Found 1180 hits with Last Name = 'mccarrick' and Initial = 'm' 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 |
|---|
Coagulation factor X
(Homo sapiens (Human)) | BDBM17284
(2-{[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-diflu...)Show SMILES CN(CC(O)=O)c1c(F)c(Oc2cccc(c2)C2=NCCN2C)nc(Oc2cc(ccc2O)C(N)=N)c1F |t:18| Show InChI InChI=1S/C25H24F2N6O5/c1-32-9-8-30-23(32)14-4-3-5-15(10-14)37-24-19(26)21(33(2)12-18(35)36)20(27)25(31-24)38-17-11-13(22(28)29)6-7-16(17)34/h3-7,10-11,34H,8-9,12H2,1-2H3,(H3,28,29)(H,35,36) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| MMDB
PDB
PubMed
| 0.110 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Coagulation factor X
(Homo sapiens (Human)) | BDBM17277
((Z,Z)BABCH | 4-{[(1Z,3Z)-3-[(4-carbamimidoylphenyl...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 0.660 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Compound (isomer) was tested in the absence of light for inhibitory activity against Human Coagulation factor X |
J Med Chem 41: 3551-6 (1998)
Article DOI: 10.1021/jm980281+
BindingDB Entry DOI: 10.7270/Q2QJ7GFX |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM17277
((Z,Z)BABCH | 4-{[(1Z,3Z)-3-[(4-carbamimidoylphenyl...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| PubMed
| 0.660 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066638
(3-[6-(5-Carbamimidoyl-2-hydroxy-phenoxy)-3,5-diflu...)Show SMILES CN(C)C(=O)c1cccc(Oc2nc(Oc3cc(ccc3O)C(N)=N)c(F)c(C)c2F)c1 Show InChI InChI=1S/C22H20F2N4O4/c1-11-17(23)20(31-14-6-4-5-13(9-14)22(30)28(2)3)27-21(18(11)24)32-16-10-12(19(25)26)7-8-15(16)29/h4-10,29H,1-3H3,(H3,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 1.80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066637
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1-meth...)Show SMILES CN1CCN=C1c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 |c:4| Show InChI InChI=1S/C23H21N5O5/c1-28-8-7-26-22(28)14-3-2-4-16(9-14)32-19-11-15(23(30)31)12-20(27-19)33-18-10-13(21(24)25)5-6-17(18)29/h2-6,9-12,29H,7-8H2,1H3,(H3,24,25)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 2.40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084175
(3,5-Bis-[1-(4-carbamimidoyl-phenyl)-meth-(Z)-ylide...)Show SMILES CCOC(=O)N1C\C(=C\c2ccc(cc2)C(N)=N)C(=O)\C(C1)=C/c1ccc(cc1)C(N)=N Show InChI InChI=1S/C24H25N5O3/c1-2-32-24(31)29-13-19(11-15-3-7-17(8-4-15)22(25)26)21(30)20(14-29)12-16-5-9-18(10-6-16)23(27)28/h3-12H,2,13-14H2,1H3,(H3,25,26)(H3,27,28)/b19-11-,20-12- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 2.5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084186
(2,9-di[1-[4-amino(imino)methylphenyl]-(Z)-methylid...)Show SMILES NC(=N)c1ccc(\C=C2\CCCCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C25H28N4O/c26-24(27)19-11-7-17(8-12-19)15-21-5-3-1-2-4-6-22(23(21)30)16-18-9-13-20(14-10-18)25(28)29/h7-16H,1-6H2,(H3,26,27)(H3,28,29)/b21-15-,22-16- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 2.80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113913
(3-[6-(3-Dimethylamino-phenoxy)-3,5-difluoro-4-meth...)Show SMILES CN(C)c1cccc(Oc2nc(Oc3cc(ccc3O)C(N)=N)c(F)c(C)c2F)c1 Show InChI InChI=1S/C21H20F2N4O3/c1-11-17(22)20(29-14-6-4-5-13(10-14)27(2)3)26-21(18(11)23)30-16-9-12(19(24)25)7-8-15(16)28/h4-10,28H,1-3H3,(H3,24,25) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066622
