Reaction Details | |||
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Report a problem with these data | |||
Target | Apelin receptor | ||
Ligand | BDBM456597 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | GTPγS Binding | ||
EC50 | 3.20±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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BDBM456597 | |||
n/a | |||
Name | BDBM456597 | ||
Synonyms: | US10736883, Example 34.0 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H19FN6O5S | ||
Mol. Mass. | 474.465 | ||
SMILES | COc1cccc(OC)c1-n1c(NS(=O)(=O)CCc2ncc(F)cn2)nnc1-c1ccco1 |(-6.72,-.03,;-5.23,-.43,;-4.14,.66,;-4.54,2.15,;-3.45,3.24,;-1.97,2.84,;-1.57,1.35,;-.08,.95,;1.01,2.04,;-2.66,.26,;-2.15,-1.73,;-.82,-2.5,;.52,-1.73,;1.85,-2.5,;1.08,-3.83,;3.19,-3.27,;2.62,-1.17,;4.16,-1.17,;4.93,.17,;6.47,.17,;7.24,1.5,;6.47,2.83,;7.24,4.17,;4.93,2.83,;4.16,1.5,;-1.14,-4.01,;-2.67,-4.17,;-3.29,-2.76,;-4.78,-2.36,;-5.48,-.99,;-7,-1.23,;-7.24,-2.75,;-5.87,-3.45,)| | ||
Structure |