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Compile Data Set for Download or QSAR

Found 191 hits with Last Name = 'stassen' and Initial = 'jm'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Thrombin and coagulation factor X


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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4.5n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human thrombin


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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15 -46.5n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Thrombin and coagulation factor X


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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20 -45.7n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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40 -43.9n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Trypsin II


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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50.3n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human trypsin


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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57 -43.0n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Trypsin


(Bos taurus (bovine))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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67 -42.6n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Trypsin


(Bos taurus (bovine))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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102 -41.5n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Trypsin


(Bos taurus (bovine))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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110 -41.3n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Thrombin and coagulation factor X


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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140 -40.7n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Thrombin and coagulation factor X


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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780 -36.3n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Plasminogen


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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1.70E+3n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human plasmin


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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3.76E+3n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human Coagulation factor Xa (fXa)


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Coagulation factor XI


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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4.10E+3 -32.0n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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PubMed
6.50E+3 -30.8n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Plasminogen


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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6.80E+3 -30.7n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor XI


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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8.20E+3 -30.2n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor XI


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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9.00E+3 -30.0n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Plasminogen


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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9.20E+3 -29.9n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Plasminogen


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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1.30E+4 -29.0n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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1.60E+4 -28.5n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Vitamin K-dependent protein C


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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2.09E+4n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human Activated protein C


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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>3.00E+4>-26.9n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor VII


(Homo sapiens (Human))
BDBM17298
PNG
(4-[({1-methyl-5-[1-(pyrrolidin-1-ylcarbonyl)cyclop...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C1(CC1)C(=O)N1CCCC1
Show InChI InChI=1S/C24H28N6O/c1-29-20-9-6-17(24(10-11-24)23(31)30-12-2-3-13-30)14-19(20)28-21(29)15-27-18-7-4-16(5-8-18)22(25)26/h4-9,14,27H,2-3,10-13,15H2,1H3,(H3,25,26)
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>4.00E+4>-26.1n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor VII


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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>4.00E+4>-26.1n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Coagulation factor VII


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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>4.00E+4>-26.1n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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4.40E+4 -25.9n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM50112086
PNG
(3-({2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-met...)
Show SMILES Cn1c(CNc2ccc(cc2)C(N)=N)nc2cc(ccc12)C(=O)N(CCC(O)=O)c1ccccn1
Show InChI InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
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4.54E+4n/an/an/an/an/an/an/an/a



Boehringer Ingelheim Pharma KG

Curated by ChEMBL


Assay Description
Inhibitory constant (Ki) was determined against human Tissue plasminogen activator (tissue plasminogen activator)


J Med Chem 45: 1757-66 (2002)


BindingDB Entry DOI: 10.7270/Q2GX49W5
More data for this
Ligand-Target Pair
Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM17295
PNG
(BIBT0871 | ethyl 2-{[(E)-{[1-(2-{[(4-carbamimidoyl...)
Show SMILES CCOC(=O)CO\N=C(\c1ccccn1)C1(CC1)c1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C29H31N7O3/c1-3-38-26(37)18-39-35-27(22-6-4-5-15-32-22)29(13-14-29)20-9-12-24-23(16-20)34-25(36(24)2)17-33-21-10-7-19(8-11-21)28(30)31/h4-12,15-16,33H,3,13-14,17-18H2,1-2H3,(H3,30,31)/b35-27-
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>5.00E+4>-25.5n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM17297
PNG
(4-[({1-methyl-5-[(2-methyl-1H-1,3-benzodiazol-1-yl...)
Show SMILES Cc1nc2ccccc2n1Cc1ccc2n(C)c(CNc3ccc(cc3)C(N)=N)nc2c1
Show InChI InChI=1S/C25H25N7/c1-16-29-20-5-3-4-6-23(20)32(16)15-17-7-12-22-21(13-17)30-24(31(22)2)14-28-19-10-8-18(9-11-19)25(26)27/h3-13,28H,14-15H2,1-2H3,(H3,26,27)
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>5.00E+4>-25.5n/an/an/an/an/a8.037



Boehringer Ingelheim Pharma KG



Assay Description
For determination of the inhibition constants (Ki), enzyme inhibition was studied at three different substrate concentrations and seven different con...