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-(3-dimethy...)Show SMILES CN(C)C(=O)c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C22H20N4O6/c1-26(2)21(28)13-4-3-5-15(8-13)31-18-10-14(22(29)30)11-19(25-18)32-17-9-12(20(23)24)6-7-16(17)27/h3-11,27H,1-2H3,(H3,23,24)(H,29,30) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 3.10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084174
(2,8-di[1-[4-amino(imino)methylphenyl]-(Z)-methylid...)Show SMILES NC(=N)c1ccc(\C=C2\CCCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C24H26N4O/c25-23(26)18-10-6-16(7-11-18)14-20-4-2-1-3-5-21(22(20)29)15-17-8-12-19(13-9-17)24(27)28/h6-15H,1-5H2,(H3,25,26)(H3,27,28)/b20-14-,21-15- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 4.60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084192
(3,5-Bis-[1-(4-carbamimidoyl-phenyl)-meth-(Z)-ylide...)Show SMILES COC(=O)C1C\C(=C\c2ccc(cc2)C(N)=N)C(=O)\C(C1)=C/c1ccc(cc1)C(N)=N Show InChI InChI=1S/C24H24N4O3/c1-31-24(30)20-12-18(10-14-2-6-16(7-3-14)22(25)26)21(29)19(13-20)11-15-4-8-17(9-5-15)23(27)28/h2-11,20H,12-13H2,1H3,(H3,25,26)(H3,27,28)/b18-10-,19-11- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 4.80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084163
(2,6-di[1-[4-amino(imino)methylphenyl]-(Z)-methylid...)Show SMILES NC(=N)c1ccc(\C=C2\CC(C\C(=C\c3ccc(cc3)C(N)=N)C2=O)c2ccccc2)cc1 Show InChI InChI=1S/C28H26N4O/c29-27(30)21-10-6-18(7-11-21)14-24-16-23(20-4-2-1-3-5-20)17-25(26(24)33)15-19-8-12-22(13-9-19)28(31)32/h1-15,23H,16-17H2,(H3,29,30)(H3,31,32)/b24-14-,25-15- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 5.20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066616
((Z,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1cccc(\C=C2\CCCC\C(=C\c3cccc(c3)C(N)=N)C2=O)c1 Show InChI InChI=1S/C23H24N4O/c24-22(25)19-9-3-5-15(13-19)11-17-7-1-2-8-18(21(17)28)12-16-6-4-10-20(14-16)23(26)27/h3-6,9-14H,1-2,7-8H2,(H3,24,25)(H3,26,27)/b17-11-,18-12- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 5.60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Compound (isomer) was tested in the absence of light for inhibitory activity against Human Coagulation factor X |
J Med Chem 41: 3551-6 (1998)
Article DOI: 10.1021/jm980281+
BindingDB Entry DOI: 10.7270/Q2QJ7GFX |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066616
((Z,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1cccc(\C=C2\CCCC\C(=C\c3cccc(c3)C(N)=N)C2=O)c1 Show InChI InChI=1S/C23H24N4O/c24-22(25)19-9-3-5-15(13-19)11-17-7-1-2-8-18(21(17)28)12-16-6-4-10-20(14-16)23(26)27/h3-6,9-14H,1-2,7-8H2,(H3,24,25)(H3,26,27)/b17-11-,18-12- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 5.60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113894
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-(3-carbami...)Show SMILES NC(=N)c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C20H17N5O5/c21-18(22)10-2-1-3-13(6-10)29-16-8-12(20(27)28)9-17(25-16)30-15-7-11(19(23)24)4-5-14(15)26/h1-9,26H,(H3,21,22)(H3,23,24)(H,27,28) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 9
(Homo sapiens (Human)) | BDBM50364378
