Compile Data Set for Download or QSAR

Found 271 hits with Last Name = 'eissenstat' and Initial = 'ma'   

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
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073270 (CHEMBL333781 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-5...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)OCc1cccnc1 Show InChI InChI=1S/C39H39N5O6/c45-36(35(23-29-14-5-2-6-15-29)44-39(48)49-26-30-16-11-20-40-25-30)24-32(22-28-12-3-1-4-13-28)42-37(46)33-18-7-8-19-34(33)43-38(47)50-27-31-17-9-10-21-41-31/h1-21,25,32,35-36,45H,22-24,26-27H2,(H,42,46)(H,43,47)(H,44,48)/t32-,35-,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073266 (CHEMBL119898 | {2-[(1S,3S,4S)-1-Benzyl-4-((2S,3S)-...) Show SMILES CCOC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C41H49N5O7/c1-4-28(3)37(46-41(51)52-5-2)39(49)44-35(25-30-18-10-7-11-19-30)36(47)26-32(24-29-16-8-6-9-17-29)43-38(48)33-21-12-13-22-34(33)45-40(50)53-27-31-20-14-15-23-42-31/h6-23,28,32,35-37,47H,4-5,24-27H2,1-3H3,(H,43,48)(H,44,49)(H,45,50)(H,46,51)/t28-,32-,35-,36-,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073253 (CHEMBL278935 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-5...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)OCc1cncs1 Show InChI InChI=1S/C37H37N5O6S/c43-34(33(20-27-13-5-2-6-14-27)42-37(46)48-24-30-22-38-25-49-30)21-29(19-26-11-3-1-4-12-26)40-35(44)31-16-7-8-17-32(31)41-36(45)47-23-28-15-9-10-18-39-28/h1-18,22,25,29,33-34,43H,19-21,23-24H2,(H,40,44)(H,41,45)(H,42,46)/t29-,33-,34-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073250 (CHEMBL333420 | {2-[(1S,3S,4S)-1-Benzyl-4-((R)-2-et...) Show SMILES CCOC(=O)N[C@H](C(C)C)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C40H47N5O7/c1-4-51-40(50)45-36(27(2)3)38(48)43-34(24-29-17-9-6-10-18-29)35(46)25-31(23-28-15-7-5-8-16-28)42-37(47)32-20-11-12-21-33(32)44-39(49)52-26-30-19-13-14-22-41-30/h5-22,27,31,34-36,46H,4,23-26H2,1-3H3,(H,42,47)(H,43,48)(H,44,49)(H,45,50)/t31-,34-,35-,36+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073269 ((2-{(1S,3S,4S)-1-Benzyl-3-hydroxy-5-phenyl-4-[(R)-...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)O[C@@H]1CCOC1 Show InChI InChI=1S/C37H40N4O7/c42-34(33(22-27-13-5-2-6-14-27)41-37(45)48-30-18-20-46-25-30)23-29(21-26-11-3-1-4-12-26)39-35(43)31-16-7-8-17-32(31)40-36(44)47-24-28-15-9-10-19-38-28/h1-17,19,29-30,33-34,42H,18,20-25H2,(H,39,43)(H,40,44)(H,41,45)/t29-,30+,33-,34-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073252 (CHEMBL324157 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-4...) Show SMILES Cc1c(O)cccc1C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C40H40N4O6/c1-27-32(19-12-21-36(27)45)38(47)43-35(24-29-15-6-3-7-16-29)37(46)25-31(23-28-13-4-2-5-14-28)42-39(48)33-18-8-9-20-34(33)44-40(49)50-26-30-17-10-11-22-41-30/h2-22,31,35,37,45-46H,23-26H2,1H3,(H,42,48)(H,43,47)(H,44,49)/t31-,35-,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073265 ((2-{(1S,2S,3R,4S)-1-Benzyl-2,3-dihydroxy-5-phenyl-...) Show SMILES