Found 199 hits with Last Name = 'khosla' and Initial = 'c' Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342570
((E)-4-bromo-3-(2-oxo-2-(pyridin-3-yl)ethylidene)in...)Show InChI InChI=1S/C15H9BrN2O2/c16-11-4-1-5-12-14(11)10(15(20)18-12)7-13(19)9-3-2-6-17-8-9/h1-8H,(H,18,20)/b10-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 250 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using ZGBC as a substrate after 30 to 60 mins by fluorometric assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342570
((E)-4-bromo-3-(2-oxo-2-(pyridin-3-yl)ethylidene)in...)Show InChI InChI=1S/C15H9BrN2O2/c16-11-4-1-5-12-14(11)10(15(20)18-12)7-13(19)9-3-2-6-17-8-9/h1-8H,(H,18,20)/b10-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 400 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342568
((E)-1-benzyl-4-chloro-3-(2-oxo-2-(pyridin-3-yl)eth...)Show SMILES Clc1cccc2N(Cc3ccccc3)C(=O)\C(=C\C(=O)c3cccnc3)c12 Show InChI InChI=1S/C22H15ClN2O2/c23-18-9-4-10-19-21(18)17(12-20(26)16-8-5-11-24-13-16)22(27)25(19)14-15-6-2-1-3-7-15/h1-13H,14H2/b17-12+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 410 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342571
((E)-5-bromo-3-(2-oxo-2-(pyridin-3-yl)ethylidene)in...)Show InChI InChI=1S/C15H9BrN2O2/c16-10-3-4-13-11(6-10)12(15(20)18-13)7-14(19)9-2-1-5-17-8-9/h1-8H,(H,18,20)/b12-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 680 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using ZGBC as a substrate after 30 to 60 mins by fluorometric assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342562
((E)-4-chloro-3-(2-oxopropylidene)indolin-2-one | C...)Show InChI InChI=1S/C11H8ClNO2/c1-6(14)5-7-10-8(12)3-2-4-9(10)13-11(7)15/h2-5H,1H3,(H,13,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 700 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342563
((E)-5-chloro-3-(2-oxopropylidene)indolin-2-one | C...)Show InChI InChI=1S/C11H8ClNO2/c1-6(14)4-9-8-5-7(12)2-3-10(8)13-11(9)15/h2-5H,1H3,(H,13,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 900 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522195
(CHEMBL1592234)Show SMILES Cc1ccc(cc1)-c1nc2Oc3c(C)cccc3Cc2c(SCC(=O)Nc2cccc(c2)C(O)=O)n1 Show InChI InChI=1S/C28H23N3O4S/c1-16-9-11-18(12-10-16)25-30-26-22(14-19-6-3-5-17(2)24(19)35-26)27(31-25)36-15-23(32)29-21-8-4-7-20(13-21)28(33)34/h3-13H,14-15H2,1-2H3,(H,29,32)(H,33,34) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
MCE PC cid PC sid UniChem
| Article PubMed
| 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using uridine, phosphoenolpyruvate, N... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342568
((E)-1-benzyl-4-chloro-3-(2-oxo-2-(pyridin-3-yl)eth...)Show SMILES Clc1cccc2N(Cc3ccccc3)C(=O)\C(=C\C(=O)c3cccnc3)c12 Show InChI InChI=1S/C22H15ClN2O2/c23-18-9-4-10-19-21(18)17(12-20(26)16-8-5-11-24-13-16)22(27)25(19)14-15-6-2-1-3-7-15/h1-13H,14H2/b17-12+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using ZGBC as a substrate after 30 to 60 mins by fluorometric assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200152
