Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456605 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 12.0±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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BDBM456605 | |||
n/a | |||
Name | BDBM456605 | ||
Synonyms: | US10736883, Example 42.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C22H24N6O5S | ||
Mol. Mass. | 484.528 | ||
SMILES | COc1cccc(OC)c1-n1c(NS(=O)(=O)[C@@H](C)Cc2ccc(C)nn2)nnc1-c1ccco1 |r,wU:16.17,(-6.18,-7.22,;-4.69,-7.62,;-3.6,-6.53,;-4,-5.05,;-2.91,-3.96,;-1.43,-4.36,;-1.03,-5.84,;.46,-6.24,;1.55,-5.15,;-2.12,-6.93,;-1.48,-8.66,;-.04,-9.21,;1.29,-8.44,;2.63,-9.21,;3.96,-9.98,;1.86,-10.55,;3.4,-7.88,;2.63,-6.54,;4.94,-7.88,;5.71,-6.54,;7.25,-6.54,;8.02,-5.21,;7.25,-3.88,;8.02,-2.54,;5.71,-3.88,;4.94,-5.21,;-.12,-10.75,;-1.61,-11.15,;-2.45,-9.86,;-3.93,-9.46,;-4.77,-8.17,;-6.26,-8.57,;-6.34,-10.1,;-4.9,-10.65,)| | ||
Structure |