O[C@H]([C@H](Cc1ccccc1)NC(=O)O[C@@H]1CCOC1)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C37H40N4O8/c42-33(34(43)32(22-26-13-5-2-6-14-26)41-37(46)49-28-18-20-47-24-28)31(21-25-11-3-1-4-12-25)39-35(44)29-16-7-8-17-30(29)40-36(45)48-23-27-15-9-10-19-38-27/h1-17,19,28,31-34,42-43H,18,20-24H2,(H,39,44)(H,40,45)(H,41,46)/t28-,31+,32+,33+,34-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073254 (Anthranilamide derivative | CHEMBL408110) Show SMILES O[C@@H]([C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C46H44N6O8/c53-41(39(27-31-15-3-1-4-16-31)49-43(55)35-21-7-9-23-37(35)51-45(57)59-29-33-19-11-13-25-47-33)42(54)40(28-32-17-5-2-6-18-32)50-44(56)36-22-8-10-24-38(36)52-46(58)60-30-34-20-12-14-26-48-34/h1-26,39-42,53-54H,27-30H2,(H,49,55)(H,50,56)(H,51,57)(H,52,58)/t39-,40-,41-,42+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	0.0700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073268 (CHEMBL331294 | {2-[(1S,2S,3R,4S)-1-Benzyl-2,3-dihy...) Show SMILES Cc1c(O)cccc1C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C40H40N4O7/c1-26-30(19-12-21-35(26)45)38(48)42-33(23-27-13-4-2-5-14-27)36(46)37(47)34(24-28-15-6-3-7-16-28)43-39(49)31-18-8-9-20-32(31)44-40(50)51-25-29-17-10-11-22-41-29/h2-22,33-34,36-37,45-47H,23-25H2,1H3,(H,42,48)(H,43,49)(H,44,50)/t33-,34-,36+,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.0900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073263 (CHEMBL117629 | {2-[(1S,3S,4S)-4-(3-Amino-2-methyl-...) Show SMILES Cc1c(N)cccc1C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C40H41N5O5/c1-27-32(19-12-20-34(27)41)38(47)44-36(24-29-15-6-3-7-16-29)37(46)25-31(23-28-13-4-2-5-14-28)43-39(48)33-18-8-9-21-35(33)45-40(49)50-26-30-17-10-11-22-42-30/h2-22,31,36-37,46H,23-26,41H2,1H3,(H,43,48)(H,44,47)(H,45,49)/t31-,36-,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.120	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073244 (CHEMBL332825 | [2-((1S,3S,4S)-1-Benzyl-4-tert-buto...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C37H42N4O6/c1-37(2,3)47-36(45)41-32(23-27-16-8-5-9-17-27)33(42)24-29(22-26-14-6-4-7-15-26)39-34(43)30-19-10-11-20-31(30)40-35(44)46-25-28-18-12-13-21-38-28/h4-21,29,32-33,42H,22-25H2,1-3H3,(H,39,43)(H,40,44)(H,41,45)/t29-,32-,33-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073262 (CHEMBL333290 | [2-((1S,2S,3R,4S)-1-Benzyl-4-tert-b...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C37H42N4O7/c1-37(2,3)48-36(46)41-31(23-26-16-8-5-9-17-26)33(43)32(42)30(22-25-14-6-4-7-15-25)39-34(44)28-19-10-11-20-29(28)40-35(45)47-24-27-18-12-13-21-38-27/h4-21,30-33,42-43H,22-24H2,1-3H3,(H,39,44)(H,40,45)(H,41,46)/t30-,31-,32-,33+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	0.130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073248 (CHEMBL119745 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-4...) Show SMILES Cc1ccccc1C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C40H40N4O5/c1-28-14-8-9-20-33(28)38(46)43-36(25-30-17-6-3-7-18-30)37(45)26-32(24-29-15-4-2-5-16-29)42-39(47)34-21-10-11-22-35(34)44-40(48)49-27-31-19-12-13-23-41-31/h2-23,32,36-37,45H,24-27H2,1H3,(H,42,47)(H,43,46)(H,44,48)/t32-,36-,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073243 ((2-{(1S,2S,3R,4S)-1-Benzyl-2,3-dihydroxy-4-[(isoxa...) Show SMILES