Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 43854   

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
Glycylpeptide N-tetradecanoyltransferase (Candida albicans (Yeast))	BDBM43854 (2-[(veratroylhydrazono)methyl]benzoic acid | 2-[[(...) Show SMILES COc1ccc(cc1OC)C(=O)NN=Cc1ccccc1C(O)=O |w:13.13| Show InChI InChI=1S/C17H16N2O5/c1-23-14-8-7-11(9-15(14)24-2)16(20)19-18-10-12-5-3-4-6-13(12)17(21)22/h3-10H,1-2H3,(H,19,20)(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	250	n/a	830	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Roche Research Center					Assay Description Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...				Chem Biol 9: 1119-28 (2002) Article DOI: 10.1016/S1074-5521(02)00240-5 BindingDB Entry DOI: 10.7270/Q2BV7F0C
					More data for this Ligand-Target Pair
DNA repair protein RAD51 homolog 1 (Homo sapiens (Human))	BDBM43854 (2-[(veratroylhydrazono)methyl]benzoic acid | 2-[[(...) Show SMILES COc1ccc(cc1OC)C(=O)NN=Cc1ccccc1C(O)=O |w:13.13| Show InChI InChI=1S/C17H16N2O5/c1-23-14-8-7-11(9-15(14)24-2)16(20)19-18-10-12-5-3-4-6-13(12)17(21)22/h3-10H,1-2H3,(H,19,20)(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	PCBioAssay	n/a	n/a	5.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
PCMD Curated by PubChem BioAssay					Assay Description Project Title: A screen for modulators of human Rad51, a key DNA repair protein Application Number: MH084119 Assay Submitter: Dr. Alex Mazin Submitte...				PubChem Bioassay (2008) BindingDB Entry DOI: 10.7270/Q2QN6558
					More data for this Ligand-Target Pair
Glycylpeptide N-tetradecanoyltransferase 1 (Homo sapiens (Human))	BDBM43854 (2-[(veratroylhydrazono)methyl]benzoic acid | 2-[[(...) Show SMILES COc1ccc(cc1OC)C(=O)NN=Cc1ccccc1C(O)=O |w:13.13| Show InChI InChI=1S/C17H16N2O5/c1-23-14-8-7-11(9-15(14)24-2)16(20)19-18-10-12-5-3-4-6-13(12)17(21)22/h3-10H,1-2H3,(H,19,20)(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.40E+5	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Roche Research Center					Assay Description Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...				Chem Biol 9: 1119-28 (2002) Article DOI: 10.1016/S1074-5521(02)00240-5 BindingDB Entry DOI: 10.7270/Q2BV7F0C
					More data for this Ligand-Target Pair