BDBM50313649 1-(1-(4-(5-(1-methyl-1H-tetrazol-5-yl)-3-phenylpyridin-2-yl)benzyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one::1-(1-{4-[5-(1-Methyl-1H-tetrazol-5-yl)-3-phenyl-pyridin-2-yl]-benzyl}-piperidin-4-yl)-1,3-dihydro-benzoimidazol-2-one::CHEMBL182101
SMILES: Cn1nnnc1-c1cnc(-c2ccc(CN3CCC(CC3)n3c4ccccc4[nH]c3=O)cc2)c(c1)-c1ccccc1
InChI Key: InChIKey=MAIWERCSNSCGHS-UHFFFAOYSA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50313649 (1-(1-(4-(5-(1-methyl-1H-tetrazol-5-yl)-3-phenylpyr...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 273 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Curated by ChEMBL | Assay Description Inhibition of Akt1 | J Med Chem 53: 1413-37 (2010) Article DOI: 10.1021/jm901132v BindingDB Entry DOI: 10.7270/Q2VD6ZK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Serine/threonine-protein kinase AKT2 (Homo sapiens (Human)) | BDBM50313649 (1-(1-(4-(5-(1-methyl-1H-tetrazol-5-yl)-3-phenylpyr...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 157 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Curated by ChEMBL | Assay Description Inhibition of Akt2 | J Med Chem 53: 1413-37 (2010) Article DOI: 10.1021/jm901132v BindingDB Entry DOI: 10.7270/Q2VD6ZK0 | |||||||||||
More data for this Ligand-Target Pair |