O[C@H]([C@H](Cc1ccccc1)NC(=O)c1ccno1)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C36H35N5O7/c42-32(33(43)30(22-25-13-5-2-6-14-25)40-35(45)31-18-20-38-48-31)29(21-24-11-3-1-4-12-24)39-34(44)27-16-7-8-17-28(27)41-36(46)47-23-26-15-9-10-19-37-26/h1-20,29-30,32-33,42-43H,21-23H2,(H,39,44)(H,40,45)(H,41,46)/t29-,30-,32-,33+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073249 (CHEMBL331199 | {2-[(1S,3S,4S)-4-(3-Amino-benzoylam...) Show SMILES Nc1cccc(c1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H39N5O5/c40-30-17-11-16-29(24-30)37(46)43-35(23-28-14-5-2-6-15-28)36(45)25-32(22-27-12-3-1-4-13-27)42-38(47)33-19-7-8-20-34(33)44-39(48)49-26-31-18-9-10-21-41-31/h1-21,24,32,35-36,45H,22-23,25-26,40H2,(H,42,47)(H,43,46)(H,44,48)/t32-,35-,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073259 (CHEMBL333407 | [2-((1S,2R,3S,4S)-1-Benzyl-4-tert-b...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C37H42N4O7/c1-37(2,3)48-36(46)41-31(23-26-16-8-5-9-17-26)33(43)32(42)30(22-25-14-6-4-7-15-25)39-34(44)28-19-10-11-20-29(28)40-35(45)47-24-27-18-12-13-21-38-27/h4-21,30-33,42-43H,22-24H2,1-3H3,(H,39,44)(H,40,45)(H,41,46)/t30-,31-,32+,33-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.450	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073261 (CHEMBL116482 | {2-[(1S,2S,3R,4S)-1-Benzyl-2,3-dihy...) Show SMILES O[C@H]([C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H38N4O7/c44-30-18-11-16-28(24-30)37(47)41-33(22-26-12-3-1-4-13-26)35(45)36(46)34(23-27-14-5-2-6-15-27)42-38(48)31-19-7-8-20-32(31)43-39(49)50-25-29-17-9-10-21-40-29/h1-21,24,33-36,44-46H,22-23,25H2,(H,41,47)(H,42,48)(H,43,49)/t33-,34-,35+,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	0.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073251 (CHEMBL118396 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-5...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)OCc1cscn1 Show InChI InChI=1S/C37H37N5O6S/c43-34(33(20-27-13-5-2-6-14-27)42-37(46)48-23-30-24-49-25-39-30)21-29(19-26-11-3-1-4-12-26)40-35(44)31-16-7-8-17-32(31)41-36(45)47-22-28-15-9-10-18-38-28/h1-18,24-25,29,33-34,43H,19-23H2,(H,40,44)(H,41,45)(H,42,46)/t29-,33-,34-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.620	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073247 (CHEMBL118513 | {2-[(1S,2S,4S)-1-Benzyl-2-hydroxy-4...) Show SMILES Cc1c(O)cccc1C(=O)N[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)Cc1ccccc1 Show InChI InChI=1S/C40H40N4O6/c1-27-32(19-12-21-36(27)45)38(47)42-31(23-28-13-4-2-5-14-28)25-37(46)35(24-29-15-6-3-7-16-29)43-39(48)33-18-8-9-20-34(33)44-40(49)50-26-30-17-10-11-22-41-30/h2-22,31,35,37,45-46H,23-26H2,1H3,(H,42,47)(H,43,48)(H,44,49)/t31-,35-,37-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.680	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073246 (CHEMBL333392 | {2-[(1S,3S,4S)-1-Benzyl-3-hydroxy-4...