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Inhibitor Report for: 3-butyl-6-benzyloxyphthalide-Mannich-base-7d

3-butyl-6-benzyloxyphthalide Mannich base derivative 7d was the most potent agent with excellent inhibitory activities on EeAChE (IC50 = 0.087 micoM), HuAChE (IC50 = 0.041 microM) and MAO-B (IC50 = 0.30 microM)


General
Type Monoamine-oxidase-inhibitor, Multitarget, Piperidine, Benzofuran
Chemical_Nomenclature 3-butyl-6-((3'-hydroxy-4'-(piperidin-1-ylmethyl)benzyl)oxy)isobenzofuran-1(3H)-one
Canonical SMILES C1=CC(=CC(=C1CN2CCCCC2)O[H])COC3=CC=C4C(=C3)C(OC4CCCC)=O
InChI InChI=1S/C26H33NO4/c1-3-4-8-24-22-12-11-21(16-23(22)26(28)31-24)30-18-19-9-10-20(25(15-19)29-2)17-27-13-6-5-7-14-27/h9-12,15-16,24H,3-8,13-14,17-18H2,1-2H3
InChIKey KAFBBPBROARMRS-UHFFFAOYSA-N
Other name(s)
________________________________________________________________________________________________
MW|409.52
Formula|C25H31NO4
CAS_number|
PubChem|
UniChem|KAFBBPBROARMRS-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | 3-butyl-6-benzyloxyphthalide-Mannich-base-7d ligand of proteins in family: ACHE
Protein | human-ACHE

References:
Search PubMed for references concerning: 3-butyl-6-benzyloxyphthalide-Mannich-base-7d
    Title: Discovery of novel 3-butyl-6-benzyloxyphthalide Mannich base derivatives as multifunctional agents against Alzheimer's disease
    Liu Z, Shi Y, Zhang X, Yu G, Li J, Cong S, Deng Y
    Ref: Bioorganic & Medicinal Chemistry, 58:116660, 2022 : PubMed