Muhammad Ali

发表

Evaluation of the thiazole Schiff bases as β\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upbeta $$\end{document}-g

M. Choudhary, Sajid Mansoor, K. Khan, 2014, Molecular Diversity.

Synergy of synthesis, computation and NMR reveals correct baulamycin structures

C. Butts, V. Aggarwal, Jingjing Wu, 2017, Nature.

Identification of the potential type 2 diabetes susceptibility genetic elements in South Asian populations

S. Batool, N. M. Ashraf, Muhammad Ali, 2020 .

2,5-Disubstituted-1,3,4-oxadiazoles: thymidine phosphorylase inhibitors

M. Choudhary, K. Khan, N. Ambreen, 2013, Medicinal Chemistry Research.

Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.

H. Ullah, L. A. Al Muqarrabun, N. Ahmat, 2018, European journal of medicinal chemistry.

Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies.

H. Ullah, L. A. Al Muqarrabun, N. Ahmat, 2018, Bioorganic & medicinal chemistry.

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 of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies.

N. Ismail, F. Rahim, K. Khan, 2015, Bioorganic & medicinal chemistry.

Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.

N. Ismail, N. Ahmat, A. Wadood, 2015, Bioorganic & medicinal chemistry.

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

N. Ismail, M. Choudhary, A. Wadood, 2015, Bioorganic chemistry.

Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitors.

Zaheer-ul-Haq, M. Lodhi, M. Choudhary, 2011, Journal of molecular graphics & modelling.

Novel quinoline derivatives as potent in vitro α-glucosidase inhibitors: in silico studies and SAR predictions

A. Rehman, N. Ismail, A. Wadood, 2015 .

Penta-1,4-Diene-3-One Oxime Derivatives Strongly Inhibit the Replicase Domain of Tobacco Mosaic Virus: Elucidation Through Molecular Docking and Density Functional Theory Mechanistic Computations

Waqar Hussain, N. Rasool, Muhammad Ali, 2018 .

Novel thiosemicarbazide–oxadiazole hybrids as unprecedented inhibitors of yeast α-glucosidase and in silico binding analysis

N. Ismail, A. Wadood, F. Rahim, 2016 .

Syntheses, characterization, in vitro antiglycation and DPPH radical scavenging activities of isatin salicylhydrazidehydrazone and its Mn (II), Co (II), Ni (II), Cu (II), and Zn (II) metal complexes

M. Y. Khuhawar, Muhammad Ali, M. Taha, 2015 .

Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities.

N. Ismail, F. Rahim, K. Khan, 2014, European journal of medicinal chemistry.

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

N. Ismail, F. Rahim, K. Khan, 2017, Bioorganic chemistry.

2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies.

U. Rashid, A. Mosaddik, Muhammad Ali, 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.

Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases.

H. Ullah, Mohsan Nawaz, A. Wadood, 2016, Bioorganic chemistry.

Synthesis, in vitro and in silico screening of 2-amino-4-aryl-6-(phenylthio) pyridine-3,5-dicarbonitriles as novel α-glucosidase inhibitors.

B. Larijani, M. Faramarzi, A. Jabbar, 2020, Bioorganic chemistry.

Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: In vitro urease inhibition and molecular docking studies.

U. Rashid, T. Mahmood, H. Ullah, 2016, Bioorganic chemistry.

Development of bis-thiobarbiturates as successful urease inhibitors and their molecular modeling studies

M. Bilal, U. Rashid, H. Ullah, 2016 .

Biology-oriented drug synthesis (BIODS), in vitro urease inhibitory activity, and in silico studies on ibuprofen derivatives

Zaheer Ul-Haq, Ruqaiya Khalil, Ajmal Khan, 2020, Molecular diversity.

Biology-oriented drug synthesis (BIODS), in vitro urease inhibitory activity, and in silico studies on ibuprofen derivatives

Zaheer Ul-Haq, Ruqaiya Khalil, Ajmal Khan, 2020, Molecular Diversity.

