Reaction Details Report a problem with these data
Target
Cholecystokinin
Ligand
BDBM50334629
Substrate
n/a
Meas. Tech.
ChEMBL_698987 (CHEMBL1646091)
IC50
>100000±n/a nM
Citation
 Kumar, D; Reddy, VB; Kumar, A; Mandal, D; Tiwari, R; Parang, K Click chemistry inspired one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles and their Src kinase inhibitory activity. Bioorg Med Chem Lett 21:449-52 (2010) [PubMed]  Article 
Target
Name:
Cholecystokinin
Synonyms:
CCK | CCKN_HUMAN
Type:
Enzyme Catalytic Domain
Mol. Mass.:
12673.30
Organism:
Homo sapiens (Human)
Description:
Cholecystokinin 0 HUMAN::P06307
Residue:
115
Sequence:
MNSGVCLCVLMAVLAAGALTQPVPPADPAGSGLQRAEEAPRRQLRVSQRTDGESRAHLGALLARYIQQARKAPSGRMSIVKNLQNLDPSHRISDRDYMGWMDFGRRSAEEYEYPS
  
Inhibitor
Name:
BDBM50334629
Synonyms:
2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone | CHEMBL1642294
Type:
Small organic molecule
Emp. Form.:
C15H17N3O
Mol. Mass.:
255.315
SMILES:
Cc1ccc(cc1)-c1cn(nn1)C1CCCCC1=O
Structure:
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