Reaction Details Report a problem with these data
Target
Cholecystokinin receptor type A
Ligand
BDBM50289201
Substrate
n/a
Meas. Tech.
ChEBML_50052
IC50
>10000±n/a nM
Citation
 González-Muñiz, R; Domínguez, Ms; Martín-Martínez, M; Herranz, R; García-López, Ms; Barber, A; Ballaz, S; Río, JD CCK-4 restricted analogues containing a 3-oxoindolizidine skeleton Bioorg Med Chem Lett 6:967-972 (1996)    Article 
Target
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:
MSHSPARQHLVESSRMDVVDSLLMNGSNITPPCELGLENETLFCLDQPQPSKEWQSALQILLYSIIFLLSVLGNTLVITVLIRNKRMRTVTNIFLLSLAVSDLMLCLFCMPFNLIPNLLKDFIFGSAVCKTTTYFMGTSVSVSTFNLVAISLERYGAICRPLQSRVWQTKSHALKVIAATWCLSFTIMTPYPIYSNLVPFTKNNNQTANMCRFLLPSDAMQQSWQTFLLLILFLLPGIVMVVAYGLISLELYQGIKFDASQKKSAKEKKPSTGSSTRYEDSDGCYLQKSRPPRKLELQQLSSGSGGSRLNRIRSSSSAANLIAKKRVIRMLIVIVVLFFLCWMPIFSANAWRAYDTVSAEKHLSGTPISFILLLSYTSSCVNPIIYCFMNKRFRLGFMATFPCCPNPGPPGVRGEVGEEEDGRTIRALLSRYSYSHMSTSAPPP
  
Inhibitor
Name:
BDBM50289201
Synonyms:
CHEMBL427492 | [(R)-1-((2S,8S,8aR)-2-Benzyl-2-carbamoyl-3-oxo-octahydro-indolizin-8-ylcarbamoyl)-2-(1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester
Type:
Small organic molecule
Emp. Form.:
C32H39N5O5
Mol. Mass.:
573.6826
SMILES:
CC(C)(C)OC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H]1CCCN2[C@@H]1C[C@@](Cc1ccccc1)(C(N)=O)C2=O
Structure:
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