Compile Data Set for Download or QSAR

Found 319 hits with Last Name = 'beutel' and Initial = 'ba'   

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
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205246 ((S)-(-)-N-(1-(3-(2-(4-isopropoxyphenoxy)thiazol-5-...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)-c2cc(on2)[C@H](C)NC(C)=O)cc1 Show InChI InChI=1S/C19H21N3O4S/c1-11(2)24-14-5-7-15(8-6-14)25-19-20-10-18(27-19)16-9-17(26-22-16)12(3)21-13(4)23/h5-12H,1-4H3,(H,21,23)/t12-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195026 (CHEMBL223100 | N-(4-(2-(4-propoxyphenoxy)thiazol-5...) Show SMILES CCCOc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-4-11-22-15-6-8-16(9-7-15)23-18-19-12-17(24-18)10-5-13(2)20-14(3)21/h6-9,12-13H,4,11H2,1-3H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195026 (CHEMBL223100 | N-(4-(2-(4-propoxyphenoxy)thiazol-5...) Show SMILES CCCOc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-4-11-22-15-6-8-16(9-7-15)23-18-19-12-17(24-18)10-5-13(2)20-14(3)21/h6-9,12-13H,4,11H2,1-3H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195040 (CHEMBL220563 | N-(4-(2-(4-(cyclopentylmethoxy)phen...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CCCC3)cc2)s1 Show InChI InChI=1S/C21H24N2O3S/c1-15(23-16(2)24)7-12-20-13-22-21(27-20)26-19-10-8-18(9-11-19)25-14-17-5-3-4-6-17/h8-11,13,15,17H,3-6,14H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189627 (CHEMBL212460 | N-{3-[4-(4-isopropoxyphenoxy)phenyl...) Show SMILES CC(C)Oc1ccc(Oc2ccc(cc2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C21H23NO3/c1-15(2)24-19-11-13-21(14-12-19)25-20-9-7-18(8-10-20)6-5-16(3)22-17(4)23/h7-16H,1-4H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203981 (CHEMBL376717 | N-(4-(2-(4-(cyclopropylmethoxy)phen...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CC3)cc2)s1 Show InChI InChI=1S/C19H20N2O3S/c1-13(21-14(2)22)3-10-18-11-20-19(25-18)24-17-8-6-16(7-9-17)23-12-15-4-5-15/h6-9,11,13,15H,4-5,12H2,1-2H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203981 (CHEMBL376717 | N-(4-(2-(4-(cyclopropylmethoxy)phen...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CC3)cc2)s1 Show InChI InChI=1S/C19H20N2O3S/c1-13(21-14(2)22)3-10-18-11-20-19(25-18)24-17-8-6-16(7-9-17)23-12-15-4-5-15/h6-9,11,13,15H,4-5,12H2,1-2H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205248 (CHEMBL220271 | N-(1-(3-(2-(4-isopropoxyphenoxy)thi...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)-c2cc(on2)C(C)NC(C)=O)cc1 Show InChI InChI=1S/C19H21N3O4S/c1-11(2)24-14-5-7-15(8-6-14)25-19-20-10-18(27-19)16-9-17(26-22-16)12(3)21-13(4)23/h5-12H,1-4H3,(H,21,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205245 (1-(4-(2-(4-(cyclopropylmethoxy)phenoxy)thiazol-5-y...) Show SMILES CNC(=O)NC(C)C#Cc1cnc(Oc2ccc(OCC3CC3)cc2)s1 Show InChI InChI=1S/C19H21N3O3S/c1-13(22-18(23)20-2)3-10-17-11-21-19(26-17)25-16-8-6-15(7-9-16)24-12-14-4-5-14/h6-9,11,13-14H,4-5,12H2,1-2H3,(H2,20,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203970 (CHEMBL232004 | N-(4-(2-(4-isobutoxy-2-methylphenox...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(C)c1 |w:17.18| Show InChI InChI=1S/C20H24N2O3S/c1-13(2)12-24-17-7-9-19(14(3)10-17)25-20-21-11-18(26-20)8-6-15(4)22-16(5)23/h7,9-11,13,15H,12H2,1-5H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195029 (CHEMBL375532 | N-(4-(2-(4-isobutoxyphenoxy)thiazol...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C19H22N2O3S/c1-13(2)12-23-16-6-8-17(9-7-16)24-19-20-11-18(25-19)10-5-14(3)21-15(4)22/h6-9,11,13-14H,12H2,1-4H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195029 (CHEMBL375532 | N-(4-(2-(4-isobutoxyphenoxy)thiazol...