Compile Data Set for Download or QSAR

Found 143 hits with Last Name = 'beyer' and Initial = 'd'   

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
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM686 (BMS-186318 analog 23 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(COC(=O)N2CCOCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C36H54N4O9/c1-35(2,3)48-32(43)38-28(20-25-10-8-7-9-11-25)30(41)22-37-23-31(42)29(39-33(44)49-36(4,5)6)21-26-12-14-27(15-13-26)24-47-34(45)40-16-18-46-19-17-40/h7-15,28-31,37,41-42H,16-24H2,1-6H3,(H,38,43)(H,39,44)/t28-,29-,30+,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM680 ((phenylmethyl)propyl]carbamic Acid, 1,1-Dimethylet...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCN2CCOC2=O)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C35H52N4O9/c1-34(2,3)47-31(42)37-27(20-24-10-8-7-9-11-24)29(40)22-36-23-30(41)28(38-32(43)48-35(4,5)6)21-25-12-14-26(15-13-25)45-18-16-39-17-19-46-33(39)44/h7-15,27-30,36,40-41H,16-23H2,1-6H3,(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM679 (BMS-186318 analog 16 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CN(C)C(=O)OCCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)cc1 |r| Show InChI InChI=1S/C35H54N4O9/c1-34(2,3)47-31(42)37-27(20-24-12-10-9-11-13-24)29(40)22-36-23-30(41)28(38-32(43)48-35(4,5)6)21-25-14-16-26(17-15-25)45-18-19-46-33(44)39(7)8/h9-17,27-30,36,40-41H,18-23H2,1-8H3,(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM676 (BMS-186318 analog 13 | [1S-[1R*, 2S*(2S*, 3R*)]-[3...) Show SMILES CC(O)COc1ccc(C[C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)cc1 |r| Show InChI InChI=1S/C33H51N3O8/c1-22(37)21-42-25-15-13-24(14-16-25)18-27(36-31(41)44-33(5,6)7)29(39)20-34-19-28(38)26(17-23-11-9-8-10-12-23)35-30(40)43-32(2,3)4/h8-16,22,26-29,34,37-39H,17-21H2,1-7H3,(H,35,40)(H,36,41)/t22?,26-,27-,28+,29+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	49	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM691 (BMS-186318 analog 28 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES COCCCCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)cc1 |r| Show InChI InChI=1S/C35H55N3O8/c1-34(2,3)45-32(41)37-28(21-25-13-9-8-10-14-25)30(39)23-36-24-31(40)29(38-33(42)46-35(4,5)6)22-26-15-17-27(18-16-26)44-20-12-11-19-43-7/h8-10,13-18,28-31,36,39-40H,11-12,19-24H2,1-7H3,(H,37,41)(H,38,42)/t28-,29-,30+,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM671 (BMS-186318 analog 8 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCc2ccccn2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H52N4O7/c1-36(2,3)47-34(44)40-30(22-26-12-8-7-9-13-26)32(42)24-38-25-33(43)31(41-35(45)48-37(4,5)6)23-27-15-17-29(18-16-27)46-21-19-28-14-10-11-20-39-28/h7-18,20,30-33,38,42-43H,19,21-25H2,1-6H3,(H,40,44)(H,41,45)/t30-,31-,32+,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM681 (BMS-186318 analog 18 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CN1CCN(CCOc2ccc(C[C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](Cc3ccccc3)NC(=O)OC(C)(C)C)cc2)C1=O |r| Show InChI InChI=1S/C36H55N5O8/c1-35(2,3)48-32(44)38-28(21-25-11-9-8-10-12-25)30(42)23-37-24-31(43)29(39-33(45)49-36(4,5)6)22-26-13-15-27(16-14-26)47-20-19-41-18-17-40(7)34(41)46/h8-16,28-31,37,42-43H,17-24H2,1-7H3,(H,38,44)(H,39,45)/t28-,29-,30+,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM672 ((phenylmethyl)propyl]carbamic Acid, 1,1-Dimethylet...