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Compile Data Set for Download or QSAR

Found 85 hits with Last Name = 'dyer' and Initial = 'dl'   
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
Prothrombin


(Homo sapiens (Human))
BDBM50122190
PNG
(CHEMBL296737 | N-(5-chloro-2-ethylcarbamoylmethoxy...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C26H29ClN4O6S/c1-3-28-25(33)16-37-23-12-10-21(27)13-20(23)14-29-24(32)15-31-18(2)9-11-22(26(31)34)30-38(35,36)17-19-7-5-4-6-8-19/h4-13,30H,3,14-17H2,1-2H3,(H,28,33)(H,29,32)
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0.0400n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122183
PNG
(CHEMBL431524 | N-(5-Chloro-2-ethylcarbamoylmethoxy...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C26H30ClN5O4/c1-3-28-24(34)17-36-22-10-9-21(27)13-20(22)15-30-23(33)16-32-18(2)14-31-25(26(32)35)29-12-11-19-7-5-4-6-8-19/h4-10,13-14H,3,11-12,15-17H2,1-2H3,(H,28,34)(H,29,31)(H,30,33)
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0.0700n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069189
PNG
(CHEMBL353431 | N-(6-Amino-2,4-dimethyl-pyridin-3-y...)
Show SMILES Cc1cc(N)nc(C)c1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C23H27N5O4S/c1-15-11-21(24)26-17(3)19(15)12-25-22(29)13-28-16(2)9-10-20(23(28)30)27-33(31,32)14-18-7-5-4-6-8-18/h4-11,27H,12-14H2,1-3H3,(H2,24,26)(H,25,29)
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0.330n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067795
PNG
(CHEMBL138855 | N-(6-Amino-2,4-dimethyl-pyridin-3-y...)
Show SMILES Cc1cc(N)nc(C)c1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C23H28N6O2/c1-15-11-20(24)28-17(3)19(15)13-26-21(30)14-29-16(2)12-27-22(23(29)31)25-10-9-18-7-5-4-6-8-18/h4-8,11-12H,9-10,13-14H2,1-3H3,(H2,24,28)(H,25,27)(H,26,30)
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0.350n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067796
PNG
(CHEMBL11157 | L-374087 | N-((6-amino-2-methylpyrid...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H25N5O4S/c1-15-8-10-19(26-32(30,31)14-17-6-4-3-5-7-17)22(29)27(15)13-21(28)24-12-18-9-11-20(23)25-16(18)2/h3-11,26H,12-14H2,1-2H3,(H2,23,25)(H,24,28)
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0.5n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067796
PNG
(CHEMBL11157 | L-374087 | N-((6-amino-2-methylpyrid...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H25N5O4S/c1-15-8-10-19(26-32(30,31)14-17-6-4-3-5-7-17)22(29)27(15)13-21(28)24-12-18-9-11-20(23)25-16(18)2/h3-11,26H,12-14H2,1-2H3,(H2,23,25)(H,24,28)
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0.5n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069190
PNG
(CHEMBL287614 | N-(1-Carbamimidoyl-piperidin-4-ylme...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C22H30N6O4S/c1-16-7-8-19(26-33(31,32)15-18-5-3-2-4-6-18)21(30)28(16)14-20(29)25-13-17-9-11-27(12-10-17)22(23)24/h2-8,17,26H,9-15H2,1H3,(H3,23,24)(H,25,29)
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0.5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069190
PNG
(CHEMBL287614 | N-(1-Carbamimidoyl-piperidin-4-ylme...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C22H30N6O4S/c1-16-7-8-19(26-33(31,32)15-18-5-3-2-4-6-18)21(30)28(16)14-20(29)25-13-17-9-11-27(12-10-17)22(23)24/h2-8,17,26H,9-15H2,1H3,(H3,23,24)(H,25,29)
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0.5n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067798
PNG
(CHEMBL336438 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES C[C@H](Cc1ccccc1)Nc1ncc(C)n(CC(=O)NCc2ccc(N)nc2C)c1=O
Show InChI InChI=1S/C23H28N6O2/c1-15(11-18-7-5-4-6-8-18)27-22-23(31)29(16(2)12-26-22)14-21(30)25-13-19-9-10-20(24)28-17(19)3/h4-10,12,15H,11,13-14H2,1-3H3,(H2,24,28)(H,25,30)(H,26,27)/t15-/m1/s1
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0.520n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50066334
PNG
((S)-1-((R)-2-Amino-2-cyclohexyl-acetyl)-pyrrolidin...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)[C@@H]1CCCN1C(=O)[C@H](N)C1CCCCC1
Show InChI InChI=1S/C24H35ClN4O4/c1-2-27-21(30)15-33-20-11-10-18(25)13-17(20)14-28-23(31)19-9-6-12-29(19)24(32)22(26)16-7-4-3-5-8-16/h10-11,13,16,19,22H,2-9,12,14-15,26H2,1H3,(H,27,30)(H,28,31)/t19-,22+/m0/s1
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0.740n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Prothrombin


