Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Lysine-specific histone demethylase 1A' and Ligand = 'BDBM456449'   

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
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM456449 (US10723742, Example 175 | US10723742, Example 185 ...) Show SMILES Cn1nnc2cc(c(F)c(F)c12)-c1ccc(cc1-c1ccc(C#N)c(F)c1)C(=O)N1[C@@H]2CC[C@H]1[C@@H](N)C2 |TLB:35:34:32.31:29| Show InChI InChI=1S/C27H21F3N6O/c1-35-26-22(33-34-35)11-19(24(29)25(26)30)17-6-4-14(27(37)36-16-5-7-23(36)21(32)10-16)8-18(17)13-2-3-15(12-31)20(28)9-13/h2-4,6,8-9,11,16,21,23H,5,7,10,32H2,1H3/t16-,21+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.140	n/a	n/a	n/a	n/a	n/a	n/a
Taiho Pharmaceutical Co., Ltd. US Patent					Assay Description The conditions for measuring inhibitory activity of compounds against LSD1 activity were determined with reference to a document available from the w...				US Patent US10723742 (2020) BindingDB Entry DOI: 10.7270/Q2TF01DB
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM456449 (US10723742, Example 175 | US10723742, Example 185 ...) Show SMILES Cn1nnc2cc(c(F)c(F)c12)-c1ccc(cc1-c1ccc(C#N)c(F)c1)C(=O)N1[C@@H]2CC[C@H]1[C@@H](N)C2 |TLB:35:34:32.31:29| Show InChI InChI=1S/C27H21F3N6O/c1-35-26-22(33-34-35)11-19(24(29)25(26)30)17-6-4-14(27(37)36-16-5-7-23(36)21(32)10-16)8-18(17)13-2-3-15(12-31)20(28)9-13/h2-4,6,8-9,11,16,21,23H,5,7,10,32H2,1H3/t16-,21+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.140	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The conditions for measuring inhibitory activity of compounds against LSD1 activity were determined with reference to a document available from the w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NC6513
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM456449 (US10723742, Example 175 | US10723742, Example 185 ...) Show SMILES Cn1nnc2cc(c(F)c(F)c12)-c1ccc(cc1-c1ccc(C#N)c(F)c1)C(=O)N1[C@@H]2CC[C@H]1[C@@H](N)C2 |TLB:35:34:32.31:29| Show InChI InChI=1S/C27H21F3N6O/c1-35-26-22(33-34-35)11-19(24(29)25(26)30)17-6-4-14(27(37)36-16-5-7-23(36)21(32)10-16)8-18(17)13-2-3-15(12-31)20(28)9-13/h2-4,6,8-9,11,16,21,23H,5,7,10,32H2,1H3/t16-,21+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.330	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The conditions for measuring inhibitory activity of compounds against LSD1 activity were determined with reference to a document available from the w...				Citation and Details BindingDB Entry DOI: 10.7270/Q2NC6513
					More data for this Ligand-Target Pair
Lysine-specific histone demethylase 1A (Homo sapiens (Human))	BDBM456449 (US10723742, Example 175 | US10723742, Example 185 ...) Show SMILES Cn1nnc2cc(c(F)c(F)c12)-c1ccc(cc1-c1ccc(C#N)c(F)c1)C(=O)N1[C@@H]2CC[C@H]1[C@@H](N)C2 |TLB:35:34:32.31:29| Show InChI InChI=1S/C27H21F3N6O/c1-35-26-22(33-34-35)11-19(24(29)25(26)30)17-6-4-14(27(37)36-16-5-7-23(36)21(32)10-16)8-18(17)13-2-3-15(12-31)20(28)9-13/h2-4,6,8-9,11,16,21,23H,5,7,10,32H2,1H3/t16-,21+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.330	n/a	n/a	n/a	n/a	n/a	n/a
Taiho Pharmaceutical Co., Ltd. US Patent					Assay Description The conditions for measuring inhibitory activity of compounds against LSD1 activity were determined with reference to a document available from the w...				US Patent US10723742 (2020) BindingDB Entry DOI: 10.7270/Q2TF01DB
					More data for this Ligand-Target Pair