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCOc2cccnc2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H52N4O8/c1-36(2,3)48-34(44)40-30(21-26-11-8-7-9-12-26)32(42)24-39-25-33(43)31(41-35(45)49-37(4,5)6)22-27-14-16-28(17-15-27)46-19-20-47-29-13-10-18-38-23-29/h7-18,23,30-33,39,42-43H,19-22,24-25H2,1-6H3,(H,40,44)(H,41,45)/t30-,31-,32+,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM674 (BMS-186318 analog 11 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCO)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C32H49N3O8/c1-31(2,3)42-29(39)34-25(18-22-10-8-7-9-11-22)27(37)20-33-21-28(38)26(35-30(40)43-32(4,5)6)19-23-12-14-24(15-13-23)41-17-16-36/h7-15,25-28,33,36-38H,16-21H2,1-6H3,(H,34,39)(H,35,40)/t25-,26-,27+,28+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	64	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM675 (BMS-186318 analog 12 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES COCCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)cc1 |r| Show InChI InChI=1S/C33H51N3O8/c1-32(2,3)43-30(39)35-26(19-23-11-9-8-10-12-23)28(37)21-34-22-29(38)27(36-31(40)44-33(4,5)6)20-24-13-15-25(16-14-24)42-18-17-41-7/h8-16,26-29,34,37-38H,17-22H2,1-7H3,(H,35,39)(H,36,40)/t26-,27-,28+,29+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	72	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM693 (BMS-186318 analog 30 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCCN2CCOCC2=O)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H56N4O9/c1-36(2,3)49-34(45)39-29(21-26-11-8-7-9-12-26)31(42)23-38-24-32(43)30(40-35(46)50-37(4,5)6)22-27-13-15-28(16-14-27)48-19-10-17-41-18-20-47-25-33(41)44/h7-9,11-16,29-32,38,42-43H,10,17-25H2,1-6H3,(H,39,45)(H,40,46)/t29-,30-,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM683 (BMS-186318 analog 20 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(CCC(=O)N2CCOCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H56N4O8/c1-36(2,3)48-34(45)39-29(22-27-10-8-7-9-11-27)31(42)24-38-25-32(43)30(40-35(46)49-37(4,5)6)23-28-14-12-26(13-15-28)16-17-33(44)41-18-20-47-21-19-41/h7-15,29-32,38,42-43H,16-25H2,1-6H3,(H,39,45)(H,40,46)/t29-,30-,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	85	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM692 (BMS-186318 analog 29 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCCN2CCOCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H58N4O8/c1-36(2,3)48-34(44)39-30(23-27-11-8-7-9-12-27)32(42)25-38-26-33(43)31(40-35(45)49-37(4,5)6)24-28-13-15-29(16-14-28)47-20-10-17-41-18-21-46-22-19-41/h7-9,11-16,30-33,38,42-43H,10,17-26H2,1-6H3,(H,39,44)(H,40,45)/t30-,31-,32+,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	86	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM685 (BMS-186318 analog 22 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCC(=O)N2CCCCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H56N4O8/c1-36(2,3)48-34(45)39-29(21-26-13-9-7-10-14-26)31(42)23-38-24-32(43)30(40-35(46)49-37(4,5)6)22-27-15-17-28(18-16-27)47-25-33(44)41-19-11-8-12-20-41/h7,9-10,13-18,29-32,38,42-43H,8,11-12,19-25H2,1-6H3,(H,39,45)(H,40,46)/t29-,30-,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM670 (BMS-186318 analog 7 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCn2ccnc2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C35H51N5O7/c1-34(2,3)46-32(43)38-28(20-25-10-8-7-9-11-25)30(41)22-37-23-31(42)29(39-33(44)47-35(4,5)6)21-26-12-14-27(15-13-26)45-19-18-40-17-16-36-24-40/h7-17,24,28-31,37,41-42H,18-23H2,1-6H3,(H,38,43)(H,39,44)/t28-,29-,30+,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM684 ((phenylmethyl)propyl]carbamic Acid, 1,1-Dimethylet...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCN2CCOCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C36H56N4O8/c1-35(2,3)47-33(43)38-29(22-26-10-8-7-9-11-26)31(41)24-37-25-32(42)30(39-34(44)48-36(4,5)6)23-27-12-14-28(15-13-27)46-21-18-40-16-19-45-20-17-40/h7-15,29-32,37,41-42H,16-25H2,1-6H3,(H,38,43)(H,39,44)/t29-,30-,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM682 (BMS-186318 analog 19 | [1S-[1R*,2S*(2S*,3R*)]]-[3-...