(CHEMBL219427 | quinolin-3-ylmethyl (S)-1-(((S)-3-b...)Show SMILES Fc1ccc2[nH]cc(C[C@H](NC(=O)OCc3cnc4ccccc4c3)C(=O)NC[C@@H]3CC(Br)=NO3)c2c1 |r,c:34| Show InChI InChI=1S/C26H23BrFN5O4/c27-24-10-19(37-33-24)13-31-25(34)23(8-17-12-30-22-6-5-18(28)9-20(17)22)32-26(35)36-14-15-7-16-3-1-2-4-21(16)29-11-15/h1-7,9,11-12,19,23,30H,8,10,13-14H2,(H,31,34)(H,32,35)/t19-,23-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342565
((E)-4-chloro-3-(2-oxo-2-(pyridin-3-yl)ethylidene)i...)Show InChI InChI=1S/C15H9ClN2O2/c16-11-4-1-5-12-14(11)10(15(20)18-12)7-13(19)9-3-2-6-17-8-9/h1-8H,(H,18,20)/b10-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342571
((E)-5-bromo-3-(2-oxo-2-(pyridin-3-yl)ethylidene)in...)Show InChI InChI=1S/C15H9BrN2O2/c16-10-3-4-13-11(6-10)12(15(20)18-13)7-14(19)9-2-1-5-17-8-9/h1-8H,(H,18,20)/b12-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342557
(5,5'-oxydiindoline-2,3-dione | CHEMBL1770389)Show InChI InChI=1S/C16H8N2O5/c19-13-9-5-7(1-3-11(9)17-15(13)21)23-8-2-4-12-10(6-8)14(20)16(22)18-12/h1-6H,(H,17,19,21)(H,18,20,22) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342583
((E)-4-chloro-3-(2-(2-methoxyphenyl)-2-oxoethyliden...)Show InChI InChI=1S/C17H12ClNO3/c1-22-15-8-3-2-5-10(15)14(20)9-11-16-12(18)6-4-7-13(16)19-17(11)21/h2-9H,1H3,(H,19,21)/b11-9+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 3.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of recombinant human TG2 V224 mutant deamidation activity using Cbz-Gln-Gly as substrate preincubated for 30 mins followed... |
Bioorg Med Chem Lett 25: 4922-6 (2015)
Article DOI: 10.1016/j.bmcl.2015.05.006 BindingDB Entry DOI: 10.7270/Q2W95C07 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342566
((E)-4-chloro-3-(2-oxo-2-phenylethylidene)indolin-2...)Show InChI InChI=1S/C16H10ClNO2/c17-12-7-4-8-13-15(12)11(16(20)18-13)9-14(19)10-5-2-1-3-6-10/h1-9H,(H,18,20)/b11-9+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 3.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522195
(CHEMBL1592234)Show SMILES Cc1ccc(cc1)-c1nc2Oc3c(C)cccc3Cc2c(SCC(=O)Nc2cccc(c2)C(O)=O)n1 Show InChI InChI=1S/C28H23N3O4S/c1-16-9-11-18(12-10-16)25-30-26-22(14-19-6-3-5-17(2)24(19)35-26)27(31-25)36-15-23(32)29-21-8-4-7-20(13-21)28(33)34/h3-13H,14-15H2,1-2H3,(H,29,32)(H,33,34) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
MCE PC cid PC sid UniChem
| Article PubMed
| 3.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using phosphoenolpyruvate, NADH and v... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342567
((E)-4-chloro-1-methyl-3-(2-oxo-2-(pyridin-3-yl)eth...)Show InChI InChI=1S/C16H11ClN2O2/c1-19-13-6-2-5-12(17)15(13)11(16(19)21)8-14(20)10-4-3-7-18-9-10/h2-9H,1H3/b11-8+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200155