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C19H22N2O3S/c1-13(2)12-23-16-6-8-17(9-7-16)24-19-20-11-18(25-19)10-5-14(3)21-15(4)22/h6-9,11,13-14H,12H2,1-4H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203978 (CHEMBL233384 | N-(4-(2-(2-chloro-4-(cyclopropylmet...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CC3)cc2Cl)s1 |w:1.0| Show InChI InChI=1S/C19H19ClN2O3S/c1-12(22-13(2)23)3-7-16-10-21-19(26-16)25-18-8-6-15(9-17(18)20)24-11-14-4-5-14/h6,8-10,12,14H,4-5,11H2,1-2H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189631 (CHEMBL376983 | N-(4-(2-(4-phenoxyphenoxy)thiazol-5...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(Oc3ccccc3)cc2)s1 Show InChI InChI=1S/C21H18N2O3S/c1-15(23-16(2)24)8-13-20-14-22-21(27-20)26-19-11-9-18(10-12-19)25-17-6-4-3-5-7-17/h3-7,9-12,14-15H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203969 (CHEMBL233004 | N-(4-(2-(2-fluoro-4-isobutoxyphenox...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(F)c1 |w:17.18| Show InChI InChI=1S/C19H21FN2O3S/c1-12(2)11-24-15-6-8-18(17(20)9-15)25-19-21-10-16(26-19)7-5-13(3)22-14(4)23/h6,8-10,12-13H,11H2,1-4H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189631 (CHEMBL376983 | N-(4-(2-(4-phenoxyphenoxy)thiazol-5...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(Oc3ccccc3)cc2)s1 Show InChI InChI=1S/C21H18N2O3S/c1-15(23-16(2)24)8-13-20-14-22-21(27-20)26-19-11-9-18(10-12-19)25-17-6-4-3-5-7-17/h3-7,9-12,14-15H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203976 (CHEMBL395345 | N-(4-(2-(2-chloro-4-isobutoxyphenox...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(Cl)c1 |w:17.18| Show InChI InChI=1S/C19H21ClN2O3S/c1-12(2)11-24-15-6-8-18(17(20)9-15)25-19-21-10-16(26-19)7-5-13(3)22-14(4)23/h6,8-10,12-13H,11H2,1-4H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195041 (CHEMBL221262 | N-(4-(2-(4-(cyclopentyloxy)phenoxy)...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OC3CCCC3)cc2)s1 Show InChI InChI=1S/C20H22N2O3S/c1-14(22-15(2)23)7-12-19-13-21-20(26-19)25-18-10-8-17(9-11-18)24-16-5-3-4-6-16/h8-11,13-14,16H,3-6H2,1-2H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195042 (CHEMBL220230 | N-(4-(2-(3-isobutoxyphenoxy)thiazol...) Show SMILES CC(C)COc1cccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c1 Show InChI InChI=1S/C19H22N2O3S/c1-13(2)12-23-16-6-5-7-17(10-16)24-19-20-11-18(25-19)9-8-14(3)21-15(4)22/h5-7,10-11,13-14H,12H2,1-4H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203975 (CHEMBL233383 | N-(4-(2-(2-chloro-4-propoxyphenoxy)...) Show SMILES CCCOc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(Cl)c1 |w:16.17| Show InChI InChI=1S/C18H19ClN2O3S/c1-4-9-23-14-6-8-17(16(19)10-14)24-18-20-11-15(25-18)7-5-12(2)21-13(3)22/h6,8,10-12H,4,9H2,1-3H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195042 (CHEMBL220230 | N-(4-(2-(3-isobutoxyphenoxy)thiazol...) Show SMILES CC(C)COc1cccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c1 Show InChI InChI=1S/C19H22N2O3S/c1-13(2)12-23-16-6-5-7-17(10-16)24-19-20-11-18(25-19)9-8-14(3)21-15(4)22/h5-7,10-11,13-14H,12H2,1-4H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205243 (CHEMBL220321 | N-(4-(2-(3-chloro-4-(cyclopropylmet...