(Homo sapiens (Human))
BDBM50067797
PNG
(CHEMBL19080 | L-37378 | N-(6-Amino-2-methyl-pyridi...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C22H26N6O2/c1-15-12-26-21(24-11-10-17-6-4-3-5-7-17)22(30)28(15)14-20(29)25-13-18-8-9-19(23)27-16(18)2/h3-9,12H,10-11,13-14H2,1-2H3,(H2,23,27)(H,24,26)(H,25,29)
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0.800n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067797
PNG
(CHEMBL19080 | L-37378 | N-(6-Amino-2-methyl-pyridi...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C22H26N6O2/c1-15-12-26-21(24-11-10-17-6-4-3-5-7-17)22(30)28(15)14-20(29)25-13-18-8-9-19(23)27-16(18)2/h3-9,12H,10-11,13-14H2,1-2H3,(H2,23,27)(H,24,26)(H,25,29)
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0.800n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069191
PNG
(CHEMBL349430 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)ccc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C23H27N5O2/c1-16-8-10-20(25-13-12-18-6-4-3-5-7-18)23(30)28(16)15-22(29)26-14-19-9-11-21(24)27-17(19)2/h3-11,25H,12-15H2,1-2H3,(H2,24,27)(H,26,29)
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2.30n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50133525
PNG
(CHEMBL115643 | N-((trans-4-aminocyclohexyl)methyl)...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NC[C@H]1CC[C@H](N)CC1 |wU:24.25,wD:27.29,(9.06,-2.5,;7.71,-3.25,;6.36,-2.48,;5.05,-3.25,;5.05,-4.76,;3.7,-5.53,;2.38,-4.76,;2,-6.25,;2.76,-3.25,;1.04,-4.02,;1.01,-2.48,;-.34,-1.71,;-.37,-.19,;.96,.63,;2.31,-.14,;2.32,-1.68,;6.36,-5.56,;6.36,-7.1,;7.71,-4.79,;9.02,-5.58,;10.36,-4.82,;10.37,-3.28,;11.69,-5.59,;13.03,-4.82,;14.37,-5.61,;15.7,-4.84,;17.03,-5.62,;17.01,-7.16,;18.35,-7.97,;15.66,-7.93,;14.35,-7.15,)|
Show InChI InChI=1S/C22H30N4O4S/c1-16-7-12-20(25-31(29,30)15-18-5-3-2-4-6-18)22(28)26(16)14-21(27)24-13-17-8-10-19(23)11-9-17/h2-7,12,17,19,25H,8-11,13-15,23H2,1H3,(H,24,27)/t17-,19-
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4.60n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289529
PNG
(CHEMBL3084745)
Show SMILES CN[C@H](Cc1ccccc1)C(=O)N1CCCC1C(=O)NC[C@H]1CC[C@H](N)CC1 |r,wU:21.22,wD:24.26,2.2,(1.75,-2.49,;3.1,-3.26,;4.43,-2.49,;4.43,-.95,;3.08,-.18,;1.75,-.95,;.42,-.18,;.42,1.37,;1.75,2.15,;3.08,1.37,;5.76,-3.26,;5.76,-4.78,;7.09,-2.47,;7.26,-.95,;8.77,-.62,;9.54,-1.95,;8.5,-3.1,;8.83,-4.61,;10.3,-5.07,;7.68,-5.63,;8.01,-7.14,;9.49,-7.62,;10.6,-6.59,;12.08,-7.05,;12.41,-8.56,;13.88,-9.03,;11.26,-9.6,;9.8,-9.12,)|
Show InChI InChI=1S/C22H34N4O2/c1-24-19(14-16-6-3-2-4-7-16)22(28)26-13-5-8-20(26)21(27)25-15-17-9-11-18(23)12-10-17/h2-4,6-7,17-20,24H,5,8-15,23H2,1H3,(H,25,27)/t17-,18-,19-,20?/m1/s1
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5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity was evaluated against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50066336
PNG
((S)-1-((R)-2-Amino-2-cyclohexyl-acetyl)-pyrrolidin...)
Show SMILES N[C@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1cc(Cl)ccc1Cl
Show InChI InChI=1S/C20H27Cl2N3O2/c21-15-8-9-16(22)14(11-15)12-24-19(26)17-7-4-10-25(17)20(27)18(23)13-5-2-1-3-6-13/h8-9,11,13,17-18H,1-7,10,12,23H2,(H,24,26)/t17-,18+/m0/s1
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5n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067791
PNG
(CHEMBL140885 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)c(Cl)nc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C22H25ClN6O2/c1-14-17(8-9-18(24)27-14)12-26-19(30)13-29-15(2)20(23)28-21(22(29)31)25-11-10-16-6-4-3-5-7-16/h3-9H,10-13H2,1-2H3,(H2,24,27)(H,25,28)(H,26,30)
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7n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122184
PNG
(CHEMBL296041 | N-(3-Chloro-benzyl)-2-(6-methyl-2-o...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCc1cccc(Cl)c1
Show InChI InChI=1S/C22H22ClN3O4S/c1-16-10-11-20(25-31(29,30)15-17-6-3-2-4-7-17)22(28)26(16)14-21(27)24-13-18-8-5-9-19(23)12-18/h2-12,25H,13-15H2,1H3,(H,24,27)
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7n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122186
PNG
(2-(3-Amino-6-methyl-2-oxo-4-trifluoromethyl-2H-pyr...)
Show SMILES CN(C)CCCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cc(c(N)c1=O)C(F)(F)F