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCC(=O)N2CCOCC2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C36H54N4O9/c1-35(2,3)48-33(44)38-28(20-25-10-8-7-9-11-25)30(41)22-37-23-31(42)29(39-34(45)49-36(4,5)6)21-26-12-14-27(15-13-26)47-24-32(43)40-16-18-46-19-17-40/h7-15,28-31,37,41-42H,16-24H2,1-6H3,(H,38,44)(H,39,45)/t28-,29-,30+,31+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM918 ((1S-(1R*,2S*(2S,3R*)))-[3-[[3-[[(1,1-Dimethylethox...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(O)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C30H45N3O7/c1-29(2,3)39-27(37)32-23(16-20-10-8-7-9-11-20)25(35)18-31-19-26(36)24(33-28(38)40-30(4,5)6)17-21-12-14-22(34)15-13-21/h7-15,23-26,31,34-36H,16-19H2,1-6H3,(H,32,37)(H,33,38)/t23-,24-,25+,26+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM673 ((phenylmethyl)propyl]carbamic Acid, 1,1-Dimethylet...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCC(O)c2cccnc2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H52N4O8/c1-36(2,3)48-34(45)40-29(19-25-11-8-7-9-12-25)31(42)22-39-23-32(43)30(41-35(46)49-37(4,5)6)20-26-14-16-28(17-15-26)47-24-33(44)27-13-10-18-38-21-27/h7-18,21,29-33,39,42-44H,19-20,22-24H2,1-6H3,(H,40,45)(H,41,46)/t29-,30-,31+,32+,33?/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM677 ((phenylmethyl)propyl]carbamic Acid, 1,1-Dimethylet...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCC(C)(C)O)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C34H53N3O8/c1-32(2,3)44-30(40)36-26(18-23-12-10-9-11-13-23)28(38)20-35-21-29(39)27(37-31(41)45-33(4,5)6)19-24-14-16-25(17-15-24)43-22-34(7,8)42/h9-17,26-29,35,38-39,42H,18-22H2,1-8H3,(H,36,40)(H,37,41)/t26-,27-,28+,29+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM914 (Aminodiol deriv. 9a | BMS-186318 analog 1 | [(S,R)...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C30H45N3O6/c1-29(2,3)38-27(36)32-23(17-21-13-9-7-10-14-21)25(34)19-31-20-26(35)24(18-22-15-11-8-12-16-22)33-28(37)39-30(4,5)6/h7-16,23-26,31,34-35H,17-20H2,1-6H3,(H,32,36)(H,33,37)/t23-,24-,25+,26+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	125	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair				3D Structure (crystal)
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM666 (BMS-186318 analog 3 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc2ncccc2c1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C33H46N4O6/c1-32(2,3)42-30(40)36-26(18-22-11-8-7-9-12-22)28(38)20-34-21-29(39)27(37-31(41)43-33(4,5)6)19-23-14-15-25-24(17-23)13-10-16-35-25/h7-17,26-29,34,38-39H,18-21H2,1-6H3,(H,36,40)(H,37,41)/t26-,27-,28+,29+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM688 (BMS-186318 analog 25 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1cccc(OCc2ccccc2)c1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H51N3O7/c1-36(2,3)46-34(43)39-30(21-26-14-9-7-10-15-26)32(41)23-38-24-33(42)31(40-35(44)47-37(4,5)6)22-28-18-13-19-29(20-28)45-25-27-16-11-8-12-17-27/h7-20,30-33,38,41-42H,21-25H2,1-6H3,(H,39,43)(H,40,44)/t30-,31-,32+,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM678 (3-{4-[(2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-4-{...