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Compile Data Set for Download or QSAR

Found 75 hits with Last Name = 'amoroso' and Initial = 'a'   
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
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385268
PNG
(CHEMBL2035292)
Show SMILES OB(O)CNC(=O)c1ccccc1[N+]([O-])=O
Show InChI InChI=1S/C8H9BN2O5/c12-8(10-5-9(13)14)6-3-1-2-4-7(6)11(15)16/h1-4,13-14H,5H2,(H,10,12)
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360n/an/an/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Binding affinity to Actinomadura sp. R39 PBP


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442248
PNG
(CHEMBL2441983)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccccc1F |w:9.9|
Show InChI InChI=1S/C17H12FNO5/c18-14-4-2-1-3-13(14)16(22)10-7-11(19-9-10)5-6-12(20)8-15(21)17(23)24/h1-7,9,19H,8H2,(H,23,24)
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400n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Non-competitive inhibition of human TdT using 3'-OH as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442215
PNG
(CHEMBL2441974)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(O)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H17NO5/c23-16-8-5-14(6-9-16)12-22-13-15(18-3-1-2-4-19(18)22)7-10-17(24)11-20(25)21(26)27/h1-10,13,23H,11-12H2,(H,26,27)
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450n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Competitive inhibition of human TdT using TTP as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442248
PNG
(CHEMBL2441983)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccccc1F |w:9.9|
Show InChI InChI=1S/C17H12FNO5/c18-14-4-2-1-3-13(14)16(22)10-7-11(19-9-10)5-6-12(20)8-15(21)17(23)24/h1-7,9,19H,8H2,(H,23,24)
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500n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Competitive inhibition of human TdT using TTP as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442215
PNG
(CHEMBL2441974)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(O)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H17NO5/c23-16-8-5-14(6-9-16)12-22-13-15(18-3-1-2-4-19(18)22)7-10-17(24)11-20(25)21(26)27/h1-10,13,23H,11-12H2,(H,26,27)
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500n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Non-competitive inhibition of human TdT using 3'-OH as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442209
PNG
(CHEMBL2441980)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccc(cc1)C#N |w:11.11|
Show InChI InChI=1S/C20H16N2O5/c1-2-27-20(26)18(24)10-17(23)8-7-16-9-15(12-22-16)19(25)14-5-3-13(11-21)4-6-14/h3-9,12,22H,2,10H2,1H3
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1.50E+3n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Competitive inhibition of human TdT using TTP as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385267
PNG
(CHEMBL2035284)
Show SMILES COc1cccc(OC)c1C(=O)NCB(O)O
Show InChI InChI=1S/C10H14BNO5/c1-16-7-4-3-5-8(17-2)9(7)10(13)12-6-11(14)15/h3-5,14-15H,6H2,1-2H3,(H,12,13)
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1.50E+3n/an/an/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Binding affinity to Actinomadura sp. R39 PBP


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
DNA nucleotidylexotransferase


(Homo sapiens (Human))
BDBM50442209
PNG
(CHEMBL2441980)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccc(cc1)C#N |w:11.11|
Show InChI InChI=1S/C20H16N2O5/c1-2-27-20(26)18(24)10-17(23)8-7-16-9-15(12-22-16)19(25)14-5-3-13(11-21)4-6-14/h3-9,12,22H,2,10H2,1H3
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1.70E+3n/an/an/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Non-competitive inhibition of human TdT using 3'-OH as substrate


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385263
PNG
(CHEMBL2035289)
Show SMILES OB(O)CNC(=O)c1ccccc1Cl
Show InChI InChI=1S/C8H9BClNO3/c10-7-4-2-1-3-6(7)8(12)11-5-9(13)14/h1-4,13-14H,5H2,(H,11,12)
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4.20E+4n/an/an/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Binding affinity to Actinomadura sp. R39 PBP