Show InChI InChI=1S/C23H29ClF3N5O4/c1-14-9-17(23(25,26)27)21(28)22(35)32(14)12-19(33)30-11-15-10-16(24)5-6-18(15)36-13-20(34)29-7-4-8-31(2)3/h5-6,9-10H,4,7-8,11-13,28H2,1-3H3,(H,29,34)(H,30,33)
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7.40n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067793
PNG
(CHEMBL139331 | N-(6-Amino-pyridin-3-ylmethyl)-2-(6...)
Show SMILES Cc1cnc(NCCc2ccccc2)c(=O)n1CC(=O)NCc1ccc(N)nc1
Show InChI InChI=1S/C21H24N6O2/c1-15-11-26-20(23-10-9-16-5-3-2-4-6-16)21(29)27(15)14-19(28)25-13-17-7-8-18(22)24-12-17/h2-8,11-12H,9-10,13-14H2,1H3,(H2,22,24)(H,23,26)(H,25,28)
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PubMed
8.30n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122187
PNG
(2-(3-Amino-6-methyl-2-oxo-4-trifluoromethyl-2H-pyr...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cc(c(N)c1=O)C(F)(F)F
Show InChI InChI=1S/C20H22ClF3N4O4/c1-3-26-17(30)10-32-15-5-4-13(21)7-12(15)8-27-16(29)9-28-11(2)6-14(20(22,23)24)18(25)19(28)31/h4-7H,3,8-10,25H2,1-2H3,(H,26,30)(H,27,29)
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8.5n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069194
PNG
(CHEMBL355441 | N-(6-Amino-pyridin-3-ylmethyl)-2-(6...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCc1ccc(N)nc1
Show InChI InChI=1S/C21H23N5O4S/c1-15-7-9-18(25-31(29,30)14-16-5-3-2-4-6-16)21(28)26(15)13-20(27)24-12-17-8-10-19(22)23-11-17/h2-11,25H,12-14H2,1H3,(H2,22,23)(H,24,27)
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11n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122181
PNG
(2-(3-Amino-6-methyl-2-oxo-2H-pyrazin-1-yl)-N-(5-ch...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cnc(N)c1=O
Show InChI InChI=1S/C18H22ClN5O4/c1-3-21-16(26)10-28-14-5-4-13(19)6-12(14)8-22-15(25)9-24-11(2)7-23-17(20)18(24)27/h4-7H,3,8-10H2,1-2H3,(H2,20,23)(H,21,26)(H,22,25)
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12n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50060751
PNG
((S)-1-((R)-2-Amino-3,3-diphenyl-propionyl)-pyrroli...)
Show SMILES N[C@H](C(c1ccccc1)c1ccccc1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(N)nc1
Show InChI InChI=1S/C26H29N5O2/c27-22-14-13-18(16-29-22)17-30-25(32)21-12-7-15-31(21)26(33)24(28)23(19-8-3-1-4-9-19)20-10-5-2-6-11-20/h1-6,8-11,13-14,16,21,23-24H,7,12,15,17,28H2,(H2,27,29)(H,30,32)/t21-,24+/m0/s1
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12n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069195
PNG
(CHEMBL354555 | N-(6-Amino-4-methyl-pyridin-3-ylmet...)
Show SMILES Cc1cc(N)ncc1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H25N5O4S/c1-15-10-20(23)24-11-18(15)12-25-21(28)13-27-16(2)8-9-19(22(27)29)26-32(30,31)14-17-6-4-3-5-7-17/h3-11,26H,12-14H2,1-2H3,(H2,23,24)(H,25,28)
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12n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122185
PNG
(2-(3-Amino-6-methyl-2-oxo-4-trifluoromethyl-2H-pyr...)
Show SMILES CNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cc(c(N)c1=O)C(F)(F)F
Show InChI InChI=1S/C19H20ClF3N4O4/c1-10-5-13(19(21,22)23)17(24)18(30)27(10)8-15(28)26-7-11-6-12(20)3-4-14(11)31-9-16(29)25-2/h3-6H,7-9,24H2,1-2H3,(H,25,29)(H,26,28)
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15n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122180
PNG
(2-(3-Amino-6-methyl-2-oxo-4-trifluoromethyl-2H-pyr...)
Show SMILES CN(C)CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cc(c(N)c1=O)C(F)(F)F
Show InChI InChI=1S/C22H27ClF3N5O4/c1-13-8-16(22(24,25)26)20(27)21(34)31(13)11-18(32)29-10-14-9-15(23)4-5-17(14)35-12-19(33)28-6-7-30(2)3/h4-5,8-9H,6-7,10-12,27H2,1-3H3,(H,28,33)(H,29,32)
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18n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067794
PNG
(CHEMBL139178 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES C[C@@H](Cc1ccccc1)Nc1ncc(C)n(CC(=O)NCc2ccc(N)nc2C)c1=O
Show InChI InChI=1S/C23H28N6O2/c1-15(11-18-7-5-4-6-8-18)27-22-23(31)29(16(2)12-26-22)14-21(30)25-13-19-9-10-20(24)28-17(19)3/h4-10,12,15H,11,13-14H2,1-3H3,(H2,24,28)(H,25,30)(H,26,27)/t15-/m0/s1
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22n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122188
