Compile Data Set for Download or QSAR

Found 93 hits with Last Name = 'radwan' 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
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50067734 ((-)-(6aR-trans)-6,6,9-trimethyl-3-pentyl-6a,7,10,1...) Show SMILES CCCCCc1cc(O)c2[C@@H]3CC(C)=CC[C@H]3C(C)(C)Oc2c1 |r,c:13| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9,12-13,16-17,22H,5-8,10-11H2,1-4H3/t16-,17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM60994 ((10R,10aR)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tet...) Show SMILES CCCCCc1cc(O)c2[C@@H]3C=C(C)CC[C@H]3C(C)(C)Oc2c1 |r,t:11| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-13,16-17,22H,5-10H2,1-4H3/t16-,17-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Similars	DrugBank Article PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092347 (CHEMBL3586106) Show SMILES [H][C@@]12CC=C(C)[C@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r,t:3| Show InChI InChI=1S/C20H19Cl2N3O2/c1-26-19-7-6-13-15(20(19)27-12-4-2-3-5-12)9-24-25-18(13)8-14-16(21)10-23-11-17(14)22/h6-7,9-12H,2-5,8H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092347 (CHEMBL3586106) Show SMILES [H][C@@]12CC=C(C)[C@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r,t:3| Show InChI InChI=1S/C20H19Cl2N3O2/c1-26-19-7-6-13-15(20(19)27-12-4-2-3-5-12)9-24-25-18(13)8-14-16(21)10-23-11-17(14)22/h6-7,9-12H,2-5,8H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	31	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM60994 ((10R,10aR)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tet...) Show SMILES CCCCCc1cc(O)c2[C@@H]3C=C(C)CC[C@H]3C(C)(C)Oc2c1 |r,t:11| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-13,16-17,22H,5-10H2,1-4H3/t16-,17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Similars	DrugBank Article PubMed	42	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092343 (CHEMBL3586110) Show SMILES [H][C@@]12CCC(COC(C)=O)=C[C@@]1([H])c1c(O)c(C(O)=O)c(CCCCC)cc1OC2(C)C |r,c:9| Show InChI InChI=1S/C24H32O6/c1-5-6-7-8-16-12-19-21(22(26)20(16)23(27)28)17-11-15(13-29-14(2)25)9-10-18(17)24(3,4)30-19/h11-12,17-18,26H,5-10,13H2,1-4H3,(H,27,28)/t17-,18-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	47	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM84880 (THC, 8 beta-OH) Show SMILES CCCCCc1cc(O)c2[C@@H]3C=C(C)[C@H](O)C[C@H]3C(C)(C)Oc2c1 |t:11| Show InChI InChI=1S/C21H30O3/c1-5-6-7-8-14-10-18(23)20-15-9-13(2)17(22)12-16(15)21(3,4)24-19(20)11-14/h9-11,15-17,22-23H,5-8,12H2,1-4H3/t15-,16-,17-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	65	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50067734 ((-)-(6aR-trans)-6,6,9-trimethyl-3-pentyl-6a,7,10,1...) Show SMILES CCCCCc1cc(O)c2[C@@H]3CC(C)=CC[C@H]3C(C)(C)Oc2c1 |r,c:13| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9,12-13,16-17,22H,5-8,10-11H2,1-4H3/t16-,17-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	78	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM84880 (THC, 8 beta-OH) Show SMILES CCCCCc1cc(O)c2[C@@H]3C=C(C)[C@H](O)C[C@H]3C(C)(C)Oc2c1 |t:11| Show InChI InChI=1S/C21H30O3/c1-5-6-7-8-14-10-18(23)20-15-9-13(2)17(22)12-16(15)21(3,4)24-19(20)11-14/h9-11,15-17,22-23H,5-8,12H2,1-4H3/t15-,16-,17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	88	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092345 (CHEMBL3586108) Show SMILES [H][C@@]12CCC(=C)[C@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r| Show InChI InChI=1S/C26H25Cl2N3O2/c1-32-25-12-11-19-21(15-30-31-24(19)14-20-22(27)16-29-17-23(20)28)26(25)33-13-7-3-6-10-18-8-4-2-5-9-18/h2,4-5,8-9,11-12,15-17H,3,6-7,10,13-14H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	