(CHEMBL1950289)Show SMILES O[C@H]1CC[C@@H](CC1)Nc1ncc2nc(Nc3c(F)cc(F)cc3F)n([C@H]3CCOC3)c2n1 |r,wU:1.0,wD:4.7,25.26,(-6.26,-6.49,;-5.49,-5.16,;-6.25,-3.82,;-5.49,-2.5,;-3.95,-2.49,;-3.17,-3.82,;-3.94,-5.16,;-3.19,-1.16,;-1.65,-1.15,;-.89,.17,;.66,.18,;1.42,-1.15,;2.92,-1.46,;3.09,-2.98,;4.42,-3.75,;5.75,-2.97,;5.74,-1.45,;4.4,-.69,;7.06,-.67,;8.41,-1.43,;9.74,-.66,;8.41,-2.97,;7.08,-3.75,;7.08,-5.29,;1.69,-3.61,;1.23,-5.08,;-.23,-5.56,;-.23,-7.1,;1.24,-7.57,;2.14,-6.32,;.66,-2.48,;-.88,-2.48,)| Show InChI InChI=1S/C21H23F3N6O2/c22-11-7-15(23)18(16(24)8-11)28-21-27-17-9-25-20(26-12-1-3-14(31)4-2-12)29-19(17)30(21)13-5-6-32-10-13/h7-9,12-14,31H,1-6,10H2,(H,27,28)(H,25,26,29)/t12-,13-,14-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| 6.20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Celgene Corporation
Curated by ChEMBL
| Assay Description
Inhibition of hexa-His-tagged JNK2 expressed in baculoviral system using GST-tagged cJun as substrate preincubated for 15 mins prior ATP addition mea... |
Bioorg Med Chem Lett 22: 1433-8 (2012)
Article DOI: 10.1016/j.bmcl.2011.12.027
BindingDB Entry DOI: 10.7270/Q2C829SK |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084170
(3,5-Bis-[1-(4-carbamimidoyl-phenyl)-meth-(Z)-ylide...)Show SMILES NC(=N)c1ccc(\C=C2\CC(C\C(=C\c3ccc(cc3)C(N)=N)C2=O)C(O)=O)cc1 Show InChI InChI=1S/C23H22N4O3/c24-21(25)15-5-1-13(2-6-15)9-17-11-19(23(29)30)12-18(20(17)28)10-14-3-7-16(8-4-14)22(26)27/h1-10,19H,11-12H2,(H3,24,25)(H3,26,27)(H,29,30)/b17-9-,18-10- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 6.90 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113925
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(2-meth...)Show SMILES Cc1nccn1-c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C23H19N5O5/c1-13-26-7-8-28(13)16-3-2-4-17(12-16)32-20-10-15(23(30)31)11-21(27-20)33-19-9-14(22(24)25)5-6-18(19)29/h2-12,29H,1H3,(H3,24,25)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 8 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113883
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1,4-di...)Show SMILES Cc1cn(C)c(n1)-c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C24H21N5O5/c1-13-12-29(2)23(27-13)15-4-3-5-17(8-15)33-20-10-16(24(31)32)11-21(28-20)34-19-9-14(22(25)26)6-7-18(19)30/h3-12,30H,1-2H3,(H3,25,26)(H,31,32) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 8.40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066636
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(1-meth...)Show SMILES Cn1ccnc1-c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C23H19N5O5/c1-28-8-7-26-22(28)14-3-2-4-16(9-14)32-19-11-15(23(30)31)12-20(27-19)33-18-10-13(21(24)25)5-6-17(18)29/h2-12,29H,1H3,(H3,24,25)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 9 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50081365
(3-(5-{3-[(Z)-amino(imino)methyl]phenoxy}-2,4-diflu...)Show SMILES Cc1c(F)c(Oc2cccc(c2)C(N)=N)cc(Oc2cccc(c2)C(N)=N)c1F Show InChI InChI=1S/C21H18F2N4O2/c1-11-18(22)16(28-14-6-2-4-12(8-14)20(24)25)10-17(19(11)23)29-15-7-3-5-13(9-15)21(26)27/h2-10H,1H3,(H3,24,25)(H3,26,27) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Washington University
Curated by ChEMBL
| Assay Description
Inhibitory constant of the compound against Coagulation factor Xa (factor Xa) |
J Med Chem 42: 3910-8 (1999)
BindingDB Entry DOI: 10.7270/Q2X63M5W |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084164
(2-[1-[4-amino(imino)methylphenyl]-(Z)-methylidene]...)Show SMILES CNC(=N)c1ccc(C=C2CCCCC(=Cc3ccc(cc3)C(N)=N)C2=O)cc1 |w:8.7,15.15| Show InChI InChI=1S/C24H26N4O/c1-28-24(27)19-12-8-17(9-13-19)15-21-5-3-2-4-20(22(21)29)14-16-6-10-18(11-7-16)23(25)26/h6-15H,2-5H2,1H3,(H3,25,26)(H2,27,28) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50370088