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(NCC3CC3)c(Cl)c2)s1 Show InChI InChI=1S/C19H20ClN3O2S/c1-12(23-13(2)24)3-7-16-11-22-19(26-16)25-15-6-8-18(17(20)9-15)21-10-14-4-5-14/h6,8-9,11-12,14,21H,4-5,10H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195044 (CHEMBL220031 | N-(4-(2-(3-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1cccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-5-7-16(10-15)23-18-19-11-17(24-18)9-8-13(3)20-14(4)21/h5-7,10-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189620 (CHEMBL208680 | N-{3-[2-(6-isopropoxy-pyridin-3-ylo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cn1 Show InChI InChI=1S/C17H19N3O3S/c1-11(2)22-16-8-6-14(9-18-16)23-17-19-10-15(24-17)7-5-12(3)20-13(4)21/h6,8-12H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195037 (CHEMBL220668 | N-(4-(2-(4-(cyclohexyloxy)phenoxy)t...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OC3CCCCC3)cc2)s1 Show InChI InChI=1S/C21H24N2O3S/c1-15(23-16(2)24)8-13-20-14-22-21(27-20)26-19-11-9-18(10-12-19)25-17-6-4-3-5-7-17/h9-12,14-15,17H,3-7H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195037 (CHEMBL220668 | N-(4-(2-(4-(cyclohexyloxy)phenoxy)t...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OC3CCCCC3)cc2)s1 Show InChI InChI=1S/C21H24N2O3S/c1-15(23-16(2)24)8-13-20-14-22-21(27-20)26-19-11-9-18(10-12-19)25-17-6-4-3-5-7-17/h9-12,14-15,17H,3-7H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203968 (CHEMBL393254 | N-(4-(2-(3-isobutoxy-2-methylphenox...) Show SMILES CC(C)COc1cccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c1C |w:18.19| Show InChI InChI=1S/C20H24N2O3S/c1-13(2)12-24-18-7-6-8-19(15(18)4)25-20-21-11-17(26-20)10-9-14(3)22-16(5)23/h6-8,11,13-14H,12H2,1-5H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189630 (CHEMBL377212 | N-(4-(2-(4-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-8-16(9-7-15)23-18-19-11-17(24-18)10-5-13(3)20-14(4)21/h6-9,11-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189630 (CHEMBL377212 | N-(4-(2-(4-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-8-16(9-7-15)23-18-19-11-17(24-18)10-5-13(3)20-14(4)21/h6-9,11-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of ACC2				Bioorg Med Chem Lett 17: 1803-7 (2007) Article DOI: 10.1016/j.bmcl.2006.12.047 BindingDB Entry DOI: 10.7270/Q28C9VXR
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189630 (CHEMBL377212 | N-(4-(2-(4-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-8-16(9-7-15)23-18-19-11-17(24-18)10-5-13(3)20-14(4)21/h6-9,11-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189630 (CHEMBL377212 | N-(4-(2-(4-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-8-16(9-7-15)23-18-19-11-17(24-18)10-5-13(3)20-14(4)21/h6-9,11-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189630 (CHEMBL377212 | N-(4-(2-(4-isopropoxyphenoxy)thiazo...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C18H20N2O3S/c1-12(2)22-15-6-8-16(9-7-15)23-18-19-11-17(24-18)10-5-13(3)20-14(4)21/h6-9,11-13H,1-4H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 1 (Homo sapiens (Human))	BDBM50205246 ((S)-(-)-N-(1-(3-(2-(4-isopropoxyphenoxy)thiazol-5-...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)-c2cc(on2)[C@H](C)NC(C)=O)cc1 Show InChI InChI=1S/C19H21N3O4S/c1-11(2)24-14-5-7-15(8-6-14)25-19-20-10-18(27-19)16-9-17(26-22-16)12(3)21-13(4)23/h5-12H,1-4H3,(H,21,23)/t12-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC1 expressed in HEK293 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase (Streptococcus pneumoniae (Firmicutes))	BDBM50137758 (2,4-Dichloro-N-[3-cyano-6-(4-hydroxy-phenyl)-4,5,6...) Show SMILES Oc1ccc(cc1)C1CCc2c(C1)sc(NC(=O)c1cc(c(Cl)cc1Cl)S(=O)(=O)N1CCOCC1)c2C#N Show InChI InChI=1S/C26H23Cl2N3O5S2/c27-21-13-22(28)24(38(34,35)31-7-9-36-10-8-31)12-19(21)25(33)30-26-20(14-29)18-6-3-16(11-23(18)37-26)15-1-4-17(32)5-2-15/h1-2,4-5,12-13,16,32H,3,6-11H2,(H,30,33)	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Antibacterial activity against UDP-MurNAc-pentapeptide synthetase from Streptococcus pneumoniae.				Bioorg Med Chem Lett 14: 267-70 (2003) BindingDB Entry DOI: 10.7270/Q2R49Q55
