Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456606 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 25.0±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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BDBM456606 | |||
n/a | |||
Name | BDBM456606 | ||
Synonyms: | US10736883, Example 43.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C23H26N6O5S | ||
Mol. Mass. | 498.555 | ||
SMILES | COc1cccc(OC)c1-n1c(NS(=O)(=O)[C@@H](C)Cc2ccc(C)nn2)nnc1-c1ccc(C)o1 |r,wU:16.17,(-5.51,-7.22,;-4.03,-7.62,;-2.94,-6.53,;-3.34,-5.05,;-2.25,-3.96,;-.76,-4.36,;-.36,-5.84,;1.13,-6.24,;2.22,-5.15,;-1.45,-6.93,;-.81,-8.66,;.63,-9.21,;1.96,-8.44,;3.3,-9.21,;4.63,-9.98,;2.53,-10.55,;4.07,-7.88,;3.3,-6.54,;5.61,-7.88,;6.38,-6.54,;7.92,-6.54,;8.69,-5.21,;7.92,-3.88,;8.69,-2.54,;6.38,-3.88,;5.61,-5.21,;.55,-10.75,;-.94,-11.15,;-1.78,-9.86,;-3.27,-9.46,;-4.11,-8.17,;-5.59,-8.57,;-5.67,-10.1,;-7.01,-10.87,;-4.24,-10.65,)| | ||
Structure |