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1 Show InChI InChI=1S/C39H38N4O6/c44-32-18-11-16-29(24-32)37(46)42-35(23-28-14-5-2-6-15-28)36(45)25-31(22-27-12-3-1-4-13-27)41-38(47)33-19-7-8-20-34(33)43-39(48)49-26-30-17-9-10-21-40-30/h1-21,24,31,35-36,44-45H,22-23,25-26H2,(H,41,47)(H,42,46)(H,43,48)/t31-,35-,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.850	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073256 (CHEMBL122006 | [2-((1S,2S,4S)-1-Benzyl-4-tert-buto...) Show SMILES CC(C)(C)OC(=O)N[C@H](C[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)Cc1ccccc1 Show InChI InChI=1S/C37H42N4O6/c1-37(2,3)47-36(45)39-29(22-26-14-6-4-7-15-26)24-33(42)32(23-27-16-8-5-9-17-27)40-34(43)30-19-10-11-20-31(30)41-35(44)46-25-28-18-12-13-21-38-28/h4-21,29,32-33,42H,22-25H2,1-3H3,(H,39,45)(H,40,43)(H,41,44)/t29-,32-,33-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.850	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073267 ((2-{(1S,3S,4S)-1-Benzyl-3-hydroxy-4-[(isoxazole-5-...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)c1ccno1 Show InChI InChI=1S/C36H35N5O6/c42-32(31(22-26-13-5-2-6-14-26)40-35(44)33-18-20-38-47-33)23-28(21-25-11-3-1-4-12-25)39-34(43)29-16-7-8-17-30(29)41-36(45)46-24-27-15-9-10-19-37-27/h1-20,28,31-32,42H,21-24H2,(H,39,43)(H,40,44)(H,41,45)/t28-,31-,32-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073264 (CHEMBL118531 | {2-[(1S,3S,4S)-4-(4-Amino-benzoylam...) Show SMILES Nc1ccc(cc1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H39N5O5/c40-30-20-18-29(19-21-30)37(46)43-35(24-28-13-5-2-6-14-28)36(45)25-32(23-27-11-3-1-4-12-27)42-38(47)33-16-7-8-17-34(33)44-39(48)49-26-31-15-9-10-22-41-31/h1-22,32,35-36,45H,23-26,40H2,(H,42,47)(H,43,46)(H,44,48)/t32-,35-,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073257 (CHEMBL325499 | {2-[(1S,2R,3S,4S)-1-Benzyl-2,3-dihy...) Show SMILES O[C@@H]([C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H38N4O7/c44-30-18-11-16-28(24-30)37(47)41-33(22-26-12-3-1-4-13-26)35(45)36(46)34(23-27-14-5-2-6-15-27)42-38(48)31-19-7-8-20-32(31)43-39(49)50-25-29-17-9-10-21-40-29/h1-21,24,33-36,44-46H,22-23,25H2,(H,41,47)(H,42,48)(H,43,49)/t33-,34-,35-,36+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073255 ((2-{(1S,3S,4S)-1-Benzyl-3-hydroxy-5-phenyl-4-[(thi...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1)[C@H](Cc1ccccc1)NC(=O)c1cscn1 Show InChI InChI=1S/C36H35N5O5S/c42-33(31(20-26-13-5-2-6-14-26)40-35(44)32-23-47-24-38-32)21-28(19-25-11-3-1-4-12-25)39-34(43)29-16-7-8-17-30(29)41-36(45)46-22-27-15-9-10-18-37-27/h1-18,23-24,28,31,33,42H,19-22H2,(H,39,43)(H,40,44)(H,41,45)/t28-,31-,33-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073258 (CHEMBL118221 | {2-[(1S,2R,3S,4S)-4-(4-Amino-benzoy...) Show SMILES Nc1ccc(cc1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H39N5O6/c40-29-20-18-28(19-21-29)37(47)42-33(23-26-11-3-1-4-12-26)35(45)36(46)34(24-27-13-5-2-6-14-27)43-38(48)31-16-7-8-17-32(31)44-39(49)50-25-30-15-9-10-22-41-30/h1-22,33-36,45-46H,23-25,40H2,(H,42,47)(H,43,48)(H,44,49)/t33-,34-,35-,36+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50073245 (CHEMBL118362 | {2-[(1S,2S,4S)-1-Benzyl-2-hydroxy-4...) Show SMILES O[C@@H](C[C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1)[C@H](Cc1ccccc1)NC(=O)c1ccccc1NC(=O)OCc1ccccn1 Show InChI InChI=1S/C39H38N4O6/c44-32-18-11-16-29(24-32)37(46)41-31(22-27-12-3-1-4-13-27)25-36(45)35(23-28-14-5-2-6-15-28)42-38(47)33-19-7-8-20-34(33)43-39(48)49-26-30-17-9-10-21-40-30/h1-21,24,31,35-36,44-45H,22-23,25-26H2,(H,41,46)(H,42,47)(H,43,48)/t31-,35-,36-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AIDS Drug Screening and Development Laboratory, SA Curated by ChEMBL					Assay Description Inhibitory activity against HIV protease				Bioorg Med Chem Lett 8: 3537-42 (1999) BindingDB Entry DOI: 10.7270/Q2HM57MB
