Found 54 hits of ec50 data for polymerid = 50000373 Target/Host (Institution) | Ligand | Target/Host 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 | pH | Temp °C |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311568
(3-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES COc1ccc(cc1Oc1ncnc(N2CCC(CC2)Oc2ncc(F)c(N)n2)c1F)C#N Show InChI InChI=1S/C21H19F2N7O3/c1-31-15-3-2-12(9-24)8-16(15)33-20-17(23)19(27-11-28-20)30-6-4-13(5-7-30)32-21-26-10-14(22)18(25)29-21/h2-3,8,10-11,13H,4-7H2,1H3,(H2,25,26,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311564
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2ncnc(Oc3ccccc3C#N)c2F)ncc1F Show InChI InChI=1S/C20H17F2N7O2/c21-14-10-25-20(28-17(14)24)30-13-5-7-29(8-6-13)18-16(22)19(27-11-26-18)31-15-4-2-1-3-12(15)9-23/h1-4,10-11,13H,5-8H2,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 4 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311570
(2-(6-(4-(4-aminopyrimidin-2-yloxy)piperidin-1-yl)-...)Show SMILES Nc1ccnc(OC2CCN(CC2)c2ncnc(Oc3ccccc3C#N)c2F)n1 Show InChI InChI=1S/C20H18FN7O2/c21-17-18(25-12-26-19(17)30-15-4-2-1-3-13(15)11-22)28-9-6-14(7-10-28)29-20-24-8-5-16(23)27-20/h1-5,8,12,14H,6-7,9-10H2,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311569
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES COc1ccc(Oc2ncnc(N3CCC(CC3)Oc3ncc(F)c(N)n3)c2F)c(c1)C#N Show InChI InChI=1S/C21H19F2N7O3/c1-31-14-2-3-16(12(8-14)9-24)33-20-17(23)19(27-11-28-20)30-6-4-13(5-7-30)32-21-26-10-15(22)18(25)29-21/h2-3,8,10-11,13H,4-7H2,1H3,(H2,25,26,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311560
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES COc1ccc(Oc2cc(ncn2)N2CCC(CC2)Oc2ncc(F)c(N)n2)c(c1)C#N Show InChI InChI=1S/C21H20FN7O3/c1-30-15-2-3-17(13(8-15)10-23)32-19-9-18(26-12-27-19)29-6-4-14(5-7-29)31-21-25-11-16(22)20(24)28-21/h2-3,8-9,11-12,14H,4-7H2,1H3,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 12 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311566
(3-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2ncnc(Oc3cccc(c3)C#N)c2F)ncc1F Show InChI InChI=1S/C20H17F2N7O2/c21-15-10-25-20(28-17(15)24)31-13-4-6-29(7-5-13)18-16(22)19(27-11-26-18)30-14-3-1-2-12(8-14)9-23/h1-3,8,10-11,13H,4-7H2,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 13 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311554
(2-(1-(6-(2-chlorophenoxy)pyrimidin-4-yl)piperidin-...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3ccccc3Cl)ncn2)ncc1F Show InChI InChI=1S/C19H18ClFN6O2/c20-13-3-1-2-4-15(13)29-17-9-16(24-11-25-17)27-7-5-12(6-8-27)28-19-23-10-14(21)18(22)26-19/h1-4,9-12H,5-8H2,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 13 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311565
(5-fluoro-2-(1-(5-fluoro-6-(4-methoxyphenoxy)pyrimi...)Show SMILES COc1ccc(Oc2ncnc(N3CCC(CC3)Oc3ncc(F)c(N)n3)c2F)cc1 Show InChI InChI=1S/C20H20F2N6O3/c1-29-12-2-4-13(5-3-12)30-19-16(22)18(25-11-26-19)28-8-6-14(7-9-28)31-20-24-10-15(21)17(23)27-20/h2-5,10-11,14H,6-9H2,1H3,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 14 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311556
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3ccccc3C#N)ncn2)ncc1F Show InChI InChI=1S/C20H18FN7O2/c21-15-11-24-20(27-19(15)23)29-14-5-7-28(8-6-14)17-9-18(26-12-25-17)30-16-4-2-1-3-13(16)10-22/h1-4,9,11-12,14H,5-8H2,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 14 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311558