((S)-quinolin-3-ylmethyl 1-((3-bromo-4,5-dihydroiso...)Show SMILES Fc1ccc2[nH]cc(C[C@H](NC(=O)OCc3cnc4ccccc4c3)C(=O)NCC3CC(Br)=NO3)c2c1 |r,c:34| Show InChI InChI=1S/C26H23BrFN5O4/c27-24-10-19(37-33-24)13-31-25(34)23(8-17-12-30-22-6-5-18(28)9-20(17)22)32-26(35)36-14-15-7-16-3-1-2-4-21(16)29-11-15/h1-7,9,11-12,19,23,30H,8,10,13-14H2,(H,31,34)(H,32,35)/t19?,23-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342553
((E)-6-chloro-3-(2-oxo-2-(pyridin-3-yl)ethylidene)i...)Show InChI InChI=1S/C15H9ClN2O2/c16-10-3-4-11-12(15(20)18-13(11)6-10)7-14(19)9-2-1-5-17-8-9/h1-8H,(H,18,20)/b12-7+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 5.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342564
((E)-6-fluoro-3-(2-oxopropylidene)indolin-2-one | C...)Show InChI InChI=1S/C11H8FNO2/c1-6(14)4-9-8-3-2-7(12)5-10(8)13-11(9)15/h2-5H,1H3,(H,13,15) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 5.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342590
((E)-4-chloro-3-(2-oxo-2-(pyridin-3-yl)ethylidene)-...)Show SMILES Clc1cccc2N(C(=O)\C(=C\C(=O)c3cccnc3)c12)c1ccccc1 Show InChI InChI=1S/C21H13ClN2O2/c22-17-9-4-10-18-20(17)16(12-19(25)14-6-5-11-23-13-14)21(26)24(18)15-7-2-1-3-8-15/h1-13H/b16-12+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 9.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of recombinant human TG2 V224 mutant deamidation activity using Cbz-Gln-Gly as substrate preincubated for 30 mins followed... |
Bioorg Med Chem Lett 25: 4922-6 (2015)
Article DOI: 10.1016/j.bmcl.2015.05.006 BindingDB Entry DOI: 10.7270/Q2W95C07 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342560
(1,1'-methylenediindoline-2,3-dione | CHEMBL1770393)Show InChI InChI=1S/C17H10N2O4/c20-14-10-5-1-3-7-12(10)18(16(14)22)9-19-13-8-4-2-6-11(13)15(21)17(19)23/h1-8H,9H2 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50132009
(3-(2-Oxo-propylidene)-1,3-dihydro-indol-2-one | CH...)Show InChI InChI=1S/C11H9NO2/c1-7(13)6-9-8-4-2-3-5-10(8)12-11(9)14/h2-6H,1H3,(H,12,14) | PDB MMDB
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| 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342559
(1,1'-(4,6-dimethyl-1,3-phenylene)bis(methylene)dii...)Show SMILES Cc1cc(C)c(CN2C(=O)C(=O)c3ccccc23)cc1CN1C(=O)C(=O)c2ccccc12 Show InChI InChI=1S/C26H20N2O4/c1-15-11-16(2)18(14-28-22-10-6-4-8-20(22)24(30)26(28)32)12-17(15)13-27-21-9-5-3-7-19(21)23(29)25(27)31/h3-12H,13-14H2,1-2H3 | PDB MMDB
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| 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200156
((S)-quinolin-3-ylmethyl 2-((((S)-3-bromo-4,5-dihyd...)Show SMILES BrC1=NO[C@H](CNC(=O)[C@@H]2CCCN2C(=O)OCc2cnc3ccccc3c2)C1 |r,t:1| Show InChI InChI=1S/C20H21BrN4O4/c21-18-9-15(29-24-18)11-23-19(26)17-6-3-7-25(17)20(27)28-12-13-8-14-4-1-2-5-16(14)22-10-13/h1-2,4-5,8,10,15,17H,3,6-7,9,11-12H2,(H,23,26)/t15-,17-/m0/s1 | PDB MMDB
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| 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342569
((E)-3-(2-oxo-2-(pyridin-3-yl)ethylidene)indolin-2-...)Show InChI InChI=1S/C15H10N2O2/c18-14(10-4-3-7-16-9-10)8-12-11-5-1-2-6-13(11)17-15(12)19/h1-9H,(H,17,19)/b12-8+ | PDB MMDB