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50471917 (CHEMBL105602) Show SMILES C[N+]1(CCn2cc(C(=O)c3cccc4ccccc34)c3ccccc23)CCOCC1 Show InChI InChI=1S/C26H27N2O2/c1-28(15-17-30-18-16-28)14-13-27-19-24(22-10-4-5-12-25(22)27)26(29)23-11-6-8-20-7-2-3-9-21(20)23/h2-12,19H,13-18H2,1H3/q+1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.89E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Displacement of [3H]CP-55940 from Cannabinoid receptor 1 of rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032571 (Anthracen-9-yl-[1-(2-morpholin-4-yl-ethyl)-1H-indo...) Show SMILES O=C(c1cn(CCN2CCOCC2)c2ccccc12)c1c2ccccc2cc2ccccc12 Show InChI InChI=1S/C29H26N2O2/c32-29(28-23-9-3-1-7-21(23)19-22-8-2-4-10-24(22)28)26-20-31(27-12-6-5-11-25(26)27)14-13-30-15-17-33-18-16-30/h1-12,19-20H,13-18H2	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.27E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032617 (CHEMBL310539 | [2,6-Dimethyl-1-(2-morpholin-4-yl-e...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2cc(C)ccc12 Show InChI InChI=1S/C24H28N2O3/c1-17-4-9-21-22(16-17)26(11-10-25-12-14-29-15-13-25)18(2)23(21)24(27)19-5-7-20(28-3)8-6-19/h4-9,16H,10-15H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.76E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032563 (CHEMBL275242 | [2-Methyl-1-(2-morpholin-4-yl-ethyl...) Show SMILES Cc1c(C(=O)c2ccc(C)cc2)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C23H26N2O2/c1-17-7-9-19(10-8-17)23(26)22-18(2)25(21-6-4-3-5-20(21)22)12-11-24-13-15-27-16-14-24/h3-10H,11-16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.08E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032591 (CHEMBL310538 | [2,7-Dimethyl-1-(2-morpholin-4-yl-e...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2c(C)cccc12 Show InChI InChI=1S/C24H28N2O3/c1-17-5-4-6-21-22(24(27)19-7-9-20(28-3)10-8-19)18(2)26(23(17)21)12-11-25-13-15-29-16-14-25/h4-10H,11-16H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.32E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032541 (CHEMBL310751 | [6-Methoxy-2-methyl-1-(2-morpholin-...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2cc(OC)ccc12 Show InChI InChI=1S/C24H28N2O4/c1-17-23(24(27)18-4-6-19(28-2)7-5-18)21-9-8-20(29-3)16-22(21)26(17)11-10-25-12-14-30-15-13-25/h4-9,16H,10-15H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	8.71E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032614 ((3-Chloro-phenyl)-[2-methyl-1-(2-morpholin-4-yl-et...) Show SMILES Cc1c(C(=O)c2cccc(Cl)c2)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C22H23ClN2O2/c1-16-21(22(26)17-5-4-6-18(23)15-17)19-7-2-3-8-20(19)25(16)10-9-24-11-13-27-14-12-24/h2-8,15H,9-14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.55E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50471922 (CHEMBL441060) Show SMILES CC(C)c1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2ccccc12 Show InChI