BDBM50348375 CHEMBL1800374

SMILES: Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1

InChI Key: InChIKey=QMAHTCRPGFEJOU-UHFFFAOYSA-N

Data: 9 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50348375   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Histone deacetylase 5 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC5 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 4 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC4 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Cereblon/Histone deacetylase 6 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC6 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 7 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC7 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 3 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC3 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 9 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC9 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC1 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC2 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50348375 (CHEMBL1800374) Show SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc(cc2)C(C)(C)C)n1 Show InChI InChI=1S/C17H20N2O2S/c1-11-9-15(21)19-16(18-11)22-10-14(20)12-5-7-13(8-6-12)17(2,3)4/h5-9H,10H2,1-4H3,(H,18,19,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
Broad Institute of Harvard and MIT Curated by ChEMBL					Assay Description Inhibition of recombinant HDAC8 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assay				Bioorg Med Chem Lett 21: 4164-9 (2011) Article DOI: 10.1016/j.bmcl.2011.05.098 BindingDB Entry DOI: 10.7270/Q20P10CT
					More data for this Ligand-Target Pair