(5-fluoro-2-(1-(6-(2-fluorophenoxy)pyrimidin-4-yl)p...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3ccccc3F)ncn2)ncc1F Show InChI InChI=1S/C19H18F2N6O2/c20-13-3-1-2-4-15(13)29-17-9-16(24-11-25-17)27-7-5-12(6-8-27)28-19-23-10-14(21)18(22)26-19/h1-4,9-12H,5-8H2,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 15 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311609
(CHEMBL1080444 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NC(=O)c1cc(ccn1)-c1cc2ccccc2s1 |r| Show InChI InChI=1S/C23H20FN5O2S/c24-17-12-29(23(31)28-21(17)25)16-6-5-15(11-16)27-22(30)18-9-14(7-8-26-18)20-10-13-3-1-2-4-19(13)32-20/h1-4,7-10,12,15-16H,5-6,11H2,(H,27,30)(H2,25,28,31)/t15-,16-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | 17 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311609
(CHEMBL1080444 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NC(=O)c1cc(ccn1)-c1cc2ccccc2s1 |r| Show InChI InChI=1S/C23H20FN5O2S/c24-17-12-29(23(31)28-21(17)25)16-6-5-15(11-16)27-22(30)18-9-14(7-8-26-18)20-10-13-3-1-2-4-19(13)32-20/h1-4,7-10,12,15-16H,5-6,11H2,(H,27,30)(H2,25,28,31)/t15-,16-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | 17 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase in anti CD3 and anti CD28 -stimulated human T cells assessed as reduction in [3H]deoxycitidine incorporation |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311548
(5-fluoro-2-(1-(6-(2-methoxyphenoxy)pyrimidin-4-yl)...)Show SMILES COc1ccccc1Oc1cc(ncn1)N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C20H21FN6O3/c1-28-15-4-2-3-5-16(15)30-18-10-17(24-12-25-18)27-8-6-13(7-9-27)29-20-23-11-14(21)19(22)26-20/h2-5,10-13H,6-9H2,1H3,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 17 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311550
(5-fluoro-2-(1-(6-(o-tolyloxy)pyrimidin-4-yl)piperi...)Show SMILES Cc1ccccc1Oc1cc(ncn1)N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C20H21FN6O2/c1-13-4-2-3-5-16(13)29-18-10-17(24-12-25-18)27-8-6-14(7-9-27)28-20-23-11-15(21)19(22)26-20/h2-5,10-12,14H,6-9H2,1H3,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 19 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311567
(4-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2ncnc(Oc3ccc(cc3)C#N)c2F)ncc1F Show InChI InChI=1S/C20H17F2N7O2/c21-15-10-25-20(28-17(15)24)31-14-5-7-29(8-6-14)18-16(22)19(27-11-26-18)30-13-3-1-12(9-23)2-4-13/h1-4,10-11,14H,5-8H2,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 20 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311551
(2-(1-(6-(biphenyl-2-yloxy)pyrimidin-4-yl)piperidin...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3ccccc3-c3ccccc3)ncn2)ncc1F Show InChI InChI=1S/C25H23FN6O2/c26-20-15-28-25(31-24(20)27)33-18-10-12-32(13-11-18)22-14-23(30-16-29-22)34-21-9-5-4-8-19(21)17-6-2-1-3-7-17/h1-9,14-16,18H,10-13H2,(H2,27,28,31) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 26 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311559
(2-(1-(6-(4-chloro-2-methylphenoxy)pyrimidin-4-yl)p...)Show SMILES Cc1cc(Cl)ccc1Oc1cc(ncn1)N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C20H20ClFN6O2/c1-12-8-13(21)2-3-16(12)30-18-9-17(25-11-26-18)28-6-4-14(5-7-28)29-20-24-10-15(22)19(23)27-20/h2-3,8-11,14H,4-7H2,1H3,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 27 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311553
