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Compile Data Set for Download or QSAR

Found 14 hits with Last Name = 'muzard' and Initial = 'm'   
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
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370431
PNG
(CHEMBL610574)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H](CC(=O)OCCCl)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C13H16ClN5O5/c14-1-2-23-7(20)3-6-9(21)10(22)13(24-6)19-5-18-8-11(15)16-4-17-12(8)19/h4-6,9-10,13,21-22H,1-3H2,(H2,15,16,17)/t6-,9-,10-,13?/m1/s1
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3.20E+3n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Inhibition of human placental AdoHcy hydrolase


Bioorg Med Chem Lett 14: 5799-802 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.050
BindingDB Entry DOI: 10.7270/Q2RN38NZ
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM84862
PNG
(5'-Deoxy-5'-thiodenosine scaffold, 6)
Show SMILES Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CS)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C10H13N5O3S/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(1-19)18-10/h2-4,6-7,10,16-17,19H,1H2,(H2,11,12,13)/t4-,6-,7-,10-/m1/s1
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4.00E+3n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Binding affinity for human placental S-adenosyl-homocysteine hydrolase


Bioorg Med Chem Lett 14: 5803-7 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.051
BindingDB Entry DOI: 10.7270/Q2MW2HX7
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370432
PNG
(CHEMBL611108)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H](CC(=O)OC2CC2(F)F)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C14H15F2N5O5/c15-14(16)2-6(14)26-7(22)1-5-9(23)10(24)13(25-5)21-4-20-8-11(17)18-3-19-12(8)21/h3-6,9-10,13,23-24H,1-2H2,(H2,17,18,19)/t5-,6?,9-,10-,13?/m1/s1
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1.70E+4n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Inhibition of human placental AdoHcy hydrolase


Bioorg Med Chem Lett 14: 5799-802 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.050
BindingDB Entry DOI: 10.7270/Q2RN38NZ
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50182453
PNG
((E)-6'-chloro-6'-cyano-5',6'-didehydro-6'-deoxyhom...)
Show SMILES Nc1ncnc2n(cnc12)[C@@H]1O[C@H](\C=C(\Cl)C#N)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C12H11ClN6O3/c13-5(2-14)1-6-8(20)9(21)12(22-6)19-4-18-7-10(15)16-3-17-11(7)19/h1,3-4,6,8-9,12,20-21H,(H2,15,16,17)/b5-1+/t6-,8-,9-,12-/m1/s1
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1.70E+4n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against AdoHcy Hydrolase


J Med Chem 49: 1223-6 (2006)


Article DOI: 10.1021/jm051023x
BindingDB Entry DOI: 10.7270/Q2RN37FV
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370433
PNG
(CHEMBL610838)
Show SMILES CSSC[C@H]1OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r|
Show InChI InChI=1S/C11H15N5O3S2/c1-20-21-2-5-7(17)8(18)11(19-5)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17-18H,2H2,1H3,(H2,12,13,14)/t5-,7-,8-,11?/m1/s1
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1.90E+4n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Binding affinity for human placental S-adenosyl-homocysteine hydrolase


Bioorg Med Chem Lett 14: 5803-7 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.051
BindingDB Entry DOI: 10.7270/Q2MW2HX7
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370435
PNG
(CHEMBL610303)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H]([C@H]2CS2)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C11H13N5O3S/c12-9-5-10(14-2-13-9)16(3-15-5)11-7(18)6(17)8(19-11)4-1-20-4/h2-4,6-8,11,17-18H,1H2,(H2,12,13,14)/t4-,6+,7-,8-,11?/m1/s1
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5.00E+4n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Binding affinity for human placental S-adenosyl-homocysteine hydrolase


Bioorg Med Chem Lett 14: 5803-7 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.051
BindingDB Entry DOI: 10.7270/Q2MW2HX7
More data for this
Ligand-Target Pair
Thymidine phosphorylase


(Escherichia coli)
BDBM50485112
PNG
(CHEMBL2030733)
Show SMILES Oc1nc(O)c2ccn(CCCCCCCCP(O)(O)=O)c2n1
Show InChI InChI=1S/C14H22N3O5P/c18-13-11-7-9-17(12(11)15-14(19)16-13)8-5-3-1-2-4-6-10-23(20,21)22/h7,9H,1-6,8,10H2,(H2,20,21,22)(H2,15,16,18,19)
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5.40E+4n/an/an/an/an/an/an/an/a



Universit£ de Caen Basse-Normandie

Curated by ChEMBL


Assay Description
Competitive inhibition of Escherichia coli thymidine phosphorylase incubated for 20 mins at room temperature followed by 5 mins incubation at 90 degC...


J Med Chem 55: 2758-68 (2012)


Article DOI: 10.1021/jm201694y
BindingDB Entry DOI: 10.7270/Q2GT5R1P
More data for this
Ligand-Target Pair
Thymidine phosphorylase


(Escherichia coli)
BDBM50485113
PNG
(CHEMBL2030728)
Show SMILES Cc1cn(Cc2cn(CCCCC(F)(F)P(O)(O)=O)nn2)c(=O)[nH]c1=O
Show InChI InChI=1S/C13H18F2N5O5P/c1-9-6-19(12(22)16-11(9)21)7-10-8-20(18-17-10)5-3-2-4-13(14,15)26(23,24)25/h6,8H,2-5,7H2,1H3,(H,16,21,22)(H2,23,24,25)
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5.80E+4n/an/an/an/an/an/an/an/a



Universit£ de Caen Basse-Normandie

Curated by ChEMBL


Assay Description
Competitive inhibition of Escherichia coli thymidine phosphorylase incubated for 20 mins at room temperature followed by 5 mins incubation at 90 degC...


