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Maryam Shekarchi

Researcher at Tehran University of Medical Sciences

Publications -  56
Citations -  914

Maryam Shekarchi is an academic researcher from Tehran University of Medical Sciences. The author has contributed to research in topics: Detection limit & Molecularly imprinted polymer. The author has an hindex of 13, co-authored 51 publications receiving 751 citations. Previous affiliations of Maryam Shekarchi include University of Tehran.

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Comparative study of rosmarinic acid content in some plants of Labiatae family.

TL;DR: RA content in different species of Labiatae was 0.0-58.5 mg g-1 of dried plants and the highest amount of RA was found in Mentha species especially M. spicata, which can be considered as a new source of rosmarinic acid.
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A validated high performance liquid chromatography method for the analysis of thymol and carvacrol in Thymus vulgaris L. volatile oil

TL;DR: A validated and reliable high performance liquid chromatography (HPLC) method has been developed for the analysis of these two components in T. vulgaris essential oil and they showed good agreement.
Journal Article

Investigating the synergistic antioxidant effects of some flavonoid and phenolic compounds

TL;DR: In this paper, the synergistic antioxidant effects of four phenolic compounds including rutin and quercetin have been investigated by FRAP (Ferric Reducing Antioxidant Power) method, and the results showed that combination of gallic acid and caffeic acid demonstrated considerable synergistic effects (137.8%) while other combinations were less potent.
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A validated method for analysis of Swerchirin in Swertia longifolia Boiss. by high performance liquid chromatography.

TL;DR: The analytical method was validated for Swerchirin as one of the most important components of the plant, with more pharmacological activities according to the validation parameters, such as, selectivity, linearity, precision, and accuracy.
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Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran-2(3H)-ylidene) methyl) pyridinium derivatives.

TL;DR: A novel series of benzofuranone-ylidene-methyl benzylpyridinium derivatives (6a-u) were synthesized as acetylcholinesterase inhibitors and it was revealed that some synthesized compounds exhibited high anticholineterase activity, among them compound 6b was the most active compound.