PNG
(CHEMBL42091 | N-(2,5-Dichloro-benzyl)-2-(6-methyl-...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCc1cc(Cl)ccc1Cl
Show InChI InChI=1S/C22H21Cl2N3O4S/c1-15-7-10-20(26-32(30,31)14-16-5-3-2-4-6-16)22(29)27(15)13-21(28)25-12-17-11-18(23)8-9-19(17)24/h2-11,26H,12-14H2,1H3,(H,25,28)
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24n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50067792
PNG
(CHEMBL141266 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)cnc(NC(C)(C)Cc2ccccc2)c1=O
Show InChI InChI=1S/C24H30N6O2/c1-16-13-27-22(29-24(3,4)12-18-8-6-5-7-9-18)23(32)30(16)15-21(31)26-14-19-10-11-20(25)28-17(19)2/h5-11,13H,12,14-15H2,1-4H3,(H2,25,28)(H,26,31)(H,27,29)
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24n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against thrombin (IIa) was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069192
PNG
(CHEMBL48929 | N-(6-Amino-2-methyl-pyridin-3-ylmeth...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1cccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C21H23N5O4S/c1-15-17(9-10-19(22)24-15)12-23-20(27)13-26-11-5-8-18(21(26)28)25-31(29,30)14-16-6-3-2-4-7-16/h2-11,25H,12-14H2,1H3,(H2,22,24)(H,23,27)
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26n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289528
PNG
(CHEMBL36397 | N-(1-Carbamimidoyl-piperidin-4-ylmet...)
Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc(C)n(CC(=O)NCC2CCN(CC2)C(N)=N)c1=O
Show InChI InChI=1S/C22H30N6O4S/c1-15-3-6-18(7-4-15)33(31,32)26-19-8-5-16(2)28(21(19)30)14-20(29)25-13-17-9-11-27(12-10-17)22(23)24/h3-8,17,26H,9-14H2,1-2H3,(H3,23,24)(H,25,29)
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29n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069193
PNG
(CHEMBL424545 | N-(4-Amino-cyclohexylmethyl)-2-(6-m...)
Show SMILES Cc1ccc(NCCc2ccccc2)c(=O)n1CC(=O)NC[C@H]1CC[C@H](N)CC1 |wU:22.23,wD:25.27,(10.88,-.69,;9.55,-1.46,;8.19,-.69,;6.86,-1.46,;6.86,-3,;5.53,-3.77,;4.19,-3,;4.19,-1.46,;2.86,-.71,;1.55,-1.48,;.22,-.73,;.19,.8,;1.5,1.58,;2.84,.83,;8.19,-3.77,;8.21,-5.32,;9.55,-3,;10.88,-3.77,;10.88,-5.32,;12.21,-6.09,;9.55,-6.09,;9.55,-7.63,;10.88,-8.4,;12.21,-7.63,;13.55,-8.4,;13.55,-9.95,;14.88,-10.72,;12.21,-10.72,;10.88,-9.95,)|
Show InChI InChI=1S/C23H32N4O2/c1-17-7-12-21(25-14-13-18-5-3-2-4-6-18)23(29)27(17)16-22(28)26-15-19-8-10-20(24)11-9-19/h2-7,12,19-20,25H,8-11,13-16,24H2,1H3,(H,26,28)/t19-,20-
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47n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards thrombin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50069193
PNG
(CHEMBL424545 | N-(4-Amino-cyclohexylmethyl)-2-(6-m...)
Show SMILES Cc1ccc(NCCc2ccccc2)c(=O)n1CC(=O)NC[C@H]1CC[C@H](N)CC1 |wU:22.23,wD:25.27,(10.88,-.69,;9.55,-1.46,;8.19,-.69,;6.86,-1.46,;6.86,-3,;5.53,-3.77,;4.19,-3,;4.19,-1.46,;2.86,-.71,;1.55,-1.48,;.22,-.73,;.19,.8,;1.5,1.58,;2.84,.83,;8.19,-3.77,;8.21,-5.32,;9.55,-3,;10.88,-3.77,;10.88,-5.32,;12.21,-6.09,;9.55,-6.09,;9.55,-7.63,;10.88,-8.4,;12.21,-7.63,;13.55,-8.4,;13.55,-9.95,;14.88,-10.72,;12.21,-10.72,;10.88,-9.95,)|
Show InChI InChI=1S/C23H32N4O2/c1-17-7-12-21(25-14-13-18-5-3-2-4-6-18)23(29)27(17)16-22(28)26-15-19-8-10-20(24)11-9-19/h2-7,12,19-20,25H,8-11,13-16,24H2,1H3,(H,26,28)/t19-,20-
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47n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289532
PNG
((1-{[(1-Carbamimidoyl-piperidin-4-ylmethyl)-carbam...)
Show SMILES Cc1ccc(NC(=O)OCc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C23H30N6O4/c1-16-7-8-19(27-23(32)33-15-18-5-3-2-4-6-18)21(31)29(16)14-20(30)26-13-17-9-11-28(12-10-17)22(24)25/h2-8,17H,9-15H2,1H3,(H3,24,25)(H,26,30)(H,27,32)
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77n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289531
PNG
(CHEMBL290947 | N-(1-{[(1-Carbamimidoyl-piperidin-4...)
Show SMILES Cc1ccc(NC(=O)CCc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C24H32N6O3/c1-17-7-9-20(28-21(31)10-8-18-5-3-2-4-6-18)23(33)30(17)16-22(32)27-15-19-11-13-29(14-12-19)24(25)26/h2-7,9,19H,8,10-16H2,1H3,(H3,25,26)(H,27,32)(H,28,31)
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95n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50289528