					More data for this Ligand-Target Pair
UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase (Streptococcus pneumoniae (Firmicutes))	BDBM50137758 (2,4-Dichloro-N-[3-cyano-6-(4-hydroxy-phenyl)-4,5,6...) Show SMILES Oc1ccc(cc1)C1CCc2c(C1)sc(NC(=O)c1cc(c(Cl)cc1Cl)S(=O)(=O)N1CCOCC1)c2C#N Show InChI InChI=1S/C26H23Cl2N3O5S2/c27-21-13-22(28)24(38(34,35)31-7-9-36-10-8-31)12-19(21)25(33)30-26-20(14-29)18-6-3-16(11-23(18)37-26)15-1-4-17(32)5-2-15/h1-2,4-5,12-13,16,32H,3,6-11H2,(H,30,33)	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories					Assay Description Inhibition of D-Ala-D-Ala adding enzyme (MurF) from Streptococcus pneumoniase.				Chem Biol Drug Des 67: 58-65 (2006) Article DOI: 10.1111/j.1747-0285.2005.00317.x BindingDB Entry DOI: 10.7270/Q2GF0S0Z
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189622 (CHEMBL208672 | {1-methyl-3-[2-(4-phenoxy-phenoxy)-...) Show SMILES CC(NC(N)=O)C#Cc1cnc(Oc2ccc(Oc3ccccc3)cc2)s1 Show InChI InChI=1S/C20H17N3O3S/c1-14(23-19(21)24)7-12-18-13-22-20(27-18)26-17-10-8-16(9-11-17)25-15-5-3-2-4-6-15/h2-6,8-11,13-14H,1H3,(H3,21,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205249 (CHEMBL222464 | methyl 4-(2-(4-(cyclopropylmethoxy)...) Show SMILES COC(=O)NC(C)C#Cc1cnc(Oc2ccc(OCC3CC3)cc2)s1 Show InChI InChI=1S/C19H20N2O4S/c1-13(21-18(22)23-2)3-10-17-11-20-19(26-17)25-16-8-6-15(7-9-16)24-12-14-4-5-14/h6-9,11,13-14H,4-5,12H2,1-2H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195020 (CHEMBL375116 | N-(4-(2-(3-(cyclohexyloxy)phenoxy)t...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2cccc(OC3CCCCC3)c2)s1 Show InChI InChI=1S/C21H24N2O3S/c1-15(23-16(2)24)11-12-20-14-22-21(27-20)26-19-10-6-9-18(13-19)25-17-7-4-3-5-8-17/h6,9-10,13-15,17H,3-5,7-8H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	26	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195015 (CHEMBL219948 | N-(4-(2-(4-(cyclohexylmethoxy)pheno...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CCCCC3)cc2)s1 Show InChI InChI=1S/C22H26N2O3S/c1-16(24-17(2)25)8-13-21-14-23-22(28-21)27-20-11-9-19(10-12-20)26-15-18-6-4-3-5-7-18/h9-12,14,16,18H,3-7,15H2,1-2H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	27	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195015 (CHEMBL219948 | N-(4-(2-(4-(cyclohexylmethoxy)pheno...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CCCCC3)cc2)s1 Show InChI InChI=1S/C22H26N2O3S/c1-16(24-17(2)25)8-13-21-14-23-22(28-21)27-20-11-9-19(10-12-20)26-15-18-6-4-3-5-7-18/h9-12,14,16,18H,3-7,15H2,1-2H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	27	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50205247 (CHEMBL219902 | N-(1-(2'-(4-isopropoxyphenoxy)-2,5'...) Show SMILES CC(C)Oc1ccc(Oc2ncc(s2)-c2ncc(s2)C(C)NC(C)=O)cc1 Show InChI InChI=1S/C19H21N3O3S2/c1-11(2)24-14-5-7-15(8-6-14)25-19-21-10-17(27-19)18-20-9-16(26-18)12(3)22-13(4)23/h5-12H,1-4H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	28	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 1 (Homo sapiens (Human))	BDBM50195040 (CHEMBL220563 | N-(4-(2-(4-(cyclopentylmethoxy)phen...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CCCC3)cc2)s1 Show InChI InChI=1S/C21H24N2O3S/c1-15(23-16(2)24)7-12-20-13-22-21(27-20)26-19-10-8-18(9-11-19)25-14-17-5-3-4-6-17/h8-11,13,15,17H,3-6,14H2,1-2H3,(H,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC1				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203972 (CHEMBL233006 | N-(4-(2-(2-chloro-4-(cyclohexylmeth...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OCC3CCCCC3)cc2Cl)s1 |w:1.0| Show InChI InChI=1S/C22H25ClN2O3S/c1-15(25-16(2)26)8-10-19-13-24-22(29-19)28-21-11-9-18(12-20(21)23)27-14-17-6-4-3-5-7-17/h9,11-13,15,17H,3-7,14H2,1-2H3,(H,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 1 (Homo sapiens (Human))	BDBM50189627 (CHEMBL212460 | N-{3-[4-(4-isopropoxyphenoxy)phenyl...) Show SMILES CC(C)Oc1ccc(Oc2ccc(cc2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C21H23NO3/c1-15(2)24-19-11-13-21(14-12-19)25-20-9-7-18(8-10-20)6-5-16(3)22-17(4)23/h7-16H,1-4H3,(H,22,23)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC1 expressed in HEK293 cells				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189615 (1-(4-(2-(4-isopropoxyphenoxy)thiazol-5-yl)but-3-yn...) Show SMILES CNC(=O)NC(C)C#Cc1cnc(Oc2ccc(OC(C)C)cc2)s1 Show InChI InChI=1S/C18H21N3O3S/c1-12(2)23-14-6-8-15(9-7-14)24-18-20-11-16(25-18)10-5-13(3)21-17(22)19-4/h6-9,11-13H,1-4H3,(H2,19,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in baculovirus/sf9 system				J Med Chem 49: 3770-3 (2006) Article DOI: 10.1021/jm060484v BindingDB Entry DOI: 10.7270/Q2M61M20
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189615 (1-(4-(2-(4-isopropoxyphenoxy)thiazol-5-yl)but-3-yn...) Show SMILES CNC(=O)NC(C)C#Cc1cnc(Oc2ccc(OC(C)C)cc2)s1 Show InChI InChI=1S/C18H21N3O3S/c1-12(2)23-14-6-8-15(9-7-14)24-18-20-11-16(25-18)10-5-13(3)21-17(22)19-4/h6-9,11-13H,1-4H3,(H2,19,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2 expressed in SF9 cells				J Med Chem 50: 1078-82 (2007) Article DOI: 10.1021/jm070035a BindingDB Entry DOI: 10.7270/Q24F1QCB
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50189615 (1-(4-(2-(4-isopropoxyphenoxy)thiazol-5-yl)but-3-yn...) Show SMILES CNC(=O)NC(C)C#Cc1cnc(Oc2ccc(OC(C)C)cc2)s1 Show InChI InChI=1S/C18H21N3O3S/c1-12(2)23-14-6-8-15(9-7-14)24-18-20-11-16(25-18)10-5-13(3)21-17(22)19-4/h6-9,11-13H,1-4H3,(H2,19,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of ACC2				Bioorg Med Chem Lett 17: 1803-7 (2007) Article DOI: 10.1016/j.bmcl.2006.12.047 BindingDB Entry DOI: 10.7270/Q28C9VXR
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203979 (CHEMBL393192 | N-(4-(2-(2-chloro-4-(cyclohexyloxy)...) Show SMILES CC(NC(C)=O)C#Cc1cnc(Oc2ccc(OC3CCCCC3)cc2Cl)s1 |w:1.0| Show InChI InChI=1S/C21H23ClN2O3S/c1-14(24-15(2)25)8-10-18-13-23-21(28-18)27-20-11-9-17(12-19(20)22)26-16-6-4-3-5-7-16/h9,11-14,16H,3-7H2,1-2H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	34	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50203983 (CHEMBL233005 | N-(4-(2-(2-bromo-4-isobutoxyphenoxy...) Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(Br)c1 |w:17.18| Show InChI InChI=1S/C19H21BrN2O3S/c1-12(2)11-24-15-6-8-18(17(20)9-15)25-19-21-10-16(26-19)7-5-13(3)22-14(4)23/h6,8-10,12-13H,11H2,1-4H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	35	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 17: 1961-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.022 BindingDB Entry DOI: 10.7270/Q2W095KS
					More data for this Ligand-Target Pair
Acetyl-CoA carboxylase 2 (Homo sapiens (Human))	BDBM50195038 (CHEMBL223372 | N-(4-(2-(4-ethoxyphenoxy)thiazol-5-...) Show SMILES CCOc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)cc1 Show InChI InChI=1S/C17H18N2O3S/c1-4-21-14-6-8-15(9-7-14)22-17-18-11-16(23-17)10-5-12(2)19-13(3)20/h6-9,11-12H,4H2,1-3H3,(H,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human recombinant ACC2				Bioorg Med Chem Lett 16: 6078-81 (2006) Article DOI: 10.1016/j.bmcl.2006.08.100 BindingDB Entry DOI: 10.7270/Q2RJ4J4W
					More data for this Ligand-Target Pair

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