(2-(1-(6-(3-chlorophenoxy)pyrimidin-4-yl)piperidin-...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3cccc(Cl)c3)ncn2)ncc1F Show InChI InChI=1S/C19H18ClFN6O2/c20-12-2-1-3-14(8-12)28-17-9-16(24-11-25-17)27-6-4-13(5-7-27)29-19-23-10-15(21)18(22)26-19/h1-3,8-11,13H,4-7H2,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 35 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311547
(5-fluoro-2-(1-(6-(3-methoxyphenoxy)pyrimidin-4-yl)...)Show SMILES COc1cccc(Oc2cc(ncn2)N2CCC(CC2)Oc2ncc(F)c(N)n2)c1 Show InChI InChI=1S/C20H21FN6O3/c1-28-14-3-2-4-15(9-14)29-18-10-17(24-12-25-18)27-7-5-13(6-8-27)30-20-23-11-16(21)19(22)26-20/h2-4,9-13H,5-8H2,1H3,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 36 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311561
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Cc1c(Oc2ccccc2C#N)ncnc1N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C21H20FN7O2/c1-13-19(26-12-27-20(13)31-17-5-3-2-4-14(17)10-23)29-8-6-15(7-9-29)30-21-25-11-16(22)18(24)28-21/h2-5,11-12,15H,6-9H2,1H3,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 54 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311552
(2-(1-(6-(4-chlorophenoxy)pyrimidin-4-yl)piperidin-...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3ccc(Cl)cc3)ncn2)ncc1F Show InChI InChI=1S/C19H18ClFN6O2/c20-12-1-3-13(4-2-12)28-17-9-16(24-11-25-17)27-7-5-14(6-8-27)29-19-23-10-15(21)18(22)26-19/h1-4,9-11,14H,5-8H2,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 57 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311549
(5-fluoro-2-(1-(6-(p-tolyloxy)pyrimidin-4-yl)piperi...)Show SMILES Cc1ccc(Oc2cc(ncn2)N2CCC(CC2)Oc2ncc(F)c(N)n2)cc1 Show InChI InChI=1S/C20H21FN6O2/c1-13-2-4-14(5-3-13)28-18-10-17(24-12-25-18)27-8-6-15(7-9-27)29-20-23-11-16(21)19(22)26-20/h2-5,10-12,15H,6-9H2,1H3,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 60 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311555
(2-(1-(6-(2-ethylphenoxy)pyrimidin-4-yl)piperidin-4...)Show SMILES CCc1ccccc1Oc1cc(ncn1)N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C21H23FN6O2/c1-2-14-5-3-4-6-17(14)30-19-11-18(25-13-26-19)28-9-7-15(8-10-28)29-21-24-12-16(22)20(23)27-21/h3-6,11-13,15H,2,7-10H2,1H3,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 61 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311557
(3-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(Oc3cccc(c3)C#N)ncn2)ncc1F Show InChI InChI=1S/C20H18FN7O2/c21-16-11-24-20(27-19(16)23)30-14-4-6-28(7-5-14)17-9-18(26-12-25-17)29-15-3-1-2-13(8-15)10-22/h1-3,8-9,11-12,14H,4-7H2,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 61 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311563
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Nc1nc(OC2CCN(CC2)c2ncnc(Oc3ccccc3C#N)c2Br)ncc1F Show InChI InChI=1S/C20H17BrFN7O2/c21-16-18(26-11-27-19(16)31-15-4-2-1-3-12(15)9-23)29-7-5-13(6-8-29)30-20-25-10-14(22)17(24)28-20/h1-4,10-11,13H,5-8H2,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 80 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311605
(CHEMBL1079600 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES COc1ccc(cc1)-c1cccc(c1)C(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C23H23FN4O3/c1-31-19-9-5-14(6-10-19)15-3-2-4-16(11-15)22(29)26-17-7-8-18(12-17)28-13-20(24)21(25)27-23(28)30/h2-6,9-11,13,17-18H,7-8,12H2,1H3,(H,26,29)(H2,25,27,30)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 100 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311562
