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D-Index & Metrics

Chemistry

D-Index
60
Citations
11729
World Ranking
9782
National Ranking
48

Overview

Muhammad Taha is affiliated with Imam Abdulrahman Bin Faisal University in Saudi Arabia. Their research spans primarily the fields of Chemistry and Medicine, with a focus on Organic Chemistry, Molecular Biology, Pharmacology, Endocrinology, Diabetes and Metabolism, and Computational Theory and Mathematics. The main topics of their research include synthesis and biological activity, natural antidiabetic agents studies, computational drug discovery methods, cholinesterase and neurodegenerative diseases, enzyme function and inhibition, synthesis and characterization of heterocyclic compounds, and click chemistry and applications.

They have published extensively with notable frequent publication venues including:

  • Journal of Molecular Structure (31 publications)
  • Arabian Journal of Chemistry (13 publications)
  • Bioorganic Chemistry (11 publications)
  • Future Medicinal Chemistry (11 publications)
  • International Journal of Biological Macromolecules (9 publications)

Their recent papers illustrate a range of biochemical and pharmacological inquiries focused on synthesis and bioactivity evaluation. Selected works include:

  • "Synthesis, DFT Studies, Molecular Docking and Biological Activity Evaluation of Thiazole-Sulfonamide Derivatives as Potent Alzheimer's Inhibitors," 2023, published in Molecules
  • "Indole acrylonitriles as potential anti-hyperglycemic agents: Synthesis, α-glucosidase inhibitory activity and molecular docking studies," 2020, published in Bioorganic & Medicinal Chemistry
  • "Synthesis, in vitro thymidine phosphorylase inhibitory activity and molecular docking study of novel pyridine-derived bis-oxadiazole bearing bis-schiff base derivatives," 2023, published in Arabian Journal of Chemistry
  • "Syntheses, in vitro α-amylase and α-glucosidase dual inhibitory activities of 4-amino-1,2,4-triazole derivatives their molecular docking and kinetic studies," 2020, published in Bioorganic & Medicinal Chemistry
  • "Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studies," 2020, published in Bioorganic Chemistry

The scientist frequently collaborates with several co-authors, including:

  • Khalid Mohammed Khan
  • Fazal Rahim
  • Syed Adnan Alı Shah
  • Abdul Wadood
  • Uzma Salar

Muhammad Taha's work reflects a multidisciplinary approach combining experimental synthesis, molecular docking techniques, and bioactivity assays relevant to pharmacological targets such as enzymes related to neurodegenerative diseases and diabetes. Their research contributes data and insights pertinent to enzyme inhibition, drug discovery methodologies, and heterocyclic compound development.

Best Publications

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

    Khalid Mohammed Khan;Momin Khan;Muhammad Ali;Muhammad Taha

  • Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.

    Fazal Rahim;Fazal Malik;Hayat Ullah;Abdul Wadood

  • Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton.

    Khalid Mohammed Khan;Fazal Rahim;Abdul Wadood;Naveen Kosar

  • Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies

    Muhammad Taha;Nor Hadiani Ismail;Salima Lalani;Muhammad Qaiser Fatmi

  • Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase inhibitory potential of thiazole analogs as new inhibitors for Alzheimer disease.

    Fazal Rahim;Muhammad Tariq Javed;Hayat Ullah;Abdul Wadood

  • Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies.

    Syahrul Imran;Muhammad Taha;Nor Hadiani Ismail;Syed Muhammad Kashif

  • Triazinoindole analogs as potent inhibitors of α-glucosidase: synthesis, biological evaluation and molecular docking studies.

    Fazal Rahim;Khadim Ullah;Hayat Ullah;Abdul Wadood

  • Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase.

    Fazal Rahim;Hayat Ullah;Muhammad Tariq Javid;Abdul Wadood

  • Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivatives

    Muhammad Taha;Syed Adnan Ali Shah;Muhammad Afifi;Syahrul Imran

  • Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas.

    Khalid Mohammed Khan;Farzana Naz;Muhammad Taha;Ajmal Khan

  • Synthesis of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking.

    Khalid Mohammed Khan;Fazal Rahim;Sobia Ahsan Halim;Muhammad Taha

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

    Fazal Rahim;Hayat Ullah;Muhammad Taha;Abdul Wadood

  • Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action

    El Hassane Anouar;Salwa Raweh;Imene Bayach;Imene Bayach;Muhammad Taha

  • 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.

    Muhammad Taha;Fazal Rahim;Syahrul Imran;Nor Hadiani Ismail

  • Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies.

    Uzma Salar;Muhammad Taha;Khalid Mohammed Khan;Nor Hadiani Ismail

  • Synthesis of novel bisindolylmethane Schiff bases and their antibacterial activity.

    Syahrul Imran;Muhammad Taha;Nor Hadiani Ismail;Khalid Mohammed Khan

  • Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives.

    Muhammad Taha;Muhammad Tariq Javid;Syahrul Imran;Manikandan Selvaraj

  • Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies.

    Muhammad Taha;Nor Hadiani Ismail;Ajmal Khan;Syed Adnan Ali Shah

  • Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents.

    Fazal Rahim;Khalid Zaman;Hayat Ullah;Muhammad Taha

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

    Uzma Salar;Khalid Mohammed Khan;Sridevi Chigurupati;Muhammad Taha

  • Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors

    Muhammad Taha;Nor Hadiani Ismail;Syahrul Imran;Muhammad Qamarruddin Bin Rokei

  • Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and kinetic studies.

    Shehryar Hameed;Kanwal;Faiza Seraj;Rafaila Rafique

Frequent Co-Authors

Khalid Mohammed Khan
Khalid Mohammed Khan University of Karachi
Fazal Rahim
Fazal Rahim Hazara University
Nor Hadiani Ismail
Nor Hadiani Ismail Universiti Teknologi MARA
Abdul Wadood
Abdul Wadood Abdul Wali Khan University Mardan
M. Iqbal Choudhary
M. Iqbal Choudhary University of Karachi
Khalid Zaman
Khalid Zaman University of Haripur
Wolfgang Voelter
Wolfgang Voelter University of Tübingen
Muhammad Sajid
Muhammad Sajid International Islamic University, Islamabad
Umer Rashid
Umer Rashid UCSI University
Mohammad Ali Faramarzi
Mohammad Ali Faramarzi Tehran University of Medical Sciences

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