Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456669 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 0.056±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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BDBM456669 | |||
n/a | |||
Name | BDBM456669 | ||
Synonyms: | US10736883, Example 116.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C23H25FN6O6S | ||
Mol. Mass. | 532.545 | ||
SMILES | CO[C@@H]([C@H](C)S(=O)(=O)Nc1nnc(-c2ccc(C)o2)n1-c1c(OC)cccc1OC)c1ncc(F)cn1 |r,wU:3.3,2.1,(5.36,-4.06,;4.02,-3.29,;4.02,-1.75,;2.69,-.98,;2.69,.56,;1.35,-1.75,;.58,-3.09,;2.12,-3.09,;.02,-.98,;-1.44,-1.46,;-1.92,-2.93,;-3.46,-2.93,;-3.94,-1.46,;-5.4,-.98,;-5.88,.48,;-7.42,.48,;-7.89,-.98,;-9.36,-1.46,;-6.65,-1.89,;-2.69,-.56,;-2.69,.98,;-4.02,1.75,;-5.36,.98,;-6.69,1.75,;-4.02,3.29,;-2.69,4.06,;-1.36,3.29,;-1.36,1.75,;-.02,.98,;1.31,1.75,;5.36,-.98,;6.69,-1.75,;8.02,-.98,;8.02,.56,;9.36,1.33,;6.69,1.33,;5.36,.56,)| | ||
Structure |