(CHEMBL84437)Show SMILES CN(C)c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C21H20N4O5/c1-25(2)14-4-3-5-15(11-14)29-18-9-13(21(27)28)10-19(24-18)30-17-8-12(20(22)23)6-7-16(17)26/h3-11,26H,1-2H3,(H3,22,23)(H,27,28) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM17278
(3-{[6-(3-carbamimidoylphenoxy)-3,5-difluoro-4-meth...)Show SMILES Cc1c(F)c(Oc2cccc(c2)C(N)=N)nc(Oc2cccc(c2)C(N)=N)c1F Show InChI InChI=1S/C20H17F2N5O2/c1-10-15(21)19(28-13-6-2-4-11(8-13)17(23)24)27-20(16(10)22)29-14-7-3-5-12(9-14)18(25)26/h2-9H,1H3,(H3,23,24)(H3,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| PubMed
| 13 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113909
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-[3-(4-meth...)Show SMILES Cc1cn(cn1)-c1cccc(Oc2cc(cc(Oc3cc(ccc3O)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C23H19N5O5/c1-13-11-28(12-26-13)16-3-2-4-17(10-16)32-20-8-15(23(30)31)9-21(27-20)33-19-7-14(22(24)25)5-6-18(19)29/h2-12,29H,1H3,(H3,24,25)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 13 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066627
(3-[6-(2-Amino-5-carbamimidoyl-phenoxy)-3,5-difluor...)Show SMILES CN(C)C(=O)c1cccc(Oc2nc(Oc3cc(ccc3N)C(N)=N)c(F)c(C)c2F)c1 Show InChI InChI=1S/C22H21F2N5O3/c1-11-17(23)20(31-14-6-4-5-13(9-14)22(30)29(2)3)28-21(18(11)24)32-16-10-12(19(26)27)7-8-15(16)25/h4-10H,25H2,1-3H3,(H3,26,27) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 14 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084160
(2-[1-[4-amino(imino)methylphenyl]-(E)-methylidene]...)Show SMILES CN(C)C(=N)c1ccc(\C=C2\CCCC\C(=C/c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C25H28N4O/c1-29(2)25(28)20-13-9-18(10-14-20)16-22-6-4-3-5-21(23(22)30)15-17-7-11-19(12-8-17)24(26)27/h7-16,28H,3-6H2,1-2H3,(H3,26,27)/b21-15+,22-16-,28-25? | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 15 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084177
(2-[1-[4-amino(imino)methylphenyl]-(Z)-methylidene]...)Show SMILES CN(C)C(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C25H28N4O/c1-29(2)25(28)20-13-9-18(10-14-20)16-22-6-4-3-5-21(23(22)30)15-17-7-11-19(12-8-17)24(26)27/h7-16,28H,3-6H2,1-2H3,(H3,26,27)/b21-15-,22-16-,28-25? | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 18 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084176
(2,6-di[1-[4-amino(imino)methylphenyl]-(Z)-methylid...)Show SMILES NC(=N)c1ccc(\C=C2\CCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C22H22N4O/c23-21(24)16-8-4-14(5-9-16)12-18-2-1-3-19(20(18)27)13-15-6-10-17(11-7-15)22(25)26/h4-13H,1-3H2,(H3,23,24)(H3,25,26)/b18-12-,19-13- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 18 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084175
(3,5-Bis-[1-(4-carbamimidoyl-phenyl)-meth-(Z)-ylide...)Show SMILES CCOC(=O)N1C\C(=C\c2ccc(cc2)C(N)=N)C(=O)\C(C1)=C/c1ccc(cc1)C(N)=N Show InChI InChI=1S/C24H25N5O3/c1-2-32-24(31)29-13-19(11-15-3-7-17(8-4-15)22(25)26)21(30)20(14-29)12-16-5-9-18(10-6-16)23(27)28/h3-12H,2,13-14H2,1H3,(H3,25,26)(H3,27,28)/b19-11-,20-12- | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113865
