Reaction Details |
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Target | Prostaglandin E2 receptor EP4 subtype |
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Ligand | BDBM285483 |
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Substrate/Competitor | n/a |
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Meas. Tech. | EP4 Antagonistic Activity Measurement |
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Temperature | 298.15±n/a K |
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IC50 | 2.70±n/a nM |
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Comments | extracted |
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Citation | Asada, M; Tani, K; Hirobe, M; Higuchi, S; Fuchibe, K; Oikawa, R; Kotani, T; Takano, H Tricyclic spiro compound US Patent US10077247 Publication Date 9/18/2018 |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin E2 receptor EP4 subtype |
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Name: | Prostaglandin E2 receptor EP4 subtype |
Synonyms: | PE2R4_HUMAN | PGE receptor EP4 subtype | PGE2 receptor EP4 subtype | PTGER2 | PTGER4 | Prostaglandin E2 receptor | Prostanoid EP4 receptor |
Type: | Enzyme |
Mol. Mass.: | 53134.53 |
Organism: | Homo sapiens (Human) |
Description: | P35408 |
Residue: | 488 |
Sequence: | MSTPGVNSSASLSPDRLNSPVTIPAVMFIFGVVGNLVAIVVLCKSRKEQKETTFYTLVCG
LAVTDLLGTLLVSPVTIATYMKGQWPGGQPLCEYSTFILLFFSLSGLSIICAMSVERYLA
INHAYFYSHYVDKRLAGLTLFAVYASNVLFCALPNMGLGSSRLQYPDTWCFIDWTTNVTA
HAAYSYMYAGFSSFLILATVLCNVLVCGALLRMHRQFMRRTSLGTEQHHAAAAASVASRG
HPAASPALPRLSDFRRRRSFRRIAGAEIQMVILLIATSLVVLICSIPLVVRVFVNQLYQP
SLEREVSKNPDLQAIRIASVNPILDPWIYILLRKTVLSKAIEKIKCLFCRIGGSRRERSG
QHCSDSQRTSSAMSGHSRSFISRELKEISSTSQTLLPDLSLPDLSENGLGGRNLLPGVPG
MGLAQEDTTSLRTLRISETSDSSQGQDSESVLLVDEAGGSGRAGPAPKGSSLQVTFPSET
LNLSEKCI
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BDBM285483 |
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n/a |
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Name | BDBM285483 |
Synonyms: | 4-[4-Cyano-2-({[(2′R,4S)-6-(5-methyl-1,3,4-oxadiazol-2-yl)-2,3-dihydrospiro[chromene-4,1′-cyclopropan]-2′-yl]carbonyl}amino)phenyl]butanoic acid | US10077247, Example 3 |
Type | Small organic molecule |
Emp. Form. | C26H24N4O5 |
Mol. Mass. | 472.4926 |
SMILES | Cc1nnc(o1)-c1ccc2OCC[C@]3(C[C@H]3C(=O)Nc3cc(ccc3CCCC(O)=O)C#N)c2c1 |r| |
Structure |
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