Compile Data Set for Download or QSAR

Found 50 hits with Last Name = 'gangopadhyay' and Initial = 'ak'   

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
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354642 (CHEMBL1834204) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccc(F)cc2F)cn1)C(O)=O |r| Show InChI InChI=1S/C24H22F2N4O4/c1-13(2)21(23(32)33)30-22(31)15-5-3-14(4-6-15)19-10-8-17(12-27-19)28-24(34)29-20-9-7-16(25)11-18(20)26/h3-13,21H,1-2H3,(H,30,31)(H,32,33)(H2,28,29,34)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354637 (CHEMBL1834440) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2F)cn1)C(O)=O |r| Show InChI InChI=1S/C24H23FN4O4/c1-14(2)21(23(31)32)29-22(30)16-9-7-15(8-10-16)19-12-11-17(13-26-19)27-24(33)28-20-6-4-3-5-18(20)25/h3-14,21H,1-2H3,(H,29,30)(H,31,32)(H2,27,28,33)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354639 (CHEMBL1834201) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccc(F)cc2)cn1)C(O)=O |r| Show InChI InChI=1S/C24H23FN4O4/c1-14(2)21(23(31)32)29-22(30)16-5-3-15(4-6-16)20-12-11-19(13-26-20)28-24(33)27-18-9-7-17(25)8-10-18/h3-14,21H,1-2H3,(H,29,30)(H,31,32)(H2,27,28,33)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354638 (CHEMBL1834200) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2cccc(F)c2)cn1)C(O)=O |r| Show InChI InChI=1S/C24H23FN4O4/c1-14(2)21(23(31)32)29-22(30)16-8-6-15(7-9-16)20-11-10-19(13-26-20)28-24(33)27-18-5-3-4-17(25)12-18/h3-14,21H,1-2H3,(H,29,30)(H,31,32)(H2,27,28,33)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM20716 ((1R,2R)-2-[(4-{4-[(phenylcarbamoyl)amino]phenyl}ph...) Show SMILES OC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)cc1 |r| Show InChI InChI=1S/C26H24N2O4/c29-24(22-7-4-8-23(22)25(30)31)19-11-9-17(10-12-19)18-13-15-21(16-14-18)28-26(32)27-20-5-2-1-3-6-20/h1-3,5-6,9-16,22-23H,4,7-8H2,(H,30,31)(H2,27,28,32)/t22-,23-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM20716 ((1R,2R)-2-[(4-{4-[(phenylcarbamoyl)amino]phenyl}ph...) Show SMILES OC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)cc1 |r| Show InChI InChI=1S/C26H24N2O4/c29-24(22-7-4-8-23(22)25(30)31)19-11-9-17(10-12-19)18-13-15-21(16-14-18)28-26(32)27-20-5-2-1-3-6-20/h1-3,5-6,9-16,22-23H,4,7-8H2,(H,30,31)(H2,27,28,32)/t22-,23-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 expressed in Sf9 cells assessed as formation of didecanoylglycerol product after 1 hr using 14C-decanoyl-CoA by beta scinti...				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354641 (CHEMBL1834203) Show SMILES COc1ccc(NC(=O)Nc2ccc(nc2)-c2ccc(cc2)C(=O)N[C@@H](C(C)C)C(O)=O)cc1 |r| Show InChI InChI=1S/C25H26N4O5/c1-15(2)22(24(31)32)29-23(30)17-6-4-16(5-7-17)21-13-10-19(14-26-21)28-25(33)27-18-8-11-20(34-3)12-9-18/h4-15,22H,1-3H3,(H,29,30)(H,31,32)(H2,27,28,33)/t22-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354631 (CHEMBL1834433) Show SMILES OC[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1)C(O)=O |r| Show InChI InChI=1S/C22H20N4O5/c27-13-18(21(29)30)25-20(28)15-8-6-14(7-9-15)16-10-11-19(23-12-16)26-22(31)24-17-4-2-1-3-5-17/h1-12,18,27H,13H2,(H,25,28)(H,29,30)(H2,23,24,26,31)/t18-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	28	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354629 (CHEMBL1834431) Show SMILES OC(=O)CNC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1 Show InChI InChI=1S/C21H18N4O4/c26-19(27)13-23-20(28)15-8-6-14(7-9-15)16-10-11-18(22-12-16)25-21(29)24-17-4-2-1-3-5-17/h1-12H,13H2,(H,23,28)(H,26,27)(H2,22,24,25,29)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354634 (CHEMBL1834436) Show SMILES CC(C)C[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1)C(O)=O |r| Show InChI InChI=1S/C25H26N4O4/c1-16(2)14-21(24(31)32)28-23(30)18-10-8-17(9-11-18)19-12-13-22(26-15-19)29-25(33)27-20-6-4-3-5-7-20/h3-13,15-16,21H,14H2,1-2H3,(H,28,30)(H,31,32)(H2,26,27,29,33)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354633 (CHEMBL1834435) Show SMILES CC(C)[C@@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O4/c1-15(2)21(23(30)31)28-22(29)17-10-8-16(9-11-17)18-12-13-20(25-14-18)27-24(32)26-19-6-4-3-5-7-19/h3-15,21H,1-2H3,(H,28,29)(H,30,31)(H2,25,26,27,32)/t21-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	51	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354636 (CHEMBL1834438) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccc(F)cc2F)nc1)C(O)=O |r| Show InChI InChI=1S/C24H22F2N4O4/c1-13(2)21(23(32)33)30-22(31)15-5-3-14(4-6-15)16-7-10-20(27-12-16)29-24(34)28-19-9-8-17(25)11-18(19)26/h3-13,21H,1-2H3,(H,30,31)(H,32,33)(H2,27,28,29,34)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	57	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354640 (CHEMBL1834202) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2OC(F)(F)F)cn1)C(O)=O |r| Show InChI InChI=1S/C25H23F3N4O5/c1-14(2)21(23(34)35)32-22(33)16-9-7-15(8-10-16)18-12-11-17(13-29-18)30-24(36)31-19-5-3-4-6-20(19)37-25(26,27)28/h3-14,21H,1-2H3,(H,32,33)(H,34,35)(H2,30,31,36)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	64	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354630 (CHEMBL1834432) Show SMILES C[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1)C(O)=O |r| Show InChI InChI=1S/C22H20N4O4/c1-14(21(28)29)24-20(27)16-9-7-15(8-10-16)17-11-12-19(23-13-17)26-22(30)25-18-5-3-2-4-6-18/h2-14H,1H3,(H,24,27)(H,28,29)(H2,23,25,26,30)/t14-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	72	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354643 (CHEMBL1834206) Show SMILES OC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(cc1)-c1ccc(Nc2nc3ccc(F)cc3s2)c(F)c1 |r| Show InChI InChI=1S/C26H20F2N2O3S/c27-17-9-11-22-23(13-17)34-26(30-22)29-21-10-8-16(12-20(21)28)14-4-6-15(7-5-14)24(31)18-2-1-3-19(18)25(32)33/h4-13,18-19H,1-3H2,(H,29,30)(H,32,33)/t18-,19-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 expressed in Sf9 cells assessed as formation of didecanoylglycerol product after 1 hr using 14C-decanoyl-CoA by beta scinti...				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354632 (CHEMBL1834434) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccccc2)nc1)C(O)=O |r| Show InChI InChI=1S/C24H24N4O4/c1-15(2)21(23(30)31)28-22(29)17-10-8-16(9-11-17)18-12-13-20(25-14-18)27-24(32)26-19-6-4-3-5-7-19/h3-15,21H,1-2H3,(H,28,29)(H,30,31)(H2,25,26,27,32)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	88	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (Homo sapiens (Human))	BDBM50354635 (CHEMBL1834437) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(NC(=O)Nc2ccc(F)cc2)nc1)C(O)=O |r| Show InChI InChI=1S/C24H23FN4O4/c1-14(2)21(23(31)32)29-22(30)16-5-3-15(4-6-16)17-7-12-20(26-13-17)28-24(33)27-19-10-8-18(25)9-11-19/h3-14,21H,1-2H3,(H,29,30)(H,31,32)(H2,26,27,28,33)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	99	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Life Sciences Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as formation of [14C]-triglyceride using [14C]oleoyl-CoA by liquid scintillation counting				Bioorg Med Chem Lett 21: 5812-7 (2011) Article DOI: 10.1016/j.bmcl.2011.07.109 BindingDB Entry DOI: 10.7270/Q28G8M29
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386129 (CHEMBL2042217) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(Cl)cc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20ClFN4O5/c1-11(2)19(21(30)31)27-20(29)18-10-17(28-33-18)12-3-6-14(7-4-12)25-22(32)26-16-8-5-13(23)9-15(16)24/h3-11,19H,1-2H3,(H,27,29)(H,30,31)(H2,25,26,32)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386149 (CHEMBL2042351) Show SMILES CC(C)[C@H](NC(=O)c1ccc(cc1)-c1ccc(Nc2nc3ccc(F)cc3s2)cc1)C(O)=O |r| Show InChI