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Chemistry

D-Index
52
Citations
8268
World Ranking
13665
National Ranking
20

Overview

Fazal Rahim is affiliated with Hazara University in Pakistan and has a research focus spanning several fields, including Chemistry, Medicine, and Biochemistry, Genetics and Molecular Biology. Their work primarily centers on Organic Chemistry, Pharmacology, Molecular Biology, Computational Theory and Mathematics, and Endocrinology, Diabetes and Metabolism.

Their scholarly output includes exploration of topics such as Synthesis and biological activity, Cholinesterase and Neurodegenerative Diseases, Computational Drug Discovery Methods, Natural Antidiabetic Agents Studies, Enzyme function and inhibition, Click Chemistry and Applications, and Enzyme Production and Characterization.

Fazal Rahim's recent publications include the following papers:

  • Synthesis, DFT Studies, Molecular Docking and Biological Activity Evaluation of Thiazole-Sulfonamide Derivatives as Potent Alzheimer's Inhibitors (2023, Molecules)
  • Synthesis, in vitro α-amylase, α-glucosidase activities and molecular docking study of new benzimidazole bearing thiazolidinone derivatives (2022, Journal of Molecular Structure)
  • Synthesis, in vitro thymidine phosphorylase inhibitory activity and molecular docking study of novel pyridine-derived bis-oxadiazole bearing bis-schiff base derivatives (2023, Arabian Journal of Chemistry)
  • Multipotent Cholinesterase Inhibitors for the Treatment of Alzheimer's Disease: Synthesis, Biological Analysis and Molecular Docking Study of Benzimidazole-Based Thiazole Derivatives (2022, Molecules)
  • Synthesis of Novel Benzimidazole-Based Thiazole Derivatives as Multipotent Inhibitors of α-Amylase and α-Glucosidase: In Vitro Evaluation along with Molecular Docking Study (2022, Molecules)

Frequent coauthors who have collaborated extensively with Fazal Rahim include:

  • Muhammad Taha
  • Hayat Ullah
  • Syed Adnan Alı Shah
  • Shoaib Khan
  • Abdul Wadood

They have published numerous articles in several academic venues, with a notable number of contributions to the following journals:

  • Journal of Molecular Structure (32 publications)
  • Chemical Data Collections (29 publications)
  • Arabian Journal of Chemistry (11 publications)
  • Molecules (10 publications)
  • Results in Chemistry (8 publications)

Best Publications

  • 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, 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 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

  • 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

  • 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

  • Synthesis of alpha amylase inhibitors based on privileged indole scaffold.

    Tayyaba Noreen;Muhammad Taha;Syahrul Imran;Sridevi Chigurupati

  • Synthesis, in vitro α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs.

    Muhammad Tariq Javid;Fazal Rahim;Muhammad Taha;Haseeb Ur Rehman

  • Synthesis, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6'-nitrobenzofuran-2'-yl)-1,3,4-oxadiazoles.

    Muhammad Taha;Nor Hadiani Ismail;Syahrul Imran;Abdul Wadood

  • Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies

    Nik Khairunissa Nik Abdullah Zawawi;Muhammad Taha;Norizan Ahmat;Abdul Wadood

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

    Muhammad Taha;Nor Hadiani Ismail;Waqas Jamil;Hesham Rashwan

  • Synthesis crystal structure of 2-methoxybenzoylhydrazones and evaluation of their α -glucosidase and urease inhibition potential

    Muhammad Taha;Nor Hadiani Ismail;Mohd Syukri Baharudin;Salima Lalani

  • Synthesis, in vitro alpha-glucosidase inhibitory potential of benzimidazole bearing bis-Schiff bases and their molecular docking study

    Fazal Rahim;Khalid Zaman;Muhammad Taha;Hayat Ullah

  • Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.

    Muhammad Taha;Syahrul Imran;Nor Hadiani Ismail;Manikandan Selvaraj

Frequent Co-Authors

Muhammad Taha
Muhammad Taha Imam Abdulrahman Bin Faisal University
Khalid Mohammed Khan
Khalid Mohammed Khan University of Karachi
Abdul Wadood
Abdul Wadood Abdul Wali Khan University Mardan
Nor Hadiani Ismail
Nor Hadiani Ismail Universiti Teknologi MARA
M. Iqbal Choudhary
M. Iqbal Choudhary University of Karachi
Khalid Zaman
Khalid Zaman University of Haripur
Muhammad Sajid
Muhammad Sajid International Islamic University, Islamabad
Umer Rashid
Umer Rashid UCSI University
Wolfgang Voelter
Wolfgang Voelter University of Tübingen
Amin Badshah
Amin Badshah Quaid-i-Azam University

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