null

SMILES: CCCCCCCCN=C(P(O)(O)O)P(O)(O)=O

InChI Key: InChIKey=UEQBZXDRWMGPJW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50113288   

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
Polyprenyl synthetase family protein (Plasmodium falciparum (isolate 3D7))	BDBM50113288 ((Octylamino-phosphono-methyl)-phosphonic acid | (o...) Show SMILES CCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:8.7| Show InChI InChI=1S/C9H23NO6P2/c1-2-3-4-5-6-7-8-10-9(17(11,12)13)18(14,15)16/h11-13,17H,2-8H2,1H3,(H2,14,15,16)	PDB KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.06E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Urbana-Champaign Curated by ChEMBL					Assay Description Inhibitory activity against Leishmania major Farnesyl diphosphate synthase				J Med Chem 47: 175-87 (2003) Article DOI: 10.1021/jm030084x BindingDB Entry DOI: 10.7270/Q2FN15N5
					More data for this Ligand-Target Pair
Geranylgeranyl pyrophosphate synthase (Homo sapiens (Human))	BDBM50113288 ((Octylamino-phosphono-methyl)-phosphonic acid | (o...) Show SMILES CCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:8.7| Show InChI InChI=1S/C9H23NO6P2/c1-2-3-4-5-6-7-8-10-9(17(11,12)13)18(14,15)16/h11-13,17H,2-8H2,1H3,(H2,14,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Illinois at Urbana-Champaign Curated by ChEMBL					Assay Description Inhibitory activity against the human recombinant geranylgeranyl diphosphate synthase (GGPPSase).				J Med Chem 45: 2185-96 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MN1
					More data for this Ligand-Target Pair