null

SMILES: [H][C@]12C=C(C)[C@@]3([H])\C(C)=C\CC\C(C)=C\[C@]4([H])C=C([C@H](C)C[C@]44OC(=O)C(=C4O)C(=O)[C@@]3(C)[C@]1([H])[C@@H](C)CC[C@@H]2O[C@@H]1O[C@H](C)[C@@H](O)[C@@H](O)[C@H]1OC(=O)c1c(C)cc(OC)cc1O)C(O)=O

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50600667   

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
Cholesterol side-chain cleavage enzyme, mitochondrial (Rattus norvegicus)	BDBM50600667 (CHEMBL5180164) Show SMILES [H][C@]12C=C(C)[C@@]3([H])\C(C)=C\CC\C(C)=C\[C@]4([H])C=C([C@H](C)C[C@]44OC(=O)C(=C4O)C(=O)[C@@]3(C)[C@]1([H])[C@@H](C)CC[C@@H]2O[C@@H]1O[C@H](C)[C@@H](O)[C@@H](O)[C@H]1OC(=O)c1c(C)cc(OC)cc1O)C(O)=O |r,c:17,27,t:2,8,13| Show InChI	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jnatprod.2c00444 BindingDB Entry DOI: 10.7270/Q2H9997N
					More data for this Ligand-Target Pair