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| 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522193
(CHEMBL4553820)Show SMILES Fc1ccc(cc1)-n1[nH]cc2c1nc(SCC(=O)Nc1ccc(Br)cc1)nc2=O Show InChI InChI=1S/C19H13BrFN5O2S/c20-11-1-5-13(6-2-11)23-16(27)10-29-19-24-17-15(18(28)25-19)9-22-26(17)14-7-3-12(21)4-8-14/h1-9,22H,10H2,(H,23,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
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| 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using uridine, phosphoenolpyruvate, N... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522193
(CHEMBL4553820)Show SMILES Fc1ccc(cc1)-n1[nH]cc2c1nc(SCC(=O)Nc1ccc(Br)cc1)nc2=O Show InChI InChI=1S/C19H13BrFN5O2S/c20-11-1-5-13(6-2-11)23-16(27)10-29-19-24-17-15(18(28)25-19)9-22-26(17)14-7-3-12(21)4-8-14/h1-9,22H,10H2,(H,23,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
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| 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using phosphoenolpyruvate, NADH and v... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342558
(5,5'-methylenediindoline-2,3-dione | CHEMBL1770390)Show InChI InChI=1S/C17H10N2O4/c20-14-10-6-8(1-3-12(10)18-16(14)22)5-9-2-4-13-11(7-9)15(21)17(23)19-13/h1-4,6-7H,5H2,(H,18,20,22)(H,19,21,23) | PDB MMDB
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| 1.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200145
(CHEMBL375426 | quinolin-3-ylmethyl 1-((3-bromo-4,5...)Show SMILES Fc1ccc2[nH]cc(CC(NC(=O)OCc3cnc4ccccc4c3)C(=O)NCC3CC(Br)=NO3)c2c1 |c:34| Show InChI InChI=1S/C26H23BrFN5O4/c27-24-10-19(37-33-24)13-31-25(34)23(8-17-12-30-22-6-5-18(28)9-20(17)22)32-26(35)36-14-15-7-16-3-1-2-4-21(16)29-11-15/h1-7,9,11-12,19,23,30H,8,10,13-14H2,(H,31,34)(H,32,35) | PDB MMDB
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| 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200154
(CHEMBL220137 | [1-[(3-bromo-4,5-dihydroisoxazol-5-...)Show SMILES Fc1ccc2c(CC(NC(=O)OCc3ccccc3)C(=O)NCC3CC(Br)=NO3)c[nH]c2c1 |c:27| Show InChI InChI=1S/C23H22BrFN4O4/c24-21-10-17(33-29-21)12-27-22(30)20(28-23(31)32-13-14-4-2-1-3-5-14)8-15-11-26-19-9-16(25)6-7-18(15)19/h1-7,9,11,17,20,26H,8,10,12-13H2,(H,27,30)(H,28,31) | PDB MMDB
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| 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200149
(CHEMBL219013 | [1-[(3-bromo-4,5-dihydroisoxazol-5-...)Show SMILES Fc1ccc2[nH]cc(CC(NC(=O)OCc3ccccc3)C(=O)NCC3CC(Br)=NO3)c2c1 |c:29| Show InChI InChI=1S/C23H22BrFN4O4/c24-21-10-17(33-29-21)12-27-22(30)20(28-23(31)32-13-14-4-2-1-3-5-14)8-15-11-26-19-7-6-16(25)9-18(15)19/h1-7,9,11,17,20,26H,8,10,12-13H2,(H,27,30)(H,28,31) | PDB MMDB
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| 1.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200147