Structure 9: 29-37 (2001)


Article DOI: 10.1016/s0969-2126(00)00551-7
BindingDB Entry DOI: 10.7270/Q2028PTC
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087126
PNG
(CHEMBL3426639)
Show SMILES COC(=O)c1ccc(F)c(c1)C(=O)Nc1cccc(c1)-c1cc(ccc1CN)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C28H22F2N4O4/c1-38-28(37)18-7-8-23(29)22(13-18)27(36)33-20-4-2-3-16(11-20)21-12-17(5-6-19(21)14-31)26(35)34-25-9-10-32-15-24(25)30/h2-13,15H,14,31H2,1H3,(H,33,36)(H,32,34,35)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087127
PNG
(CHEMBL3426637)
Show SMILES COC(=O)c1cccc(c1)C(=O)Nc1cccc(c1)-c1cc(ccc1CN)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C28H23FN4O4/c1-37-28(36)20-6-2-5-18(12-20)26(34)32-22-7-3-4-17(13-22)23-14-19(8-9-21(23)15-30)27(35)33-25-10-11-31-16-24(25)29/h2-14,16H,15,30H2,1H3,(H,32,34)(H,31,33,35)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087167
PNG
(CHEMBL3426727)
Show SMILES NCc1ccc(cc1-c1cccc(c1)C(=O)Nc1ccc(CC(=O)OC2CCCC2)cc1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C33H31FN4O4/c34-29-20-36-15-14-30(29)38-33(41)24-10-11-25(19-35)28(18-24)22-4-3-5-23(17-22)32(40)37-26-12-8-21(9-13-26)16-31(39)42-27-6-1-2-7-27/h3-5,8-15,17-18,20,27H,1-2,6-7,16,19,35H2,(H,37,40)(H,36,38,41)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087166
PNG
(CHEMBL3426728)
Show SMILES NCc1ccc(cc1-c1cccc(c1)C(=O)Nc1ccc(CC(=O)OC2CCCOC2)cc1)C(=O)Nc1ccncc1F
Show InChI InChI=1/C33H31FN4O5/c34-29-19-36-13-12-30(29)38-33(41)24-8-9-25(18-35)28(17-24)22-3-1-4-23(16-22)32(40)37-26-10-6-21(7-11-26)15-31(39)43-27-5-2-14-42-20-27/h1,3-4,6-13,16-17,19,27H,2,5,14-15,18,20,35H2,(H,37,40)(H,36,38,41)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087165
PNG
(CHEMBL3426729)
Show SMILES CN1CCC(CC1)OC(=O)Cc1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C34H34FN5O4/c1-40-15-12-28(13-16-40)44-32(41)17-22-5-9-27(10-6-22)38-33(42)24-4-2-3-23(18-24)29-19-25(7-8-26(29)20-36)34(43)39-31-11-14-37-21-30(31)35/h2-11,14,18-19,21,28H,12-13,15-17,20,36H2,1H3,(H,38,42)(H,37,39,43)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087138
PNG
(CHEMBL3426730)
Show SMILES CCCOC(=O)c1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C30H27FN4O4/c1-2-14-39-30(38)19-8-10-24(11-9-19)34-28(36)21-5-3-4-20(15-21)25-16-22(6-7-23(25)17-32)29(37)35-27-12-13-33-18-26(27)31/h3-13,15-16,18H,2,14,17,32H2,1H3,(H,34,36)(H,33,35,37)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087137
PNG
(CHEMBL3426731)
Show SMILES COC(=O)c1ccc(cc1)C(=O)Nc1cccc(c1)-c1cc(ccc1CN)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C28H23FN4O4/c1-37-28(36)18-7-5-17(6-8-18)26(34)32-22-4-2-3-19(13-22)23-14-20(9-10-21(23)15-30)27(35)33-25-11-12-31-16-24(25)29/h2-14,16H,15,30H2,1H3,(H,32,34)(H,31,33,35)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087136
PNG
(CHEMBL3426732)
Show SMILES NCc1ccc(cc1-c1cccc(NC(=O)c2ccc(cc2)C(O)=O)c1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C27H21FN4O4/c28-23-15-30-11-10-24(23)32-26(34)19-8-9-20(14-29)22(13-19)18-2-1-3-21(12-18)31-25(33)16-4-6-17(7-5-16)27(35)36/h1-13,15H,14,29H2,(H,31,33)(H,35,36)(H,30,32,34)