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCC(O)=O)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C33H49N3O9/c1-32(2,3)44-30(41)35-25(18-22-10-8-7-9-11-22)27(37)20-34-21-28(38)26(36-31(42)45-33(4,5)6)19-23-12-14-24(15-13-23)43-17-16-29(39)40/h7-15,25-28,34,37-38H,16-21H2,1-6H3,(H,35,41)(H,36,42)(H,39,40)/t25-,26-,27+,28+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM668 (BMS-186318 analog 5 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1cccc(O)c1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C30H45N3O7/c1-29(2,3)39-27(37)32-23(16-20-11-8-7-9-12-20)25(35)18-31-19-26(36)24(33-28(38)40-30(4,5)6)17-21-13-10-14-22(34)15-21/h7-15,23-26,31,34-36H,16-19H2,1-6H3,(H,32,37)(H,33,38)/t23-,24-,25+,26+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM689 (BMS-186318 analog 26 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCCCc2nc3ccccc3o2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C40H54N4O8/c1-39(2,3)51-37(47)43-31(23-27-13-8-7-9-14-27)33(45)25-41-26-34(46)32(44-38(48)52-40(4,5)6)24-28-18-20-29(21-19-28)49-22-12-17-36-42-30-15-10-11-16-35(30)50-36/h7-11,13-16,18-21,31-34,41,45-46H,12,17,22-26H2,1-6H3,(H,43,47)(H,44,48)/t31-,32-,33+,34+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	280	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM669 (BMS-186318 analog 6 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccccc1O)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C30H45N3O7/c1-29(2,3)39-27(37)32-22(16-20-12-8-7-9-13-20)25(35)18-31-19-26(36)23(33-28(38)40-30(4,5)6)17-21-14-10-11-15-24(21)34/h7-15,22-23,25-26,31,34-36H,16-19H2,1-6H3,(H,32,37)(H,33,38)/t22-,23-,25+,26+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM687 (BMS-186318 analog 24 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C37H51N3O7/c1-36(2,3)46-34(43)39-30(21-26-13-9-7-10-14-26)32(41)23-38-24-33(42)31(40-35(44)47-37(4,5)6)22-27-17-19-29(20-18-27)45-25-28-15-11-8-12-16-28/h7-20,30-33,38,41-42H,21-25H2,1-6H3,(H,39,43)(H,40,44)/t30-,31-,32+,33+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM690 (BMS-186318 analog 27 | tert-butyl N-[(2S,3R)-4-{[(...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccc(OCc2nc3ccccc3o2)cc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C38H50N4O8/c1-37(2,3)49-35(45)41-29(20-25-12-8-7-9-13-25)31(43)22-39-23-32(44)30(42-36(46)50-38(4,5)6)21-26-16-18-27(19-17-26)47-24-34-40-28-14-10-11-15-33(28)48-34/h7-19,29-32,39,43-44H,20-24H2,1-6H3,(H,41,45)(H,42,46)/t29-,30-,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
Dimer of Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM665 (BMS-186318 analog 2 | [1S-[1R*,2S*(2S*,3R*)]]-[3-[...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC[C@@H](O)[C@H](Cc1ccncc1)NC(=O)OC(C)(C)C |r| Show InChI InChI=1S/C29H44N4O6/c1-28(2,3)38-26(36)32-22(16-20-10-8-7-9-11-20)24(34)18-31-19-25(35)23(17-21-12-14-30-15-13-21)33-27(37)39-29(4,5)6/h7-15,22-25,31,34-35H,16-19H2,1-6H3,(H,32,36)(H,33,37)/t22-,23-,24+,25+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	5.5	37
Bristol-Myers Squibb Company					Assay Description IC50 values are determined by inhibition of the cleavage of the peptidic substrate [V-S-Q-N-(beta-naphthylalanine)-P-I-V]. The IC50 value represents ...				J Med Chem 39: 1991-2007 (1996) Article DOI: 10.1021/jm950717a BindingDB Entry DOI: 10.7270/Q2VX0DQ2
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205383 ((5-{4-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1ccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)cc1 Show InChI InChI=1S/C25H19NO6S/c27-20-10-9-19(23(30)24(20)31)15-2-1-3-16(12-15)25(32)26-17-6-4-14(5-7-17)21-11-8-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	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	570	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205368 ((5-{3-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1cccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)c1 Show InChI InChI=1S/C25H19NO6S/c27-20-9-8-19(23(30)24(20)31)14-3-1-5-16(11-14)25(32)26-17-6-2-4-15(12-17)21-10-7-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	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	740	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205383 ((5-{4-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1ccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)cc1 Show InChI InChI=1S/C25H19NO6S/c27-20-10-9-19(23(30)24(20)31)15-2-1-3-16(12-15)25(32)26-17-6-4-14(5-7-17)21-11-8-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	790	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
