127729-01-5Relevant academic research and scientific papers
Synthesis, antitumour activities and molecular docking of thiocarboxylic acid ester-based NSAID scaffolds: COX-2 inhibition and mechanistic studies
El-Azab, Adel S.,Abdel-Aziz, Alaa A.-M.,Abou-Zeid, Laila A.,El-Husseiny, Walaa M.,ElMorsy, Ahmad M.,El-Gendy, Manal A.,El-Sayed, Magda A.-A.
, p. 989 - 998 (2018)
A new series of NSAID thioesters were synthesized and evaluated for their in vitro antitumor effects against a panel of four human tumor cell lines, namely: HepG2, MCF-7, HCT-116 and Caco-2, using the MTT assay. Compared to the reference drugs 5-FU, afati
Enzymatic resolution of (RS)-2-arylpropionic acid thioesters by Candida rugosa lipase-catalyzed thiotransesterification or hydrolysis in organic solvents
Chang, Chun-Sheng,Tsai, Shau-Wei,Lin, Chun-Nan
, p. 2799 - 2807 (1998)
An enzymatic resolution process was developed to produce (S)-naproxen ester, (S)-naproxen or (S)-ibuprofen from the corresponding racemic thioesters by using lipase-catalyzed thiotransesterification or hydrolysis in organic solvents. Enzyme activity is greatly enhanced when activated naproxen thioesters containing an electron-withdrawing group are the substrates. Unlike other lipases, Candida rugosa lipase may discern the sulfur moiety of the thioesters, and yields lower enzyme activity when compared to the corresponding oxygen-containing analogues. Enzyme performances were further compared under various conditions, i.e. different combinations of reaction type (thiotransesterification or hydrolysis), solvent (isooctane or cyclohexane), substrate (naproxen or ibuprofen thioesters) and lipase sources.
A new mild method for the synthesis of esters and benzenethiol esters by activation of pyridine-2-thiol or benzothiazol-2-thiol esters by methyl iodide
Ravi,Mereyala
, p. 6089 - 6090 (2007/10/02)
Activation of in-situ generated pyridine-2-thiol or benzothiazol-2-thiol esters by methyl iodide at room temperature in presence of alcohols and benzenethiol yields the corresponding esters and thiol esters.