InChI=1S/C25H22FN3O3S/c1-14(2)22(24(31)32)29-23(30)17-5-3-15(4-6-17)16-7-10-19(11-8-16)27-25-28-20-12-9-18(26)13-21(20)33-25/h3-14,22H,1-2H3,(H,27,28)(H,29,30)(H,31,32)/t22-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386120 (CHEMBL2042201) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccccc2Cl)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21ClN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-7-9-14(10-8-13)24-22(31)25-16-6-4-3-5-15(16)23/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386126 (CHEMBL2042213) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(C)c(C)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C24H26N4O5/c1-13(2)21(23(30)31)27-22(29)20-12-19(28-33-20)16-6-9-17(10-7-16)25-24(32)26-18-8-5-14(3)15(4)11-18/h5-13,21H,1-4H3,(H,27,29)(H,30,31)(H2,25,26,32)/t21-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386122 (CHEMBL2042204) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cccc(Cl)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21ClN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-6-8-15(9-7-13)24-22(31)25-16-5-3-4-14(23)10-16/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386145 (CHEMBL2042347) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(C)ccc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C23H23FN4O5/c1-12(2)20(22(30)31)27-21(29)19-11-17(28-33-19)14-5-7-15(8-6-14)25-23(32)26-18-10-13(3)4-9-16(18)24/h4-12,20H,1-3H3,(H,27,29)(H,30,31)(H2,25,26,32)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386137 (CHEMBL2042339) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccccc2C(F)(F)F)cc1)C(O)=O |r| Show InChI InChI=1S/C23H21F3N4O5/c1-12(2)19(21(32)33)29-20(31)18-11-17(30-35-18)13-7-9-14(10-8-13)27-22(34)28-16-6-4-3-5-15(16)23(24,25)26/h3-12,19H,1-2H3,(H,29,31)(H,32,33)(H2,27,28,34)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386136 (CHEMBL2042338) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cccc(C)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C23H24N4O5/c1-13(2)20(22(29)30)26-21(28)19-12-18(27-32-19)15-7-9-16(10-8-15)24-23(31)25-17-6-4-5-14(3)11-17/h4-13,20H,1-3H3,(H,26,28)(H,29,30)(H2,24,25,31)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386131 (CHEMBL2042221) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(F)cc2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21FN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-3-7-15(8-4-13)24-22(31)25-16-9-5-14(23)6-10-16/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386132 (CHEMBL2042223) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(C)cc2)cc1)C(O)=O |r| Show InChI InChI=1S/C23H24N4O5/c1-13(2)20(22(29)30)26-21(28)19-12-18(27-32-19)15-6-10-17(11-7-15)25-23(31)24-16-8-4-14(3)5-9-16/h4-13,20H,1-3H3,(H,26,28)(H,29,30)(H2,24,25,31)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386130 (CHEMBL2042219) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(F)cc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20F2N4O5/c1-11(2)19(21(30)31)27-20(29)18-10-17(28-33-18)12-3-6-14(7-4-12)25-22(32)26-16-8-5-13(23)9-15(16)24/h3-11,19H,1-2H3,(H,27,29)(H,30,31)(H2,25,26,32)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386133 (CHEMBL2042334) Show SMILES COc1ccc(NC(=O)Nc2ccc(cc2)-c2cc(on2)C(=O)N[C@@H](C(C)C)C(O)=O)cc1 |r| Show InChI InChI=1S/C23H24N4O6/c1-13(2)20(22(29)30)26-21(28)19-12-18(27-33-19)14-4-6-15(7-5-14)24-23(31)25-16-8-10-17(32-3)11-9-16/h4-13,20H,1-3H3,(H,26,28)(H,29,30)(H2,24,25,31)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386124 (CHEMBL2042210) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cccc(c2)C(F)(F)F)cc1)C(O)=O |r| Show InChI InChI=1S/C23H21F3N4O5/c1-12(2)19(21(32)33)29-20(31)18-11-17(30-35-18)13-6-8-15(9-7-13)27-22(34)28-16-5-3-4-14(10-16)23(24,25)26/h3-12,19H,1-2H3,(H,29,31)(H,32,33)(H2,27,28,34)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386148 (CHEMBL2042350) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(F)ccc2C)cc1)C(O)=O |r| Show InChI InChI=1S/C23H23FN4O5/c1-12(2)20(22(30)31)27-21(29)19-11-18(28-33-19)14-5-8-16(9-6-14)25-23(32)26-17-10-15(24)7-4-13(17)3/h4-12,20H,1-3H3,(H,27,29)(H,30,31)(H2,25,26,32)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386140 (CHEMBL2042342) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(F)cc(F)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20F2N4O5/c1-11(2)19(21(30)31)27-20(29)18-10-17(28-33-18)12-3-5-15(6-4-12)25-22(32)26-16-8-13(23)7-14(24)9-16/h3-11,19H,1-2H3,(H,27,29)(H,30,31)(H2,25,26,32)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386139 (CHEMBL2042341) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(F)c(F)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20F2N4O5/c1-11(2)19(21(30)31)27-20(29)18-10-17(28-33-18)12-3-5-13(6-4-12)25-22(32)26-14-7-8-15(23)16(24)9-14/h3-11,19H,1-2H3,(H,27,29)(H,30,31)(H2,25,26,32)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386138 (CHEMBL2042340) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(cc2)C(F)(F)F)cc1)C(O)=O |r| Show InChI InChI=1S/C23H21F3N4O5/c1-12(2)19(21(32)33)29-20(31)18-11-17(30-35-18)13-3-7-15(8-4-13)27-22(34)28-16-9-5-14(6-10-16)23(24,25)26/h3-12,19H,1-2H3,(H,29,31)(H,32,33)(H2,27,28,34)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386135 (CHEMBL2042337) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccccc2C)cc1)C(O)=O |r| Show InChI InChI=1S/C23H24N4O5/c1-13(2)20(22(29)30)26-21(28)19-12-18(27-32-19)15-8-10-16(11-9-15)24-23(31)25-17-7-5-4-6-14(17)3/h4-13,20H,1-3H3,(H,26,28)(H,29,30)(H2,24,25,31)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386143 (CHEMBL2042345) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(C)cc2C)cc1)C(O)=O |r| Show InChI InChI=1S/C24H26N4O5/c1-13(2)21(23(30)31)27-22(29)20-12-19(28-33-20)16-6-8-17(9-7-16)25-24(32)26-18-10-5-14(3)11-15(18)4/h5-13,21H,1-4H3,(H,27,29)(H,30,31)(H2,25,26,32)/t21-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386127 (CHEMBL2042215) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(Cl)cc2Oc2ccccc2)cc1)C(O)=O |r| Show InChI InChI=1S/C28H25ClN4O6/c1-16(2)25(27(35)36)32-26(34)24-15-22(33-39-24)17-8-11-19(12-9-17)30-28(37)31-21-13-10-18(29)14-23(21)38-20-6-4-3-5-7-20/h3-16,25H,1-2H3,(H,32,34)(H,35,36)(H2,30,31,37)/t25-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386147 (CHEMBL2042349) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(F)cc2C)cc1)C(O)=O |r| Show InChI InChI=1S/C23H23FN4O5/c1-12(2)20(22(30)31)27-21(29)19-11-18(28-33-19)14-4-7-16(8-5-14)25-23(32)26-17-9-6-15(24)10-13(17)3/h4-12,20H,1-3H3,(H,27,29)(H,30,31)(H2,25,26,32)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386134 (CHEMBL2042336) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cccc(F)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21FN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-6-8-15(9-7-13)24-22(31)25-16-5-3-4-14(23)10-16/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386144 (CHEMBL2042346) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(C)cc(C)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C24H26N4O5/c1-13(2)21(23(30)31)27-22(29)20-12-19(28-33-20)16-5-7-17(8-6-16)25-24(32)26-18-10-14(3)9-15(4)11-18/h5-13,21H,1-4H3,(H,27,29)(H,30,31)(H2,25,26,32)/t21-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.14E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386151 (CHEMBL2042352) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(Nc2nc3ccc(F)cc3s2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H19FN4O4S/c1-11(2)19(21(29)30)26-20(28)17-10-16(27-31-17)12-3-6-14(7-4-12)24-22-25-15-8-5-13(23)9-18(15)32-22/h3-11,19H,1-2H3,(H,24,25)(H,26,28)(H,29,30)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386123 (CHEMBL2042207) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(Cl)cc2)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21ClN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-3-7-15(8-4-13)24-22(31)25-16-9-5-14(23)6-10-16/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.24E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386141 (CHEMBL2042343) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2cc(F)ccc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20F2N4O5/c1-11(2)19(21(30)31)27-20(29)18-10-16(28-33-18)12-3-6-14(7-4-12)25-22(32)26-17-9-13(23)5-8-15(17)24/h3-11,19H,1-2H3,(H,27,29)(H,30,31)(H2,25,26,32)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.41E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386119 (CHEMBL2042335) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccccc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21FN4O5/c1-12(2)19(21(29)30)26-20(28)18-11-17(27-32-18)13-7-9-14(10-8-13)24-22(31)25-16-6-4-3-5-15(16)23/h3-12,19H,1-2H3,(H,26,28)(H,29,30)(H2,24,25,31)/t19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.41E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386146 (CHEMBL2042348) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2ccc(C)c(F)c2)cc1)C(O)=O |r| Show InChI InChI=1S/C23H23FN4O5/c1-12(2)20(22(30)31)27-21(29)19-11-18(28-33-19)14-5-8-15(9-6-14)25-23(32)26-16-7-4-13(3)17(24)10-16/h4-12,20H,1-3H3,(H,27,29)(H,30,31)(H2,25,26,32)/t20-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.78E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386142 (CHEMBL2042344) Show SMILES CC(C)[C@H](NC(=O)c1cc(no1)-c1ccc(NC(=O)Nc2c(F)cccc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C22H20F2N4O5/c1-11(2)18(21(30)31)26-20(29)17-10-16(28-33-17)12-6-8-13(9-7-12)25-22(32)27-19-14(23)4-3-5-15(19)24/h3-11,18H,1-2H3,(H,26,29)(H,30,31)(H2,25,27,32)/t18-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.85E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386128 (CHEMBL2042216) Show SMILES CC(C)[C@H](NC(=O)c1ncc(o1)-c1ccc(NC(=O)Nc2ccc(Cl)cc2Oc2ccccc2)cc1)C(O)=O |r| Show InChI InChI=1S/C28H25ClN4O6/c1-16(2)24(27(35)36)33-25(34)26-30-15-23(39-26)17-8-11-19(12-9-17)31-28(37)32-21-13-10-18(29)14-22(21)38-20-6-4-3-5-7-20/h3-16,24H,1-2H3,(H,33,34)(H,35,36)(H2,31,32,37)/t24-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.30E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386150 (CHEMBL2042220) Show SMILES CC(C)[C@H](NC(=O)c1nc(no1)-c1ccc(NC(=O)Nc2ccc(F)cc2F)cc1)C(O)=O |r| Show InChI InChI=1S/C21H19F2N5O5/c1-10(2)16(20(30)31)26-18(29)19-27-17(28-33-19)11-3-6-13(7-4-11)24-21(32)25-15-8-5-12(22)9-14(15)23/h3-10,16H,1-2H3,(H,26,29)(H,30,31)(H2,24,25,32)/t16-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.59E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386121 (CHEMBL2042202) Show SMILES CC(C)[C@H](NC(=O)c1ncc(o1)-c1ccc(NC(=O)Nc2ccccc2Cl)cc1)C(O)=O |r| Show InChI InChI=1S/C22H21ClN4O5/c1-12(2)18(21(29)30)27-19(28)20-24-11-17(32-20)13-7-9-14(10-8-13)25-22(31)26-16-6-4-3-5-15(16)23/h3-12,18H,1-2H3,(H,27,28)(H,29,30)(H2,25,26,31)/t18-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.82E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair
Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (Homo sapiens (Human))	BDBM50386125 (CHEMBL2042211) Show SMILES CC(C)[C@H](NC(=O)c1ncc(o1)-c1ccc(NC(=O)Nc2cccc(c2)C(F)(F)F)cc1)C(O)=O |r| Show InChI InChI=1S/C23H21F3N4O5/c1-12(2)18(21(32)33)30-19(31)20-27-11-17(35-20)13-6-8-15(9-7-13)28-22(34)29-16-5-3-4-14(10-16)23(24,25)26/h3-12,18H,1-2H3,(H,30,31)(H,32,33)(H2,28,29,34)/t18-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.58E+5	n/a	n/a	n/a	n/a	n/a	n/a
Piramal Healthcare Limited Curated by ChEMBL					Assay Description Inhibition of human DGAT1 assessed as conversion of [14C]-oleoyl-CoA to [14C]-triglyceride after 10 mins by scintillation counting				Eur J Med Chem 54: 324-42 (2012) Article DOI: 10.1016/j.ejmech.2012.05.016 BindingDB Entry DOI: 10.7270/Q25B03HK
					More data for this Ligand-Target Pair