Evaluation of the thiazole Schiff bases as $$\upbeta $$β-glucuronidase inhibitors and their in silico studies

M. Choudhary, Sajid Mansoor, K. Khan, 2014, Molecular Diversity.

Synthesis of bis-Schiff bases of isatins and their antiglycation activity.

M. Choudhary, Momin Khan, K. Khan, 2009, Bioorganic & medicinal chemistry.

Synthesis, SAR elucidations and molecular docking study of newly designed isatin based oxadiazole analogs as potent inhibitors of thymidine phosphorylase.

Mohsan Nawaz, A. Wadood, S. Shah, 2018, Bioorganic chemistry.

2,5-Disubstituted-1,3,4-oxadiazoles: thymidine phosphorylase inhibitors

M. Choudhary, K. Khan, N. Ambreen, 2013, Medicinal Chemistry Research.

Identification of potent urease inhibitors via ligand- and structure-based virtual screening and in vitro assays.

Shahnaz Perveen, Abdul Wadood, Zaheer Ul-Haq, 2010, Journal of molecular graphics & modelling.

3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies.

N. Ismail, A. Wadood, F. Rahim, 2017, Bioorganic chemistry.

5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study.

Sajda Ashraf, Zaheer Ul-Haq, M. Lodhi, 2018, Bioorganic chemistry.

Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.

N. Ismail, F. Rahim, K. Khan, 2017, European journal of medicinal chemistry.

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

N. Ismail, A. Wadood, F. Rahim, 2016, Bioorganic chemistry.

Effects of skeletal modifications of ciprofloxacin on antibacterial, antifungal and cytotoxic activities

K. Khan, N. Sultana, Muhammad Ali, 2007 .

Inhibition potential of phenyl linked benzimidazole-triazolothiadiazole modular hybrids against β-glucuronidase and their interactions thereof.

N. Uddin, F. Rahim, K. Khan, 2020, International journal of biological macromolecules.

Regio‐ and Stereoselective Homologation of 1,2‐Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3‐Diols and Sch 725674

V. Aggarwal, E. L. Myers, Muhammad Ali, 2016, Angewandte Chemie.

Synthesis, Evaluation of Antioxidant Activity and Crystal Structure of 2,4-Dimethylbenzoylhydrazones

N. Ismail, E. Hussain, Muhammad Ali, 2013, Molecules.

Synthesis, molecular structure, quantum mechanical studies and urease inhibition assay of two new isatin derived sulfonylhydrazides

A. M. Qureshi, Z. Iqbal, A. Asiri, 2017 .

Pharmacological importance of an ethnobotanical plant: Capsicum annuum L.

F. A. Khan, T. Mahmood, Muhammad Ali, 2014, Natural product research.

Synthesis of benzimidazole derivatives as potent inhibitors for α-amylase and their molecular docking study in management of type-II diabetes

N. Uddin, M. Bangesh, Fahad Khan, 2021, Journal of Molecular Structure.

Synthesis of a series of new 6-nitrobenzofuran-2-carbohydrazide derivatives with cytotoxic and antioxidant activity

S. Yeap, N. Ismail, S. Shah, 2017 .

Synthesis and screening of (E)-3-(2-benzylidenehydrazinyl)-5,6-diphenyl-1,2,4-triazine analogs as novel dual inhibitors of α-amylase and α-glucosidase.

N. Ullah, A. Wadood, K. Khan, 2020, Bioorganic chemistry.

Synthesis of alpha amylase inhibitors based on privileged indole scaffold.

Faisal Nawaz, H. Ullah, N. Ismail, 2017, Bioorganic chemistry.

Synthesis of indole-2-hydrazones in search of potential leishmanicidal agents

N. Ismail, Muhammad Ali, M. Taha, 2014, Medicinal Chemistry Research.

Rational design of bis-indolylmethane-oxadiazole hybrids as inhibitors of thymidine phosphorylase.

