Compile Data Set for Download or QSAR

Found 16 hits with Last Name = 'palcic' and Initial = 'mm'   

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
N-acetyllactosaminide alpha-1,3-galactosyltransferase (Bos taurus)	BDBM50389789 (CHEMBL1229737) Show SMILES OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2cc(-c3ccc(C=O)s3)c(=O)[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C20H26N2O18P2S/c23-4-7-1-2-11(43-7)8-3-22(20(31)21-17(8)30)18-15(28)13(26)10(37-18)6-36-41(32,33)40-42(34,35)39-19-16(29)14(27)12(25)9(5-24)38-19/h1-4,9-10,12-16,18-19,24-29H,5-6H2,(H,32,33)(H,34,35)(H,21,30,31)/t9-,10-,12+,13-,14+,15-,16-,18-,19-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	9.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of East Anglia Curated by ChEMBL					Assay Description Inhibition of alpha-1,3-GalT in bovine after 15 mins by Dixon plot analysis				J Med Chem 55: 2015-24 (2012) Article DOI: 10.1021/jm201154p BindingDB Entry DOI: 10.7270/Q28W3FCH
					More data for this Ligand-Target Pair
N-acetyllactosaminide alpha-1,3-galactosyltransferase (Bos taurus)	BDBM50389786 (CHEMBL2070378) Show SMILES OC[C@H]1O[C@H](CCP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2cc(-c3ccc(C=O)s3)c(=O)[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C22H30N2O17P2S/c25-6-9-1-2-14(44-9)10-5-24(22(33)23-20(10)32)21-19(31)17(29)13(40-21)8-38-43(36,37)41-42(34,35)4-3-11-15(27)18(30)16(28)12(7-26)39-11/h1-2,5-6,11-13,15-19,21,26-31H,3-4,7-8H2,(H,34,35)(H,36,37)(H,23,32,33)/t11-,12-,13-,15+,16+,17-,18-,19-,21-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of East Anglia Curated by ChEMBL					Assay Description Inhibition of alpha-1,3-GalT in bovine after 15 mins by Dixon plot analysis				J Med Chem 55: 2015-24 (2012) Article DOI: 10.1021/jm201154p BindingDB Entry DOI: 10.7270/Q28W3FCH
					More data for this Ligand-Target Pair
N-acetyllactosaminide alpha-1,3-galactosyltransferase (Bos taurus)	BDBM50389788 (CHEMBL2070375) Show SMILES OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2cc(-c3ccccc3)c(=O)[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C21H28N2O17P2/c24-7-11-13(25)15(27)17(29)20(38-11)39-42(34,35)40-41(32,33)36-8-12-14(26)16(28)19(37-12)23-6-10(18(30)22-21(23)31)9-4-2-1-3-5-9/h1-6,11-17,19-20,24-29H,7-8H2,(H,32,33)(H,34,35)(H,22,30,31)/t11-,12-,13+,14-,15+,16-,17-,19-,20-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	7.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of East Anglia Curated by ChEMBL					Assay Description Inhibition of alpha-1,3-GalT in bovine after 15 mins by Dixon plot analysis				J Med Chem 55: 2015-24 (2012) Article DOI: 10.1021/jm201154p BindingDB Entry DOI: 10.7270/Q28W3FCH
					More data for this Ligand-Target Pair
N-acetyllactosaminide alpha-1,3-galactosyltransferase (Bos taurus)	BDBM50389787 (CHEMBL2070376) Show SMILES OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n2cc(-c3ccco3)c(=O)[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C19H26N2O18P2/c22-5-9-11(23)13(25)15(27)18(37-9)38-41(32,33)39-40(30,31)35-6-10-12(24)14(26)17(36-10)21-4-7(8-2-1-3-34-8)16(28)20-19(21)29/h1-4,9-15,17-18,22-27H,5-6H2,(H,30,31)(H,32,33)(H,20,28,29)/t9-,10-,11+,12-,13+,14-,15-,17-,18-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of East Anglia Curated by ChEMBL					Assay Description Inhibition of alpha-1,3-GalT in bovine after 15 mins by Dixon plot analysis				J Med Chem 55: 2015-24 (2012) Article DOI: 10.1021/jm201154p BindingDB Entry DOI: 10.7270/Q28W3FCH
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.17E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427446 (CHEMBL477507) Show SMILES OC[C@@H](O)[C@@H](O)[C@@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O |r| Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4+,6-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.61E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.65E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Competitive inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by Michaelis-Menten equation analysis in presence of m...				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427445 (CHEMBL1235497) Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O |r| Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	5.71E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427446 (CHEMBL477507) Show SMILES OC[C@@H](O)[C@@H](O)[C@@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O |r| Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4+,6-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427445 (CHEMBL1235497) Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O |r| Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	2.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.89E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	1.82E+5	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Binding affinity to human blood group B Galactosyltransferase by STD NMR analysis in presence of magnesium ions				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427445 (CHEMBL1235497) Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O |r| Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	n/a	2.30E+6	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Binding affinity to human blood group B Galactosyltransferase after 300 secs by SPR analysis				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair
Histo-blood group ABO system transferase (Homo sapiens (Human))	BDBM50427444 (CHEMBL2326313) Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	2.54E+5	n/a	n/a	n/a	n/a	n/a
University of Hamburg Curated by ChEMBL					Assay Description Binding affinity to human blood group B Galactosyltransferase after 300 secs by SPR analysis				J Med Chem 56: 2150-4 (2013) Article DOI: 10.1021/jm300642a BindingDB Entry DOI: 10.7270/Q26T0P01
					More data for this Ligand-Target Pair