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Compile Data Set for Download or QSAR

Found 286 hits with Last Name = 'mesch' and Initial = 's'   
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))
BDBM50443853
PNG
(CHEMBL3091519 | US20230391761, Reference 1)
Show SMILES CN1CCN(CC1)C(=O)[C@H](CNC(=O)c1ccc(Cl)s1)NS(=O)(=O)c1cccc(N2CCCC2=O)c1C |r|
Show InChI InChI=1S/C24H30ClN5O5S2/c1-16-18(30-10-4-7-22(30)31)5-3-6-20(16)37(34,35)27-17(24(33)29-13-11-28(2)12-14-29)15-26-23(32)19-8-9-21(25)36-19/h3,5-6,8-9,17,27H,4,7,10-15H2,1-2H3,(H,26,32)/t17-/m0/s1
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TBA



Citation and Details
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50443853
PNG
(CHEMBL3091519 | US20230391761, Reference 1)
Show SMILES CN1CCN(CC1)C(=O)[C@H](CNC(=O)c1ccc(Cl)s1)NS(=O)(=O)c1cccc(N2CCCC2=O)c1C |r|
Show InChI InChI=1S/C24H30ClN5O5S2/c1-16-18(30-10-4-7-22(30)31)5-3-6-20(16)37(34,35)27-17(24(33)29-13-11-28(2)12-14-29)15-26-23(32)19-8-9-21(25)36-19/h3,5-6,8-9,17,27H,4,7,10-15H2,1-2H3,(H,26,32)/t17-/m0/s1
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639340
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-{[(5-chloro-2...)
Show SMILES Cc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639343
PNG
(3-(1-Methyl-1H-imidazol-2-yl)propyl 3-[(5-chloroth...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639321
PNG
(Methyl 3-{[(5-chloro-2-thienyl)carbonyl]amino}-N-{...)
Show SMILES COC(=O)[C@H](CNC(=O)c1ccc(Cl)s1)NS(=O)(=O)c1cccc(N2CCCC2=O)c1C |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639346
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
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Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639322
PNG
(Methyl 3-[(5-chlorothiophene-2-carbonyl)amino]-N-[...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OC)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639344
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES Cc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639342
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-{[(5-chloro-2...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639346
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639338
PNG
(Methyl 3-[(5-chlorothiophene-2-carbonyl)amino]-N-{...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OC)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639342
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-{[(5-chloro-2...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639339
PNG
(Methyl 3-[(5-chlorothiophene-2-carbonyl)amino]-N-{...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OC)N1CC[C@@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639348
PNG
(3-(1-Methyl-1H-imidazol-2-yl)propyl 3-[(5-chloroth...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639341
PNG
(2-(1-Methyl-1H-imidazol-5-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1cncn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639341
PNG
(2-(1-Methyl-1H-imidazol-5-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1cncn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639347
PNG
(3-(1-Methyl-1H-imidazol-2-yl)propyl 3-[(5-chloroth...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639345
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES Cc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
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More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639319
PNG
(2-(Dimethylamino)ethyl 3-{[(5-chloro-2-thienyl)car...)
Show SMILES CN(C)CCOC(=O)[C@H](CNC(=O)c1ccc(Cl)s1)NS(=O)(=O)c1cccc(N2CCCC2=O)c1C |r|
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More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639340
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-{[(5-chloro-2...)
Show SMILES Cc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639343
PNG
(3-(1-Methyl-1H-imidazol-2-yl)propyl 3-[(5-chloroth...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCCc1nccn1C)N1CCCC1=O |r|
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More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506203
PNG
(CHEMBL4452312)
Show SMILES COc1ccccc1CC(=O)Nc1ccc(Oc2cccc(Cl)c2)c(c1)S(N)(=O)=O
Show InChI InChI=1S/C21H19ClN2O5S/c1-28-18-8-3-2-5-14(18)11-21(25)24-16-9-10-19(20(13-16)30(23,26)27)29-17-7-4-6-15(22)12-17/h2-10,12-13H,11H2,1H3,(H,24,25)(H2,23,26,27)
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n/an/a 2n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506156
PNG
(CHEMBL4471140)
Show SMILES NS(=O)(=O)c1cc(NC(=O)Cc2ccccc2Cl)ccc1OCc1ccccc1
Show InChI InChI=1S/C21H19ClN2O4S/c22-18-9-5-4-8-16(18)12-21(25)24-17-10-11-19(20(13-17)29(23,26)27)28-14-15-6-2-1-3-7-15/h1-11,13H,12,14H2,(H,24,25)(H2,23,26,27)
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Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM639320
PNG
(1-Methylpiperidin-4-yl 3-{[(5-chloro-2-thienyl)car...)
Show SMILES CN1CCC(CC1)OC(=O)[C@H](CNC(=O)c1ccc(Cl)s1)NS(=O)(=O)c1cccc(N2CCCC2=O)c1C |r|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
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PC sid
UniChem
n/an/a 2.30n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639346
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
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n/an/a 4n/an/an/an/an/an/a


