BDBM50274441 1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-ethanone::CHEMBL483770

SMILES: CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O

InChI Key: InChIKey=KFTALYXDAWXLJE-UHFFFAOYSA-N

Data: 7 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 7 hits for monomerid = 50274441   

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
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of human sPLA2 group 2A				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Mus musculus)	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	KEGG UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse sPLA2 group 2A				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Phospholipase A2 group IIA (Rattus norvegicus)	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of rat sPLA2 group 2A				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Group X secretory phospholipase A2 (Mus musculus)	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse sPLA2 group 10				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Phospholipase A2 group V (Mus musculus)	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse sPLA2 group 5				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Group X secretory phospholipase A2 (Homo sapiens (Human))	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of human sPLA2 group 10				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair
Secretory phospholipase A2, group V (sPLA2-V) (Homo sapiens (Human))	BDBM50274441 (1-(3-Acetyl-5-dodecyl-2,4,6-trihydroxy-phenyl)-eth...) Show SMILES CCCCCCCCCCCCc1c(O)c(C(C)=O)c(O)c(C(C)=O)c1O Show InChI InChI=1S/C22H34O5/c1-4-5-6-7-8-9-10-11-12-13-14-17-20(25)18(15(2)23)22(27)19(16(3)24)21(17)26/h25-27H,4-14H2,1-3H3	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of human sPLA2 group 5				Bioorg Med Chem Lett 18: 5415-9 (2008) Article DOI: 10.1016/j.bmcl.2008.09.041 BindingDB Entry DOI: 10.7270/Q2CJ8DB1
					More data for this Ligand-Target Pair