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM39809
PNG
(Acylglycineboronic acid, 6)
Show SMILES OB(O)CNC(=O)Cc1ccccc1
Show InChI InChI=1S/C9H12BNO3/c12-9(11-7-10(13)14)6-8-4-2-1-3-5-8/h1-5,13-14H,6-7H2,(H,11,12)
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1.25E+5n/an/an/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Binding affinity to Actinomadura sp. R39 PBP


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385268
PNG
(CHEMBL2035292)
Show SMILES OB(O)CNC(=O)c1ccccc1[N+]([O-])=O
Show InChI InChI=1S/C8H9BN2O5/c12-8(10-5-9(13)14)6-3-1-2-4-7(6)11(15)16/h1-4,13-14H,5H2,(H,10,12)
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n/an/a 600n/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Inhibition of Actinomadura sp. R39 PBP using S2d as substrate incubated for 60 mins prior to substrate addition by DTNB-based spectrophotometry


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385267
PNG
(CHEMBL2035284)
Show SMILES COc1cccc(OC)c1C(=O)NCB(O)O
Show InChI InChI=1S/C10H14BNO5/c1-16-7-4-3-5-8(17-2)9(7)10(13)12-6-11(14)15/h3-5,14-15H,6H2,1-2H3,(H,12,13)
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n/an/a 1.30E+3n/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Inhibition of Actinomadura sp. R39 PBP using S2d as substrate incubated for 60 mins prior to substrate addition by DTNB-based spectrophotometry


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385266
PNG
(CHEMBL2035295)
Show SMILES OB(O)CNC(=O)c1ccccc1C(F)(F)F
Show InChI InChI=1S/C9H9BF3NO3/c11-9(12,13)7-4-2-1-3-6(7)8(15)14-5-10(16)17/h1-4,16-17H,5H2,(H,14,15)
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n/an/a 1.50E+4n/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Inhibition of Actinomadura sp. R39 PBP using S2d as substrate incubated for 60 mins prior to substrate addition by DTNB-based spectrophotometry


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
Penicillin-binding protein 2


(Staphylococcus aureus)
BDBM50500470
PNG
(CHEMBL3746902)
Show SMILES CSc1ccc2n(Cc3ccc(Cl)c(Cl)c3)c(C)c(CCN)c2c1
Show InChI InChI=1S/C19H20Cl2N2S/c1-12-15(7-8-22)16-10-14(24-2)4-6-19(16)23(12)11-13-3-5-17(20)18(21)9-13/h3-6,9-10H,7-8,11,22H2,1-2H3
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n/an/a 2.07E+4n/an/an/an/an/an/a



University of Ljubljana

Curated by ChEMBL


Assay Description
Inhibition of Staphylococcus aureus PBP2 transglycosylase activity after 30 mins by continous fluorescence assay


J Med Chem 58: 9712-21 (2015)


Article DOI: 10.1021/acs.jmedchem.5b01482
BindingDB Entry DOI: 10.7270/Q2F47S40
More data for this
Ligand-Target Pair
D-alanyl-D-alanine carboxypeptidase


(Actinomadura sp. (strain R39))
BDBM50385262
PNG
(CHEMBL2035285)
Show SMILES OB(O)CNC(=O)c1c(F)cccc1F
Show InChI InChI=1S/C8H8BF2NO3/c10-5-2-1-3-6(11)7(5)8(13)12-4-9(14)15/h1-3,14-15H,4H2,(H,12,13)
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n/an/a 3.50E+4n/an/an/an/an/an/a



Universit£ de Li£ge

Curated by ChEMBL


Assay Description
Inhibition of Actinomadura sp. R39 PBP using S2d as substrate incubated for 60 mins prior to substrate addition by DTNB-based spectrophotometry


Bioorg Med Chem 20: 3915-24 (2012)