(3-[6-(5-Carbamimidoyl-2,3-dihydroxy-phenoxy)-3,5-d...)Show SMILES CN(C)C(=O)c1cccc(Oc2nc(Oc3cc(cc(O)c3O)C(N)=N)c(F)c(C)c2F)c1 Show InChI InChI=1S/C22H20F2N4O5/c1-10-16(23)20(32-13-6-4-5-11(7-13)22(31)28(2)3)27-21(17(10)24)33-15-9-12(19(25)26)8-14(29)18(15)30/h4-9,29-30H,1-3H3,(H3,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 23 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066617
(2-(5-Carbamimidoyl-2-hydroxy-phenoxy)-6-(3-imidazo...)Show SMILES NC(=N)c1ccc(O)c(Oc2cc(cc(Oc3cccc(c3)-n3ccnc3)n2)C(O)=O)c1 Show InChI InChI=1S/C22H17N5O5/c23-21(24)13-4-5-17(28)18(8-13)32-20-10-14(22(29)30)9-19(26-20)31-16-3-1-2-15(11-16)27-7-6-25-12-27/h1-12,28H,(H3,23,24)(H,29,30) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| PubMed
| 26 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50066615
((E,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C/c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 29 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Compound (isomer) was tested in the absence of light for inhibitory activity against trypsin. |
J Med Chem 41: 3551-6 (1998)
Article DOI: 10.1021/jm980281+
BindingDB Entry DOI: 10.7270/Q2QJ7GFX |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50066615
((E,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C/c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 29 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084191
(2-[1-[4-amino(imino)methylphenyl]-(E)-methylidene]...)Show SMILES NC(=N)c1ccc(\C=C2\CCCCC\C(=C/c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C24H26N4O/c25-23(26)18-10-6-16(7-11-18)14-20-4-2-1-3-5-21(22(20)29)15-17-8-12-19(13-9-17)24(27)28/h6-15H,1-5H2,(H3,25,26)(H3,27,28)/b20-14-,21-15+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084164
(2-[1-[4-amino(imino)methylphenyl]-(Z)-methylidene]...)Show SMILES CNC(=N)c1ccc(C=C2CCCCC(=Cc3ccc(cc3)C(N)=N)C2=O)cc1 |w:8.7,15.15| Show InChI InChI=1S/C24H26N4O/c1-28-24(27)19-12-8-17(9-13-19)15-21-5-3-2-4-20(22(21)29)14-16-6-10-18(11-7-16)23(25)26/h6-15H,2-5H2,1H3,(H3,25,26)(H2,27,28) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| 30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM17277
((Z,Z)BABCH | 4-{[(1Z,3Z)-3-[(4-carbamimidoylphenyl...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14- | PDB
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| 33 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Compound (isomer) was tested in the absence of light for inhibitory activity against trypsin. |
J Med Chem 41: 3551-6 (1998)
Article DOI: 10.1021/jm980281+
BindingDB Entry DOI: 10.7270/Q2QJ7GFX |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Serine protease 1
(Bos taurus (bovine)) | BDBM17277
((Z,Z)BABCH | 4-{[(1Z,3Z)-3-[(4-carbamimidoylphenyl...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C23H24N4O/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)28)14-16-7-11-18(12-8-16)23(26)27/h5-14H,1-4H2,(H3,24,25)(H3,26,27)/b19-13-,20-14- | PDB
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| 33 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50165509
(CHEMBL372847 | Naphthalene-1-carboxylic acid (7-ca...)Show SMILES NC(=N)c1ccc2ccc(CN(CCc3ccc(F)cc3)C(=O)c3cccc4ccccc34)cc2c1 Show InChI InChI=1S/C31H26FN3O/c32-27-14-9-21(10-15-27)16-17-35(31(36)29-7-3-5-24-4-1-2-6-28(24)29)20-22-8-11-23-12-13-25(30(33)34)19-26(23)18-22/h1-15,18-19H,16-17,20H2,(H3,33,34) | PDB