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n/an/a 1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087169
PNG
(CHEMBL3426725)
Show SMILES NCc1ccc(cc1-c1cccc(c1)C(=O)Nc1ccc(CC(=O)OC2CCOCC2)cc1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C33H31FN4O5/c34-29-20-36-13-10-30(29)38-33(41)24-6-7-25(19-35)28(18-24)22-2-1-3-23(17-22)32(40)37-26-8-4-21(5-9-26)16-31(39)43-27-11-14-42-15-12-27/h1-10,13,17-18,20,27H,11-12,14-16,19,35H2,(H,37,40)(H,36,38,41)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087170
PNG
(CHEMBL3426724)
Show SMILES CC[C@@H](C)OC(=O)Cc1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1 |r|
Show InChI InChI=1/C32H31FN4O4/c1-3-20(2)41-30(38)15-21-7-11-26(12-8-21)36-31(39)23-6-4-5-22(16-23)27-17-24(9-10-25(27)18-34)32(40)37-29-13-14-35-19-28(29)33/h4-14,16-17,19-20H,3,15,18,34H2,1-2H3,(H,36,39)(H,35,37,40)/t20-/s2
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087122
PNG
(CHEMBL3426647)
Show SMILES CC(C)OC(=O)Cc1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C31H29FN4O4/c1-19(2)40-29(37)14-20-6-10-25(11-7-20)35-30(38)22-5-3-4-21(15-22)26-16-23(8-9-24(26)17-33)31(39)36-28-12-13-34-18-27(28)32/h3-13,15-16,18-19H,14,17,33H2,1-2H3,(H,35,38)(H,34,36,39)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087125
PNG
(CHEMBL3426640)
Show SMILES COCCOC(=O)c1ccc(F)c(c1)C(=O)Nc1cccc(c1)-c1cc(ccc1CN)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C30H26F2N4O5/c1-40-11-12-41-30(39)20-7-8-25(31)24(15-20)29(38)35-22-4-2-3-18(13-22)23-14-19(5-6-21(23)16-33)28(37)36-27-9-10-34-17-26(27)32/h2-10,13-15,17H,11-12,16,33H2,1H3,(H,35,38)(H,34,36,37)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087130
PNG
(CHEMBL3426625)
Show SMILES COC(=O)Cc1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C29H25FN4O4/c1-38-27(35)13-18-5-9-23(10-6-18)33-28(36)20-4-2-3-19(14-20)24-15-21(7-8-22(24)16-31)29(37)34-26-11-12-32-17-25(26)30/h2-12,14-15,17H,13,16,31H2,1H3,(H,33,36)(H,32,34,37)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087131
PNG
(CHEMBL3426624)
Show SMILES COC(=O)c1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C28H23FN4O4/c1-37-28(36)17-7-9-22(10-8-17)32-26(34)19-4-2-3-18(13-19)23-14-20(5-6-21(23)15-30)27(35)33-25-11-12-31-16-24(25)29/h2-14,16H,15,30H2,1H3,(H,32,34)(H,31,33,35)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087134
PNG
(CHEMBL3426620)
Show SMILES NCc1ccc(cc1-c1cccc(c1)C(=O)Nc1ccccc1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C26H21FN4O2/c27-23-16-29-12-11-24(23)31-26(33)19-9-10-20(15-28)22(14-19)17-5-4-6-18(13-17)25(32)30-21-7-2-1-3-8-21/h1-14,16H,15,28H2,(H,30,32)(H,29,31,33)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087275
PNG
(CHEMBL3426644)
Show SMILES NCc1ccc(cc1-c1cccc(NC(=O)c2cccc(c2)C(O)=O)c1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C27H21FN4O4/c28-23-15-30-10-9-24(23)32-26(34)18-7-8-20(14-29)22(13-18)16-3-2-6-21(12-16)31-25(33)17-4-1-5-19(11-17)27(35)36/h1-13,15H,14,29H2,(H,31,33)(H,35,36)(H,30,32,34)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 2


