Reaction Details |
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Target | Cholecystokinin receptor type A |
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Ligand | BDBM50286896 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_50038 |
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IC50 | 433±n/a nM |
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Citation | Semple, G; Ryder, H; Kendrick, DA; Szelke, M; Ohta, M; Satoh, M; Nishida, A; Akuzawa, S; Miyata, K Synthesis and biological activity of 5-heteroaryl benzodiazepines: analogues of YM022 Bioorg Med Chem Lett6:55-58 (1996) Article |
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More Info.: | Get all data from this article, Assay Method |
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Cholecystokinin receptor type A |
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Name: | Cholecystokinin receptor type A |
Synonyms: | CCKAR_RAT | Cckar | Cholecystokinin peripheral | Cholecystokinin receptor | Cholecystokinin receptor type A |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 49676.37 |
Organism: | RAT |
Description: | Cholecystokinin central 0 RAT::P30551 |
Residue: | 444 |
Sequence: | MSHSPARQHLVESSRMDVVDSLLMNGSNITPPCELGLENETLFCLDQPQPSKEWQSALQI
LLYSIIFLLSVLGNTLVITVLIRNKRMRTVTNIFLLSLAVSDLMLCLFCMPFNLIPNLLK
DFIFGSAVCKTTTYFMGTSVSVSTFNLVAISLERYGAICRPLQSRVWQTKSHALKVIAAT
WCLSFTIMTPYPIYSNLVPFTKNNNQTANMCRFLLPSDAMQQSWQTFLLLILFLLPGIVM
VVAYGLISLELYQGIKFDASQKKSAKEKKPSTGSSTRYEDSDGCYLQKSRPPRKLELQQL
SSGSGGSRLNRIRSSSSAANLIAKKRVIRMLIVIVVLFFLCWMPIFSANAWRAYDTVSAE
KHLSGTPISFILLLSYTSSCVNPIIYCFMNKRFRLGFMATFPCCPNPGPPGVRGEVGEEE
DGRTIRALLSRYSYSHMSTSAPPP
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BDBM50286896 |
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n/a |
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Name | BDBM50286896 |
Synonyms: | 1-(3,3-Dimethyl-2-oxo-butyl)-5-thiazol-2-yl-3-[(m-tolylamino-methyl)-amino]-1,3-dihydro-benzo[e][1,4]diazepin-2-one | CHEMBL435447 |
Type | Small organic molecule |
Emp. Form. | C26H29N5O2S |
Mol. Mass. | 475.606 |
SMILES | Cc1cccc(NCNC2N=C(c3nccs3)c3ccccc3N(CC(=O)C(C)(C)C)C2=O)c1 |t:10| |
Structure |
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