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| 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibition constant towards human coagulation factor X |
Bioorg Med Chem Lett 15: 2249-52 (2005)
Article DOI: 10.1016/j.bmcl.2005.03.019
BindingDB Entry DOI: 10.7270/Q2V40W0H |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM17283
((2S)-3-(7-carbamimidoylnaphthalen-2-yl)-2-(4-{[(3S...)Show SMILES CC(=N)N1CC[C@@H](C1)Oc1ccc(cc1)[C@H](Cc1ccc2ccc(cc2c1)C(N)=N)C(O)=O |r| Show InChI InChI=1S/C26H28N4O3/c1-16(27)30-11-10-23(15-30)33-22-8-6-19(7-9-22)24(26(31)32)13-17-2-3-18-4-5-20(25(28)29)14-21(18)12-17/h2-9,12,14,23-24,27H,10-11,13,15H2,1H3,(H3,28,29)(H,31,32)/t23-,24-/m0/s1 | PDB
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| 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50364378
(CHEMBL1950289)Show SMILES O[C@H]1CC[C@@H](CC1)Nc1ncc2nc(Nc3c(F)cc(F)cc3F)n([C@H]3CCOC3)c2n1 |r,wU:1.0,wD:4.7,25.26,(-6.26,-6.49,;-5.49,-5.16,;-6.25,-3.82,;-5.49,-2.5,;-3.95,-2.49,;-3.17,-3.82,;-3.94,-5.16,;-3.19,-1.16,;-1.65,-1.15,;-.89,.17,;.66,.18,;1.42,-1.15,;2.92,-1.46,;3.09,-2.98,;4.42,-3.75,;5.75,-2.97,;5.74,-1.45,;4.4,-.69,;7.06,-.67,;8.41,-1.43,;9.74,-.66,;8.41,-2.97,;7.08,-3.75,;7.08,-5.29,;1.69,-3.61,;1.23,-5.08,;-.23,-5.56,;-.23,-7.1,;1.24,-7.57,;2.14,-6.32,;.66,-2.48,;-.88,-2.48,)| Show InChI InChI=1S/C21H23F3N6O2/c22-11-7-15(23)18(16(24)8-11)28-21-27-17-9-25-20(26-12-1-3-14(31)4-2-12)29-19(17)30(21)13-5-6-32-10-13/h7-9,12-14,31H,1-6,10H2,(H,27,28)(H,25,26,29)/t12-,13-,14-/m0/s1 | PDB
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Article
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| 44 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Celgene Corporation
Curated by ChEMBL
| Assay Description
Inhibition of hexa-His-tagged JNK1 expressed in baculoviral system using GST-tagged c-Jun as substrate preincubated for 15 mins prior ATP addition me... |
Bioorg Med Chem Lett 22: 1433-8 (2012)
Article DOI: 10.1016/j.bmcl.2011.12.027
BindingDB Entry DOI: 10.7270/Q2C829SK |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Serine protease 1
(Bos taurus (bovine)) | BDBM50066616
((Z,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1cccc(\C=C2\CCCC\C(=C\c3cccc(c3)C(N)=N)C2=O)c1 Show InChI InChI=1S/C23H24N4O/c24-22(25)19-9-3-5-15(13-19)11-17-7-1-2-8-18(21(17)28)12-16-6-4-10-20(14-16)23(26)27/h3-6,9-14H,1-2,7-8H2,(H3,24,25)(H3,26,27)/b17-11-,18-12- | PDB
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| 44 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Compound (isomer) was tested in the absence of light for inhibitory activity against trypsin. |
J Med Chem 41: 3551-6 (1998)
Article DOI: 10.1021/jm980281+
BindingDB Entry DOI: 10.7270/Q2QJ7GFX |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50066616
((Z,Z)-2,7-Bis(4-amidinobenzylidine)cycloheptan-1-o...)Show SMILES NC(=N)c1cccc(\C=C2\CCCC\C(=C\c3cccc(c3)C(N)=N)C2=O)c1 Show InChI InChI=1S/C23H24N4O/c24-22(25)19-9-3-5-15(13-19)11-17-7-1-2-8-18(21(17)28)12-16-6-4-10-20(14-16)23(26)27/h3-6,9-14H,1-2,7-8H2,(H3,24,25)(H3,26,27)/b17-11-,18-12- | PDB
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| 44 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084180
(4-[3-[1-(4-Carbamimidoyl-phenyl)-meth-(Z)-ylidene]...)Show SMILES NC(=N)c1ccc(\C=C2\CCCC\C(=C\c3ccc(cc3)C(N)=O)C2=O)cc1 Show InChI InChI=1S/C23H23N3O2/c24-22(25)17-9-5-15(6-10-17)13-19-3-1-2-4-20(21(19)27)14-16-7-11-18(12-8-16)23(26)28/h5-14H,1-4H2,(H3,24,25)(H2,26,28)/b19-13-,20-14- | PDB