Article DOI: 10.1016/j.bmc.2012.04.018
BindingDB Entry DOI: 10.7270/Q200034N
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442207
PNG
(CHEMBL2441981)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(cn1Cc1ccc(F)cc1)C(=O)c1ccccc1 |w:11.11|
Show InChI InChI=1S/C26H22FNO5/c1-2-33-26(32)24(30)15-23(29)13-12-22-14-20(25(31)19-6-4-3-5-7-19)17-28(22)16-18-8-10-21(27)11-9-18/h3-14,17H,2,15-16H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442208
PNG
(CHEMBL2440137)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(cn1Cc1ccccc1)C(=O)c1ccccc1 |w:11.11|
Show InChI InChI=1S/C26H23NO5/c1-2-32-26(31)24(29)16-23(28)14-13-22-15-21(25(30)20-11-7-4-8-12-20)18-27(22)17-19-9-5-3-6-10-19/h3-15,18H,2,16-17H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442209
PNG
(CHEMBL2441980)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccc(cc1)C#N |w:11.11|
Show InChI InChI=1S/C20H16N2O5/c1-2-27-20(26)18(24)10-17(23)8-7-16-9-15(12-22-16)19(25)14-5-3-13(11-21)4-6-14/h3-9,12,22H,2,10H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442210
PNG
(CHEMBL2441979)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1cccc(F)c1 |w:11.11|
Show InChI InChI=1S/C19H16FNO5/c1-2-26-19(25)17(23)10-16(22)7-6-15-9-13(11-21-15)18(24)12-4-3-5-14(20)8-12/h3-9,11,21H,2,10H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442211
PNG
(CHEMBL2441978)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccc(F)cc1 |w:11.11|
Show InChI InChI=1S/C19H16FNO5/c1-2-26-19(25)17(23)10-16(22)8-7-15-9-13(11-21-15)18(24)12-3-5-14(20)6-4-12/h3-9,11,21H,2,10H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442212
PNG
(CHEMBL2441977)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cc(c[nH]1)C(=O)c1ccccc1F |w:11.11|
Show InChI InChI=1S/C19H16FNO5/c1-2-26-19(25)17(23)10-14(22)8-7-13-9-12(11-21-13)18(24)15-5-3-4-6-16(15)20/h3-9,11,21H,2,10H2,1H3
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442213
PNG
(CHEMBL2441976)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(CC(=O)N2CCOCC2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C20H20N2O6/c23-15(11-18(24)20(26)27)6-5-14-12-22(17-4-2-1-3-16(14)17)13-19(25)21-7-9-28-10-8-21/h1-6,12H,7-11,13H2,(H,26,27)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442214
PNG
(CHEMBL2441975)
Show SMILES CN(C)C(=O)Cn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:9.8|
Show InChI InChI=1S/C18H18N2O5/c1-19(2)17(23)11-20-10-12(14-5-3-4-6-15(14)20)7-8-13(21)9-16(22)18(24)25/h3-8,10H,9,11H2,1-2H3,(H,24,25)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442215
PNG
(CHEMBL2441974)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(O)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H17NO5/c23-16-8-5-14(6-9-16)12-22-13-15(18-3-1-2-4-19(18)22)7-10-17(24)11-20(25)21(26)27/h1-10,13,23H,11-12H2,(H,26,27)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442216
PNG
(CHEMBL2441973)
Show SMILES COc1ccc(Cn2cc(C=CC(=O)CC(=O)C(O)=O)c3ccccc23)cc1 |w:10.9|
Show InChI InChI=1S/C22H19NO5/c1-28-18-10-6-15(7-11-18)13-23-14-16(19-4-2-3-5-20(19)23)8-9-17(24)12-21(25)22(26)27/h2-11,14H,12-13H2,1H3,(H,26,27)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442217
PNG
(CHEMBL2441972)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(cc2)C#N)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C22H16N2O4/c23-12-15-5-7-16(8-6-15)13-24-14-17(19-3-1-2-4-20(19)24)9-10-18(25)11-21(26)22(27)28/h1-10,14H,11,13H2,(H,27,28)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442218
PNG
(CHEMBL2441971)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(Cl)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H16ClNO4/c22-16-8-5-14(6-9-16)12-23-13-15(18-3-1-2-4-19(18)23)7-10-17(24)11-20(25)21(26)27/h1-10,13H,11-12H2,(H,26,27)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442219
