Tommonaro_2015_J.Enzyme.Inhib.Med.Chem_30_333

Reference

Title : Further in vitro biological activity evaluation of amino-, thio- and ester-derivatives of avarol - Tommonaro_2015_J.Enzyme.Inhib.Med.Chem_30_333
Author(s) : Tommonaro G , Pejin B , Iodice C , Tafuto A , De Rosa S
Ref : J Enzyme Inhib Med Chem , 30 :333 , 2015
Abstract :

The acetylcholinesterase inhibitory and/or antitumour activities of amino-, thio- and ester-derivatives of avarol selected were evaluated for the first time at in vitro conditions. Avarol-3',4'-dithioglycol (1) and avarol-4'-(3)mercaptopropionic acid (3) were shown to be the best inhibitors of the enzyme tested (0.50 microg and IC50 0.05 mM and 0.50 microg and IC50 0.12 mM, respectively), while 4'-tryptamine-avarone (9) and avarol-3'-(3)mercaptopropionic acid (2) exhibited the highest cytotoxicity against the human breast T-47D cancer cell line (IC50 0.66 microg/mL and 1.25 microg/mL, respectively). According to experimental data obtained, the sesquiterpenoid hydroquinone structure of bioactive avarol derivatives may inspire development of new pharmacologically useful substances to be used in the treatment of Alzheimer's disease and/or human breast tumour.

PubMedSearch : Tommonaro_2015_J.Enzyme.Inhib.Med.Chem_30_333
PubMedID: 24939096

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Citations formats

Tommonaro G, Pejin B, Iodice C, Tafuto A, De Rosa S (2015)
Further in vitro biological activity evaluation of amino-, thio- and ester-derivatives of avarol
J Enzyme Inhib Med Chem 30 :333

Tommonaro G, Pejin B, Iodice C, Tafuto A, De Rosa S (2015)
J Enzyme Inhib Med Chem 30 :333