Compile Data Set for Download or QSAR

Found 21 hits Enz. Inhib. hit(s) with all data for entry = 8751   

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
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013820 (CHEMBL3265274 | US10323013, Compound 34) Show SMILES NC(=N)N1CCc2c(C1)c(=O)oc1c(C=O)c(O)ccc21 Show InChI InChI=1S/C14H13N3O4/c15-14(16)17-4-3-7-8-1-2-11(19)10(6-18)12(8)21-13(20)9(7)5-17/h1-2,6,19H,3-5H2,(H3,15,16)	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	47	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013802 (CHEMBL3265261 | US10323013, Compound 21b) Show SMILES Oc1ccc2c3CCN(Cc3c(=O)oc2c1C=O)C(=O)OCC=C Show InChI InChI=1S/C17H15NO6/c1-2-7-23-17(22)18-6-5-10-11-3-4-14(20)13(9-19)15(11)24-16(21)12(10)8-18/h2-4,9,20H,1,5-8H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	US Patent	n/a	n/a	111	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013817 (CHEMBL3265271 | US10323013, Compound 31) Show SMILES Oc1ccc2c3CCN(Cc4ccccc4)Cc3c(=O)oc2c1C=O Show InChI InChI=1S/C20H17NO4/c22-12-17-18(23)7-6-15-14-8-9-21(10-13-4-2-1-3-5-13)11-16(14)20(24)25-19(15)17/h1-7,12,23H,8-11H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	113	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013814 (CHEMBL3265270 | US10323013, Compound 30) Show SMILES CN1CCc2c(C1)c(=O)oc1c(C=O)c(O)ccc21 Show InChI InChI=1S/C14H13NO4/c1-15-5-4-8-9-2-3-12(17)11(7-16)13(9)19-14(18)10(8)6-15/h2-3,7,17H,4-6H2,1H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013819 (CHEMBL3265273 | US10323013, Compound 33) Show SMILES CC(=C)CN1CCc2c(C1)c(=O)oc1c(C=O)c(O)ccc21 Show InChI InChI=1S/C17H17NO4/c1-10(2)7-18-6-5-11-12-3-4-15(20)14(9-19)16(12)22-17(21)13(11)8-18/h3-4,9,20H,1,5-8H2,2H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	255	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013818 (CHEMBL3265272 | US10323013, Compound 32) Show SMILES Oc1ccc2c3CCN(Cc4ccc(F)cc4)Cc3c(=O)oc2c1C=O Show InChI InChI=1S/C20H16FNO4/c21-13-3-1-12(2-4-13)9-22-8-7-14-15-5-6-18(24)17(11-23)19(15)26-20(25)16(14)10-22/h1-6,11,24H,7-10H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	303	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013813 (CHEMBL3265269 | US10323013, Compound 29) Show SMILES CC(=O)N1CCc2c(C1)c(=O)oc1c(C=O)c(O)ccc21 Show InChI InChI=1S/C15H13NO5/c1-8(18)16-5-4-9-10-2-3-13(19)12(7-17)14(10)21-15(20)11(9)6-16/h2-3,7,19H,4-6H2,1H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	312	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013812 (CHEMBL3265268 | US10323013, Compound 28) Show SMILES Oc1ccc2c3CCNCc3c(=O)oc2c1C1OCCCO1 Show InChI InChI=1S/C16H17NO5/c18-12-3-2-10-9-4-5-17-8-11(9)15(19)22-14(10)13(12)16-20-6-1-7-21-16/h2-3,16-18H,1,4-8H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	US Patent	n/a	n/a	1.23E+3	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM416659 (US10323013, Compound 37 | allyl 7-(3-ethoxy-3-oxop...) Show SMILES CCOC(=O)C=Cc1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C21H21NO7/c1-3-11-28-21(26)22-10-9-13-14-5-7-17(23)15(6-8-18(24)27-4-2)19(14)29-20(25)16(13)12-22/h3,5-8,23H,1,4,9-12H2,2H3/b8-6+	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013807 (CHEMBL3265264 | US10323013, Compound 24) Show SMILES Oc1ccc2c3CCN(Cc3c(=O)oc2c1C1OCCCO1)C(=O)OCC=C Show InChI InChI=1S/C20H21NO7/c1-2-8-27-20(24)21-7-6-12-13-4-5-15(22)16(19-25-9-3-10-26-19)17(13)28-18(23)14(12)11-21/h2,4-5,19,22H,1,3,6-11H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	3.