(CHEMBL410077 | [1-[(3-bromo-4,5-dihydroisoxazol-5-...)Show SMILES BrC1=NOC(CNC(=O)C(Cc2c[nH]c3ncccc23)NC(=O)OCc2ccccc2)C1 |t:1| Show InChI InChI=1S/C22H22BrN5O4/c23-19-10-16(32-28-19)12-26-21(29)18(9-15-11-25-20-17(15)7-4-8-24-20)27-22(30)31-13-14-5-2-1-3-6-14/h1-8,11,16,18H,9-10,12-13H2,(H,24,25)(H,26,29)(H,27,30) | PDB MMDB
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Similars
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| 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM81791
(Dopamine + GPP(NH)p | GPP(NH)P(+) | GPP(NH)p(-) | ...)Show SMILES Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)NP(O)(O)=O)[C@@H](O)[C@H]1O Show InChI InChI=1S/C10H17N6O13P3/c11-10-13-7-4(8(19)14-10)12-2-16(7)9-6(18)5(17)3(28-9)1-27-32(25,26)29-31(23,24)15-30(20,21)22/h2-3,5-6,9,17-18H,1H2,(H,25,26)(H3,11,13,14,19)(H4,15,20,21,22,23,24)/t3-,5-,6-,9-/m1/s1 | PDB MMDB
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Similars
| Article PubMed
| 2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Competitive inhibition of recombinant human TG2 V224 mutant deamidation activity using Cbz-Gln-Gly as substrate preincubated for 30 mins followed by ... |
Bioorg Med Chem Lett 25: 4922-6 (2015)
Article DOI: 10.1016/j.bmcl.2015.05.006 BindingDB Entry DOI: 10.7270/Q2W95C07 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200151
(CHEMBL374790 | quinolin-3-ylmethyl (S)-1-(((S)-3-b...)Show SMILES Oc1ccc(C[C@H](NC(=O)OCc2cnc3ccccc3c2)C(=O)NC[C@@H]2CC(Br)=NO2)cc1 |r,c:31| Show InChI InChI=1S/C24H23BrN4O5/c25-22-11-19(34-29-22)13-27-23(31)21(10-15-5-7-18(30)8-6-15)28-24(32)33-14-16-9-17-3-1-2-4-20(17)26-12-16/h1-9,12,19,21,30H,10-11,13-14H2,(H,27,31)(H,28,32)/t19-,21-/m0/s1 | PDB MMDB
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| CHEMBL PC cid PC sid UniChem
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| 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522198
(CHEMBL4434988)Show SMILES Cc1cc(C)cc(NC(=O)CSCn2[nH]nc3c2nc(Cc2ccc(F)cc2)nc3=O)c1 Show InChI InChI=1S/C22H21FN6O2S/c1-13-7-14(2)9-17(8-13)24-19(30)11-32-12-29-21-20(27-28-29)22(31)26-18(25-21)10-15-3-5-16(23)6-4-15/h3-9,28H,10-12H2,1-2H3,(H,24,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| PC cid PC sid UniChem
| Article PubMed
| 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using uridine, phosphoenolpyruvate, N... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200153
(CHEMBL384892 | quinolin-3-ylmethyl 1-((3-bromo-4,5...)Show SMILES Oc1ccc2[nH]cc(CC(NC(=O)OCc3cnc4ccccc4c3)C(=O)NCC3CC(Br)=NO3)c2c1 |c:34| Show InChI InChI=1S/C26H24BrN5O5/c27-24-10-19(37-32-24)13-30-25(34)23(8-17-12-29-22-6-5-18(33)9-20(17)22)31-26(35)36-14-15-7-16-3-1-2-4-21(16)28-11-15/h1-7,9,11-12,19,23,29,33H,8,10,13-14H2,(H,30,34)(H,31,35) | PDB MMDB
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Similars
| Article PubMed
| 3.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50216771