(2-(6-(4-(4-amino-5-fluoropyrimidin-2-yloxy)piperid...)Show SMILES Cc1nc(Oc2ccccc2C#N)cc(n1)N1CCC(CC1)Oc1ncc(F)c(N)n1 Show InChI InChI=1S/C21H20FN7O2/c1-13-26-18(10-19(27-13)31-17-5-3-2-4-14(17)11-23)29-8-6-15(7-9-29)30-21-25-12-16(22)20(24)28-21/h2-5,10,12,15H,6-9H2,1H3,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 140 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311544
(2-(2-(1-(6-(benzo[b]thiophen-2-yl)pyrimidin-4-yl)p...)Show SMILES Nc1nc(OCCC2CCN(CC2)c2cc(ncn2)-c2cc3ccccc3s2)ncc1F Show InChI InChI=1S/C23H23FN6OS/c24-17-13-26-23(29-22(17)25)31-10-7-15-5-8-30(9-6-15)21-12-18(27-14-28-21)20-11-16-3-1-2-4-19(16)32-20/h1-4,11-15H,5-10H2,(H2,25,26,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 160 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311608
(CHEMBL1079784 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Cc1cc(Cl)ccc1-c1cccc(c1)C(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C23H22ClFN4O2/c1-13-9-16(24)5-8-19(13)14-3-2-4-15(10-14)22(30)27-17-6-7-18(11-17)29-12-20(25)21(26)28-23(29)31/h2-5,8-10,12,17-18H,6-7,11H2,1H3,(H,27,30)(H2,26,28,31)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 170 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311607
(CHEMBL1076274 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NC(=O)c1cccc(c1)-c1cccc(Cl)c1 |r| Show InChI InChI=1S/C22H20ClFN4O2/c23-16-6-2-4-14(10-16)13-3-1-5-15(9-13)21(29)26-17-7-8-18(11-17)28-12-19(24)20(25)27-22(28)30/h1-6,9-10,12,17-18H,7-8,11H2,(H,26,29)(H2,25,27,30)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 180 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311599
(CHEMBL1079759 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1ccc(Cl)cc1 |r| Show InChI InChI=1S/C21H20ClFN4O3S/c22-15-6-4-13(5-7-15)14-2-1-3-18(10-14)31(29,30)26-16-8-9-17(11-16)27-12-19(23)20(24)25-21(27)28/h1-7,10,12,16-17,26H,8-9,11H2,(H2,24,25,28)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 240 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311606
(CHEMBL1079783 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NC(=O)c1cccc(c1)-c1ccc(Cl)cc1 |r| Show InChI InChI=1S/C22H20ClFN4O2/c23-16-6-4-13(5-7-16)14-2-1-3-15(10-14)21(29)26-17-8-9-18(11-17)28-12-19(24)20(25)27-22(28)30/h1-7,10,12,17-18H,8-9,11H2,(H,26,29)(H2,25,27,30)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 270 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311603
(CHEMBL1079432 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Cc1cc(Cl)ccc1-c1cccc(c1)S(=O)(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C22H22ClFN4O3S/c1-13-9-15(23)5-8-19(13)14-3-2-4-18(10-14)32(30,31)27-16-6-7-17(11-16)28-12-20(24)21(25)26-22(28)29/h2-5,8-10,12,16-17,27H,6-7,11H2,1H3,(H2,25,26,29)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 290 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311594
(CHEMBL1082101 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES COc1ccc(cc1)-c1cccc(c1)S(=O)(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C22H23FN4O4S/c1-31-18-9-5-14(6-10-18)15-3-2-4-19(11-15)32(29,30)26-16-7-8-17(12-16)27-13-20(23)21(24)25-22(27)28/h2-6,9-11,13,16-17,26H,7-8,12H2,1H3,(H2,24,25,28)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 300 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311545
