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10 similar compounds to monomer 50440148

Wt: 375.4
BDBM50440149
Wt: 393.4
BDBM50440150
Wt: 361.4
BDBM50440152
Wt: 361.4
BDBM50440153
Wt: 379.4
BDBM50440154
Wt: 347.4
BDBM50440162
Wt: 347.4
BDBM50440163
Wt: 365.4
BDBM50440164
Wt: 403.5
BDBM50440178
Wt: 435.5
BDBM50440182

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 21 hits for monomerid = 50440149,50440150,50440152,50440153,50440154,50440162,50440163,50440164,50440178,50440182   
Target
(Institution)
LigandTarget
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Deoxycytidine kinase


(Homo sapiens)
BDBM50440178
PNG
(CHEMBL2426568)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(OC)c(O)c1
Show InChI InChI=1S/C18H21N5O2S2/c1-3-4-14-11(9-26-18-22-15(19)8-16(20)23-18)21-17(27-14)10-5-6-13(25-2)12(24)7-10/h5-8,24H,3-4,9H2,1-2H3,(H4,19,20,22,23)
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8.90n/an/an/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Apparent inhibition of human dCK by steady-state kinetic assay


J Med Chem 57: 9480-94 (2014)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Deoxycytidine kinase


(Homo sapiens)
BDBM50440178
PNG
(CHEMBL2426568)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(OC)c(O)c1
Show InChI InChI=1S/C18H21N5O2S2/c1-3-4-14-11(9-26-18-22-15(19)8-16(20)23-18)21-17(27-14)10-5-6-13(25-2)12(24)7-10/h5-8,24H,3-4,9H2,1-2H3,(H4,19,20,22,23)
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n/an/a 26n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Apparent inhibition of human dCK assessed as phosphorylation activity by spectroscopic NADH-dependent enzyme-coupled assay


J Med Chem 57: 9480-94 (2014)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Deoxycytidine kinase


(Mus musculus)
BDBM50440152
PNG
(CHEMBL2426557)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cccc(F)c1
Show InChI InChI=1S/C16H16FN5S2/c1-2-12-11(8-23-16-21-13(18)7-14(19)22-16)20-15(24-12)9-4-3-5-10(17)6-9/h3-7H,2,8H2,1H3,(H4,18,19,21,22)
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n/an/a 510n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440153
PNG
(CHEMBL2426460)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C16H16FN5S2/c1-2-12-11(8-23-16-21-13(18)7-14(19)22-16)20-15(24-12)9-3-5-10(17)6-4-9/h3-7H,2,8H2,1H3,(H4,18,19,21,22)
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n/an/a 265n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440154
PNG
(CHEMBL2426459)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C16H15F2N5S2/c1-2-12-11(7-24-16-22-13(19)6-14(20)23-16)21-15(25-12)8-3-9(17)5-10(18)4-8/h3-6H,2,7H2,1H3,(H4,19,20,22,23)
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n/an/a 620n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440162
PNG
(CHEMBL2426591)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1cccc(F)c1
Show InChI InChI=1S/C15H14FN5S2/c1-8-11(7-22-15-20-12(17)6-13(18)21-15)19-14(23-8)9-3-2-4-10(16)5-9/h2-6H,7H2,1H3,(H4,17,18,20,21)
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n/an/a 255n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440163
PNG
(CHEMBL2426590)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C15H14FN5S2/c1-8-11(7-22-15-20-12(17)6-13(18)21-15)19-14(23-8)9-2-4-10(16)5-3-9/h2-6H,7H2,1H3,(H4,17,18,20,21)
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n/an/a 395n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440164
PNG
(CHEMBL2426589)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C15H13F2N5S2/c1-7-11(6-23-15-21-12(18)5-13(19)22-15)20-14(24-7)8-2-9(16)4-10(17)3-8/h2-5H,6H2,1H3,(H4,18,19,21,22)
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n/an/a 595n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440178
PNG
(CHEMBL2426568)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(OC)c(O)c1
Show InChI InChI=1S/C18H21N5O2S2/c1-3-4-14-11(9-26-18-22-15(19)8-16(20)23-18)21-17(27-14)10-5-6-13(25-2)12(24)7-10/h5-8,24H,3-4,9H2,1-2H3,(H4,19,20,22,23)
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n/an/a 19n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Deoxycytidine kinase


