Compile Data Set for Download or QSAR

Found 8 hits with Last Name = 'paessens' and Initial = 'a'   

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)	BDBM50282499 (Bis-((R)-1-{(S)-3-methyl-2-[(S)-3-(2-methyl-propan...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)N[C@H](Cc1ccccc1)P(O)(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C62H79N4O10PS2/c1-41(2)55(65-57(67)49(39-78(73,74)61(5,6)7)37-47-31-21-29-45-27-17-19-33-51(45)47)59(69)63-53(35-43-23-13-11-14-24-43)77(71,72)54(36-44-25-15-12-16-26-44)64-60(70)56(42(3)4)66-58(68)50(40-79(75,76)62(8,9)10)38-48-32-22-30-46-28-18-20-34-52(46)48/h11-34,41-42,49-50,53-56H,35-40H2,1-10H3,(H,63,69)(H,64,70)(H,65,67)(H,66,68)(H,71,72)/t49-,50-,53+,54+,55+,56+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282499 (Bis-((R)-1-{(S)-3-methyl-2-[(S)-3-(2-methyl-propan...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)N[C@H](Cc1ccccc1)P(O)(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C62H79N4O10PS2/c1-41(2)55(65-57(67)49(39-78(73,74)61(5,6)7)37-47-31-21-29-45-27-17-19-33-51(45)47)59(69)63-53(35-43-23-13-11-14-24-43)77(71,72)54(36-44-25-15-12-16-26-44)64-60(70)56(42(3)4)66-58(68)50(40-79(75,76)62(8,9)10)38-48-32-22-30-46-28-18-20-34-52(46)48/h11-34,41-42,49-50,53-56H,35-40H2,1-10H3,(H,63,69)(H,64,70)(H,65,67)(H,66,68)(H,71,72)/t49-,50-,53+,54+,55+,56+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282495 (Bis-((R)-1-{(S)-3-methyl-2-[(S)-3-(2-methyl-propan...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)N[C@H](Cc1ccccc1)P(N)(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C62H80N5O9PS2/c1-41(2)55(66-57(68)49(39-78(73,74)61(5,6)7)37-47-31-21-29-45-27-17-19-33-51(45)47)59(70)64-53(35-43-23-13-11-14-24-43)77(63,72)54(36-44-25-15-12-16-26-44)65-60(71)56(42(3)4)67-58(69)50(40-79(75,76)62(8,9)10)38-48-32-22-30-46-28-18-20-34-52(46)48/h11-34,41-42,49-50,53-56H,35-40H2,1-10H3,(H2,63,72)(H,64,70)(H,65,71)(H,66,68)(H,67,69)/t49-,50-,53+,54+,55+,56+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282495 (Bis-((R)-1-{(S)-3-methyl-2-[(S)-3-(2-methyl-propan...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)N[C@H](Cc1ccccc1)P(N)(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C62H80N5O9PS2/c1-41(2)55(66-57(68)49(39-78(73,74)61(5,6)7)37-47-31-21-29-45-27-17-19-33-51(45)47)59(70)64-53(35-43-23-13-11-14-24-43)77(63,72)54(36-44-25-15-12-16-26-44)65-60(71)56(42(3)4)67-58(69)50(40-79(75,76)62(8,9)10)38-48-32-22-30-46-28-18-20-34-52(46)48/h11-34,41-42,49-50,53-56H,35-40H2,1-10H3,(H2,63,72)(H,64,70)(H,65,71)(H,66,68)(H,67,69)/t49-,50-,53+,54+,55+,56+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282500 (({(S)-3-Methyl-2-[2-((S)-2-methyl-propane-2-sulfon...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)NCP(O)(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C48H67N4O10PS2/c1-31(2)41(51-43(53)37(27-64(59,60)47(5,6)7)25-35-21-15-19-33-17-11-13-23-39(33)35)45(55)49-29-63(57,58)30-50-46(56)42(32(3)4)52-44(54)38(28-65(61,62)48(8,9)10)26-36-22-16-20-34-18-12-14-24-40(34)36/h11-24,31-32,37-38,41-42H,25-30H2,1-10H3,(H,49,55)(H,50,56)(H,51,53)(H,52,54)(H,57,58)/t37-,38-,41+,42+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282496 (Bis-({(S)-3-methyl-2-[(S)-3-(2-methyl-propane-2-su...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)NCP(N)(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C48H68N5O9PS2/c1-31(2)41(52-43(54)37(27-64(59,60)47(5,6)7)25-35-21-15-19-33-17-11-13-23-39(33)35)45(56)50-29-63(49,58)30-51-46(57)42(32(3)4)53-44(55)38(28-65(61,62)48(8,9)10)26-36-22-16-20-34-18-12-14-24-40(34)36/h11-24,31-32,37-38,41-42H,25-30H2,1-10H3,(H2,49,58)(H,50,56)(H,51,57)(H,52,54)(H,53,55)/t37-,38-,41+,42+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282498 (Bis-({(S)-3-methyl-2-[(S)-3-(2-methyl-propane-2-su...) Show SMILES CC(C)[C@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(=O)NCP(=O)(CNC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C)NN Show InChI InChI=1S/C48H69N6O9PS2/c1-31(2)41(52-43(55)37(27-65(60,61)47(5,6)7)25-35-21-15-19-33-17-11-13-23-39(33)35)45(57)50-29-64(59,54-49)30-51-46(58)42(32(3)4)53-44(56)38(28-66(62,63)48(8,9)10)26-36-22-16-20-34-18-12-14-24-40(34)36/h11-24,31-32,37-38,41-42H,25-30,49H2,1-10H3,(H,50,57)(H,51,58)(H,52,55)(H,53,56)(H,54,59)/t37-,38-,41+,42+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	8.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50282497 (Bis-({(S)-3-methyl-2-[(S)-3-(2-methyl-propane-2-su...) Show SMILES COP(=O)(CNC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C)CNC(=O)[C@@H](NC(=O)[C@H](Cc1cccc2ccccc12)CS(=O)(=O)C(C)(C)C)C(C)C Show InChI InChI=1S/C49H69N4O10PS2/c1-32(2)42(52-44(54)38(28-65(59,60)48(5,6)7)26-36-22-16-20-34-18-12-14-24-40(34)36)46(56)50-30-64(58,63-11)31-51-47(57)43(33(3)4)53-45(55)39(29-66(61,62)49(8,9)10)27-37-23-17-21-35-19-13-15-25-41(35)37/h12-25,32-33,38-39,42-43H,26-31H2,1-11H3,(H,50,56)(H,51,57)(H,52,54)(H,53,55)/t38-,39-,42+,43+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	950	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity if the compound was determined against HIV protease				Bioorg Med Chem Lett 4: 1191-1194 (1994) Article DOI: 10.1016/S0960-894X(01)80327-9 BindingDB Entry DOI: 10.7270/Q28G8KM2
					More data for this Ligand-Target Pair