Shazia Parveen

Dr. Shazia Parveen

Faculty of Science, Chemistry Department, Taibah University, Yanbu Branch, 46423, Yanbu, Saudi Arabia.
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 September 2012 in Journal of Photochemistry and Photobiology B: Biology
Verified
Journal Article
Closed access
FAFarukh Arjmand
Farukh Arjmand
SPShazia Parveen
Shazia Parveen
Mohd AfzalMohd Afzal
Mohd Afzal
MSMohd. Shahid
Mohd. Shahid

20 May 2020 in Applied Organometallic Chemistry
Verified
Journal Article
Closed access
PDF file
SPShazia Parveen
Shazia Parveen

1 March 2012 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
FAFarukh Arjmand
Farukh Arjmand
SPShazia Parveen
Shazia Parveen
Mohd AfzalMohd Afzal
Mohd Afzal
LTLoic Toupet
Loic Toupet
THTaibi Ben Hadda
Taibi Ben Hadda

8 August 2019 in RSC Advances
Verified
Journal Article
Open access
PDF file
SPShazia Parveen
Shazia Parveen
FAFarukh Arjmand
Farukh Arjmand
STSartaj Tabassum
Sartaj Tabassum
Polymer therapeutics encompasses polymer–drug conjugates that are nano-sized, multicomponent constructs already in the clinic as antitumor compounds, either as single agents or in combination with other organic drug scaffolds.


11 December 2019 in Journal of Biomolecular Structure and Dynamics
Verified
Journal Article
Closed access
RARua Alnoman
Rua Alnoman
SPShazia Parveen
Shazia Parveen
Mohamed E HagarMohamed E Hagar
Mohamed E Hagar
HAHoda A. Ahmed
Hoda A. Ahmed
JKJulian G. Knight
Julian G. Knight
A new chiral BODIPY–based fluorescent compound, 5‒bromo‒4,4‒difluoro‒3(S)‒1‒phenylethyl)amino)BODIPY, 4 was synthesized for biomedical applications. Optical, antimicrobial, antioxidant properties of the compound 4 are investigated. The partition coefficient suggested that the compound 4 has the potential to be developed as an active antibacterial and antioxidant candidate. In this context, antibacterial assay was carried out for compound 4 against various bacterial strains, revealing maximum inhibition zone (24 ± 2.19 mm) in Escherichia coli. Moreover, results of antioxidant activity of compound 4 revealed IC50 values to be greater than ascorbic acid. Molecular docking has given brief insight about the binding of the compound 4, suggesting that it has a strong potential to inhibit bacterial target enzymes viz., DNA gyrase, enzymes in the type II fatty acid synthesis and Ddl (D‒alanine:D‒alanine ligase) in peptidoglycan synthesis. The molecular geometry and electrostatic potential of compound 4, was established by DFT (Density Functional Theory) calculations.