Reaction Details Report a problem with these data
Target
Cholecystokinin receptor type A
Ligand
BDBM50008005
Substrate
n/a
Meas. Tech.
ChEMBL_49714 (CHEMBL661791)
IC50
15±n/a nM
Citation
 Shiosaki, K; Lin, CW; Kopecka, H; Bianchi, B; Miller, T; Stashko, M; Witte, D Minor structural differences in Boc-CCK-4 derivatives dictate affinity and selectivity for CCK-A and CCK-B receptors. J Med Chem 40:1169-72 (1997) [PubMed]  Article 
Target
Name:
Cholecystokinin receptor type A
Synonyms:
CCK-A receptor | CCK-AR | CCK1-R | CCKAR | CCKAR_CAVPO | Cholecystokinin A receptor | Cholecystokinin receptor type A | Cholecystokinin-1 receptor
Type:
n/a
Mol. Mass.:
48229.77
Organism:
Cavia porcellus
Description:
n/a
Residue:
430
Sequence:
MDVVDSLFVNGSNITSACELGFENETLFCLDRPRPSKEWQPAVQILLYSLIFLLSVLGNTLVITVLIRNKRMRTVTNIFLLSLAVSDLMLCLFCMPFNLIPSLLKDFIFGSAVCKTTTYFMGTSVSVSTFNLVAISLERYGAICKPLQSRVWQTKSHALKVIAATWCLSFTIMTPYPIYSNLVPFTKNNNQTGNMCRFLLPNDVMQQTWHTFLLLILFLIPGIVMMVAYGLISLELYQGIKFDAIQKKSAKERKTSTGSSGPMEDSDGCYLQKSRHPRKLELRQLSPSSSGSNRINRIRSSSSTANLMAKKRVIRMLIVIVVLFFLCWMPIFSANAWRAYDTVSAERHLSGTPISFILLLSYTSSCVNPIIYCFMNKRFRLGFMATFPCCPNPGTPGVRGEMGEEEEGRTTGASLSRYSYSHMSTSAPPP
  
Inhibitor
Name:
BDBM50008005
Synonyms:
3-(3-{(S)-5-[2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-5-[1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-carboxy-ethylcarbamoyl]-pentyl}-ureido)-benzoic acid methyl ester | 3-(3-{5-[2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-5-[1-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-2-carboxy-ethylcarbamoyl]-pentyl}-ureido)-benzoic acid methyl ester | CHEMBL17284
Type:
Small organic molecule
Emp. Form.:
C44H54N8O11
Mol. Mass.:
870.9466
SMILES:
COC(=O)c1cccc(NC(=O)NCCCC[C@H](NC(=O)C(Cc2c[nH]c3ccccc23)NC(=O)OC(C)(C)C)C(=O)NC(CC(O)=O)C(=O)NC(Cc2ccccc2)C(N)=O)c1
Structure:
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