Reaction Details | |||
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Target | 5-hydroxytryptamine receptor 5A | ||
Ligand | BDBM135782 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Binding Inhibition Assay | ||
pH | 7.5±n/a | ||
Temperature | 298.15±n/a K | ||
Ki | 1.6±n/a nM | ||
Comments | extracted | ||
Citation | Kinoyama, I; Miyazaki, T; Koganemaru, Y; Washio, T; Hamaguchi, W Nitrogenous-ring acylguanidine derivative US Patent US8853242 Publication Date 10/7/2014 | ||
More Info.: | Get all data from this article, Assay Method | ||
5-hydroxytryptamine receptor 5A | |||
Name: | 5-hydroxytryptamine receptor 5A | ||
Synonyms: | 5-HT-5 | 5-HT-5A | 5-hydroxytryptamine receptor 5 (5-HT5) | 5-hydroxytryptamine receptor 5A (5-HT5A) | 5HT5A_HUMAN | HTR5A | Serotonin (5-HT) receptor | Serotonin receptor 5A | ||
Type: | Enzyme | ||
Mol. Mass.: | 40266.25 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P47898 | ||
Residue: | 357 | ||
Sequence: |
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BDBM135782 | |||
n/a | |||
Name | BDBM135782 | ||
Synonyms: | US8853242, 147 | ||
Type | Small organic molecule | ||
Emp. Form. | C17H11ClF2N4O | ||
Mol. Mass. | 360.745 | ||
SMILES | NC(N)=NC(=O)c1ccc2c(F)cnc(-c3c(F)cccc3Cl)c2c1 |(6,-.77,;4.67,,;4.67,1.54,;3.33,-.77,;2,,;2,1.54,;.67,-.77,;.67,-2.31,;-.67,-3.08,;-2,-2.31,;-3.33,-3.08,;-3.33,-4.62,;-4.67,-2.31,;-4.67,-.77,;-3.33,,;-3.33,1.54,;-2,2.31,;-.67,1.54,;-2,3.85,;-3.33,4.62,;-4.67,3.85,;-4.67,2.31,;-6,1.54,;-2,-.77,;-.67,,)| | ||
Structure |