PNG
(CHEMBL2441970)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(F)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H16FNO4/c22-16-8-5-14(6-9-16)12-23-13-15(18-3-1-2-4-19(18)23)7-10-17(24)11-20(25)21(26)27/h1-10,13H,11-12H2,(H,26,27)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442220
PNG
(CHEMBL2441969)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccccc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C21H17NO4/c23-17(12-20(24)21(25)26)11-10-16-14-22(13-15-6-2-1-3-7-15)19-9-5-4-8-18(16)19/h1-11,14H,12-13H2,(H,25,26)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442221
PNG
(CHEMBL2441968)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(-c2ccc(Cl)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C20H14ClNO4/c21-14-6-8-15(9-7-14)22-12-13(17-3-1-2-4-18(17)22)5-10-16(23)11-19(24)20(25)26/h1-10,12H,11H2,(H,25,26)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442222
PNG
(CHEMBL2441967)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(-c2ccc(O)cc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C20H15NO5/c22-15-9-6-14(7-10-15)21-12-13(17-3-1-2-4-18(17)21)5-8-16(23)11-19(24)20(25)26/h1-10,12,22H,11H2,(H,25,26)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442223
PNG
(CHEMBL2441966)
Show SMILES OC(=O)C(=O)CC(=O)C=Cc1cn(-c2ccccc2)c2ccccc12 |w:9.9|
Show InChI InChI=1S/C20H15NO4/c22-16(12-19(23)20(24)25)11-10-14-13-21(15-6-2-1-3-7-15)18-9-5-4-8-17(14)18/h1-11,13H,12H2,(H,24,25)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442224
PNG
(CHEMBL2441965)
Show SMILES CC(=C)Cn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:7.6|
Show InChI InChI=1S/C18H17NO4/c1-12(2)10-19-11-13(15-5-3-4-6-16(15)19)7-8-14(20)9-17(21)18(22)23/h3-8,11H,1,9-10H2,2H3,(H,22,23)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442225
PNG
(CHEMBL2441964)
Show SMILES [#6]\[#6](-[#6])=[#6]\n1cc(-[#6]=[#6]-[#6](=O)-[#6]-[#6](=O)-[#6](-[#8])=O)c2ccccc12 |w:7.6|
Show InChI InChI=1S/C18H17NO4/c1-12(2)10-19-11-13(15-5-3-4-6-16(15)19)7-8-14(20)9-17(21)18(22)23/h3-8,10-11H,9H2,1-2H3,(H,22,23)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442226
PNG
(CHEMBL2441963)
Show SMILES C\C=C\Cn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:7.6|
Show InChI InChI=1S/C18H17NO4/c1-2-3-10-19-12-13(15-6-4-5-7-16(15)19)8-9-14(20)11-17(21)18(22)23/h2-9,12H,10-11H2,1H3,(H,22,23)/b3-2+,9-8?
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442227
PNG
(CHEMBL2441962)
Show SMILES C\C=C\n1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:6.5|
Show InChI InChI=1S/C17H15NO4/c1-2-9-18-11-12(14-5-3-4-6-15(14)18)7-8-13(19)10-16(20)17(21)22/h2-9,11H,10H2,1H3,(H,21,22)/b8-7?,9-2+
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442228
PNG
(CHEMBL2441961)
Show SMILES CC(C)CCn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:8.7|
Show InChI InChI=1S/C19H21NO4/c1-13(2)9-10-20-12-14(16-5-3-4-6-17(16)20)7-8-15(21)11-18(22)19(23)24/h3-8,12-13H,9-11H2,1-2H3,(H,23,24)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442229
PNG
(CHEMBL2441960)
Show SMILES CCCCn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:7.6|
Show InChI InChI=1S/C18H19NO4/c1-2-3-10-19-12-13(15-6-4-5-7-16(15)19)8-9-14(20)11-17(21)18(22)23/h4-9,12H,2-3,10-11H2,1H3,(H,22,23)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442230
PNG
(CHEMBL2441959)
Show SMILES CCCn1cc(C=CC(=O)CC(=O)C(O)=O)c2ccccc12 |w:6.5|
Show InChI InChI=1S/C17H17NO4/c1-2-9-18-11-12(14-5-3-4-6-15(14)18)7-8-13(19)10-16(20)17(21)22/h3-8,11H,2,9-10H2,1H3,(H,21,22)
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442231
PNG
(CHEMBL2441958)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(CC(=O)N2CCOCC2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C22H24N2O6/c1-2-30-22(28)20(26)13-17(25)8-7-16-14-24(19-6-4-3-5-18(16)19)15-21(27)23-9-11-29-12-10-23/h3-8,14H,2,9-13,15H2,1H3