(Homo sapiens)
BDBM50440182
PNG
(CHEMBL2426564)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(OCCO)c1
Show InChI InChI=1S/C19H22FN5O2S2/c1-2-3-15-14(10-28-19-24-16(21)9-17(22)25-19)23-18(29-15)11-6-12(20)8-13(7-11)27-5-4-26/h6-9,26H,2-5,10H2,1H3,(H4,21,22,24,25)
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n/an/a 2.80n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440149
PNG
(CHEMBL2426560)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C17H18FN5S2/c1-2-3-13-12(9-24-17-22-14(19)8-15(20)23-17)21-16(25-13)10-4-6-11(18)7-5-10/h4-8H,2-3,9H2,1H3,(H4,19,20,22,23)
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n/an/a 37n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440150
PNG
(CHEMBL2426559)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C17H17F2N5S2/c1-2-3-13-12(8-25-17-23-14(20)7-15(21)24-17)22-16(26-13)9-4-10(18)6-11(19)5-9/h4-7H,2-3,8H2,1H3,(H4,20,21,23,24)
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n/an/a 173n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440152
PNG
(CHEMBL2426557)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cccc(F)c1
Show InChI InChI=1S/C16H16FN5S2/c1-2-12-11(8-23-16-21-13(18)7-14(19)22-16)20-15(24-12)9-4-3-5-10(17)6-9/h3-7H,2,8H2,1H3,(H4,18,19,21,22)
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n/an/a 11n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440153
PNG
(CHEMBL2426460)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C16H16FN5S2/c1-2-12-11(8-23-16-21-13(18)7-14(19)22-16)20-15(24-12)9-3-5-10(17)6-4-9/h3-7H,2,8H2,1H3,(H4,18,19,21,22)
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n/an/a 83n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440154
PNG
(CHEMBL2426459)
Show SMILES CCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C16H15F2N5S2/c1-2-12-11(7-24-16-22-13(19)6-14(20)23-16)21-15(25-12)8-3-9(17)5-10(18)4-8/h3-6H,2,7H2,1H3,(H4,19,20,22,23)
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n/an/a 162n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440162
PNG
(CHEMBL2426591)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1cccc(F)c1
Show InChI InChI=1S/C15H14FN5S2/c1-8-11(7-22-15-20-12(17)6-13(18)21-15)19-14(23-8)9-3-2-4-10(16)5-9/h2-6H,7H2,1H3,(H4,17,18,20,21)
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n/an/a 92n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440163
PNG
(CHEMBL2426590)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C15H14FN5S2/c1-8-11(7-22-15-20-12(17)6-13(18)21-15)19-14(23-8)9-2-4-10(16)5-3-9/h2-6H,7H2,1H3,(H4,17,18,20,21)
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n/an/a 230n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440164
PNG
(CHEMBL2426589)
Show SMILES Cc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C15H13F2N5S2/c1-7-11(6-23-15-21-12(18)5-13(19)22-15)20-14(24-7)8-2-9(16)4-10(17)3-8/h2-5H,6H2,1H3,(H4,18,19,21,22)
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n/an/a 150n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Homo sapiens)
BDBM50440178
PNG
(CHEMBL2426568)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(OC)c(O)c1
Show InChI InChI=1S/C18H21N5O2S2/c1-3-4-14-11(9-26-18-22-15(19)8-16(20)23-18)21-17(27-14)10-5-6-13(25-2)12(24)7-10/h5-8,24H,3-4,9H2,1-2H3,(H4,19,20,22,23)
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n/an/a 19n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of dCK in human CCRF-CEM cells assessed as inhibition of [3H]-dC uptake by scintillation counting analysis


J Med Chem 57: 9480-94 (2014)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Deoxycytidine kinase


(Mus musculus)
BDBM50440149
PNG
(CHEMBL2426560)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1ccc(F)cc1
Show InChI InChI=1S/C17H18FN5S2/c1-2-3-13-12(9-24-17-22-14(19)8-15(20)23-17)21-16(25-13)10-4-6-11(18)7-5-10/h4-8H,2-3,9H2,1H3,(H4,19,20,22,23)
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n/an/a 170n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair
Deoxycytidine kinase


(Mus musculus)
BDBM50440150
PNG
(CHEMBL2426559)
Show SMILES CCCc1sc(nc1CSc1nc(N)cc(N)n1)-c1cc(F)cc(F)c1
Show InChI InChI=1S/C17H17F2N5S2/c1-2-3-13-12(8-25-17-23-14(20)7-15(21)24-17)22-16(26-13)9-4-10(18)6-11(19)5-9/h4-7H,2-3,8H2,1H3,(H4,20,21,23,24)
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PubMed
n/an/a 385n/an/an/an/an/an/a



California NanoSystems Institute

Curated by ChEMBL


Assay Description
Inhibition of dCK in mouse L1210 cells assessed as inhibition of tritiated deoxycytidine [3H]-dC uptake


J Med Chem 56: 6696-708 (2013)

More data for this
Ligand-Target Pair