Compile Data Set for Download or QSAR

Found 83 hits Enz. Inhib. hit(s) with all data for entry = 10921   

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
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578446 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-chloropheny...) Show SMILES CN[C@@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(Cl)cc1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578479 ((S)—N-(2-(2-(dimethylamino)ethoxy)-5-fluoro-4-(1H-...) Show SMILES CN[C@H](C(=O)Nc1cc(F)c(cc1OCCN(C)C)-c1cn[nH]c1)c1cccc(OC)c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.60	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578424 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-chlorophenyl)-2...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(Cl)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578438 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphen...) Show SMILES CNCCN[C@@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.80	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578449 (3-(2-((4-(1H-pyrazol-4-yl)phenyl)amino)-1-(methyla...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(c1)C(=O)NC Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.90	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578470 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES COc1cccc(c1)C(NCCN1CCOCC1)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578435 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-(dimethyla...) Show SMILES COc1cccc(c1)[C@@H](NCCN(C)C)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	2.90	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578454 (N-(2-(2-(dimethylamino)ethoxy)-5-fluoro-4-(1H-pyra...) Show SMILES CNC(C(=O)Nc1cc(F)c(cc1OCCN(C)C)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578409 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(2-methoxyphenyl)-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccccc1OC |$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578410 ((S)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphen...) Show SMILES CN[C@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r,$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 [1-535] (Homo sapiens (Human))	BDBM578438 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphen...) Show SMILES CNCCN[C@@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578415 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(p-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(C)cc1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578420 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-chlorophenyl)-2...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(Cl)c1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578415 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(p-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(C)cc1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578411 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578423 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-fluorophenyl)-2...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(F)cc1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	4.80	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578476 (N-(3-methoxy-4-(1H-pyrazol-4-yl)phenyl)-2-((2-meth...) Show SMILES COCCNC(C(=O)Nc1ccc(-c2cn[nH]c2)c(OC)c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578430 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES CNCCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578417 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(3-...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	6.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578421 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-chlorophenyl)-2...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(Cl)cc1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	6.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578461 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES CNCCCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	6.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578418 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(methylamino)-2-(m...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(C)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	6.80	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578453 (N-(2-(3-(dimethylamino)propoxy)-5-fluoro-4-(1H-pyr...) Show SMILES CNC(C(=O)Nc1cc(F)c(cc1OCCCN(C)C)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	7.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 [1-535] (Homo sapiens (Human))	BDBM578435 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-(dimethyla...) Show SMILES COc1cccc(c1)[C@@H](NCCN(C)C)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	7.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578471 (N-(2-(2-(dimethylamino)ethoxy)-5-fluoro-4-(1H-pyra...) Show SMILES COCCN(C)C(C(=O)Nc1cc(F)c(cc1OCCN(C)C)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	8.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578457 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-((3-(dimethylamino...) Show SMILES COc1cccc(c1)C(NCCCN(C)C)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	8.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578426 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-chlorophenyl)-2...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(Cl)cc1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	8.90	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578431 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-(dimethylamino...) Show SMILES COc1cccc(c1)C(NCCN(C)C)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578422 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-fluorophenyl)-2...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(F)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 [1-535] (Homo sapiens (Human))	BDBM578409 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(2-methoxyphenyl)-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccccc1OC |$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578412 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphen...) Show SMILES CN[C@@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r,$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578460 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-amino-2-oxoeth...) Show SMILES COc1cccc(c1)C(NCC(N)=O)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578433 ((R)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-methoxyeth...) Show SMILES COCCN[C@@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578440 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(2-methoxypyridin-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccnc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578413 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-methoxyphenyl)-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(OC)cc1 |$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	15.4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578455 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES COCCCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578458 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-((2-(dimethylamino...) Show SMILES COc1cccc(c1)C(NCC(=O)N(C)C)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578472 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES COc1cccc(c1)C(NCCN1CCCC1)C(=O)Nc1ccc(cc1)-c1cn[nH]c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578475 (N-(3-fluoro-4-(1H-pyrazol-4-yl)phenyl)-2-((2-metho...) Show SMILES COCCNC(C(=O)Nc1ccc(-c2cn[nH]c2)c(F)c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 [1-535] (Homo sapiens (Human))	BDBM578411 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphenyl)-...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578447 (N-(2-fluoro-5-methoxy-4-(1H-pyrazol-4-yl)phenyl)-2...) Show SMILES CNC(C(=O)Nc1cc(OC)c(cc1F)-c1cn[nH]c1)c1cccc(OC)c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578441 (Methyl 3-(2-((4-(1H-pyrazol-4-yl)phenyl)amino)-1-(...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(c1)C(=O)OC Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578414 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(4-...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(OC)cc1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	21	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578427 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-fluoro-4-methox...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(OC)c(F)c1 |$;HN;;;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	21	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578439 ((S)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methoxyphen...) Show SMILES CNCCN[C@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC)c1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578428 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-(difluoromethox...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(OC(F)F)c1 |$;N;;;;;;;;;;;;;;;;;;;;;O;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578445 ((S)—N-(4-(1H-pyrazol-4-yl)phenyl)-2-(4-chloropheny...) Show SMILES CN[C@H](C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(Cl)cc1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578419 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(3-...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1cccc(F)c1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578444 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(3-methyl-1H-indaz...) Show SMILES CNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc2c(C)n[nH]c2c1 Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair
Rho-associated protein kinase 2 [1-552] (Homo sapiens (Human))	BDBM578416 (N-(4-(1H-pyrazol-4-yl)phenyl)-2-(ethylamino)-2-(4-...) Show SMILES CCNC(C(=O)Nc1ccc(cc1)-c1cn[nH]c1)c1ccc(F)cc1 |$;;HN;;;;;;;;;;;;;;;;;;;;;;$| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Compounds activities were measured by Z'-lyte kinase kit (ThermoFisher Scientific). The percent inhibition rate was calculated by normalizing the...				Citation and Details BindingDB Entry DOI: 10.7270/Q2R78JGS
					More data for this Ligand-Target Pair

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