((2S)-2-{[(2S)-1-[(2S)-2-[(2S)-2-{[(2S)-1-[(2S)-4-c...)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCNC(=O)C=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(O)=O Show InChI InChI=1S/C41H59N9O11/c1-24(2)21-29(40(59)50-20-8-13-32(50)38(57)48-30(41(60)61)22-25-9-4-3-5-10-25)47-36(55)27(16-18-44-34(53)23-51)45-37(56)31-12-7-19-49(31)39(58)28(14-15-33(42)52)46-35(54)26-11-6-17-43-26/h3-5,9-10,23-24,26-32,43H,6-8,11-22H2,1-2H3,(H2,42,52)(H,44,53)(H,45,56)(H,46,54)(H,47,55)(H,48,57)(H,60,61)/t26-,27-,28-,29-,30-,31-,32-/m0/s1 | PDB MMDB
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| CHEMBL KEGG PC cid PC sid UniChem
Similars
| Article PubMed
| 4.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 |
Bioorg Med Chem 15: 6253-61 (2007)
Article DOI: 10.1016/j.bmc.2007.06.020 BindingDB Entry DOI: 10.7270/Q24Q7TQ3 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200159
((S)-quinolin-3-ylmethyl 1-((3-bromo-4,5-dihydroiso...)Show SMILES Oc1ccc(C[C@H](NC(=O)OCc2cnc3ccccc3c2)C(=O)NCC2CC(Br)=NO2)cc1 |r,c:31| Show InChI InChI=1S/C24H23BrN4O5/c25-22-11-19(34-29-22)13-27-23(31)21(10-15-5-7-18(30)8-6-15)28-24(32)33-14-16-9-17-3-1-2-4-20(17)26-12-16/h1-9,12,19,21,30H,10-11,13-14H2,(H,27,31)(H,28,32)/t19?,21-/m0/s1 | PDB MMDB
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Similars
| Article PubMed
| 4.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342561
((2-oxoindolin-3-ylidene)indolin-2-one | (E)-[3,3'-...)Show InChI InChI=1S/C16H10N2O2/c19-15-13(9-5-1-3-7-11(9)17-15)14-10-6-2-4-8-12(10)18-16(14)20/h1-8H,(H,17,19)(H,18,20)/b14-13+ | PDB MMDB
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| Article PubMed
| 4.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human transglutaminase 2 using Cbz-Gln-Gly as a substrate by GDH-coupled assay |
Bioorg Med Chem Lett 21: 2692-6 (2011)
Article DOI: 10.1016/j.bmcl.2010.12.037 BindingDB Entry DOI: 10.7270/Q2CN7471 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM59188
(Dihydroisoxazole, 3e)Show SMILES BrC1=NOC(CNC(=O)[C@H](Cc2ccccc2)NC(=O)Oc2ccc3ccccc3c2)C1 |r,t:1| Show InChI InChI=1S/C24H22BrN3O4/c25-22-14-20(32-28-22)15-26-23(29)21(12-16-6-2-1-3-7-16)27-24(30)31-19-11-10-17-8-4-5-9-18(17)13-19/h1-11,13,20-21H,12,14-15H2,(H,26,29)(H,27,30)/t20?,21-/m0/s1 | PDB MMDB
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| PC cid PC sid UniChem
Similars
| Article PubMed
| 4.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a | 7.2 | n/a |
Stanford University
| Assay Description Recombinant of human TG2 was expressed in E.coli and purified to >90% homogeneity. |
Chem Biol 12: 469-75 (2005)
Article DOI: 10.1016/j.chembiol.2005.02.007 BindingDB Entry DOI: 10.7270/Q2XK8D0V |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342582
((E)-4-chloro-3-(2-(4-chlorophenyl)-2-oxoethylidene...)Show InChI InChI=1S/C16H9Cl2NO2/c17-10-6-4-9(5-7-10)14(20)8-11-15-12(18)2-1-3-13(15)19-16(11)21/h1-8H,(H,19,21)/b11-8+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 4.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of recombinant human TG2 V224 mutant deamidation activity using Cbz-Gln-Gly as substrate preincubated for 30 mins followed... |