InChI=1S/C25H30N2O2/c1-18(2)20-8-10-21(11-9-20)25(28)24-19(3)27(23-7-5-4-6-22(23)24)13-12-26-14-16-29-17-15-26/h4-11,18H,12-17H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.12E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50368231 (CHEMBL337134) Show SMILES C[C@@H](CN1CCOCC1)n1c(C)c(C(=O)c2ccccc2F)c2ccccc12 Show InChI InChI=1S/C23H25FN2O2/c1-16(15-25-11-13-28-14-12-25)26-17(2)22(19-8-4-6-10-21(19)26)23(27)18-7-3-5-9-20(18)24/h3-10,16H,11-15H2,1-2H3/t16-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.12E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Displacement of [3H]CP-55940 from Cannabinoid receptor 1 of rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032566 (CHEMBL78710 | [2-Methyl-1-(2-morpholin-4-yl-ethyl)...) Show SMILES Cc1c(C(=O)c2cccc3ncccc23)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C25H25N3O2/c1-18-24(25(29)20-7-4-9-22-19(20)8-5-11-26-22)21-6-2-3-10-23(21)28(18)13-12-27-14-16-30-17-15-27/h2-11H,12-17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.51E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032576 ((2-Methoxy-phenyl)-[2-methyl-1-(2-morpholin-4-yl-e...) Show SMILES COc1ccccc1C(=O)c1c(C)n(CCN2CCOCC2)c2ccccc12 Show InChI InChI=1S/C23H26N2O3/c1-17-22(23(26)19-8-4-6-10-21(19)27-2)18-7-3-5-9-20(18)25(17)12-11-24-13-15-28-16-14-24/h3-10H,11-16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.58E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50213819 (CHEMBL421497) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CC2CCCCN2C)c2ccccc12 Show InChI InChI=1S/C24H28N2O2/c1-17-23(24(27)18-11-13-20(28-3)14-12-18)21-9-4-5-10-22(21)26(17)16-19-8-6-7-15-25(19)2/h4-5,9-14,19H,6-8,15-16H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.82E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032572 ((4-Methoxy-phenyl)-[2-methyl-1-(2-thiomorpholin-4-...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCSCC2)c2ccccc12 Show InChI InChI=1S/C23H26N2O2S/c1-17-22(23(26)18-7-9-19(27-2)10-8-18)20-5-3-4-6-21(20)25(17)12-11-24-13-15-28-16-14-24/h3-10H,11-16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.04E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032553 (CHEMBL12914 | [2-Methyl-1-(2-morpholin-4-yl-ethyl)...) Show SMILES Cc1c(C(=O)c2cccc(C)c2)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C23H26N2O2/c1-17-6-5-7-19(16-17)23(26)22-18(2)25(21-9-4-3-8-20(21)22)11-10-24-12-14-27-15-13-24/h3-9,16H,10-15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.09E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50009862 (CHEMBL12566 | {1-[2-(2-Hydroxy-morpholin-4-yl)-eth...) Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2ccccc2n1CCN1CCOC(O)C1 Show InChI InChI=1S/C26H26N2O3/c1-18-25(26(30)21-11-6-8-19-7-2-3-9-20(19)21)22-10-4-5-12-23(22)28(18)14-13-27-15-16-31-24(29)17-27/h2-12,24,29H,13-17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.24E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Displacement of [3H]CP-55940 from Cannabinoid receptor 1 of rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032546 (CHEMBL78701 | [7-Fluoro-2-methyl-1-(2-morpholin-4-...