E-selectin (Homo sapiens (Human))	BDBM50205396 (3-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-benzoi...) Show SMILES OC(=O)c1cccc(NC(=O)Cc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C15H13NO6/c17-11-4-8(5-12(18)14(11)20)6-13(19)16-10-3-1-2-9(7-10)15(21)22/h1-5,7,17-18,20H,6H2,(H,16,19)(H,21,22)	PDB MMDB NCI pathway 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	800	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human E-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205377 (CHEMBL220254 | {2'-[(3,4,5-trihydroxybenzoyl)oxy]-...) Show SMILES OC(=O)Cc1cccc(c1)-c1ccccc1OC(=O)c1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C21H16O7/c22-16-10-14(11-17(23)20(16)26)21(27)28-18-7-2-1-6-15(18)13-5-3-4-12(8-13)9-19(24)25/h1-8,10-11,22-23,26H,9H2,(H,24,25)	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	870	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
E-selectin (Homo sapiens (Human))	BDBM50205385 (CHEMBL220255 | {3-[2-(3,4,5-trihydroxy-phenyl)-ace...) Show SMILES OC(=O)Cc1cccc(NC(=O)Cc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C16H15NO6/c18-12-5-10(6-13(19)16(12)23)7-14(20)17-11-3-1-2-9(4-11)8-15(21)22/h1-6,18-19,23H,7-8H2,(H,17,20)(H,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human E-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205394 ((5-{2-[(2',3',4'-trihydroxy-biphenyl-4-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)c1ccc(cc1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C25H19NO6S/c27-20-11-10-17(23(30)24(20)31)14-5-7-15(8-6-14)25(32)26-19-4-2-1-3-18(19)21-12-9-16(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	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	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205368 ((5-{3-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1cccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)c1 Show InChI InChI=1S/C25H19NO6S/c27-20-9-8-19(23(30)24(20)31)14-3-1-5-16(11-14)25(32)26-17-6-2-4-15(12-17)21-10-7-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205396 (3-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-benzoi...) Show SMILES OC(=O)c1cccc(NC(=O)Cc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C15H13NO6/c17-11-4-8(5-12(18)14(11)20)6-13(19)16-10-3-1-2-9(7-10)15(21)22/h1-5,7,17-18,20H,6H2,(H,16,19)(H,21,22)	PDB MMDB NCI pathway 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	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205403 (5-{2-[(2'3',4'-hydroxy-biphenyl-3-carbonyl)-amino]...) Show SMILES OC(=O)c1ccc(s1)-c1ccccc1NC(=O)c1cccc(c1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C24H17NO6S/c26-18-9-8-15(21(27)22(18)28)13-4-3-5-14(12-13)23(29)25-17-7-2-1-6-16(17)19-10-11-20(32-19)24(30)31/h1-12,26-28H,(H,25,29)(H,30,31)	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	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
