLVAACFSLCGPLLSARTRARRPESKATNATLDPRSFLLRNPNDKYEPFWEDEE
KNESGLTEYRLVSINKSSPLQKQLPAFISEDASGYLTSSWLTLFVPSVYTGVFVVSLPLN
IMAIVVFILKMKVKKPAVVYMLHLATADVLFVSVLPFKISYYFSGSDWQFGSELCRFVTA
AFYCNMYASILLMTVISIDRFLAVVYPMQSLSWRTLGRASFTCLAIWALAIAGVVPLLLK
EQTIQVPGLNITTCHDVLNETLLEGYYAYYFSAFSAVFFFVPLIISTVCYVSIIRCLSSS
AVANRSKKSRALFLSAAVFCIFIICFGPTNVLLIAHYSFLSHTSTTEAAYFAYLLCVCVS
SISCCIDPLIYYYASSECQRYVYSILCCKESSDPSSYNSSGQLMASKMDTCSSNLNNSIY
KKLLT
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BDBM230743 |
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n/a |
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Name | BDBM230743 |
Synonyms: | US9340530, 78 |
Type | Small organic molecule |
Emp. Form. | C24H23F2N3O |
Mol. Mass. | 407.4557 |
SMILES | C[C@H]1NC(=O)C2CC(F)(F)[C@@H](C)[C@H](\C=C\c3ccc(cn3)-c3ccccc3C#N)C12 |r| |
Structure |
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