flavonol glycosides from euphorbia microsciadia bioss. with their immunomodulatory activities

Authors

sayyed mustafa ghannadian isfahan pharmaceutical sciences research center, isfahan university of medical sciences, isfahan, iran.sfahan pharmaceutical sciences research center, isfahan university of medical sciences, isfahan, iran.

abdul majid ayatollahi school of pharmacy and phytochemistry research centre, shahid beheshti university of medical sciences, tehran, iran.

suleiman afsharypour faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran.

sumaira hareem dr. panjwani center for molecular medicine and drug research, sciences, university of karachi, karachi-75270, pakistan.

abstract

four known flavonoids: quercetin 3-o-β-d-rutinoside (q3rut), myricetin 3-o-β-d-galactopyranoside (m3gal), quercetin 3-o-β-d-galactopyranoside (q3gal) and quercetin 3-o-β-d-glucopyranoside (q3glc), for the first time were isolated from aerial parts of euphorbia microsciadia. the chemical structure of them was elucidated on the basis of 1 and 2 d-nmr spectra and different spectroscopic techniques. the immunomodulatory activities of isolated compounds were compared using standard t-cell proliferation assay. these data showed that lymphocyte suppression activity of flavonoids (1-4) were comparatively lower than prednisolon as a standard drug. immunosuppressive activity of flavonoids with hydroxyl groups at both 3′-and 4′-positions in their b-ring (q3gal) were more than those with 3′-,4′-and 5′-hydroxyl substitution (m3gal). in these compounds, q3gal showed the most inhibitory activity, whereas m3gal showed the least lymphocyte antiprolifeartive activity.

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Journal title:
the iranian journal of pharmaceutical research

جلد ۱۱، شماره ۳، صفحات ۹۲۵-۹۳۰

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