Compile Data Set for Download or QSAR

Found 60 hits Enz. Inhib. hit(s) with all data for entry = 50015210   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583918 (CHEMBL4791134) Show SMILES CS(=O)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583916 (CHEMBL4786320) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	21	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50526790 (CHEMBL4555799) Show SMILES Clc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C17H18ClN5/c18-14-10-21-17(22-11-4-3-7-19-8-11)23-16(14)13-9-20-15-6-2-1-5-12(13)15/h1-2,5-6,9-11,19-20H,3-4,7-8H2,(H,21,22,23)/t11-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583916 (CHEMBL4786320) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50526790 (CHEMBL4555799) Show SMILES Clc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C17H18ClN5/c18-14-10-21-17(22-11-4-3-7-19-8-11)23-16(14)13-9-20-15-6-2-1-5-12(13)15/h1-2,5-6,9-11,19-20H,3-4,7-8H2,(H,21,22,23)/t11-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583918 (CHEMBL4791134) Show SMILES CS(=O)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583925 (CHEMBL4782954) Show SMILES CS(=O)(=O)c1c(ccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F)C#N |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	33	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583922 (CHEMBL4786555) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583922 (CHEMBL4786555) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583916 (CHEMBL4786320) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	42	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583922 (CHEMBL4786555) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	52	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583925 (CHEMBL4782954) Show SMILES CS(=O)(=O)c1c(ccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F)C#N |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583919 (CHEMBL5083688) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2cc(ccc12)C#N |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583921 (CHEMBL4779443) Show SMILES CS(=O)(=O)c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	69	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583920 (CHEMBL4786843) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	71	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583927 (CHEMBL5088381) Show SMILES Cl.Cc1noc(C)c1-c1ccc2c(c[nH]c2n1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	75	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583918 (CHEMBL4791134) Show SMILES CS(=O)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	78	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583919 (CHEMBL5083688) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2cc(ccc12)C#N |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	86	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583927 (CHEMBL5088381) Show SMILES Cl.Cc1noc(C)c1-c1ccc2c(c[nH]c2n1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583920 (CHEMBL4786843) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	95	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50526790 (CHEMBL4555799) Show SMILES Clc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C17H18ClN5/c18-14-10-21-17(22-11-4-3-7-19-8-11)23-16(14)13-9-20-15-6-2-1-5-12(13)15/h1-2,5-6,9-11,19-20H,3-4,7-8H2,(H,21,22,23)/t11-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	102	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583923 (CHEMBL4786592) Show SMILES CP(C)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	102	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583924 (CHEMBL4790490) Show SMILES Cc1noc(C)c1-c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	112	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583920 (CHEMBL4786843) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	128	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583921 (CHEMBL4779443) Show SMILES CS(=O)(=O)c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	133	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583917 (CHEMBL4800180) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	135	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583924 (CHEMBL4790490) Show SMILES Cc1noc(C)c1-c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	138	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583928 (CHEMBL5080711) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	156	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583927 (CHEMBL5088381) Show SMILES Cl.Cc1noc(C)c1-c1ccc2c(c[nH]c2n1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	189	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583926 (CHEMBL4798916) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2c(c(ccc12)C#N)S(C)(=O)=O |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	215	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583925 (CHEMBL4782954) Show SMILES CS(=O)(=O)c1c(ccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F)C#N |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	284	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583923 (CHEMBL4786592) Show SMILES CP(C)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	286	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583921 (CHEMBL4779443) Show SMILES CS(=O)(=O)c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	299	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583919 (CHEMBL5083688) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2cc(ccc12)C#N |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	347	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583923 (CHEMBL4786592) Show SMILES CP(C)(=O)c1cccc2c(c[nH]c12)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	414	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583917 (CHEMBL4800180) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	430	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583924 (CHEMBL4790490) Show SMILES Cc1noc(C)c1-c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	460	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583928 (CHEMBL5080711) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	572	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583928 (CHEMBL5080711) Show SMILES CC1(C)CNC[C@H](C1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	771	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583926 (CHEMBL4798916) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2c(c(ccc12)C#N)S(C)(=O)=O |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	907	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583917 (CHEMBL4800180) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	923	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583926 (CHEMBL4798916) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2c(c(ccc12)C#N)S(C)(=O)=O |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 12 (Homo sapiens)	BDBM50583929 (SY-5609 | SY5609 | Sy 5609 | Sy-5609) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50583929 (SY-5609 | SY5609 | Sy 5609 | Sy-5609) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	1.92E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-dependent kinase 2/G1/S-specific cyclin-E1 (Homo sapiens (Human))	BDBM50583929 (SY-5609 | SY5609 | Sy 5609 | Sy-5609) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2c(c(ccc12)C#N)P(C)(C)=O)C(F)(F)F |r| Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	5.52E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as substrate in presence of ATP by mobility shift assay				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-H/Cyclin-dependent kinase 7 (Homo sapiens (Human))	BDBM50526790 (CHEMBL4555799) Show SMILES Clc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI InChI=1S/C17H18ClN5/c18-14-10-21-17(22-11-4-3-7-19-8-11)23-16(14)13-9-20-15-6-2-1-5-12(13)15/h1-2,5-6,9-11,19-20H,3-4,7-8H2,(H,21,22,23)/t11-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	0.330	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavable 6His tagged full length cyclinH (1 to 323 residues) (unknown origi...				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-H/Cyclin-dependent kinase 7 (Homo sapiens (Human))	BDBM50583919 (CHEMBL5083688) Show SMILES FC(F)(F)c1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2cc(ccc12)C#N |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	0.0900	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavable 6His tagged full length cyclinH (1 to 323 residues) (unknown origi...				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-H/Cyclin-dependent kinase 7 (Homo sapiens (Human))	BDBM50583920 (CHEMBL4786843) Show SMILES CC1(C)CC[C@@H](CN1)Nc1ncc(c(n1)-c1c[nH]c2ccccc12)C(F)(F)F |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	0.340	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavable 6His tagged full length cyclinH (1 to 323 residues) (unknown origi...				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-H/Cyclin-dependent kinase 7 (Homo sapiens (Human))	BDBM50583921 (CHEMBL4779443) Show SMILES CS(=O)(=O)c1ccc2c(c[nH]c2c1)-c1nc(N[C@H]2CCCNC2)ncc1C(F)(F)F |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	0.100	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavable 6His tagged full length cyclinH (1 to 323 residues) (unknown origi...				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair
Cyclin-H/Cyclin-dependent kinase 7 (Homo sapiens (Human))	BDBM50583917 (CHEMBL4800180) Show SMILES CCc1cnc(N[C@H]2CCCNC2)nc1-c1c[nH]c2ccccc12 |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Molecular Design, Inc. Curated by ChEMBL					Assay Description Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavable 6His tagged full length cyclinH (1 to 323 residues) (unknown origi...				J Med Chem 47: 4818-28 (2004) Article DOI: 10.1021/acs.jmedchem.1c01171 BindingDB Entry DOI: 10.7270/Q2736VSR
					More data for this Ligand-Target Pair

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