PNG
(CHEMBL36397 | N-(1-Carbamimidoyl-piperidin-4-ylmet...)
Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc(C)n(CC(=O)NCC2CCN(CC2)C(N)=N)c1=O
Show InChI InChI=1S/C22H30N6O4S/c1-15-3-6-18(7-4-15)33(31,32)26-19-8-5-16(2)28(21(19)30)14-20(29)25-13-17-9-11-27(12-10-17)22(23)24/h3-8,17,26H,9-14H2,1-2H3,(H3,23,24)(H,25,29)
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140n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human trypsin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289526
PNG
(CHEMBL37035 | N-(1-{[(1-Carbamimidoyl-piperidin-4-...)
Show SMILES Cc1ccc(NC(=O)CC(c2ccccc2)c2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C30H36N6O3/c1-21-12-13-26(29(39)36(21)20-28(38)33-19-22-14-16-35(17-15-22)30(31)32)34-27(37)18-25(23-8-4-2-5-9-23)24-10-6-3-7-11-24/h2-13,22,25H,14-20H2,1H3,(H3,31,32)(H,33,38)(H,34,37)
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166n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122182
PNG
(2-(3-Amino-6-methyl-2-oxo-4-trifluoromethyl-2H-pyr...)
Show SMILES Cc1cc(c(N)c(=O)n1CC(=O)NCc1ccc(N)nc1C)C(F)(F)F
Show InChI InChI=1S/C16H18F3N5O2/c1-8-5-11(16(17,18)19)14(21)15(26)24(8)7-13(25)22-6-10-3-4-12(20)23-9(10)2/h3-5H,6-7,21H2,1-2H3,(H2,20,23)(H,22,25)
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340n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50289532
PNG
((1-{[(1-Carbamimidoyl-piperidin-4-ylmethyl)-carbam...)
Show SMILES Cc1ccc(NC(=O)OCc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C23H30N6O4/c1-16-7-8-19(27-23(32)33-15-18-5-3-2-4-6-18)21(31)29(16)14-20(30)26-13-17-9-11-28(12-10-17)22(24)25/h2-8,17H,9-15H2,1H3,(H3,24,25)(H,26,30)(H,27,32)
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350n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human trypsin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50069190
PNG
(CHEMBL287614 | N-(1-Carbamimidoyl-piperidin-4-ylme...)
Show SMILES Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C22H30N6O4S/c1-16-7-8-19(26-33(31,32)15-18-5-3-2-4-6-18)21(30)28(16)14-20(29)25-13-17-9-11-27(12-10-17)22(23)24/h2-8,17,26H,9-15H2,1H3,(H3,23,24)(H,25,29)
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570n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human trypsin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50289533
PNG
(CHEMBL34306 | N-(1-{[(1-Carbamimidoyl-piperidin-4-...)
Show SMILES Cc1ccc(NC(=O)c2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C22H28N6O3/c1-15-7-8-18(26-20(30)17-5-3-2-4-6-17)21(31)28(15)14-19(29)25-13-16-9-11-27(12-10-16)22(23)24/h2-8,16H,9-14H2,1H3,(H3,23,24)(H,25,29)(H,26,30)
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690n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human thrombin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50289526
PNG
(CHEMBL37035 | N-(1-{[(1-Carbamimidoyl-piperidin-4-...)
Show SMILES Cc1ccc(NC(=O)CC(c2ccccc2)c2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C30H36N6O3/c1-21-12-13-26(29(39)36(21)20-28(38)33-19-22-14-16-35(17-15-22)30(31)32)34-27(37)18-25(23-8-4-2-5-9-23)24-10-6-3-7-11-24/h2-13,22,25H,14-20H2,1H3,(H3,31,32)(H,33,38)(H,34,37)
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890n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human trypsin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM50122189
PNG
(2-(3-Amino-6-methyl-2-oxo-2H-pyrazin-1-yl)-N-(6-am...)
Show SMILES Cc1nc(N)ccc1CNC(=O)Cn1c(C)cnc(N)c1=O
Show InChI InChI=1S/C14H18N6O2/c1-8-5-18-13(16)14(22)20(8)7-12(21)17-6-10-3-4-11(15)19-9(10)2/h3-5H,6-7H2,1-2H3,(H2,15,19)(H2,16,18)(H,17,21)
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900n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of thrombin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50289531
PNG
(CHEMBL290947 | N-(1-{[(1-Carbamimidoyl-piperidin-4...)
Show SMILES Cc1ccc(NC(=O)CCc2ccccc2)c(=O)n1CC(=O)NCC1CCN(CC1)C(N)=N
Show InChI InChI=1S/C24H32N6O3/c1-17-7-9-20(28-21(31)10-8-18-5-3-2-4-6-18)23(33)30(17)16-22(32)27-15-19-11-13-29(14-12-19)24(25)26/h2-7,9,19H,8,10-16H2,1H3,(H3,25,26)(H,27,32)(H,28,31)
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940n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity against human trypsin