E-selectin (Homo sapiens (Human))	BDBM50205371 (4-methyl-3-[3-(3,4,5-trihydroxy-phenyl)-propionyla...) Show SMILES Cc1ccc(cc1NC(=O)CCc1cc(O)c(O)c(O)c1)C(O)=O Show InChI InChI=1S/C17H17NO6/c1-9-2-4-11(17(23)24)8-12(9)18-15(21)5-3-10-6-13(19)16(22)14(20)7-10/h2,4,6-8,19-20,22H,3,5H2,1H3,(H,18,21)(H,23,24)	PDB MMDB NCI pathway 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	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human E-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205396 (3-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-benzoi...) Show SMILES OC(=O)c1cccc(NC(=O)Cc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C15H13NO6/c17-11-4-8(5-12(18)14(11)20)6-13(19)16-10-3-1-2-9(7-10)15(21)22/h1-5,7,17-18,20H,6H2,(H,16,19)(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205377 (CHEMBL220254 | {2'-[(3,4,5-trihydroxybenzoyl)oxy]-...) Show SMILES OC(=O)Cc1cccc(c1)-c1ccccc1OC(=O)c1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C21H16O7/c22-16-10-14(11-17(23)20(16)26)21(27)28-18-7-2-1-6-15(18)13-5-3-4-12(8-13)9-19(24)25/h1-8,10-11,22-23,26H,9H2,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205394 ((5-{2-[(2',3',4'-trihydroxy-biphenyl-4-carbonyl)-a...) Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)c1ccc(cc1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C25H19NO6S/c27-20-11-10-17(23(30)24(20)31)14-5-7-15(8-6-14)25(32)26-19-4-2-1-3-18(19)21-12-9-16(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205403 (5-{2-[(2'3',4'-hydroxy-biphenyl-3-carbonyl)-amino]...) Show SMILES OC(=O)c1ccc(s1)-c1ccccc1NC(=O)c1cccc(c1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C24H17NO6S/c26-18-9-8-15(21(27)22(18)28)13-4-3-5-14(12-13)23(29)25-17-7-2-1-6-16(17)19-10-11-20(32-19)24(30)31/h1-12,26-28H,(H,25,29)(H,30,31)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205385 (CHEMBL220255 | {3-[2-(3,4,5-trihydroxy-phenyl)-ace...) Show SMILES OC(=O)Cc1cccc(NC(=O)Cc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C16H15NO6/c18-12-5-10(6-13(19)16(12)23)7-14(20)17-11-3-1-2-9(4-11)8-15(21)22/h1-6,18-19,23H,7-8H2,(H,17,20)(H,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205375 (CHEMBL220419 | {3-[3-(3,4,5-trihydroxy-phenyl)-pro...) Show SMILES OC(=O)Cc1cccc(NC(=O)CCc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C17H17NO6/c19-13-7-11(8-14(20)17(13)24)4-5-15(21)18-12-3-1-2-10(6-12)9-16(22)23/h1-3,6-8,19-20,24H,4-5,9H2,(H,18,21)(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
L-selectin (Homo sapiens (Human))	BDBM50205375 (CHEMBL220419 | {3-[3-(3,4,5-trihydroxy-phenyl)-pro...) Show SMILES OC(=O)Cc1cccc(NC(=O)CCc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C17H17NO6/c19-13-7-11(8-14(20)17(13)24)4-5-15(21)18-12-3-1-2-10(6-12)9-16(22)23/h1-3,6-8,19-20,24H,4-5,9H2,(H,18,21)(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human L-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
E-selectin (Homo sapiens (Human))	BDBM50205375 (CHEMBL220419 | {3-[3-(3,4,5-trihydroxy-phenyl)-pro...) Show SMILES OC(=O)Cc1cccc(NC(=O)CCc2cc(O)c(O)c(O)c2)c1 Show InChI InChI=1S/C17H17NO6/c19-13-7-11(8-14(20)17(13)24)4-5-15(21)18-12-3-1-2-10(6-12)9-16(22)23/h1-3,6-8,19-20,24H,4-5,9H2,(H,18,21)(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human E-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair
P-selectin (Homo sapiens (Human))	BDBM50205384 ((5-{2-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-ph...) Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)Cc1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C20H17NO6S/c22-15-7-11(8-16(23)20(15)27)9-18(24)21-14-4-2-1-3-13(14)17-6-5-12(28-17)10-19(25)26/h1-8,22-23,27H,9-10H2,(H,21,24)(H,25,26)	PDB MMDB NCI pathway 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	2.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Revotar Biopharmaceuticals AG Curated by ChEMBL					Assay Description Inhibition of human P-selectin after 2 hrs				J Med Chem 50: 1101-15 (2007) Article DOI: 10.1021/jm060536g BindingDB Entry DOI: 10.7270/Q2TB17Q6
					More data for this Ligand-Target Pair

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