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013825 (CHEMBL3265279 | US10323013, Compound 40) Show SMILES OC(=O)c1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C17H15NO7/c1-2-7-24-17(23)18-6-5-9-10-3-4-12(19)13(15(20)21)14(10)25-16(22)11(9)8-18/h2-4,19H,1,5-8H2,(H,20,21)	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	4.11E+3	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM416662 (3-allyl 7-methyl 8-hydroxy-5-oxo-4,5-dihydro-1H-ch...) Show SMILES COC(=O)C1C2OC(=O)C3=C(CCN(C3)C(=O)OCC=C)C2=CC=C1O |c:23,25,t:9| Show InChI InChI=1S/C18H19NO7/c1-3-8-25-18(23)19-7-6-10-11-4-5-13(20)14(17(22)24-2)15(11)26-16(21)12(10)9-19/h3-5,14-15,20H,1,6-9H2,2H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013808 (CHEMBL3265265 | US10323013, Compound 25) Show SMILES Oc1ccc2c3CCN(Cc3c(=O)oc2c1C1SCCCS1)C(=O)OCC=C Show InChI InChI=1S/C20H21NO5S2/c1-2-8-25-20(24)21-7-6-12-13-4-5-15(22)16(19-27-9-3-10-28-19)17(13)26-18(23)14(12)11-21/h2,4-5,19,22H,1,3,6-11H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	1.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013821 (CHEMBL3265275 | US10323013, Compound 35) Show SMILES COCOc1ccc2c3CCN(Cc3c(=O)oc2c1C=O)C(=O)OCC=C Show InChI InChI=1S/C19H19NO7/c1-3-8-25-19(23)20-7-6-12-13-4-5-16(26-11-24-2)15(10-21)17(13)27-18(22)14(12)9-20/h3-5,10H,1,6-9,11H2,2H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013822 (CHEMBL3265276 | US10323013, Compound 36) Show SMILES CC(=O)c1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C18H17NO6/c1-3-8-24-18(23)19-7-6-11-12-4-5-14(21)15(10(2)20)16(12)25-17(22)13(11)9-19/h3-5,21H,1,6-9H2,2H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013810 (CHEMBL3265267 | US10323013, Compound 27) Show SMILES C=CCOC(=O)N1CCc2c(C1)c(=O)oc1c(C=O)c(OCc3ccccc3)ccc21 Show InChI InChI=1S/C24H21NO6/c1-2-12-29-24(28)25-11-10-17-18-8-9-21(30-15-16-6-4-3-5-7-16)20(14-26)22(18)31-23(27)19(17)13-25/h2-9,14H,1,10-13,15H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM416660 (US10323013, Compound 38 | allyl 8-hydroxy-7-(2-(me...) Show SMILES CS(=O)(=O)C=Cc1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C19H19NO7S/c1-3-9-26-19(23)20-8-6-12-13-4-5-16(21)14(7-10-28(2,24)25)17(13)27-18(22)15(12)11-20/h3-5,7,10,21H,1,6,8-9,11H2,2H3/b10-7+	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013803 (CHEMBL3265262 | US10323013, Compound 22) Show SMILES OCc1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C17H17NO6/c1-2-7-23-17(22)18-6-5-10-11-3-4-14(20)13(9-19)15(11)24-16(21)12(10)8-18/h2-4,19-20H,1,5-9H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013827 (CHEMBL3265281 | US10323013, Compound 42) Show SMILES CON(C)C(=O)c1c(O)ccc2c3CCN(Cc3c(=O)oc12)C(=O)OCC=C Show InChI InChI=1S/C19H20N2O7/c1-4-9-27-19(25)21-8-7-11-12-5-6-14(22)15(17(23)20(2)26-3)16(12)28-18(24)13(11)10-21/h4-6,22H,1,7-10H2,2-3H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM50013809 (CHEMBL3265266 | US10323013, Compound 26) Show SMILES COc1ccc2c3CCN(Cc3c(=O)oc2c1C=O)C(=O)OCC=C Show InChI InChI=1S/C18H17NO6/c1-3-8-24-18(22)19-7-6-11-12-4-5-15(23-2)14(10-20)16(12)25-17(21)13(11)9-19/h3-5,10H,1,6-9H2,2H3	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase/endoribonuclease IRE1 (Homo sapiens (Human))	BDBM416640 (US10323013, Compound 23 | allyl 8-hydroxy-7-chloro...) Show SMILES Oc1ccc2c3CCN(Cc3c(=O)oc2c1Cl)C(=O)OCC=C Show InChI InChI=1S/C16H14ClNO5/c1-2-7-22-16(21)18-6-5-9-10-3-4-12(19)13(17)14(10)23-15(20)11(9)8-18/h2-4,19H,1,5-8H2	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. US Patent					Assay Description All compounds were evaluated by FRET-suppression assay in side-by-side experiments using 21b as a control inhibitor (Table 2). Protection of the alde...				US Patent US10323013 (2019) BindingDB Entry DOI: 10.7270/Q24J0HH9
					More data for this Ligand-Target Pair