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Compile Data Set for Download or QSAR

Found 14 hits Enz. Inhib. hit(s) with Target = 'Ribonucleoside-diphosphate reductase subunit M2'   
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
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50198892
PNG
(3-AP | 3-aminopyridine-2-carboxaldehyde thiosemica...)
Show SMILES NC(=S)N\N=C\c1ncccc1N
Show InChI InChI=1S/C7H9N5S/c8-5-2-1-3-10-6(5)4-11-12-7(9)13/h1-4H,8H2,(H3,9,12,13)/b11-4+
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Article
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n/an/a 185n/an/an/an/an/an/a



Case Western Reserve University

Curated by ChEMBL


Assay Description
Inhibition of human RRM2 expressed in Escherichia coli BL21-codon plus(DE3) using [14C]-ADP as substrate after 3 mins by liquid scintillation countin...


J Med Chem 61: 666-680 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00530
BindingDB Entry DOI: 10.7270/Q2W098CB
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051772
PNG
((Z)-N'-(5-amino-6-formylpyridin-2-yl)carbamohydraz...)
Show SMILES NC(=S)NNc1ccc(N)c(C=O)n1
Show InChI InChI=1S/C7H9N5OS/c8-4-1-2-6(10-5(4)3-13)11-12-7(9)14/h1-3H,8H2,(H,10,11)(H3,9,12,14)
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n/an/a 820n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051768
PNG
((1Z,N'E)-N'-((3-(methylamino)pyridin-2-yl)methylen...)
Show SMILES CNc1cccnc1C=NNC(N)=S |w:8.8|
Show InChI InChI=1S/C8H11N5S/c1-10-6-3-2-4-11-7(6)5-12-13-8(9)14/h2-5,10H,1H3,(H3,9,13,14)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051776
PNG
((1Z,N'E)-N'-((5-(ethylamino)pyridin-2-yl)methylene...)
Show SMILES CCNc1ccc(C=NNC(N)=S)nc1 |w:7.6|
Show InChI InChI=1S/C9H13N5S/c1-2-11-7-3-4-8(12-5-7)6-13-14-9(10)15/h3-6,11H,2H2,1H3,(H3,10,14,15)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051769
PNG
((1Z,N'E)-N'-((5-(methylamino)pyridin-2-yl)methylen...)
Show SMILES CNc1ccc(C=NNC(N)=S)nc1 |w:6.5|
Show InChI InChI=1S/C8H11N5S/c1-10-6-2-3-7(11-4-6)5-12-13-8(9)14/h2-5,10H,1H3,(H3,9,13,14)
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n/an/a 1.30E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051775
PNG
((1Z,N'E)-N'-((5-(allylamino)pyridin-2-yl)methylene...)
Show SMILES NC(=S)NN=Cc1ccc(NCC=C)cn1 |w:5.5|
Show InChI InChI=1S/C10H13N5S/c1-2-5-12-8-3-4-9(13-6-8)7-14-15-10(11)16/h2-4,6-7,12H,1,5H2,(H3,11,15,16)
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n/an/a 1.40E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051767
PNG
((1Z,N'E)-N'-((5-(propylamino)pyridin-2-yl)methylen...)
Show SMILES CCCNc1ccc(C=NNC(N)=S)nc1 |w:8.7|
Show InChI InChI=1S/C10H15N5S/c1-2-5-12-8-3-4-9(13-6-8)7-14-15-10(11)16/h3-4,6-7,12H,2,5H2,1H3,(H3,11,15,16)
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n/an/a 1.40E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051774
PNG
((1Z,N'E)-N'-((3-(allylamino)pyridin-2-yl)methylene...)
Show SMILES NC(=S)NN=Cc1ncccc1NCC=C |w:5.5|
Show InChI InChI=1S/C10H13N5S/c1-2-5-12-8-4-3-6-13-9(8)7-14-15-10(11)16/h2-4,6-7,12H,1,5H2,(H3,11,15,16)
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n/an/a 1.70E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051777
PNG
((1Z,N'E)-N'-((5-(aminomethyl)pyridin-2-yl)methylen...)
Show SMILES NCc1ccc(C=NNC(N)=S)nc1 |w:6.5|
Show InChI InChI=1S/C8H11N5S/c9-3-6-1-2-7(11-4-6)5-12-13-8(10)14/h1-2,4-5H,3,9H2,(H3,10,13,14)
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n/an/a 2.50E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051766
PNG
((1Z,N'E)-N'-((5-(butylamino)pyridin-2-yl)methylene...)
Show SMILES CCCCNc1ccc(C=NNC(N)=S)nc1 |w:9.8|
Show InChI InChI=1S/C11H17N5S/c1-2-3-6-13-9-4-5-10(14-7-9)8-15-16-11(12)17/h4-5,7-8,13H,2-3,6H2,1H3,(H3,12,16,17)
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n/an/a 2.50E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051773
PNG
((Z)-N'-(3-amino-6-formylpyridin-2-yl)carbamohydraz...)
Show SMILES NC(=S)NNc1nc(C=O)ccc1N
Show InChI InChI=1S/C7H9N5OS/c8-5-2-1-4(3-13)10-6(5)11-12-7(9)14/h1-3H,8H2,(H,10,11)(H3,9,12,14)
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n/an/a 2.70E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051771
PNG
((1Z,N'E)-N'-((3,5-diaminopyridin-2-yl)methylene)ca...)
Show SMILES NC(=S)NN=Cc1ncc(N)cc1N |w:4.3|
Show InChI InChI=1S/C7H10N6S/c8-4-1-5(9)6(11-2-4)3-12-13-7(10)14/h1-3H,8-9H2,(H3,10,13,14)
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n/an/a 9.00E+3n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50051770
PNG
((1Z,N'E)-N'-((5-amino-4-(morpholinomethyl)pyridin-...)
Show SMILES NC(=S)NN=Cc1cc(CN2CCOCC2)c(N)cn1 |w:4.3|
Show InChI InChI=1S/C12H18N6OS/c13-11-7-15-10(6-16-17-12(14)20)5-9(11)8-18-1-3-19-4-2-18/h5-7H,1-4,8,13H2,(H3,14,17,20)
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n/an/a 1.10E+4n/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibitory activity against CDP reductase.


J Med Chem 39: 2586-93 (1996)


Article DOI: 10.1021/jm9600454
BindingDB Entry DOI: 10.7270/Q2KS6QN9
More data for this
Ligand-Target Pair
Ribonucleoside-diphosphate reductase subunit M2


(Homo sapiens (Human))
BDBM50247408
PNG
(CHEMBL4067105)
Show SMILES Oc1ccccc1C(=O)N\N=C\c1c(O)ccc2ccccc12
Show InChI InChI=1S/C18H14N2O3/c21-16-8-4-3-7-14(16)18(23)20-19-11-15-13-6-2-1-5-12(13)9-10-17(15)22/h1-11,21-22H,(H,20,23)/b19-11+
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n/an/a 1.23E+5n/an/an/an/an/an/a



Case Western Reserve University

Curated by ChEMBL


Assay Description
Inhibition of human RRM2 expressed in Escherichia coli BL21-codon plus(DE3) using [14C]-ADP as substrate after 3 mins by liquid scintillation countin...


J Med Chem 61: 666-680 (2018)


Article DOI: 10.1021/acs.jmedchem.7b00530
BindingDB Entry DOI: 10.7270/Q2W098CB
More data for this
Ligand-Target Pair