Uzma Salar

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2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study.

A. Wadood, K. Khan, M. Taha, 2018, European journal of medicinal chemistry.

Aryl hydrazones linked thiazolyl coumarin hybrids as potential urease inhibitors

Zaheer Ul-Haq, M. Lodhi, K. Khan, 2021, Journal of the Iranian Chemical Society.

1-[(4'-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies.

A. Wadood, K. Khan, Muhammad Riaz, 2018, Bioorganic chemistry.

Diversified Thiazole Substituted Coumarins and Chromones as Non- Cytotoxic ROS and NO Inhibitors

A. Jabeen, K. Khan, S. Perveen, 2020 .

Synthesis, in vitro $$\alpha $$α-glucosidase inhibitory activity, and in silico study of (E)-thiosemicarbazones and (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives

A. Wadood, K. Khan, Muhammad Riaz, 2018, Molecular Diversity.

Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs.

H. Ullah, N. Ismail, A. Wadood, 2016, Bioorganic chemistry.

Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors

N. Ismail, F. Rahim, K. Khan, 2015, Medicinal Chemistry Research.

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

N. Ismail, A. Wadood, K. Khan, 2017, European journal of medicinal chemistry.

WITHDRAWN: 2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors

M. Choudhary, S. Saad, K. Khan, 2014 .

Evaluation of synthetic 2-aryl quinoxaline derivatives as α-amylase, α-glucosidase, acetylcholinesterase, and butyrylcholinesterase inhibitors.

P. Taslimi, F. Saleem, K. Khan, 2022, International journal of biological macromolecules.

2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.

S. T. Moin, M. Choudhary, S. Saad, 2015, Bioorganic & medicinal chemistry.

Synthesis, in vitro, and in silico studies of newly functionalized quinazolinone analogs for the identification of potent α-glucosidase inhibitors

B. Larijani, M. Faramarzi, Ayaz Anwar, 2021, Journal of the Iranian Chemical Society.

New Hybrid Hydrazinyl Thiazole Substituted Chromones: As Potential α-Amylase Inhibitors and Radical (DPPH & ABTS) Scavengers

A. Wadood, K. Khan, S. Vijayabalan, 2017, Scientific Reports.

Coumarin and Biscoumarin Inhibit in Vitro Obesity Model

M. Choudhary, K. Khan, A. Ejaz, 2016 .

Discovery of New N-hydrazinecarbothioamide Indazole Hybrids: As Potential Radical (ABTS and DPPH) Scavengers

K. Khan, S. Perveen, Arshia, 2020 .

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies.

N. Ismail, F. Rahim, K. Khan, 2016, Bioorganic chemistry.

Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.

N. Ismail, K. Khan, M. Taha, 2017, Bioorganic chemistry.

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

Qurat-Ul-Ain, N. Ismail, A. Wadood, 2017, European journal of medicinal chemistry.

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

N. Ismail, A. Wadood, K. Khan, 2016, Bioorganic & medicinal chemistry.

Atenolol thiourea hybrid as potent urease inhibitors: Design, biology-oriented drug synthesis, inhibitory activity screening, and molecular docking studies.

A. Wadood, K. Khan, Muhammad Ali Versiani, 2019, Bioorganic chemistry.

Synthesis, in vitro urease inhibitory activity, and molecular docking studies of thiourea and urea derivatives.

F. Begum, K. Khan, S. Perveen, 2018, Bioorganic chemistry.