117	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092345 (CHEMBL3586108) Show SMILES [H][C@@]12CCC(=C)[C@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r| Show InChI InChI=1S/C26H25Cl2N3O2/c1-32-25-12-11-19-21(15-30-31-24(19)14-20-22(27)16-29-17-23(20)28)26(25)33-13-7-3-6-10-18-8-4-2-5-9-18/h2,4-5,8-9,11-12,15-17H,3,6-7,10,13-14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	129	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092344 (CHEMBL3586109) Show SMILES [H][C@@]12O[C@]1(C)CC[C@]1([H])[C@]2([H])c2c(O)cc(CCCCC)cc2OC1(C)C |r| Show InChI InChI=1S/C20H19Cl2N3O3/c1-27-19-7-6-13-15(20(19)28-12-4-2-3-5-12)11-25(26)24-18(13)8-14-16(21)9-23-10-17(14)22/h6-7,9-12H,2-5,8H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	224	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092344 (CHEMBL3586109) Show SMILES [H][C@@]12O[C@]1(C)CC[C@]1([H])[C@]2([H])c2c(O)cc(CCCCC)cc2OC1(C)C |r| Show InChI InChI=1S/C20H19Cl2N3O3/c1-27-19-7-6-13-15(20(19)28-12-4-2-3-5-12)11-25(26)24-18(13)8-14-16(21)9-23-10-17(14)22/h6-7,9-12H,2-5,8H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	335	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092346 (CHEMBL3586107) Show SMILES [H][C@@]12CC=C(C)[C@@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r,t:3| Show InChI InChI=1S/C26H23Cl2N3O/c1-32-26-13-12-19-22(20(26)11-7-3-6-10-18-8-4-2-5-9-18)15-30-31-25(19)14-21-23(27)16-29-17-24(21)28/h2,4-5,7-9,11-13,15-17H,3,6,10,14H2,1H3/b11-7+	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	830	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092343 (CHEMBL3586110) Show SMILES [H][C@@]12CCC(COC(C)=O)=C[C@@]1([H])c1c(O)c(C(O)=O)c(CCCCC)cc1OC2(C)C |r,c:9| Show InChI InChI=1S/C24H32O6/c1-5-6-7-8-16-12-19-21(22(26)20(16)23(27)28)17-11-15(13-29-14(2)25)9-10-18(17)24(3,4)30-19/h11-12,17-18,26H,5-10,13H2,1-4H3,(H,27,28)/t17-,18-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	912	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092348 (CHEMBL3586104) Show SMILES [H][C@@]12C=C(C)[C@@H](O)C[C@@]1([H])C(C)(C)Oc1cc(CCCCC)cc(O)c21 |r,t:2| Show InChI InChI=1S/C26H21Cl2N3O/c1-32-26-13-12-19-22(20(26)11-7-3-6-10-18-8-4-2-5-9-18)15-30-31-25(19)14-21-23(27)16-29-17-24(21)28/h2,4-5,8-9,12-13,15-17H,3,6,10,14H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	1.91E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092342 (CHEMBL3586111) Show SMILES [H][C@@]12CC[C@](C)(O)[C@@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r| Show InChI InChI=1S/C21H32O4/c1-5-6-7-8-13-11-15(22)18-16(12-13)25-20(2,3)14-9-10-21(4,24)19(23)17(14)18/h11-12,14,17,19,22-24H,5-10H2,1-4H3/t14-,17-,19+,21+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.14E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092348 (CHEMBL3586104) Show SMILES [H][C@@]12C=C(C)[C@@H](O)C[C@@]1([H])C(C)(C)Oc1cc(CCCCC)cc(O)c21 |r,t:2| Show InChI InChI=1S/C26H21Cl2N3O/c1-32-26-13-12-19-22(20(26)11-7-3-6-10-18-8-4-2-5-9-18)15-30-31-25(19)14-21-23(27)16-29-17-24(21)28/h2,4-5,8-9,12-13,15-17H,3,6,10,14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	3.22E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50092346 (CHEMBL3586107) Show SMILES [H][C@@]12CC=C(C)[C@@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r,t:3| Show InChI InChI=1S/C26H23Cl2N3O/c1-32-26-13-12-19-22(20(26)11-7-3-6-10-18-8-4-2-5-9-18)15-30-31-25(19)14-21-23(27)16-29-17-24(21)28/h2,4-5,7-9,11-13,15-17H,3,6,10,14H2,1H3/b11-7+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.27E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50092342 (CHEMBL3586111) Show SMILES [H][C@@]12CC[C@](C)(O)[C@@H](O)[C@@]1([H])c1c(O)cc(CCCCC)cc1OC2(C)C |r| Show InChI InChI=1S/C21H32O4/c1-5-6-7-8-13-11-15(22)18-16(12-13)25-20(2,3)14-9-10-21(4,24)19(23)17(14)18/h11-12,14,17,19,22-24H,5-10H2,1-4H3/t14-,17-,19+,21+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.67E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from full length human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by scintillation counting analysi...				J Nat Prod 78: 1271-6 (2015) Article DOI: 10.1021/acs.jnatprod.5b00065 BindingDB Entry DOI: 10.7270/Q2SQ923K
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50491190 (CHEMBL2375656) Show SMILES COc1cc(O)c2c(CC(=O)CCCC(=O)CCC[C@@H](C)OC2=O)c1 |r| Show InChI InChI=1S/C19H24O6/c1-12-5-3-6-14(20)7-4-8-15(21)9-13-10-16(24-2)11-17(22)18(13)19(23)25-12/h10-12,22H,3-9H2,1-2H3/t12-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.31E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Mississippi Curated by ChEMBL					Assay Description Displacement of [3H]-enkephalin from human delta opioid receptor transfected in CHOK1 cells after 60 mins				J Nat Prod 76: 824-8 (2013) Article DOI: 10.1021/np300653d BindingDB Entry DOI: 10.7270/Q2W95D30
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50030474 (Avandamet | Avandaryl | Avandia | BRL-49653 | CHEB...) Show SMILES CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccccn1 Show InChI InChI=1S/C18H19N3O3S/c1-21(16-4-2-3-9-19-16)10-11-24-14-7-5-13(6-8-14)12-15-17(22)20-18(23)25-15/h2-9,15H,10-12H2,1H3,(H,20,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid PDB UniChem Similars	DrugBank PDB Article PubMed	n/a	n/a	292	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50030474 (Avandamet | Avandaryl | Avandia | BRL-49653 | CHEB...) Show SMILES CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccccn1 Show InChI InChI=1S/C18H19N3O3S/c1-21(16-4-2-3-9-19-16)10-11-24-14-7-5-13(6-8-14)12-15-17(22)20-18(23)25-15/h2-9,15H,10-12H2,1H3,(H,20,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid PDB UniChem Similars	DrugBank PDB Article PubMed	n/a	n/a	298	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair				3D Structure (crystal)
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269543 (CHEMBL4068985) Show SMILES COc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)S(=O)(=O)NC(=O)NC2CCCCC2)nc2ccccc2c1=O Show InChI InChI=1S/C30H31N5O6S2/c1-41-23-15-13-22(14-16-23)35-28(37)25-9-5-6-10-26(25)33-30(35)42-19-27(36)31-21-11-17-24(18-12-21)43(39,40)34-29(38)32-20-7-3-2-4-8-20/h5-6,9-18,20H,2-4,7-8,19H2,1H3,(H,31,36)(H2,32,34,38)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50211660 (CHEMBL3915254) Show SMILES Cc1nc2ccccc2n(CC(=O)Nc2ccc(cc2)S(=O)(=O)NC(=S)NC2CCCCC2)c1=O Show InChI InChI=1S/C24H27N5O4S2/c1-16-23(31)29(21-10-6-5-9-20(21)25-16)15-22(30)26-18-11-13-19(14-12-18)35(32,33)28-24(34)27-17-7-3-2-4-8-17/h5-6,9-14,17H,2-4,7-8,15H2,1H3,(H,26,30)(H2,27,28,34)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269553 (CHEMBL4104828) Show SMILES Cc1nc2ccc(Br)cc2c(=O)n1CC(=O)Nc1ccc(cc1)S(=O)(=O)NC(=O)NC1CCCCC1 Show InChI InChI=1S/C24H26BrN5O5S/c1-15-26-21-12-7-16(25)13-20(21)23(32)30(15)14-22(31)27-18-8-10-19(11-9-18)36(34,35)29-24(33)28-17-5-3-2-4-6-17/h7-13,17H,2-6,14H2,1H3,(H,27,31)(H2,28,29,33)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	353	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50211669 (CHEMBL3943220) Show SMILES CCCCNC(=S)NS(=O)(=O)c1ccc(NC(=O)Cn2c3ccccc3nc(C)c2=O)cc1 