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| 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50084160
(2-[1-[4-amino(imino)methylphenyl]-(E)-methylidene]...)Show SMILES CN(C)C(=N)c1ccc(\C=C2\CCCC\C(=C/c3ccc(cc3)C(N)=N)C2=O)cc1 Show InChI InChI=1S/C25H28N4O/c1-29(2)25(28)20-13-9-18(10-14-20)16-22-6-4-3-5-21(23(22)30)15-17-7-11-19(12-8-17)24(26)27/h7-16,28H,3-6H2,1-2H3,(H3,26,27)/b21-15+,22-16-,28-25? | PDB
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| 52 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of human coagulation factor Xa (Xa) in a purified enzyme system. |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084193
(2,6-di[1-[4-amino(imino)methylphenyl]-(E)-methylid...)Show SMILES NC(=N)c1ccc(\C=C2/CC(C\C(=C/c3ccc(cc3)C(N)=N)C2=O)c2ccccc2)cc1 Show InChI InChI=1S/C28H26N4O/c29-27(30)21-10-6-18(7-11-21)14-24-16-23(20-4-2-1-3-5-20)17-25(26(24)33)15-19-8-12-22(13-9-19)28(31)32/h1-15,23H,16-17H2,(H3,29,30)(H3,31,32)/b24-14+,25-15+ | PDB
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| 56 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50066620
(2,6-Bis-(3-carbamimidoyl-phenoxy)-isonicotinic aci...)Show SMILES NC(=N)c1cccc(Oc2cc(cc(Oc3cccc(c3)C(N)=N)n2)C(O)=O)c1 Show InChI InChI=1S/C20H17N5O4/c21-18(22)11-3-1-5-14(7-11)28-16-9-13(20(26)27)10-17(25-16)29-15-6-2-4-12(8-15)19(23)24/h1-10H,(H3,21,22)(H3,23,24)(H,26,27) | PDB
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| 59 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084183
(3-[1-(4-Carbamimidoyl-phenyl)-meth-(E)-ylidene]-5-...)Show SMILES CCOC(=O)N1C\C(=C\c2ccc(cc2)C(N)=N)C(=O)\C(C1)=C\c1ccc(cc1)C(N)=N Show InChI InChI=1S/C24H25N5O3/c1-2-32-24(31)29-13-19(11-15-3-7-17(8-4-15)22(25)26)21(30)20(14-29)12-16-5-9-18(10-6-16)23(27)28/h3-12H,2,13-14H2,1H3,(H3,25,26)(H3,27,28)/b19-11-,20-12+ | PDB
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| 61 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50113916
(4-Amino-3-[6-(3-dimethylamino-phenoxy)-3,5-difluor...)Show SMILES CN(C)c1cccc(Oc2nc(Oc3cc(ccc3N)C(N)=N)c(F)c(C)c2F)c1 Show InChI InChI=1S/C21H21F2N5O2/c1-11-17(22)20(29-14-6-4-5-13(10-14)28(2)3)27-21(18(11)23)30-16-9-12(19(25)26)7-8-15(16)24/h4-10H,24H2,1-3H3,(H3,25,26) | PDB
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| 64 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
Inhibitory constant against human coagulation factor Xa (fXa) |
J Med Chem 45: 2484-93 (2002)
BindingDB Entry DOI: 10.7270/Q24J0FTH |
More data for this
Ligand-Target Pair | |
Serine protease 1
(Bos taurus (bovine)) | BDBM50084178
(3,5-Bis-[1-(4-carbamimidoyl-phenyl)-meth-(E)-ylide...)Show SMILES COC(=O)C1C\C(=C/c2ccc(cc2)C(N)=N)C(=O)\C(C1)=C\c1ccc(cc1)C(N)=N Show InChI InChI=1S/C24H24N4O3/c1-31-24(30)20-12-18(10-14-2-6-16(7-3-14)22(25)26)21(29)19(13-20)11-15-4-8-17(9-5-15)23(27)28/h2-11,20H,12-13H2,1H3,(H3,25,26)(H3,27,28)/b18-10+,19-11+ | PDB
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| 72 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Berlex Biosciences
Curated by ChEMBL
| Assay Description
In vitro inhibition of bovine trypsin(Trp). |
J Med Chem 42: 5415-25 (2000)
BindingDB Entry DOI: 10.7270/Q2TT4Q5S |
More data for this
Ligand-Target Pair | |
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