null

SMILES: [H][C@@]12CC[C@@]3(C)CC4=CC(=O)[C@@]5([H])[C@@](C)(CO)[C@H](O)CC[C@]5(C)[C@@]4([H])CC[C@]3([H])[C@@]1(C)CC[C@H](O)[C@]2(C)C(O)=O

InChI Key: InChIKey=BATRMLNFDUPFQV-MTFRJUANSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50092534   

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
Acetylcholinesterase (Homo sapiens (Human))	BDBM50092534 (CHEMBL3586202) Show SMILES [H][C@@]12CC[C@@]3(C)CC4=CC(=O)[C@@]5([H])[C@@](C)(CO)[C@H](O)CC[C@]5(C)[C@@]4([H])CC[C@]3([H])[C@@]1(C)CC[C@H](O)[C@]2(C)C(O)=O |r,t:7| Show InChI InChI=1S/C30H46O6/c1-26-11-8-21-28(3,13-10-23(34)30(21,5)25(35)36)20(26)7-6-18-17(15-26)14-19(32)24-27(18,2)12-9-22(33)29(24,4)16-31/h14,18,20-24,31,33-34H,6-13,15-16H2,1-5H3,(H,35,36)/t18-,20-,21+,22+,23-,24+,26-,27+,28+,29-,30+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Catholic University of Daegu Curated by ChEMBL					Assay Description Inhibition of AChE (unknown origin) using acetylthiocholine as substrate assessed as substrate hydrolysis by spectrophotometric/Ellman method				Bioorg Med Chem 23: 3126-34 (2015) Article DOI: 10.1016/j.bmc.2015.04.080 BindingDB Entry DOI: 10.7270/Q24X59JZ
					More data for this Ligand-Target Pair
Beta-secretase 1 (Homo sapiens (Human))	BDBM50092534 (CHEMBL3586202) Show SMILES [H][C@@]12CC[C@@]3(C)CC4=CC(=O)[C@@]5([H])[C@@](C)(CO)[C@H](O)CC[C@]5(C)[C@@]4([H])CC[C@]3([H])[C@@]1(C)CC[C@H](O)[C@]2(C)C(O)=O |r,t:7| Show InChI InChI=1S/C30H46O6/c1-26-11-8-21-28(3,13-10-23(34)30(21,5)25(35)36)20(26)7-6-18-17(15-26)14-19(32)24-27(18,2)12-9-22(33)29(24,4)16-31/h14,18,20-24,31,33-34H,6-13,15-16H2,1-5H3,(H,35,36)/t18-,20-,21+,22+,23-,24+,26-,27+,28+,29-,30+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Catholic University of Daegu Curated by ChEMBL					Assay Description Inhibition of human recombinant BACE1 by fluorescence resonance energy transfer (FRET) assay				Bioorg Med Chem 23: 3126-34 (2015) Article DOI: 10.1016/j.bmc.2015.04.080 BindingDB Entry DOI: 10.7270/Q24X59JZ
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50092534 (CHEMBL3586202) Show SMILES [H][C@@]12CC[C@@]3(C)CC4=CC(=O)[C@@]5([H])[C@@](C)(CO)[C@H](O)CC[C@]5(C)[C@@]4([H])CC[C@]3([H])[C@@]1(C)CC[C@H](O)[C@]2(C)C(O)=O |r,t:7| Show InChI InChI=1S/C30H46O6/c1-26-11-8-21-28(3,13-10-23(34)30(21,5)25(35)36)20(26)7-6-18-17(15-26)14-19(32)24-27(18,2)12-9-22(33)29(24,4)16-31/h14,18,20-24,31,33-34H,6-13,15-16H2,1-5H3,(H,35,36)/t18-,20-,21+,22+,23-,24+,26-,27+,28+,29-,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Catholic University of Daegu Curated by ChEMBL					Assay Description Inhibition of BChE (unknown origin) using butyrylthiocholine as substrate assessed as substrate hydrolysis by spectrophotometric/Ellman method				Bioorg Med Chem 23: 3126-34 (2015) Article DOI: 10.1016/j.bmc.2015.04.080 BindingDB Entry DOI: 10.7270/Q24X59JZ
					More data for this Ligand-Target Pair