Show InChI InChI=1S/C22H25N5O4S2/c1-3-4-13-23-22(32)26-33(30,31)17-11-9-16(10-12-17)25-20(28)14-27-19-8-6-5-7-18(19)24-15(2)21(27)29/h5-12H,3-4,13-14H2,1-2H3,(H,25,28)(H2,23,26,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	369	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269548 (CHEMBL4069917) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(OC)cc2)cc1 Show InChI InChI=1S/C28H29N5O6S2/c1-3-4-17-29-27(36)32-41(37,38)22-15-9-19(10-16-22)30-25(34)18-40-28-31-24-8-6-5-7-23(24)26(35)33(28)20-11-13-21(39-2)14-12-20/h5-16H,3-4,17-18H2,1-2H3,(H,30,34)(H2,29,32,36)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	369	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269511 (CHEMBL4072706) Show SMILES Cc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)S(=O)(=O)NC(=O)Nc2ccccc2)nc2ccccc2c1=O Show InChI InChI=1S/C30H25N5O5S2/c1-20-11-15-23(16-12-20)35-28(37)25-9-5-6-10-26(25)33-30(35)41-19-27(36)31-22-13-17-24(18-14-22)42(39,40)34-29(38)32-21-7-3-2-4-8-21/h2-18H,19H2,1H3,(H,31,36)(H2,32,34,38)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	371	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269510 (CHEMBL4085687) Show SMILES Cc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)S(=O)(=O)NC(=O)NC2CCCCC2)nc2ccccc2c1=O Show InChI InChI=1S/C30H31N5O5S2/c1-20-11-15-23(16-12-20)35-28(37)25-9-5-6-10-26(25)33-30(35)41-19-27(36)31-22-13-17-24(18-14-22)42(39,40)34-29(38)32-21-7-3-2-4-8-21/h5-6,9-18,21H,2-4,7-8,19H2,1H3,(H,31,36)(H2,32,34,38)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	402	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269552 (CHEMBL4080597) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccc(NC(=O)Cn2c(CC)nc3ccccc3c2=O)cc1 Show InChI InChI=1S/C23H27N5O5S/c1-3-5-14-24-23(31)27-34(32,33)17-12-10-16(11-13-17)25-21(29)15-28-20(4-2)26-19-9-7-6-8-18(19)22(28)30/h6-13H,3-5,14-15H2,1-2H3,(H,25,29)(H2,24,27,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	408	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269542 (CHEMBL4093428) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(C)cc2)cc1 Show InChI InChI=1S/C28H29N5O5S2/c1-3-4-17-29-27(36)32-40(37,38)22-15-11-20(12-16-22)30-25(34)18-39-28-31-24-8-6-5-7-23(24)26(35)33(28)21-13-9-19(2)10-14-21/h5-16H,3-4,17-18H2,1-2H3,(H,30,34)(H2,29,32,36)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	434	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549123 (CHEMBL4779272) Show SMILES C\C(=N/NC(=O)c1cc(ccc1Cl)[N+]([O-])=O)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(C)cc2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	452	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269549 (CHEMBL4097121) Show SMILES Cc1nc2ccccc2c(=O)n1CC(=O)Nc1ccc(cc1)S(=O)(=O)NC(=O)NC1CCCCC1 Show InChI InChI=1S/C24H27N5O5S/c1-16-25-21-10-6-5-9-20(21)23(31)29(16)15-22(30)26-18-11-13-19(14-12-18)35(33,34)28-24(32)27-17-7-3-2-4-8-17/h5-6,9-14,17H,2-4,7-8,15H2,1H3,(H,26,30)(H2,27,28,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	464	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50211676 (CHEMBL3899514) Show SMILES Cc1nc2ccccc2n(CC(=O)Nc2ccc(cc2)S(=O)(=O)NC(=O)NC2CCCCC2)c1=O Show InChI InChI=1S/C24H27N5O5S/c1-16-23(31)29(21-10-6-5-9-20(21)25-16)15-22(30)26-18-11-13-19(14-12-18)35(33,34)28-24(32)27-17-7-3-2-4-8-17/h5-6,9-14,17H,2-4,7-8,15H2,1H3,(H,26,30)(H2,27,28,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	482	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50211656 (CHEMBL3959627) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccc(NC(=O)Cn2c3ccccc3nc(C)c2=O)cc1 