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Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

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antibodypedia
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n/an/a 4.5n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

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antibodypedia
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n/an/a 4.60n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

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antibodypedia
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n/an/a 4.90n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639346
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC sid
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n/an/a 4.90n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506173
PNG
(CHEMBL4589444)
Show SMILES NS(=O)(=O)c1cc(NC(=O)Cc2ccccc2Cl)ccc1OCC1CCC1
Show InChI InChI=1S/C19H21ClN2O4S/c20-16-7-2-1-6-14(16)10-19(23)22-15-8-9-17(18(11-15)27(21,24)25)26-12-13-4-3-5-13/h1-2,6-9,11,13H,3-5,10,12H2,(H,22,23)(H2,21,24,25)
KEGG

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n/an/a 5n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
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PC sid
UniChem
n/an/a 5.20n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

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antibodypedia
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n/an/a 5.30n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
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n/an/a 5.80n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

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antibodypedia
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n/an/a 5.90n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639349
PNG
(2-(1-Methyl-1H-imidazol-2-yl)ethyl 3-[(5-chlorothi...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCc1nccn1C)N1CC[C@H](O)C1=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem
n/an/a 6n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506179
PNG
(CHEMBL4579583)
Show SMILES COc1cccc(Oc2ccc(NC(=O)Cc3ccccc3Cl)cc2S(N)(=O)=O)c1
Show InChI InChI=1S/C21H19ClN2O5S/c1-28-16-6-4-7-17(13-16)29-19-10-9-15(12-20(19)30(23,26)27)24-21(25)11-14-5-2-3-8-18(14)22/h2-10,12-13H,11H2,1H3,(H,24,25)(H2,23,26,27)
KEGG

UniProtKB/SwissProt

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n/an/a 8n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506184
PNG
(CHEMBL4447043)
Show SMILES NS(=O)(=O)c1cc(NC(=O)Cc2c(F)cccc2Cl)ccc1Oc1cccc(Cl)c1
Show InChI InChI=1S/C20H15Cl2FN2O4S/c21-12-3-1-4-14(9-12)29-18-8-7-13(10-19(18)30(24,27)28)25-20(26)11-15-16(22)5-2-6-17(15)23/h1-10H,11H2,(H,25,26)(H2,24,27,28)
KEGG

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n/an/a 9n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639322
PNG
(Methyl 3-[(5-chlorothiophene-2-carbonyl)amino]-N-[...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OC)N1CCCC1=O |r|
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n/an/a 9.70n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506187
PNG
(CHEMBL4522504)
Show SMILES Cc1ccccc1CC(=O)Nc1ccc(Oc2cccc(Cl)c2)c(c1)S(N)(=O)=O
Show InChI InChI=1S/C21H19ClN2O4S/c1-14-5-2-3-6-15(14)11-21(25)24-17-9-10-19(20(13-17)29(23,26)27)28-18-8-4-7-16(22)12-18/h2-10,12-13H,11H2,1H3,(H,24,25)(H2,23,26,27)
KEGG

UniProtKB/SwissProt

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n/an/a 10n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
Prothrombin


(Homo sapiens (Human))
BDBM639348
PNG
(3-(1-Methyl-1H-imidazol-2-yl)propyl 3-[(5-chloroth...)
Show SMILES CCc1c(cccc1S(=O)(=O)N[C@@H](CNC(=O)c1ccc(Cl)s1)C(=O)OCCCc1nccn1C)N1CC[C@@H](O)C1=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC cid
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n/an/a 10n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506180
PNG
(CHEMBL4556573)
Show SMILES NS(=O)(=O)c1cc(NC(=O)Cc2ccccc2Cl)ccc1Oc1ccccc1
Show InChI InChI=1S/C20H17ClN2O4S/c21-17-9-5-4-6-14(17)12-20(24)23-15-10-11-18(19(13-15)28(22,25)26)27-16-7-2-1-3-8-16/h1-11,13H,12H2,(H,23,24)(H2,22,25,26)
KEGG

UniProtKB/SwissProt

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n/an/a 10n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
P2X purinoceptor 4


(Homo sapiens (Human))
BDBM50506201
PNG
(CHEMBL4516176)
Show SMILES NS(=O)(=O)c1cc(NC(=O)Cc2ccccc2Cl)ccc1Oc1ccccc1Cl
Show InChI InChI=1S/C20H16Cl2N2O4S/c21-15-6-2-1-5-13(15)11-20(25)24-14-9-10-18(19(12-14)29(23,26)27)28-17-8-4-3-7-16(17)22/h1-10,12H,11H2,(H,24,25)(H2,23,26,27)
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
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n/an/a 13n/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Antagonist activity at human P2X4 receptor tranfected in HEK293 cells assessed as inhibition of Bz-ATP-induced calcium influx incubated for 30 mins a...


J Med Chem 62: 11194-11217 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01304
BindingDB Entry DOI: 10.7270/Q2M048RW
More data for this
Ligand-Target Pair
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