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442232
PNG
(CHEMBL2441957)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(CC(=O)N(C)C)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C20H22N2O5/c1-4-27-20(26)18(24)11-15(23)10-9-14-12-22(13-19(25)21(2)3)17-8-6-5-7-16(14)17/h5-10,12H,4,11,13H2,1-3H3
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Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442233
PNG
(CHEMBL2441956)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(O)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C23H21NO5/c1-2-29-23(28)22(27)13-19(26)12-9-17-15-24(21-6-4-3-5-20(17)21)14-16-7-10-18(25)11-8-16/h3-12,15,25H,2,13-14H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442234
PNG
(CHEMBL2442004)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(OC)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C24H23NO5/c1-3-30-24(28)23(27)14-19(26)11-10-18-16-25(22-7-5-4-6-21(18)22)15-17-8-12-20(29-2)13-9-17/h4-13,16H,3,14-15H2,1-2H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442235
PNG
(CHEMBL2442003)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(cc2)C#N)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C24H20N2O4/c1-2-30-24(29)23(28)13-20(27)12-11-19-16-26(22-6-4-3-5-21(19)22)15-18-9-7-17(14-25)8-10-18/h3-12,16H,2,13,15H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442236
PNG
(CHEMBL2442002)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(Cl)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C23H20ClNO4/c1-2-29-23(28)22(27)13-19(26)12-9-17-15-25(21-6-4-3-5-20(17)21)14-16-7-10-18(24)11-8-16/h3-12,15H,2,13-14H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442237
PNG
(CHEMBL2442001)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccc(F)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C23H20FNO4/c1-2-29-23(28)22(27)13-19(26)12-9-17-15-25(21-6-4-3-5-20(17)21)14-16-7-10-18(24)11-8-16/h3-12,15H,2,13-14H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442238
PNG
(CHEMBL2442000)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(Cc2ccccc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C23H21NO4/c1-2-28-23(27)22(26)14-19(25)13-12-18-16-24(15-17-8-4-3-5-9-17)21-11-7-6-10-20(18)21/h3-13,16H,2,14-15H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442239
PNG
(CHEMBL2441999)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(-c2ccc(Cl)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C22H18ClNO4/c1-2-28-22(27)21(26)13-18(25)12-7-15-14-24(17-10-8-16(23)9-11-17)20-6-4-3-5-19(15)20/h3-12,14H,2,13H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442240
PNG
(CHEMBL2441998)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(-c2ccc(O)cc2)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C22H19NO5/c1-2-28-22(27)21(26)13-18(25)10-7-15-14-23(16-8-11-17(24)12-9-16)20-6-4-3-5-19(15)20/h3-12,14,24H,2,13H2,1H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
DNA polymerase beta


(Homo sapiens (Human))
BDBM50442241
PNG
(CHEMBL2441996)
Show SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cn(CC(C)=C)c2ccccc12 |w:11.11|
Show InChI InChI=1S/C20H21NO4/c1-4-25-20(24)19(23)11-16(22)10-9-15-13-21(12-14(2)3)18-8-6-5-7-17(15)18/h5-10,13H,2,4,11-12H2,1,3H3
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n/an/a>4.00E+4n/an/an/an/an/an/a



Sapienza" Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of human recombinant DNA polymerase beta


J Med Chem 56: 7431-41 (2013)


Article DOI: 10.1021/jm4010187
BindingDB Entry DOI: 10.7270/Q2H70H8G
More data for this
Ligand-Target Pair
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