(5-fluoro-2-(1-(6-phenoxypyrimidin-4-yl)piperidin-4...)Show InChI InChI=1S/C19H19FN6O2/c20-15-11-22-19(25-18(15)21)28-14-6-8-26(9-7-14)16-10-17(24-12-23-16)27-13-4-2-1-3-5-13/h1-5,10-12,14H,6-9H2,(H2,21,22,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 340 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311571
(2-(6-(4-(4-amino-2-oxopyrimidin-1(2H)-yloxy)piperi...)Show SMILES Nc1ccn(OC2CCN(CC2)c2ncnc(Oc3ccccc3C#N)c2F)c(=O)n1 Show InChI InChI=1S/C20H18FN7O3/c21-17-18(24-12-25-19(17)30-15-4-2-1-3-13(15)11-22)27-8-5-14(6-9-27)31-28-10-7-16(23)26-20(28)29/h1-4,7,10,12,14H,5-6,8-9H2,(H2,23,26,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | 350 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311600
(CHEMBL1079760 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1cccc(Cl)c1 |r| Show InChI InChI=1S/C21H20ClFN4O3S/c22-15-5-1-3-13(9-15)14-4-2-6-18(10-14)31(29,30)26-16-7-8-17(11-16)27-12-19(23)20(24)25-21(27)28/h1-6,9-10,12,16-17,26H,7-8,11H2,(H2,24,25,28)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 360 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311595
(CHEMBL1079397 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1ccc(cc1)C#N |r| Show InChI InChI=1S/C22H20FN5O3S/c23-20-13-28(22(29)26-21(20)25)18-9-8-17(11-18)27-32(30,31)19-3-1-2-16(10-19)15-6-4-14(12-24)5-7-15/h1-7,10,13,17-18,27H,8-9,11H2,(H2,25,26,29)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 390 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311601
(CHEMBL1079415 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1ccccc1Cl |r| Show InChI InChI=1S/C21H20ClFN4O3S/c22-18-7-2-1-6-17(18)13-4-3-5-16(10-13)31(29,30)26-14-8-9-15(11-14)27-12-19(23)20(24)25-21(27)28/h1-7,10,12,14-15,26H,8-9,11H2,(H2,24,25,28)/t14-,15-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 430 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311593
(CHEMBL1081189 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Cc1ccc(cc1)-c1cccc(c1)S(=O)(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C22H23FN4O3S/c1-14-5-7-15(8-6-14)16-3-2-4-19(11-16)31(29,30)26-17-9-10-18(12-17)27-13-20(23)21(24)25-22(27)28/h2-8,11,13,17-18,26H,9-10,12H2,1H3,(H2,24,25,28)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 500 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311602
(CHEMBL1079771 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1ccc(Cl)cc1Cl |r| Show InChI InChI=1S/C21H19Cl2FN4O3S/c22-13-4-7-17(18(23)9-13)12-2-1-3-16(8-12)32(30,31)27-14-5-6-15(10-14)28-11-19(24)20(25)26-21(28)29/h1-4,7-9,11,14-15,27H,5-6,10H2,(H2,25,26,29)/t14-,15-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 530 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311592
(CHEMBL1081006 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(c1)-c1ccccc1 |r| Show InChI InChI=1S/C21H21FN4O3S/c22-19-13-26(21(27)24-20(19)23)17-10-9-16(12-17)25-30(28,29)18-8-4-7-15(11-18)14-5-2-1-3-6-14/h1-8,11,13,16-17,25H,9-10,12H2,(H2,23,24,27)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 600 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311542
(2-(1-(6-(benzo[b]thiophen-2-yl)pyrimidin-4-yl)pipe...)Show SMILES Nc1nc(OC2CCN(CC2)c2cc(ncn2)-c2cc3ccccc3s2)ncc1F Show InChI InChI=1S/C21H19FN6OS/c22-15-11-24-21(27-20(15)23)29-14-5-7-28(8-6-14)19-10-16(25-12-26-19)18-9-13-3-1-2-4-17(13)30-18/h1-4,9-12,14H,5-8H2,(H2,23,24,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 700 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311543