Bioorg Med Chem Lett 25: 4922-6 (2015)
Article DOI: 10.1016/j.bmcl.2015.05.006 BindingDB Entry DOI: 10.7270/Q2W95C07 |
More data for this Ligand-Target Pair | |
Uridine-cytidine kinase 2
(Homo sapiens) | BDBM50522198
(CHEMBL4434988)Show SMILES Cc1cc(C)cc(NC(=O)CSCn2[nH]nc3c2nc(Cc2ccc(F)cc2)nc3=O)c1 Show InChI InChI=1S/C22H21FN6O2S/c1-13-7-14(2)9-17(8-13)24-19(30)11-32-12-29-21-20(27-28-29)22(31)26-18(25-21)10-15-3-5-16(23)6-4-15/h3-9,28H,10-12H2,1-2H3,(H,24,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| 5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of C-terminally His6-tagged human UCK2 expressed in Escherichia coli BL21(DE3) cells using phosphoenolpyruvate, NADH and v... |
Bioorg Med Chem Lett 29: 2559-2564 (2019)
Article DOI: 10.1016/j.bmcl.2019.08.010 BindingDB Entry DOI: 10.7270/Q2DZ0CQZ |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200146
(CHEMBL216391 | quinolin-3-ylmethyl 1-((3-bromo-4,5...)Show SMILES COc1ccc2[nH]cc(CC(NC(=O)OCc3cnc4ccccc4c3)C(=O)NCC3CC(Br)=NO3)c2c1 |c:35| Show InChI InChI=1S/C27H26BrN5O5/c1-36-19-6-7-23-21(10-19)18(13-30-23)9-24(26(34)31-14-20-11-25(28)33-38-20)32-27(35)37-15-16-8-17-4-2-3-5-22(17)29-12-16/h2-8,10,12-13,20,24,30H,9,11,14-15H2,1H3,(H,31,34)(H,32,35) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 5.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM59187
(Dihydroisoxazole, 3d)Show SMILES BrC1=NOC(CNC(=O)[C@H](Cc2ccccc2)NC(=O)OCCc2ccccc2)C1 |r,t:1| Show InChI InChI=1S/C22H24BrN3O4/c23-20-14-18(30-26-20)15-24-21(27)19(13-17-9-5-2-6-10-17)25-22(28)29-12-11-16-7-3-1-4-8-16/h1-10,18-19H,11-15H2,(H,24,27)(H,25,28)/t18?,19-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 6.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | 7.2 | n/a |
Stanford University
| Assay Description Recombinant of human TG2 was expressed in E.coli and purified to >90% homogeneity. |
Chem Biol 12: 469-75 (2005)
Article DOI: 10.1016/j.chembiol.2005.02.007 BindingDB Entry DOI: 10.7270/Q2XK8D0V |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200157
((S)-quinolin-3-ylmethyl 2-(((3-bromo-4,5-dihydrois...)Show SMILES BrC1=NOC(CNC(=O)N2CCC[C@H]2C(=O)OCc2ccc3ccccc3n2)C1 |r,t:1| Show InChI InChI=1S/C20H21BrN4O4/c21-18-10-15(29-24-18)11-22-20(27)25-9-3-6-17(25)19(26)28-12-14-8-7-13-4-1-2-5-16(13)23-14/h1-2,4-5,7-8,15,17H,3,6,9-12H2,(H,22,27)/t15?,17-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| 6.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50200148
(CHEMBL375595 | benzyl (S)-1-(((S)-3-bromo-4,5-dihy...)Show SMILES Oc1ccc(C[C@H](NC(=O)OCc2ccccc2)C(=O)NC[C@@H]2CC(Br)=NO2)cc1 |r,c:26| Show InChI InChI=1S/C21H22BrN3O5/c22-19-11-17(30-25-19)12-23-20(27)18(10-14-6-8-16(26)9-7-14)24-21(28)29-13-15-4-2-1-3-5-15/h1-9,17-18,26H,10-13H2,(H,23,27)(H,24,28)/t17-,18-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| 6.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TG2 expressed in Escherichia coli |
J Med Chem 49: 7493-501 (2006)
