BDBM50338873 CHEMBL1684800::N-(5-Amino-1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-5-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido)-2-methylbenzamide
SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
InChI Key InChIKey=ZJDFSKSBQBPOSK-UHFFFAOYSA-N
Data 20 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 20 hits for monomerid = 50338873
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Human)
Hanyang University
Curated by ChEMBL
Hanyang University
Curated by ChEMBL
Affinity DataIC50: 2.13nMAssay Description:Inhibition of CDK2/cyclin EMore data for this Ligand-Target Pair
Affinity DataIC50: >2.00E+4nMAssay Description:inhibition of JNK3More data for this Ligand-Target Pair
Affinity DataIC50: 2.73nMAssay Description:inhibition of GSK3-betaMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 1/G2/mitotic-specific cyclin-B1/G2/mitotic-specific cyclin-B2/G2/mitotic-specific cyclin-B3(Human)
Hanyang University
Curated by ChEMBL
Hanyang University
Curated by ChEMBL
Affinity DataIC50: 3.20nMAssay Description:Inhibition of CDK1/cyclin BMore data for this Ligand-Target Pair
TargetDual specificity mitogen-activated protein kinase kinase 1(Human)
Hanyang University
Curated by ChEMBL
Hanyang University
Curated by ChEMBL
Affinity DataIC50: 51.6nMAssay Description:inhibition of IGF-1RMore data for this Ligand-Target Pair
Affinity DataIC50: 107nMAssay Description:Inhibition of C-Raf assessed as [33P]gamma-ATP incorporation into substrate after 40 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataIC50: 1.59E+3nMAssay Description:inhibition of JNK1a1 at 10 uMMore data for this Ligand-Target Pair
Affinity DataIC50: 3.02E+3nMAssay Description:inhibition of mTORMore data for this Ligand-Target Pair
Affinity DataIC50: 1.14E+4nMAssay Description:Inhibition of ERK2More data for this Ligand-Target Pair