Bioorg Med Chem Lett 7: 1497-1500 (1997)


Article DOI: 10.1016/S0960-894X(97)00257-6
BindingDB Entry DOI: 10.7270/Q2P55P15
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50067795
PNG
(CHEMBL138855 | N-(6-Amino-2,4-dimethyl-pyridin-3-y...)
Show SMILES Cc1cc(N)nc(C)c1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C23H28N6O2/c1-15-11-20(24)28-17(3)19(15)13-26-21(30)14-29-16(2)12-27-22(23(29)31)25-10-9-18-7-5-4-6-8-18/h4-8,11-12H,9-10,13-14H2,1-3H3,(H2,24,28)(H,25,27)(H,26,30)
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1.00E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against trypsin was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Trypsin


(Homo sapiens (Human))
BDBM50122183
PNG
(CHEMBL431524 | N-(5-Chloro-2-ethylcarbamoylmethoxy...)
Show SMILES CCNC(=O)COc1ccc(Cl)cc1CNC(=O)Cn1c(C)cnc(NCCc2ccccc2)c1=O
Show InChI InChI=1S/C26H30ClN5O4/c1-3-28-24(34)17-36-22-10-9-21(27)13-20(22)15-30-23(33)16-32-18(2)14-31-25(26(32)35)29-12-11-19-7-5-4-6-8-19/h4-10,13-14H,3,11-12,15-17H2,1-2H3,(H,28,34)(H,29,31)(H,30,33)
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1.00E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of trypsin in human plasma


