Compile Data Set for Download or QSAR

Found 72 hits with Last Name = 'sieber' and Initial = 'sa'   

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
Fatty acid synthase (Homo sapiens (Human))	BDBM50242245 (CHEMBL4081658) Show SMILES CCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C30H37N3O8/c1-3-11-23-25(41-28(23)36)27(35)31-17-10-16-24(29(37)39-18-21-12-6-4-7-13-21)33-26(34)20(2)32-30(38)40-19-22-14-8-5-9-15-22/h4-9,12-15,20,23-25H,3,10-11,16-19H2,1-2H3,(H,31,35)(H,32,38)(H,33,34)/t20-,23-,24-,25+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of FAS thioster domain (unknown origin)				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242243 (CHEMBL4059718) Show SMILES CC(C)C[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C31H39N3O8/c1-20(2)17-24-26(42-29(24)37)28(36)32-16-10-15-25(30(38)40-18-22-11-6-4-7-12-22)34-27(35)21(3)33-31(39)41-19-23-13-8-5-9-14-23/h4-9,11-14,20-21,24-26H,10,15-19H2,1-3H3,(H,32,36)(H,33,39)(H,34,35)/t21-,24-,25-,26+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of FAS thioster domain (unknown origin)				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242221 (CHEMBL4084033) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-3-4-5-12-18-26-28(44-31(26)39)30(38)34-20-13-19-27(32(40)42-21-24-14-8-6-9-15-24)36-29(37)23(2)35-33(41)43-22-25-16-10-7-11-17-25/h6-11,14-17,23,26-28H,3-5,12-13,18-22H2,1-2H3,(H,34,38)(H,35,41)(H,36,37)/t23-,26-,27-,28+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of FAS thioster domain (unknown origin)				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242232 (CHEMBL4071106) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccc(cc1)C#C |r| Show InChI InChI=1S/C36H45N3O8/c1-4-6-7-11-16-29-31(47-35(29)43)33(41)37-22-13-12-17-30(39-36(44)46-24-27-14-9-8-10-15-27)32(40)38-25(3)34(42)45-23-28-20-18-26(5-2)19-21-28/h2,8-10,14-15,18-21,25,29-31H,4,6-7,11-13,16-17,22-24H2,1,3H3,(H,37,41)(H,38,40)(H,39,44)/t25-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST-tagged VEGFR2 (D807 to V1356 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242223 (CHEMBL4091800) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-33(27)41)31(39)35-21-14-13-20-28(37-34(42)44-23-26-17-10-7-11-18-26)30(38)36-24(2)32(40)43-22-25-15-8-6-9-16-25/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,38)(H,37,42)/t24-,27-,28-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Alcohol dehydrogenase 1A (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	460	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of ADH1 (unknown origin) preincubated for 2 hrs followed by substrate/NAD+ addition				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242244 (CHEMBL4073670) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-32(27)40)31(39)35-21-14-13-20-28(33(41)43-22-25-15-8-6-9-16-25)37-30(38)24(2)36-34(42)44-23-26-17-10-7-11-18-26/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,42)(H,37,38)/t24-,27-,28-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242222 (CHEMBL4062314) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)c1ccc(Br)cc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H42BrN3O7/c1-3-4-5-9-14-26-28(44-32(26)41)31(40)35-20-11-10-15-27(33(42)43-21-23-12-7-6-8-13-23)37-29(38)22(2)36-30(39)24-16-18-25(34)19-17-24/h6-8,12-13,16-19,22,26-28H,3-5,9-11,14-15,20-21H2,1-2H3,(H,35,40)(H,36,39)(H,37,38)/t22-,26-,27-,28+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242224 (CHEMBL4070939) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@@H]1NC(=O)N([C@@H](C)C(=O)OCc2ccccc2)C1=O |r| Show InChI InChI=1S/C27H37N3O7/c1-3-4-5-9-14-20-22(37-26(20)34)23(31)28-16-11-10-15-21-24(32)30(27(35)29-21)18(2)25(33)36-17-19-12-7-6-8-13-19/h6-8,12-13,18,20-22H,3-5,9-11,14-17H2,1-2H3,(H,28,31)(H,29,35)/t18-,20-,21-,22+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST-tagged VEGFR2 (D807 to V1356 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Tyrosine-protein kinase ABL2 (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	540	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged ABL2 (M1 to P650 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242242 (CHEMBL4100488) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Tyrosine-protein kinase ABL2 (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	685	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged ABL2 (M1 to P650 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242221 (CHEMBL4084033) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-3-4-5-12-18-26-28(44-31(26)39)30(38)34-20-13-19-27(32(40)42-21-24-14-8-6-9-15-24)36-29(37)23(2)35-33(41)43-22-25-16-10-7-11-17-25/h6-11,14-17,23,26-28H,3-5,12-13,18-22H2,1-2H3,(H,34,38)(H,35,41)(H,36,37)/t23-,26-,27-,28+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242231 (CHEMBL4098160) Show SMILES CCCCCC[C@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.19E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 1 (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.28E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST-tagged VEGFR1 (K784 to I1338 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242226 (CHEMBL4081526) Show SMILES CCCCCC[C@@H]1[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27+,29+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.38E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242223 (CHEMBL4091800) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-33(27)41)31(39)35-21-14-13-20-28(37-34(42)44-23-26-17-10-7-11-18-26)30(38)36-24(2)32(40)43-22-25-15-8-6-9-16-25/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,38)(H,37,42)/t24-,27-,28-,29+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 1 (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST-tagged VEGFR1 (K784 to I1338 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate aft...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242221 (CHEMBL4084033) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-3-4-5-12-18-26-28(44-31(26)39)30(38)34-20-13-19-27(32(40)42-21-24-14-8-6-9-15-24)36-29(37)23(2)35-33(41)43-22-25-16-10-7-11-17-25/h6-11,14-17,23,26-28H,3-5,12-13,18-22H2,1-2H3,(H,34,38)(H,35,41)(H,36,37)/t23-,26-,27-,28+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242228 (CHEMBL4066131) Show SMILES CCCCCC[C@]1(C)[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29+,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.18E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242227 (CHEMBL4087502) Show SMILES CCCCCC[C@@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.43E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242227 (CHEMBL4087502) Show SMILES CCCCCC[C@@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.61E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242225 (CHEMBL4099536) Show SMILES CCCCCC[C@@H]1[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-33(27)41)31(39)35-21-14-13-20-28(37-34(42)44-23-26-17-10-7-11-18-26)30(38)36-24(2)32(40)43-22-25-15-8-6-9-16-25/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,38)(H,37,42)/t24-,27+,28-,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.71E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242222 (CHEMBL4062314) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)c1ccc(Br)cc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H42BrN3O7/c1-3-4-5-9-14-26-28(44-32(26)41)31(40)35-20-11-10-15-27(33(42)43-21-23-12-7-6-8-13-23)37-29(38)22(2)36-30(39)24-16-18-25(34)19-17-24/h6-8,12-13,16-19,22,26-28H,3-5,9-11,14-15,20-21H2,1-2H3,(H,35,40)(H,36,39)(H,37,38)/t22-,26-,27-,28+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.81E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Mast/stem cell growth factor receptor Kit (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged c-KIT (T544 to V976 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate ...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242244 (CHEMBL4073670) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-32(27)40)31(39)35-21-14-13-20-28(33(41)43-22-25-15-8-6-9-16-25)37-30(38)24(2)36-34(42)44-23-26-17-10-7-11-18-26/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,42)(H,37,38)/t24-,27-,28-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242228 (CHEMBL4066131) Show SMILES CCCCCC[C@]1(C)[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29+,35+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.11E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242244 (CHEMBL4073670) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-32(27)40)31(39)35-21-14-13-20-28(33(41)43-22-25-15-8-6-9-16-25)37-30(38)24(2)36-34(42)44-23-26-17-10-7-11-18-26/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,42)(H,37,38)/t24-,27-,28-,29+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.17E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-5 (Homo sapiens (Human))	BDBM50242231 (CHEMBL4098160) Show SMILES CCCCCC[C@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.39E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242242 (CHEMBL4100488) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.51E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242231 (CHEMBL4098160) Show SMILES CCCCCC[C@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.62E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242227 (CHEMBL4087502) Show SMILES CCCCCC[C@@]1(C)[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29-,35-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.74E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242232 (CHEMBL4071106) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccc(cc1)C#C |r| Show InChI InChI=1S/C36H45N3O8/c1-4-6-7-11-16-29-31(47-35(29)43)33(41)37-22-13-12-17-30(39-36(44)46-24-27-14-9-8-10-15-27)32(40)38-25(3)34(42)45-23-28-20-18-26(5-2)19-21-28/h2,8-10,14-15,18-21,25,29-31H,4,6-7,11-13,16-17,22-24H2,1,3H3,(H,37,41)(H,38,40)(H,39,44)/t25-,29-,30-,31+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242228 (CHEMBL4066131) Show SMILES CCCCCC[C@]1(C)[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C35H47N3O8/c1-4-5-6-14-21-35(3)29(46-33(35)42)31(40)36-22-15-13-20-28(32(41)44-23-26-16-9-7-10-17-26)38-30(39)25(2)37-34(43)45-24-27-18-11-8-12-19-27/h7-12,16-19,25,28-29H,4-6,13-15,20-24H2,1-3H3,(H,36,40)(H,37,43)(H,38,39)/t25-,28-,29+,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 3 (Homo sapiens (Human))	BDBM50518790 (CHEMBL4465918) Show SMILES Oc1cc2N(C[C@@H](CCl)c2c2ccccc12)C(=O)CCCC(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21 |r| Show InChI InChI=1S/C31H28Cl2N2O4/c32-14-18-16-34(24-12-26(36)20-6-1-3-8-22(20)30(18)24)28(38)10-5-11-29(39)35-17-19(15-33)31-23-9-4-2-7-21(23)27(37)13-25(31)35/h1-4,6-9,12-13,18-19,36-37H,5,10-11,14-17H2/t18-,19-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged VEGFR3 (N799 to R1298 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrat...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242221 (CHEMBL4084033) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-3-4-5-12-18-26-28(44-31(26)39)30(38)34-20-13-19-27(32(40)42-21-24-14-8-6-9-15-24)36-29(37)23(2)35-33(41)43-22-25-16-10-7-11-17-25/h6-11,14-17,23,26-28H,3-5,12-13,18-22H2,1-2H3,(H,34,38)(H,35,41)(H,36,37)/t23-,26-,27-,28+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.35E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM24567 ((2S)-1-[(2S,3S)-3-hexyl-4-oxooxetan-2-yl]tridecan-...) Show SMILES CCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)OC(=O)[C@H](CC(C)C)NC=O |r| Show InChI InChI=1S/C29H53NO5/c1-5-7-9-11-12-13-14-15-16-18-24(34-29(33)26(30-22-31)20-23(3)4)21-27-25(28(32)35-27)19-17-10-8-6-2/h22-27H,5-21H2,1-4H3,(H,30,31)/t24-,25-,26-,27-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	DrugBank Article PubMed	n/a	n/a	4.63E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242222 (CHEMBL4062314) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)[C@H](C)NC(=O)c1ccc(Br)cc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H42BrN3O7/c1-3-4-5-9-14-26-28(44-32(26)41)31(40)35-20-11-10-15-27(33(42)43-21-23-12-7-6-8-13-23)37-29(38)22(2)36-30(39)24-16-18-25(34)19-17-24/h6-8,12-13,16-19,22,26-28H,3-5,9-11,14-15,20-21H2,1-2H3,(H,35,40)(H,36,39)(H,37,38)/t22-,26-,27-,28+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.81E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242224 (CHEMBL4070939) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@@H]1NC(=O)N([C@@H](C)C(=O)OCc2ccccc2)C1=O |r| Show InChI InChI=1S/C27H37N3O7/c1-3-4-5-9-14-20-22(37-26(20)34)23(31)28-16-11-10-15-21-24(32)30(27(35)29-21)18(2)25(33)36-17-19-12-7-6-8-13-19/h6-8,12-13,18,20-22H,3-5,9-11,14-17H2,1-2H3,(H,28,31)(H,29,35)/t18-,20-,21-,22+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.55E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Alcohol dehydrogenase 1A (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of ADH1 (unknown origin) preincubated for 2 hrs followed by substrate/NAD+ addition				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242224 (CHEMBL4070939) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@@H]1NC(=O)N([C@@H](C)C(=O)OCc2ccccc2)C1=O |r| Show InChI InChI=1S/C27H37N3O7/c1-3-4-5-9-14-20-22(37-26(20)34)23(31)28-16-11-10-15-21-24(32)30(27(35)29-21)18(2)25(33)36-17-19-12-7-6-8-13-19/h6-8,12-13,18,20-22H,3-5,9-11,14-17H2,1-2H3,(H,28,31)(H,29,35)/t18-,20-,21-,22+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.93E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Mast/stem cell growth factor receptor Kit (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged c-KIT (T544 to V976 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrate ...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242226 (CHEMBL4081526) Show SMILES CCCCCC[C@@H]1[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27+,29+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.37E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-1 (Homo sapiens (Human))	BDBM50242226 (CHEMBL4081526) Show SMILES CCCCCC[C@@H]1[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27+,29+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242242 (CHEMBL4100488) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-2-3-4-11-18-26-29(44-31(26)39)30(38)34-20-13-12-19-27(32(40)42-22-24-14-7-5-8-15-24)36-28(37)21-35-33(41)43-23-25-16-9-6-10-17-25/h5-10,14-17,26-27,29H,2-4,11-13,18-23H2,1H3,(H,34,38)(H,35,41)(H,36,37)/t26-,27-,29+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.56E+3	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 3 (Homo sapiens (Human))	BDBM50518789 (CHEMBL4473548) Show SMILES C[C@@H]1CN(C(=O)CCCC(=O)N2C[C@@H](C)c3c2cc(O)c2ccccc32)c2cc(O)c3ccccc3c12 |r| Show InChI InChI=1S/C31H30N2O4/c1-18-16-32(24-14-26(34)20-8-3-5-10-22(20)30(18)24)28(36)12-7-13-29(37)33-17-19(2)31-23-11-6-4-9-21(23)27(35)15-25(31)33/h3-6,8-11,14-15,18-19,34-35H,7,12-13,16-17H2,1-2H3/t18-,19-/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Albert Ludwigs University Freiburg Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal GST/His6-tagged VEGFR3 (N799 to R1298 residues) expressed in sf9 cells using Poly(Glu,Tyr) 4:1 as substrat...				J Nat Prod 82: 16-26 (2019) Article DOI: 10.1021/acs.jnatprod.8b00233 BindingDB Entry DOI: 10.7270/Q2FX7DVS
					More data for this Ligand-Target Pair
Fatty acid synthase (Homo sapiens (Human))	BDBM50242225 (CHEMBL4099536) Show SMILES CCCCCC[C@@H]1[C@H](OC1=O)C(=O)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C34H45N3O8/c1-3-4-5-12-19-27-29(45-33(27)41)31(39)35-21-14-13-20-28(37-34(42)44-23-26-17-10-7-11-18-26)30(38)36-24(2)32(40)43-22-25-15-8-6-9-16-25/h6-11,15-18,24,27-29H,3-5,12-14,19-23H2,1-2H3,(H,35,39)(H,36,38)(H,37,42)/t24-,27+,28-,29-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins...				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair
Proteasome subunit beta type-2 (Homo sapiens (Human))	BDBM50242221 (CHEMBL4084033) Show SMILES CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)OCc1ccccc1 |r| Show InChI InChI=1S/C33H43N3O8/c1-3-4-5-12-18-26-28(44-31(26)39)30(38)34-20-13-19-27(32(40)42-21-24-14-8-6-9-15-24)36-29(37)23(2)35-33(41)43-22-25-16-10-7-11-17-25/h6-11,14-17,23,26-28H,3-5,12-13,18-22H2,1-2H3,(H,34,38)(H,35,41)(H,36,37)/t23-,26-,27-,28+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Baylor University Curated by ChEMBL					Assay Description Inhibition of the binding of [3H]C18-Platelet activating factor to human platelet membrane preparation				Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 72 total )  |  Next  |  Last  >>

Jump to: