BDBM50378212 CHEMBL575450

SMILES: CC(C)n1cnc2c(NCc3ccc(cc3)-c3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc12

InChI Key: InChIKey=OQBHUKNHTKIHKA-YHBQERECSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50378212   

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
CDK2/Cyclin E/G1/S-specific cyclin E2 (Homo sapiens (Human))	BDBM50378212 (CHEMBL575450) Show SMILES CC(C)n1cnc2c(NCc3ccc(cc3)-c3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc12 |r,wU:25.26,wD:28.30,(15.79,-2.71,;16.81,-1.56,;18.32,-1.86,;16.32,-.1,;17.21,1.15,;16.3,2.39,;14.84,1.9,;13.51,2.66,;13.5,4.2,;12.16,4.96,;10.83,4.19,;10.84,2.64,;9.51,1.87,;8.17,2.64,;8.16,4.17,;9.49,4.95,;6.85,1.87,;5.51,2.63,;4.18,1.86,;4.18,.31,;5.51,-.46,;6.85,.32,;12.18,1.88,;12.18,.35,;10.85,-.43,;10.86,-1.97,;12.19,-2.73,;12.19,-4.28,;10.86,-5.05,;10.86,-6.59,;9.52,-4.28,;9.52,-2.74,;13.52,-.42,;14.85,.37,)| Show InChI InChI=1S/C27H33N7/c1-18(2)34-17-30-24-25(32-27(33-26(24)34)31-23-14-12-22(28)13-15-23)29-16-19-8-10-21(11-9-19)20-6-4-3-5-7-20/h3-11,17-18,22-23H,12-16,28H2,1-2H3,(H2,29,31,32,33)/t22-,23-	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.100	n/a	n/a	n/a	n/a	n/a	n/a
AMRI Curated by ChEMBL					Assay Description Inhibition of Cdk2/cyclinE				Bioorg Med Chem Lett 19: 6613-7 (2009) Article DOI: 10.1016/j.bmcl.2009.10.011 BindingDB Entry DOI: 10.7270/Q2M32WPQ
					More data for this Ligand-Target Pair
CDK2/Cyclin A/Cyclin A1 (Homo sapiens (Human))	BDBM50378212 (CHEMBL575450) Show SMILES CC(C)n1cnc2c(NCc3ccc(cc3)-c3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc12 |r,wU:25.26,wD:28.30,(15.79,-2.71,;16.81,-1.56,;18.32,-1.86,;16.32,-.1,;17.21,1.15,;16.3,2.39,;14.84,1.9,;13.51,2.66,;13.5,4.2,;12.16,4.96,;10.83,4.19,;10.84,2.64,;9.51,1.87,;8.17,2.64,;8.16,4.17,;9.49,4.95,;6.85,1.87,;5.51,2.63,;4.18,1.86,;4.18,.31,;5.51,-.46,;6.85,.32,;12.18,1.88,;12.18,.35,;10.85,-.43,;10.86,-1.97,;12.19,-2.73,;12.19,-4.28,;10.86,-5.05,;10.86,-6.59,;9.52,-4.28,;9.52,-2.74,;13.52,-.42,;14.85,.37,)| Show InChI InChI=1S/C27H33N7/c1-18(2)34-17-30-24-25(32-27(33-26(24)34)31-23-14-12-22(28)13-15-23)29-16-19-8-10-21(11-9-19)20-6-4-3-5-7-20/h3-11,17-18,22-23H,12-16,28H2,1-2H3,(H2,29,31,32,33)/t22-,23-	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
AMRI Curated by ChEMBL					Assay Description Inhibition of recombinant CDK2/cyclin A				Bioorg Med Chem Lett 19: 6608-12 (2009) Article DOI: 10.1016/j.bmcl.2009.10.025 BindingDB Entry DOI: 10.7270/Q2445NFT
					More data for this Ligand-Target Pair
CDK2/Cyclin E/G1/S-specific cyclin E2 (Homo sapiens (Human))	BDBM50378212 (CHEMBL575450) Show SMILES CC(C)n1cnc2c(NCc3ccc(cc3)-c3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc12 |r,wU:25.26,wD:28.30,(15.79,-2.71,;16.81,-1.56,;18.32,-1.86,;16.32,-.1,;17.21,1.15,;16.3,2.39,;14.84,1.9,;13.51,2.66,;13.5,4.2,;12.16,4.96,;10.83,4.19,;10.84,2.64,;9.51,1.87,;8.17,2.64,;8.16,4.17,;9.49,4.95,;6.85,1.87,;5.51,2.63,;4.18,1.86,;4.18,.31,;5.51,-.46,;6.85,.32,;12.18,1.88,;12.18,.35,;10.85,-.43,;10.86,-1.97,;12.19,-2.73,;12.19,-4.28,;10.86,-5.05,;10.86,-6.59,;9.52,-4.28,;9.52,-2.74,;13.52,-.42,;14.85,.37,)| Show InChI InChI=1S/C27H33N7/c1-18(2)34-17-30-24-25(32-27(33-26(24)34)31-23-14-12-22(28)13-15-23)29-16-19-8-10-21(11-9-19)20-6-4-3-5-7-20/h3-11,17-18,22-23H,12-16,28H2,1-2H3,(H2,29,31,32,33)/t22-,23-	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
AMRI Curated by ChEMBL					Assay Description Inhibition of recombinant CDK2/cyclin E				Bioorg Med Chem Lett 19: 6608-12 (2009) Article DOI: 10.1016/j.bmcl.2009.10.025 BindingDB Entry DOI: 10.7270/Q2445NFT
					More data for this Ligand-Target Pair
CDK2/Cyclin A/Cyclin A1 (Homo sapiens (Human))	BDBM50378212 (CHEMBL575450) Show SMILES CC(C)n1cnc2c(NCc3ccc(cc3)-c3ccccc3)nc(N[C@H]3CC[C@H](N)CC3)nc12 |r,wU:25.26,wD:28.30,(15.79,-2.71,;16.81,-1.56,;18.32,-1.86,;16.32,-.1,;17.21,1.15,;16.3,2.39,;14.84,1.9,;13.51,2.66,;13.5,4.2,;12.16,4.96,;10.83,4.19,;10.84,2.64,;9.51,1.87,;8.17,2.64,;8.16,4.17,;9.49,4.95,;6.85,1.87,;5.51,2.63,;4.18,1.86,;4.18,.31,;5.51,-.46,;6.85,.32,;12.18,1.88,;12.18,.35,;10.85,-.43,;10.86,-1.97,;12.19,-2.73,;12.19,-4.28,;10.86,-5.05,;10.86,-6.59,;9.52,-4.28,;9.52,-2.74,;13.52,-.42,;14.85,.37,)| Show InChI InChI=1S/C27H33N7/c1-18(2)34-17-30-24-25(32-27(33-26(24)34)31-23-14-12-22(28)13-15-23)29-16-19-8-10-21(11-9-19)20-6-4-3-5-7-20/h3-11,17-18,22-23H,12-16,28H2,1-2H3,(H2,29,31,32,33)/t22-,23-	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
AMRI Curated by ChEMBL					Assay Description Inhibition of recombinant Cdk2/cyclinA				Bioorg Med Chem Lett 19: 6613-7 (2009) Article DOI: 10.1016/j.bmcl.2009.10.011 BindingDB Entry DOI: 10.7270/Q2M32WPQ
					More data for this Ligand-Target Pair