Bioorg Med Chem Lett 13: 161-4 (2002)


BindingDB Entry DOI: 10.7270/Q2348JQ0
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50067793
PNG
(CHEMBL139331 | N-(6-Amino-pyridin-3-ylmethyl)-2-(6...)
Show SMILES Cc1cnc(NCCc2ccccc2)c(=O)n1CC(=O)NCc1ccc(N)nc1
Show InChI InChI=1S/C21H24N6O2/c1-15-11-26-20(23-10-9-16-5-3-2-4-6-16)21(29)27(15)14-19(28)25-13-17-7-8-18(22)24-12-17/h2-8,11-12H,9-10,13-14H2,1H3,(H2,22,24)(H,23,26)(H,25,28)
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1.20E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against trypsin was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50069195
PNG
(CHEMBL354555 | N-(6-Amino-4-methyl-pyridin-3-ylmet...)
Show SMILES Cc1cc(N)ncc1CNC(=O)Cn1c(C)ccc(NS(=O)(=O)Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H25N5O4S/c1-15-10-20(23)24-11-18(15)12-25-21(28)13-27-16(2)8-9-19(22(27)29)26-32(30,31)14-17-6-4-3-5-7-17/h3-11,26H,12-14H2,1-2H3,(H2,23,24)(H,25,28)
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1.50E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Binding affinity towards trypsin was evaluated


Bioorg Med Chem Lett 8: 817-22 (1999)


BindingDB Entry DOI: 10.7270/Q2JH3K9Z
More data for this
Ligand-Target Pair
Serine protease 1


(Homo sapiens (Human))
BDBM50067798
PNG
(CHEMBL336438 | N-(6-Amino-2-methyl-pyridin-3-ylmet...)
Show SMILES C[C@H](Cc1ccccc1)Nc1ncc(C)n(CC(=O)NCc2ccc(N)nc2C)c1=O
Show InChI InChI=1S/C23H28N6O2/c1-15(11-18-7-5-4-6-8-18)27-22-23(31)29(16(2)12-26-22)14-21(30)25-13-19-9-10-20(24)28-17(19)3/h4-10,12,15H,11,13-14H2,1-3H3,(H2,24,28)(H,25,30)(H,26,27)/t15-/m1/s1
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1.50E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound against trypsin was determined


J Med Chem 41: 4466-74 (1998)


Article DOI: 10.1021/jm980368v
BindingDB Entry DOI: 10.7270/Q2KK99X0
More data for this
Ligand-Target Pair
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