J Med Chem 55: 2758-68 (2012)


Article DOI: 10.1021/jm201694y
BindingDB Entry DOI: 10.7270/Q2GT5R1P
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370430
PNG
(CHEMBL610300)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H](CC(=O)OCCF)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C13H16FN5O5/c14-1-2-23-7(20)3-6-9(21)10(22)13(24-6)19-5-18-8-11(15)16-4-17-12(8)19/h4-6,9-10,13,21-22H,1-3H2,(H2,15,16,17)/t6-,9-,10-,13?/m1/s1
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7.50E+4n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Inhibition of human placental AdoHcy hydrolase


Bioorg Med Chem Lett 14: 5799-802 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.050
BindingDB Entry DOI: 10.7270/Q2RN38NZ
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370436
PNG
(CHEMBL611107)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@@H](CSSC[C@H]2OC([C@H](O)[C@@H]2O)n2cnc3c(N)ncnc23)[C@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C20H24N10O6S2/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(35-19)1-37-38-2-8-12(32)14(34)20(36-8)30-6-28-10-16(22)24-4-26-18(10)30/h3-8,11-14,19-20,31-34H,1-2H2,(H2,21,23,25)(H2,22,24,26)/t7-,8+,11-,12+,13-,14+,19?,20?
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9.60E+4n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Binding affinity for human placental S-adenosyl-homocysteine hydrolase


Bioorg Med Chem Lett 14: 5803-7 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.051
BindingDB Entry DOI: 10.7270/Q2MW2HX7
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370434
PNG
(CHEMBL610588)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H]([C@@H]2CS2)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C11H13N5O3S/c12-9-5-10(14-2-13-9)16(3-15-5)11-7(18)6(17)8(19-11)4-1-20-4/h2-4,6-8,11,17-18H,1H2,(H2,12,13,14)/t4-,6-,7+,8+,11?/m0/s1
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1.05E+5n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Binding affinity for human placental S-adenosyl-homocysteine hydrolase


Bioorg Med Chem Lett 14: 5803-7 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.051
BindingDB Entry DOI: 10.7270/Q2MW2HX7
More data for this
Ligand-Target Pair
Thymidine phosphorylase


(Escherichia coli)
BDBM50485111
PNG
(CHEMBL368694)
Show SMILES Nc1c(Br)c(=O)[nH]c(=O)n1CCCCCCCCP(O)(O)=O
Show InChI InChI=1S/C12H21BrN3O5P/c13-9-10(14)16(12(18)15-11(9)17)7-5-3-1-2-4-6-8-22(19,20)21/h1-8,14H2,(H,15,17,18)(H2,19,20,21)
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1.42E+5n/an/an/an/an/an/an/an/a



Universit£ de Caen Basse-Normandie

Curated by ChEMBL


Assay Description
Competitive inhibition of Escherichia coli thymidine phosphorylase incubated for 20 mins at room temperature followed by 5 mins incubation at 90 degC...


J Med Chem 55: 2758-68 (2012)


Article DOI: 10.1021/jm201694y
BindingDB Entry DOI: 10.7270/Q2GT5R1P
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Rattus norvegicus)
BDBM50366378
PNG
(CHEMBL604650)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@](F)(CO)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C10H12FN5O4/c11-10(1-17)6(19)5(18)9(20-10)16-3-15-4-7(12)13-2-14-8(4)16/h2-3,5-6,9,17-19H,1H2,(H2,12,13,14)/t5-,6+,9?,10-/m1/s1
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1.66E+5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory constant against rat liver S-adenosyl-L-homocysteine hydrolase


Bioorg Med Chem Lett 5: 1455-1460 (1995)


Article DOI: 10.1016/0960-894X(95)00256-S
BindingDB Entry DOI: 10.7270/Q2C53MBT
More data for this
Ligand-Target Pair
Adenosylhomocysteinase


(Homo sapiens (Human))
BDBM50370429
PNG
(CHEMBL610573)
Show SMILES Nc1ncnc2n(cnc12)C1O[C@H](CC(=O)OC2CC2(Cl)Cl)[C@@H](O)[C@H]1O |r|
Show InChI InChI=1S/C14H15Cl2N5O5/c15-14(16)2-6(14)26-7(22)1-5-9(23)10(24)13(25-5)21-4-20-8-11(17)18-3-19-12(8)21/h3-6,9-10,13,23-24H,1-2H2,(H2,17,18,19)/t5-,6?,9-,10-,13?/m1/s1
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7.50E+5n/an/an/an/an/an/an/an/a



UMR 6519

Curated by ChEMBL


Assay Description
Inhibition of human placental AdoHcy hydrolase


Bioorg Med Chem Lett 14: 5799-802 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.050
BindingDB Entry DOI: 10.7270/Q2RN38NZ
More data for this
Ligand-Target Pair