Reaction Details |
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Target | Cholecystokinin receptor type A |
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Ligand | BDBM50185261 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_343639 (CHEMBL860998) |
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IC50 | 195±n/a nM |
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Citation | De Luca, S; Saviano, M; Lassiani, L; Yannakopoulou, K; Stefanidou, P; Aloj, L; Morelli, G; Varnavas, A Anthranilic acid based CCK1 receptor antagonists and CCK-8 have a common step in their"receptor desmodynamic processes". J Med Chem49:2456-62 (2006) [PubMed] 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: | CCK-A receptor | CCK-AR | CCK1-R | CCKAR | CCKAR_HUMAN | CCKRA | Cholecystokinin receptor | Cholecystokinin receptor type A | Cholecystokinin-1 Receptor |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 47859.34 |
Organism: | Homo sapiens (Human) |
Description: | Stable expression of human CCK-1 receptors in HEK 293 cells. |
Residue: | 428 |
Sequence: | MDVVDSLLVNGSNITPPCELGLENETLFCLDQPRPSKEWQPAVQILLYSLIFLLSVLGNT
LVITVLIRNKRMRTVTNIFLLSLAVSDLMLCLFCMPFNLIPNLLKDFIFGSAVCKTTTYF
MGTSVSVSTFNLVAISLERYGAICKPLQSRVWQTKSHALKVIAATWCLSFTIMTPYPIYS
NLVPFTKNNNQTANMCRFLLPNDVMQQSWHTFLLLILFLIPGIVMMVAYGLISLELYQGI
KFEASQKKSAKERKPSTTSSGKYEDSDGCYLQKTRPPRKLELRQLSTGSSSRANRIRSNS
SAANLMAKKRVIRMLIVIVVLFFLCWMPIFSANAWRAYDTASAERRLSGTPISFILLLSY
TSSCVNPIIYCFMNKRFRLGFMATFPCCPNPGPPGARGEVGEEEEGGTTGASLSRFSYSH
MSASVPPQ
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BDBM50185261 |
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n/a |
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Name | BDBM50185261 |
Synonyms: | 4-(3,4-dichlorobenzamido)-5-((3-methoxypropyl)(pentyl)amino)-5-oxopentanoic acid | CHEMBL206025 | LOXIGLUMIDE |
Type | Small organic molecule |
Emp. Form. | C21H30Cl2N2O5 |
Mol. Mass. | 461.379 |
SMILES | CCCCCN(CCCOC)C(=O)C(CCC(O)=O)NC(=O)c1ccc(Cl)c(Cl)c1 |
Structure |
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