Article DOI: 10.1021/jm060839a BindingDB Entry DOI: 10.7270/Q2280771 |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM59186
(Dihydroisoxazole, 3c)Show SMILES BrC1=NOC(CNC(=O)[C@H](Cc2ccccc2)NC(=O)Oc2cccnc2)C1 |r,t:1| Show InChI InChI=1S/C19H19BrN4O4/c20-17-10-15(28-24-17)12-22-18(25)16(9-13-5-2-1-3-6-13)23-19(26)27-14-7-4-8-21-11-14/h1-8,11,15-16H,9-10,12H2,(H,22,25)(H,23,26)/t15?,16-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 7.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a | 7.2 | n/a |
Stanford University
| Assay Description Recombinant of human TG2 was expressed in E.coli and purified to >90% homogeneity. |
Chem Biol 12: 469-75 (2005)
Article DOI: 10.1016/j.chembiol.2005.02.007 BindingDB Entry DOI: 10.7270/Q2XK8D0V |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM59190
(Dihydroisoxazole, 4)Show SMILES Oc1ccc2[nH]cc(C[C@H](NC(=O)OCC3=Cc4ccccc4S3(=O)=O)C(=O)NCC3CC(Br)=NO3)c2c1 |r,c:35,t:15| Show InChI InChI=1S/C25H23BrN4O7S/c26-23-10-17(37-30-23)12-28-24(32)21(8-15-11-27-20-6-5-16(31)9-19(15)20)29-25(33)36-13-18-7-14-3-1-2-4-22(14)38(18,34)35/h1-7,9,11,17,21,27,31H,8,10,12-13H2,(H,28,32)(H,29,33)/t17?,21-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 7.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a | 7.2 | n/a |
Stanford University
| Assay Description Recombinant of human TG2 was expressed in E.coli and purified to >90% homogeneity. |
Chem Biol 12: 469-75 (2005)
Article DOI: 10.1016/j.chembiol.2005.02.007 BindingDB Entry DOI: 10.7270/Q2XK8D0V |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM59185
(Dihydroisoxazole, 3b)Show SMILES Oc1ccc(C[C@H](NC(=O)Oc2ccncc2)C(=O)NCC2CC(Br)=NO2)cc1 |r,c:25| Show InChI InChI=1S/C19H19BrN4O5/c20-17-10-15(29-24-17)11-22-18(26)16(9-12-1-3-13(25)4-2-12)23-19(27)28-14-5-7-21-8-6-14/h1-8,15-16,25H,9-11H2,(H,22,26)(H,23,27)/t15?,16-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 8.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | 7.2 | n/a |
Stanford University
| Assay Description Recombinant of human TG2 was expressed in E.coli and purified to >90% homogeneity. |
Chem Biol 12: 469-75 (2005)
Article DOI: 10.1016/j.chembiol.2005.02.007 BindingDB Entry DOI: 10.7270/Q2XK8D0V |
More data for this Ligand-Target Pair | |
Protein-glutamine gamma-glutamyltransferase 2
(Homo sapiens (Human)) | BDBM50342569
((E)-3-(2-oxo-2-(pyridin-3-yl)ethylidene)indolin-2-...)Show InChI InChI=1S/C15H10N2O2/c18-14(10-4-3-7-16-9-10)8-12-11-5-1-2-6-13(11)17-15(12)19/h1-9H,(H,17,19)/b12-8+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 8.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Stanford University
Curated by ChEMBL
| Assay Description Non-competitive inhibition of recombinant human TG2 V224 mutant deamidation activity using Cbz-Gln-Gly as substrate preincubated for 30 mins followed... |
Bioorg Med Chem Lett 25: 4922-6 (2015)
Article DOI: 10.1016/j.bmcl.2015.05.006 BindingDB Entry DOI: 10.7270/Q2W95C07 |
More data for this Ligand-Target Pair | |