electrochemical synthesis of novel 1,3-indandione derivatives and evaluation of their antiplatelet aggregation activities

نویسندگان

salimeh amidi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

farzad kobarfard 1- department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. 2- phytochemistry research center, shahid beheshti university of medical sciences, tehran, iran.

abdolmajid bayandori moghaddam department of engineering science, college of engineering, university of tehran, p.o. box 11155-4563, tehran, iran.

kimia tabib department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

چکیده

electrochemical oxidation of some selected catechol derivatives, using cyclic voltammetry, in the presence of different 2-aryl-1,3-indandiones as nucleophiles, resulted in electrochemical synthesis of new 1,3- indandione derivatives in an undivided cell in good yield and purity. a michael addition mechanism was proposed for the formation of the analogs based on the reaction conditions which were provided in electrochemical cell. the in-vitro antiplatelet and anticoagulant activity of these compounds was evaluated, using arachidonic acid (aa) and adenosine diphosphate (adp) as the platelet aggregation inducers. the results show that the incorporation of catechol ring in 1,3-indandione nucleus leads to the emergence of antiplatelet aggregation activity in these compounds. the compounds may exert their antiaggregation activity by interfering with the arachidonic acid pathway.

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Electrochemical Synthesis of Novel 1,3-Indandione Derivatives and Evaluation of Their Antiplatelet Aggregation Activities

Electrochemical oxidation of some selected catechol derivatives, using cyclic voltammetry, in the presence of different 2-aryl-1,3-indandiones as nucleophiles, resulted in electrochemical synthesis of new 1,3- indandione derivatives in an undivided cell in good yield and purity. A Michael addition mechanism was proposed for the formation of the analogs based on the reaction conditions which wer...

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Electrochemical Synthesis of Novel 1,3-Indandione Derivatives and Evaluation of Their Antiplatelet Aggregation Activities

Electrochemical oxidation of some selected catechol derivatives, using cyclic voltammetry, in the presence of different 2-aryl-1,3-indandiones as nucleophiles, resulted in electrochemical synthesis of new 1,3- indandione derivatives in an undivided cell in good yield and purity. A Michael addition mechanism was proposed for the formation of the analogs based on the reaction conditions which wer...

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Electrochemical Synthesis of Novel 1,3-Indandione Derivatives and Evaluation of Their Antiplatelet Aggregation Activities

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عنوان ژورنال:
the iranian journal of pharmaceutical research

جلد ۱۲، شماره Supplement، صفحات ۹۱-۱۰۳

کلمات کلیدی
[ ' e l e c t r o c h e m i c a l s y n t h e s i s ' , 1 , 3 , ' i n d a n d i o n e ' , ' p l a t e l e t a g g r e g a t i o n i n h i b i t i o n ' ]

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