(2-((1-(6-(benzo[b]thiophen-2-yl)pyrimidin-4-yl)pip...)Show SMILES Nc1nc(OCC2CCN(CC2)c2cc(ncn2)-c2cc3ccccc3s2)ncc1F Show InChI InChI=1S/C22H21FN6OS/c23-16-11-25-22(28-21(16)24)30-12-14-5-7-29(8-6-14)20-10-17(26-13-27-20)19-9-15-3-1-2-4-18(15)31-19/h1-4,9-11,13-14H,5-8,12H2,(H2,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 790 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311546
(5-fluoro-2-(1-(6-(4-methoxyphenoxy)pyrimidin-4-yl)...)Show SMILES COc1ccc(Oc2cc(ncn2)N2CCC(CC2)Oc2ncc(F)c(N)n2)cc1 Show InChI InChI=1S/C20H21FN6O3/c1-28-13-2-4-14(5-3-13)29-18-10-17(24-12-25-18)27-8-6-15(7-9-27)30-20-23-11-16(21)19(22)26-20/h2-5,10-12,15H,6-9H2,1H3,(H2,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 890 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of dCK in human CCRF-CEM assessed as inhibition of Ara-C phosohorylation |
Bioorg Med Chem Lett 19: 6780-3 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.082 BindingDB Entry DOI: 10.7270/Q2HM58K9 |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311604
(CHEMBL1079433 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NC(=O)c1cccc(c1)-c1ccccc1 |r| Show InChI InChI=1S/C22H21FN4O2/c23-19-13-27(22(29)26-20(19)24)18-10-9-17(12-18)25-21(28)16-8-4-7-15(11-16)14-5-2-1-3-6-14/h1-8,11,13,17-18H,9-10,12H2,(H,25,28)(H2,24,26,29)/t17-,18-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 910 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311596
(CHEMBL1079398 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cccc(c1)S(=O)(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C22H23FN4O5S2/c1-33(29,30)18-9-5-14(6-10-18)15-3-2-4-19(11-15)34(31,32)26-16-7-8-17(12-16)27-13-20(23)21(24)25-22(27)28/h2-6,9-11,13,16-17,26H,7-8,12H2,1H3,(H2,24,25,28)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311591
(CHEMBL1081005 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1cccc(Br)c1 |r| Show InChI InChI=1S/C15H16BrFN4O3S/c16-9-2-1-3-12(6-9)25(23,24)20-10-4-5-11(7-10)21-8-13(17)14(18)19-15(21)22/h1-3,6,8,10-11,20H,4-5,7H2,(H2,18,19,22)/t10-,11-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.80E+3 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311590
(CHEMBL1081909 | N-((1S,3S)-3-(4-amino-5-fluoro-2-o...)Show SMILES Nc1nc(=O)n(cc1F)[C@H]1CC[C@@H](C1)NS(=O)(=O)c1ccc(cc1)-c1ccccc1 |r| Show InChI InChI=1S/C21H21FN4O3S/c22-19-13-26(21(27)24-20(19)23)17-9-8-16(12-17)25-30(28,29)18-10-6-15(7-11-18)14-4-2-1-3-5-14/h1-7,10-11,13,16-17,25H,8-9,12H2,(H2,23,24,27)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5.50E+3 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |
Deoxycytidine kinase
(Homo sapiens (Human)) | BDBM50311597
(3'-(N-((1S,3S)-3-(4-amino-5-fluoro-2-oxopyrimidin-...)Show SMILES NC(=O)c1ccc(cc1)-c1cccc(c1)S(=O)(=O)N[C@H]1CC[C@@H](C1)n1cc(F)c(N)nc1=O |r| Show InChI InChI=1S/C22H22FN5O4S/c23-19-12-28(22(30)26-20(19)24)17-9-8-16(11-17)27-33(31,32)18-3-1-2-15(10-18)13-4-6-14(7-5-13)21(25)29/h1-7,10,12,16-17,27H,8-9,11H2,(H2,25,29)(H2,24,26,30)/t16-,17-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5.90E+3 | n/a | n/a | n/a | n/a |
Princ
Curated by ChEMBL
| Assay Description Inhibition of deoxycytidine kinase-mediated arabinoside C-induced cytotoxicity |
Bioorg Med Chem Lett 19: 6784-7 (2009)
Article DOI: 10.1016/j.bmcl.2009.09.081 BindingDB Entry DOI: 10.7270/Q2CV4HVK |
More data for this Ligand-Target Pair | |