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Umer Rashid

Researcher at Universiti Putra Malaysia

Publications -  410
Citations -  14133

Umer Rashid is an academic researcher from Universiti Putra Malaysia. The author has contributed to research in topics: Catalysis & Biodiesel. The author has an hindex of 51, co-authored 381 publications receiving 10081 citations. Previous affiliations of Umer Rashid include University of Gujrat & Universiti Teknologi Petronas.

Papers
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Synthesis, pharmacological evaluation and Molecular modelling studies of pregnenolone derivatives as inhibitors of human dihydrofolate reductase.

Muhammad Bilal Tufail, +7 more
- 01 Apr 2021 - 
TL;DR: In this paper, a base-catalyzed Claisen-Schmidt condensation reaction was used to synthesize chalcone derivatives of pregnenolone by cyclization reaction.
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Crude extract and isolated bioactive compounds from Notholirion thomsonianum (Royale) Stapf as multitargets antidiabetic agents: in-vitro and molecular docking approaches.

Mater H. Mahnashi, +8 more
TL;DR: In this paper, Notholirion thomsonianum extracts were evaluated for α-glucosidase, α-amylase and antioxidant activities and the structures of isolated compounds were confirmed with NMR and MS analyses.
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Characterization of newly synthesized ZrFe 2 O 5 nanomaterial and investigations of its tremendous photocatalytic properties under visible light irradiation

Shaukat Ali Shahid, +6 more
- 01 Jan 2013 - 
TL;DR: In this paper, high functional ZrFe2O5 nanoparticles were synthesized using coprecipitation technique and the chemical composition of nanomaterials was studied by energy-dispersive X-ray (EDX).
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Organotin (IV) based complexes as promiscuous antibacterials: Synthesis, in vitro, in silico pharmacokinetic and docking studies

Wajid Rehman, +9 more
- 15 Sep 2014 - 
TL;DR: Among various synthesized organotin (IV) complexes, compound 5 was found as potent antibacterial agent against various bacterial strains as well as in silico binding to different antibacterial targets.
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2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies.

Muhammad Taha, +8 more
- 01 Oct 2019 - 
TL;DR: Thiadiazole derivatives synthesized from methyl 4-methoxybenzoate via hydrazide and thio-hydrazide intermediates evaluated for their potential against β-glucuronidase enzyme exhibited superior activity potential than the standard d-saccharic acid-1,4-lactone.