(Homo sapiens (Human))
BDBM50087270
PNG
(CHEMBL3426645)
Show SMILES NCc1ccc(cc1-c1cccc(NC(=O)c2cc(ccc2F)C(O)=O)c1)C(=O)Nc1ccncc1F
Show InChI InChI=1S/C27H20F2N4O4/c28-22-7-6-17(27(36)37)12-21(22)26(35)32-19-3-1-2-15(10-19)20-11-16(4-5-18(20)13-30)25(34)33-24-8-9-31-14-23(24)29/h1-12,14H,13,30H2,(H,32,35)(H,36,37)(H,31,33,34)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK2 expressed in baculovirus-infected insect cells using long S6 kinase peptide as substrate by radiometr...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 1


(Homo sapiens (Human))
BDBM50087130
PNG
(CHEMBL3426625)
Show SMILES COC(=O)Cc1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C29H25FN4O4/c1-38-27(35)13-18-5-9-23(10-6-18)33-28(36)20-4-2-3-19(14-20)24-15-21(7-8-22(24)16-31)29(37)34-26-11-12-32-17-25(26)30/h2-12,14-15,17H,13,16,31H2,1H3,(H,33,36)(H,32,34,37)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK1 expressed in insect cells using long S6 kinase peptide as substrate by radiometric assay in presence ...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 1


(Homo sapiens (Human))
BDBM50087131
PNG
(CHEMBL3426624)
Show SMILES COC(=O)c1ccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)cc1
Show InChI InChI=1S/C28H23FN4O4/c1-37-28(36)17-7-9-22(10-8-17)32-26(34)19-4-2-3-18(13-19)23-14-20(5-6-21(23)15-30)27(35)33-25-11-12-31-16-24(25)29/h2-14,16H,15,30H2,1H3,(H,32,34)(H,31,33,35)
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n/an/a<1n/an/an/an/an/an/a



Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK1 expressed in insect cells using long S6 kinase peptide as substrate by radiometric assay in presence ...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
Rho-associated protein kinase 1


(Homo sapiens (Human))
BDBM50087132
PNG
(CHEMBL3426623)
Show SMILES COC(=O)Cc1cccc(NC(=O)c2cccc(c2)-c2cc(ccc2CN)C(=O)Nc2ccncc2F)c1
Show InChI InChI=1S/C29H25FN4O4/c1-38-27(35)13-18-4-2-7-23(12-18)33-28(36)20-6-3-5-19(14-20)24-15-21(8-9-22(24)16-31)29(37)34-26-10-11-32-17-25(26)30/h2-12,14-15,17H,13,16,31H2,1H3,(H,33,36)(H,32,34,37)
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Agoralaan Abis

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged ROCK1 expressed in insect cells using long S6 kinase peptide as substrate by radiometric assay in presence ...


J Med Chem 58: 4309-24 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00308
BindingDB Entry DOI: 10.7270/Q2H41T4R
More data for this
Ligand-Target Pair
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