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Mariya al-Rashida

Researcher at Forman Christian College

Publications -  85
Citations -  1586

Mariya al-Rashida is an academic researcher from Forman Christian College. The author has contributed to research in topics: Carbonic anhydrase & Docking (molecular). The author has an hindex of 16, co-authored 78 publications receiving 939 citations. Previous affiliations of Mariya al-Rashida include University of the Punjab & COMSATS Institute of Information Technology.

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Schiff bases in medicinal chemistry: a patent review (2010-2015).

TL;DR: This review aims to provide a comprehensive overview of the various patented therapeutic applications of Schiff bases and their metal complexes from 2010 to 2015 and has been used to coordinate almost all d-block metals as well as lanthanides.
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Quinazoline and quinazolinone as important medicinal scaffolds: a comparative patent review (2011-2016).

TL;DR: This review covers recent efforts in the synthesis and biological screening of quinazoline/quinazolinone based compounds from 2011–2016, and focuses on the promising anticancer activity of qu inazoline and quinzolinone containing compounds.
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Therapeutic potentials of ecto-nucleoside triphosphate diphosphohydrolase, ecto-nucleotide pyrophosphatase/phosphodiesterase, ecto-5'-nucleotidase, and alkaline phosphatase inhibitors.

TL;DR: Most recent and significant advances in field of NTPDase, NPP, AP, and e5NT inhibitors is being discussed in detail in anticipation of providing prolific leads and relevant background for research groups interested in synthesis of selective ecto‐nucleotidase inhibitors.
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Multicomponent reactions (MCR) in medicinal chemistry: a patent review (2010-2020).

TL;DR: Application of MCRs is the recent advancement in the field of drug design and discovery which will expectedly lead to the development of medicinally important heterocyclic compounds with a vast range of biological activities.
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In search of new α-glucosidase inhibitors: Imidazolylpyrazole derivatives.

TL;DR: In this paper, a series of imidazolyl pyrazoles (2a-2k) were synthesized in good to excellent yields from a mixture of three precursors: aryl(hetaryl)pyrazole-4-carbaldehydes (1a-1k), benzil and ammonium acetate.