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2c(F)cccc12 Show InChI InChI=1S/C23H25FN2O3/c1-16-21(23(27)17-6-8-18(28-2)9-7-17)19-4-3-5-20(24)22(19)26(16)11-10-25-12-14-29-15-13-25/h3-9H,10-15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.24E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032586 (CHEMBL310741 | [6-Bromo-2-methyl-1-(2-morpholin-4-...) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2cc(Br)ccc12 Show InChI InChI=1S/C23H25BrN2O3/c1-16-22(23(27)17-3-6-19(28-2)7-4-17)20-8-5-18(24)15-21(20)26(16)10-9-25-11-13-29-14-12-25/h3-8,15H,9-14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.45E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032619 (CHEMBL309700 | [2-Methyl-1-(2-morpholin-4-yl-ethyl...) Show SMILES Cc1c(C(=O)c2ccc3ncccc3c2)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C25H25N3O2/c1-18-24(25(29)20-8-9-22-19(17-20)5-4-10-26-22)21-6-2-3-7-23(21)28(18)12-11-27-13-15-30-16-14-27/h2-10,17H,11-16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.51E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50471921 (CHEMBL302991) Show SMILES COc1ccc(cc1)C(=O)c1c(C)n(CC2CCCN2C)c2ccccc12 Show InChI InChI=1S/C23H26N2O2/c1-16-22(23(26)17-10-12-19(27-3)13-11-17)20-8-4-5-9-21(20)25(16)15-18-7-6-14-24(18)2/h4-5,8-13,18H,6-7,14-15H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.57E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032618 (CHEMBL78992 | [1-(2-Morpholin-4-yl-ethyl)-1H-indol...) Show SMILES O=C(c1cn(CCN2CCOCC2)c2ccccc12)c1ccc2ncccc2c1 Show InChI InChI=1S/C24H23N3O2/c28-24(19-7-8-22-18(16-19)4-3-9-25-22)21-17-27(23-6-2-1-5-20(21)23)11-10-26-12-14-29-15-13-26/h1-9,16-17H,10-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.57E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50009868 ((4-Methoxy-phenyl)-[1-(2-morpholin-4-yl-ethyl)-1H-...) Show SMILES COc1ccc(cc1)C(=O)c1cn(CCN2CCOCC2)c2ccccc12 Show InChI InChI=1S/C22H24N2O3/c1-26-18-8-6-17(7-9-18)22(25)20-16-24(21-5-3-2-4-19(20)21)11-10-23-12-14-27-15-13-23/h2-9,16H,10-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.82E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Displacement of [3H]CP-55940 from Cannabinoid receptor 1 of rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50032551 (Benzofuran-2-yl-[2-methyl-1-(2-morpholin-4-yl-ethy...) Show SMILES Cc1c(C(=O)c2cc3ccccc3o2)c2ccccc2n1CCN1CCOCC1 Show InChI InChI=1S/C24H24N2O3/c1-17-23(24(27)22-16-18-6-2-5-9-21(18)29-22)19-7-3-4-8-20(19)26(17)11-10-25-12-14-28-15-13-25/h2-9,16H,10-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.02E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50009868 ((4-Methoxy-phenyl)-[1-(2-morpholin-4-yl-ethyl)-1H-...) Show SMILES COc1ccc(cc1)C(=O)c1cn(CCN2CCOCC2)c2ccccc12 Show InChI InChI=1S/C22H24N2O3/c1-26-18-8-6-17(7-9-18)22(25)20-16-24(21-5-3-2-4-19(20)21)11-10-23-12-14-27-15-13-23/h2-9,16H,10-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.24E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Research Division Curated by ChEMBL					Assay Description Cannabinoid receptor 1 binding affinity by measuring its ability to displace [3H]WIN-55212-2 in rat forebrain membranes				J Med Chem 41: 4521-32 (1998) Article DOI: 10.1021/jm980305c BindingDB Entry DOI: 10.7270/Q2XD14F0
					More data for this Ligand-Target Pair

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