U. Rashid, S. Imran, Muhammad Ali, 2018, Bioorganic & medicinal chemistry.

Identification of Potent COVID-19 Main Protease (Mpro) Inhibitors from Natural Polyphenols: An in Silico Strategy Unveils a Hope against CORONA

V. Eyupoglu, Iqra Sarfraz, Muhammad Ali, 2020 .

Characterization of Rheumatoid Arthritis Risk-Associated SNPs and Identification of Novel Therapeutic Sites Using an In-Silico Approach

Z. Islam, Hamed A. El‐Serehy, S. Al‐Farraj, 2021, Biology.

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors.

N. Ismail, F. Rahim, S. Imran, 2015, Bioorganic chemistry.

Studies on the expression and processing of human proinsulin derivatives encoded by different DNA constructs.

N. Rashid, M. Akhtar, F. Aslam, 2013, Biochimica et biophysica acta.

Prediction of putative epitope‐based vaccine against all corona virus strains for the Chinese population: Approach toward development of vaccine

S. Batool, N. M. Ashraf, Muhammad Ali, 2020, Microbiology and immunology.

Synthesis of symmetrical bis-Schiff base-disulfide hybrids as highly effective anti-leishmanial agents.

N. Ismail, A. Al-Harrasi, F. Rahim, 2020, Bioorganic chemistry.

Molecular hybridization conceded exceptionally potent quinolinyl-oxadiazole hybrids through phenyl linked thiosemicarbazide antileishmanial scaffolds: In silico validation and SAR studies.

N. Uddin, U. Rashid, N. Ismail, 2017, Bioorganic chemistry.

Synthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent β-Glucuronidase Inhibitors

Yasser A. Bamarouf, Mohammed A. Alqahtani, Z. Zakaria, 2019, Molecules.

Identification of bisindolylmethane–hydrazone hybrids as novel inhibitors of β-glucuronidase, DFT, and in silico SAR intimations

N. Uddin, N. Ismail, S. Imran, 2016 .

Synthesis of 2-phenyl-1H-imidazo[4,5-b]pyridine as type 2 diabetes inhibitors and molecular docking studies

N. Uddin, N. Ismail, S. Imran, 2017, Medicinal Chemistry Research.

Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mellitus.

H. Ullah, N. Ismail, F. Rahim, 2017, Bioorganic chemistry.

Successful computer guided planned synthesis of (4R)-thiazolidine carboxylic acid and its 2-substituted analogues as urease inhibitors

M. Lodhi, M. Choudhary, Z. Ullah, 2006, Molecular Diversity.

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.

Discovery of novel oxindole derivatives as potent α-glucosidase inhibitors.

M. Yousaf, Z. Hussain, A. Wadood, 2014, Bioorganic & medicinal chemistry.

Synthesis, β-Glucuronidase Inhibition, and Molecular Docking Studies of 1,2,4-Triazole Hydrazones

Muhammad Ali, M. Taha, K. Khan, 2018, Journal of the Iranian Chemical Society.

Synthesis of indole-2-hydrazones in search of potential leishmanicidal agents

N. Ismail, Muhammad Ali, M. Taha, 2014, Medicinal Chemistry Research.

Data-mining approach for screening of rare genetic elements associated with predisposition of prostate cancer in South-Asian populations

N. Zeeshan, K. Sughra, S. Batool, 2019, Turkish Journal of Biochemistry.

Two New Octulosonic Acid Derivatives and a New Cyclohexanecarboxylic Acid Derivative from Erigeron bonariensis L.

Afsar Khan, A. Zahoor, S. Khan, 2012 .

Synthesis of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies.

N. Ismail, F. Rahim, K. Khan, 2015, Bioorganic & medicinal chemistry.

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

N. Ismail, F. Rahim, K. Khan, 2017, Bioorganic chemistry.