Show InChI InChI=1S/C22H25N5O5S/c1-3-4-13-23-22(30)26-33(31,32)17-11-9-16(10-12-17)25-20(28)14-27-19-8-6-5-7-18(19)24-15(2)21(27)29/h5-12H,3-4,13-14H2,1-2H3,(H,25,28)(H2,23,26,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	491	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269551 (CHEMBL4088467) Show SMILES CCc1nc2ccccc2c(=O)n1CC(=O)Nc1ccc(cc1)S(=O)(=O)NC(=O)NC1CCCCC1 Show InChI InChI=1S/C25H29N5O5S/c1-2-22-28-21-11-7-6-10-20(21)24(32)30(22)16-23(31)26-18-12-14-19(15-13-18)36(34,35)29-25(33)27-17-8-4-3-5-9-17/h6-7,10-15,17H,2-5,8-9,16H2,1H3,(H,26,31)(H2,27,29,33)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	590	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
DNA topoisomerase 2-alpha (Homo sapiens (Human))	BDBM50468489 (CHEMBL1305588) Show SMILES C1CCC(CC1)Nc1nc2ccccc2n2cnnc12 Show InChI InChI=1S/C15H17N5/c1-2-6-11(7-3-1)17-14-15-19-16-10-20(15)13-9-5-4-8-12(13)18-14/h4-5,8-11H,1-3,6-7H2,(H,17,18)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Inhibition of human topoisomerase 2 using supercoiled pHOT1 DNA as substrate after 30 mins by agarose gel electrophoresis				Eur J Med Chem 155: 117-134 (2018) Article DOI: 10.1016/j.ejmech.2018.06.004 BindingDB Entry DOI: 10.7270/Q2TT4TN9
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549119 (CHEMBL4763393) Show SMILES Cc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)C(=O)Nc2ccc(Cl)cc2)nc2ccccc2c1=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	684	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549115 (CHEMBL4784161) Show SMILES Cc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)S(=O)(=O)Nc2nc(C)cc(C)n2)nc2ccccc2c1=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	707	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549116 (CHEMBL4781567) Show SMILES CC(=O)NS(=O)(=O)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(C)cc2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	721	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
DNA topoisomerase 2-alpha (Homo sapiens (Human))	BDBM50468484 (CHEMBL4288104) Show SMILES COc1cccc(NC(=O)CSc2nnc3c4nncn4c4ccccc4n23)c1 Show InChI InChI=1S/C19H15N7O2S/c1-28-13-6-4-5-12(9-13)21-16(27)10-29-19-24-23-18-17-22-20-11-25(17)14-7-2-3-8-15(14)26(18)19/h2-9,11H,10H2,1H3,(H,21,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	850	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Inhibition of human topoisomerase 2 using supercoiled pHOT1 DNA as substrate after 30 mins by agarose gel electrophoresis				Eur J Med Chem 155: 117-134 (2018) Article DOI: 10.1016/j.ejmech.2018.06.004 BindingDB Entry DOI: 10.7270/Q2TT4TN9
					More data for this Ligand-Target Pair
DNA topoisomerase 2-alpha (Homo sapiens (Human))	BDBM22984 ((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...) Show SMILES COc1cccc2C(=O)c3c(O)c4C[C@](O)(C[C@H](O[C@H]5C[C@H](N)[C@H](O)[C@H](C)O5)c4c(O)c3C(=O)c12)C(=O)CO |r| Show InChI InChI=1S/C27H29NO11/c1-10-22(31)13(28)6-17(38-10)39-15-8-27(36,16(30)9-29)7-12-19(15)26(35)21-20(24(12)33)23(32)11-4-3-5-14(37-2)18(11)25(21)34/h3-5,10,13,15,17,22,29,31,33,35-36H,6-9,28H2,1-2H3/t10-,13-,15-,17-,22+,27-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	880	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Inhibition of human topoisomerase 2 using supercoiled pHOT1 DNA as substrate after 30 mins by agarose gel electrophoresis				Eur J Med Chem 155: 117-134 (2018) Article DOI: 10.1016/j.ejmech.2018.06.004 BindingDB Entry DOI: 10.7270/Q2TT4TN9
					More data for this Ligand-Target Pair
