Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456600 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 3.60±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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BDBM456600 | |||
n/a | |||
Name | BDBM456600 | ||
Synonyms: | US10736883, Example 37.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C21H21ClN6O5S | ||
Mol. Mass. | 504.947 | ||
SMILES | COc1cccc(OC)c1-n1c(NS(=O)(=O)[C@@H](C)Cc2ncc(Cl)cn2)nnc1-c1ccco1 |r,wU:16.17,(-6.29,-7.06,;-4.8,-7.45,;-3.71,-6.36,;-4.11,-4.88,;-3.02,-3.79,;-1.53,-4.19,;-1.14,-5.67,;.35,-6.07,;1.44,-4.98,;-2.23,-6.76,;-1.59,-8.49,;-.15,-9.04,;1.19,-8.27,;2.52,-9.04,;3.85,-9.81,;1.75,-10.38,;3.29,-7.71,;2.52,-6.38,;4.83,-7.71,;5.6,-6.38,;7.14,-6.38,;7.91,-5.04,;7.14,-3.71,;7.91,-2.37,;5.6,-3.71,;4.83,-5.04,;-.23,-10.58,;-1.72,-10.98,;-2.56,-9.69,;-4.04,-9.29,;-4.88,-8,;-6.37,-8.4,;-6.45,-9.93,;-5.01,-10.49,)| | ||
Structure |