null

SMILES: CCOC(=O)C[C@H](C[C@]1(C)C2CC[C@]3(C)C(CCC3C2CCC1=O)C(C)CCCC(C)C)C(O)=O

InChI Key: InChIKey=SVZKSTLFKNEAPQ-PFTDNVHHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50067836   

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
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha (Homo sapiens (Human))	BDBM50067836 ((S)-2-[(3aR,6R)-3-(1,5-Dimethyl-hexyl)-3a,6-dimeth...) Show SMILES CCOC(=O)C[C@H](C[C@]1(C)C2CC[C@]3(C)C(CCC3C2CCC1=O)C(C)CCCC(C)C)C(O)=O Show InChI InChI=1S/C30H50O5/c1-7-35-27(32)17-21(28(33)34)18-30(6)25-15-16-29(5)23(20(4)10-8-9-19(2)3)12-13-24(29)22(25)11-14-26(30)31/h19-25H,7-18H2,1-6H3,(H,33,34)/t20?,21-,22?,23?,24?,25?,29-,30-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	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
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human Farnesyltransferase				J Med Chem 41: 4492-501 (1998) Article DOI: 10.1021/jm980356+ BindingDB Entry DOI: 10.7270/Q23779DQ
					More data for this Ligand-Target Pair