DNA topoisomerase 2-alpha (Homo sapiens (Human))	BDBM50468485 (CHEMBL4286850) Show SMILES Fc1ccc(NC(=O)CSc2nnc3c4nncn4c4ccccc4n23)cc1 Show InChI InChI=1S/C18H12FN7OS/c19-11-5-7-12(8-6-11)21-15(27)9-28-18-24-23-17-16-22-20-10-25(16)13-3-1-2-4-14(13)26(17)18/h1-8,10H,9H2,(H,21,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	940	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Inhibition of human topoisomerase 2 using supercoiled pHOT1 DNA as substrate after 30 mins by agarose gel electrophoresis				Eur J Med Chem 155: 117-134 (2018) Article DOI: 10.1016/j.ejmech.2018.06.004 BindingDB Entry DOI: 10.7270/Q2TT4TN9
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50269550 (CHEMBL4089408) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccc(NC(=O)Cn2c(C)nc3ccccc3c2=O)cc1 Show InChI InChI=1S/C22H25N5O5S/c1-3-4-13-23-22(30)26-33(31,32)17-11-9-16(10-12-17)25-20(28)14-27-15(2)24-19-8-6-5-7-18(19)21(27)29/h5-12H,3-4,13-14H2,1-2H3,(H,25,28)(H2,23,26,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	980	n/a	n/a	n/a	n/a	n/a	n/a
Pharmaceutical Chemistry Department, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt. Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma green from GST-tagged PPARgamma-LBD (unknown origin) by fluorescence polarization assay				Bioorg Med Chem 25: 4723-4744 (2017) Article DOI: 10.1016/j.bmc.2017.07.015 BindingDB Entry DOI: 10.7270/Q2DZ0BTW
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549122 (CHEMBL4794044) Show SMILES C\C(=N/NC(N)=S)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(C)cc2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549124 (CHEMBL4777885) Show SMILES C\C(=N/NC(=O)c1ccccc1O)c1ccc(NC(=O)CSc2nc3ccccc3c(=O)n2-c2ccc(C)cc2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
DNA topoisomerase 2-alpha (Homo sapiens (Human))	BDBM50468490 (CHEMBL4291398) Show SMILES Sc1nnc2c3nncn3c3ccccc3n12 Show InChI InChI=1S/C10H6N6S/c17-10-14-13-9-8-12-11-5-15(8)6-3-1-2-4-7(6)16(9)10/h1-5H,(H,14,17)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.06E+3	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Inhibition of human topoisomerase 2 using supercoiled pHOT1 DNA as substrate after 30 mins by agarose gel electrophoresis				Eur J Med Chem 155: 117-134 (2018) Article DOI: 10.1016/j.ejmech.2018.06.004 BindingDB Entry DOI: 10.7270/Q2TT4TN9
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50549117 (CHEMBL4749461) Show SMILES Cc1ccc(cc1)-n1c(SCC(=O)Nc2ccc(cc2)C(=O)NNC(=O)c2ccccc2O)nc2ccccc2c1=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.06E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of human VEGFR2 incubated for 2.5 hrs by ELISA				Citation and Details Article DOI: 10.1016/j.bmc.2020.115872 BindingDB Entry DOI: 10.7270/Q2KH0RZQ
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50211677 (CHEMBL3977442) Show SMILES O=C(NC1CCCCC1)NS(=O)(=O)c1ccc(NCC(=O)N2CC(=O)Nc3ccccc23)cc1 Show InChI InChI=1S/C23H27N5O5S/c29-21-15-28(20-9-5-4-8-19(20)26-21)22(30)14-24-16-10-12-18(13-11-16)34(32,33)27-23(31)25-17-6-2-1-3-7-17/h4-5,8-13,17,24H,1-3,6-7,14-15H2,(H,26,29)(H2,25,27,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.14E+3	n/a	n/a	n/a	n/a	n/a	n/a
Al-Azhar University Curated by ChEMBL					Assay Description Displacement of fluormone-PPARgamma Green from recombinant human N-terminal GST-tagged PPARgamma-LBD by fluorescence polarization assay				Bioorg Med Chem 25: 1496-1513 (2017) Article DOI: 10.1016/j.bmc.2017.01.015 BindingDB Entry DOI: 10.7270/Q2H13463
					More data for this Ligand-Target Pair

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