Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456571 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 28.0±n/a nM | ||
Citation | Brown, M; Chen, N; Chen, X; Chen, Y; Cheng, AC; Connors, RV; Deignan, J; Dransfield, PJ; Du, X; Fu, Z; Harvey, JS; Heath, JA; Heumann, LV; Houze, J; Kayser, F; Khakoo, AY; Kopecky, D; Lai, S; Ma, Z; Medina, JC; Mihalic, JT; Olson, SH; Pattaropong, V; Swaminath, G; Wang, X; Wanska, M; Yeh, W Triazole furan compounds as agonists of the APJ receptor US Patent US10736883 Publication Date 8/11/2020 | ||
More Info.: | Get all data from this article, Assay Method | ||
Apelin receptor | |||
Name: | Apelin receptor | ||
Synonyms: | AGTRL1 | APJ | APJ_HUMAN | APLNR | Angiotensin receptor-like 1 | Apelin receptor | Apelin receptor (APJ) | G-protein coupled receptor APJ | G-protein coupled receptor HG11 | ||
Type: | Enzyme Catalytic Domain | ||
Mol. Mass.: | 42664.06 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P35414 | ||
Residue: | 380 | ||
Sequence: |
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BDBM456571 | |||
n/a | |||
Name | BDBM456571 | ||
Synonyms: | US10736883, Example 8.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C23H22FN7O5S | ||
Mol. Mass. | 527.528 | ||
SMILES | COc1cccc(OC)c1-n1c(NS(=O)(=O)[C@@H](C)Cc2ncc(F)c3[nH]cnc23)nnc1-c1ccco1 |r,wU:16.17,(-7.89,9.28,;-6.56,8.51,;-5.22,9.28,;-5.22,10.82,;-3.89,11.59,;-2.56,10.82,;-2.56,9.28,;-1.22,8.51,;.11,9.28,;-3.89,8.51,;-3.89,6.97,;-2.64,6.07,;-1.18,6.54,;-.09,5.45,;.68,4.12,;-.86,4.12,;1.24,6.22,;1.24,7.76,;2.58,5.45,;3.91,6.22,;3.91,7.76,;5.24,8.53,;6.58,7.76,;7.91,8.53,;6.58,6.22,;7.72,5.19,;7.1,3.79,;5.56,3.95,;5.24,5.45,;-3.12,4.6,;-4.66,4.6,;-5.14,6.07,;-6.6,6.54,;-7.08,8.01,;-8.62,8.01,;-9.09,6.54,;-7.85,5.64,)| | ||
Structure |