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Muhammad A. Rashid

Researcher at University of Karachi

Publications -  83
Citations -  845

Muhammad A. Rashid is an academic researcher from University of Karachi. The author has contributed to research in topics: Biology & Medicine. The author has an hindex of 15, co-authored 63 publications receiving 622 citations. Previous affiliations of Muhammad A. Rashid include University of Agriculture, Faisalabad & University of Burgos.

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Antioxidant, antimicrobial, antitumor, and cytotoxic activities of an important medicinal plant (Euphorbia royleana) from Pakistan.

Aisha Ashraf, +3 more
- 01 Mar 2015 - 
TL;DR: Investigation of extracts of fresh Euphorbia royleana found that investigated extracts have potential for isolation of antioxidant and antimicrobial compounds for the pharmaceutical industry.
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Fine Tuning the Optoelectronic Properties of Triphenylamine Based Donor Molecules for Organic Solar Cells

Muhammad Adnan, +7 more
- 27 Jun 2017 - 
TL;DR: In this paper, the electron donor materials M1-M3 (for organic solar cells) and diphenylamine (DPA) were used for the first time in a solar cell.
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Chemical composition, antioxidant, antitumor, anticancer and cytotoxic effects of Psidium guajava leaf extracts.

Aisha Ashraf, +5 more
- 03 Feb 2016 - 
TL;DR: The present study demonstrates that P. guajava leaf extracts play a substantial role against cancer and down-modulate inflammatory nuclear factor kB.
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Thermodynamic solution properties of pefloxacin mesylate and its interactions with organized assemblies of anionic surfactant, sodium dodecyl sulphate

Muhammad Usman, +4 more
- 10 Dec 2013 - 
TL;DR: The physicochemical behavior of antibiotic amphiphilic drug pefloxacin mesylate (PFM) and its interaction with anionic surfactant, sodium dodecyl sulfate (SDS) was reported in this paper.
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Straightforward Synthesis of Dihydrobenzo[a]fluorenes through Au(I)-Catalyzed Formal [3 + 3] Cycloadditions

Patricia García-García, +4 more
- 31 Aug 2012 - 
TL;DR: Dihydrobenzo[a]fluorene derivatives have been prepared by a formal intramolecular [3 + 3] cycloaddition of o-alkynylstyrenes bearing a secondary alkyl group at the β-position of the styrene moiety.