Muhammad Ashraf

4.5k total citations
103 papers, 2.0k citations indexed

About

Muhammad Ashraf is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Muhammad Ashraf has authored 103 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Organic Chemistry, 33 papers in Pharmacology and 31 papers in Molecular Biology. Recurrent topics in Muhammad Ashraf's work include Synthesis and biological activity (49 papers), Cholinesterase and Neurodegenerative Diseases (21 papers) and Synthesis and Characterization of Heterocyclic Compounds (17 papers). Muhammad Ashraf is often cited by papers focused on Synthesis and biological activity (49 papers), Cholinesterase and Neurodegenerative Diseases (21 papers) and Synthesis and Characterization of Heterocyclic Compounds (17 papers). Muhammad Ashraf collaborates with scholars based in Pakistan, Saudi Arabia and Malaysia. Muhammad Ashraf's co-authors include Abdul Jabbar, Shafqat Hussain, Muhammad Ali, Muhammad Saleem, Yong Sup Lee, Abdul Wadood, Ayesha Shaukat, Khalid Mohammed Khan, Muhammad Yar and Naheed Riaz and has published in prestigious journals such as Phytochemistry, Natural Product Reports and International Journal of Biological Macromolecules.

In The Last Decade

Muhammad Ashraf

95 papers receiving 1.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Muhammad Ashraf Pakistan 26 1.2k 518 514 315 240 103 2.0k
Uzma Salar Pakistan 31 2.0k 1.7× 703 1.4× 295 0.6× 560 1.8× 189 0.8× 118 2.6k
Manikandan Selvaraj Malaysia 25 1.0k 0.9× 406 0.8× 229 0.4× 339 1.1× 125 0.5× 52 1.5k
Maryam Mohammadi‐Khanaposhtani Iran 30 1.9k 1.6× 718 1.4× 491 1.0× 559 1.8× 73 0.3× 112 2.6k
Syahrul Imran Malaysia 36 2.3k 2.0× 851 1.6× 291 0.6× 879 2.8× 216 0.9× 92 3.1k
Aftab Alam Pakistan 25 997 0.8× 474 0.9× 177 0.3× 205 0.7× 49 0.2× 98 1.6k
Kanwal Pakistan 22 810 0.7× 318 0.6× 134 0.3× 275 0.9× 109 0.5× 48 1.2k
Gianluigi Lauro Italy 25 513 0.4× 755 1.5× 470 0.9× 54 0.2× 256 1.1× 89 1.6k
Muhammad Athar Abbasi Pakistan 20 646 0.5× 440 0.8× 219 0.4× 124 0.4× 25 0.1× 184 1.4k
Zha‐Jun Zhan China 25 540 0.5× 1.2k 2.3× 797 1.6× 51 0.2× 291 1.2× 163 2.4k
K. Suresh Babu India 23 505 0.4× 577 1.1× 271 0.5× 95 0.3× 104 0.4× 92 1.5k

Countries citing papers authored by Muhammad Ashraf

Since Specialization
Citations

This map shows the geographic impact of Muhammad Ashraf's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Muhammad Ashraf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Muhammad Ashraf more than expected).

Fields of papers citing papers by Muhammad Ashraf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Muhammad Ashraf. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Muhammad Ashraf. The network helps show where Muhammad Ashraf may publish in the future.

Co-authorship network of co-authors of Muhammad Ashraf

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Ashraf. A scholar is included among the top collaborators of Muhammad Ashraf based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Muhammad Ashraf. Muhammad Ashraf is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
3.
Munir, Zuhair A., Azizur Rehman, Muhammad Athar Abbasi, et al.. (2025). Synthesis, biological analysis and computational studies of substituted 1,2,4-triazoles: FMO, MEP and docking investigations. Journal of Molecular Structure. 1338. 142276–142276. 2 indexed citations
5.
Amjad, Hira, Muhammad Athar Abbasi, Sabahat Zahra Siddiqui, et al.. (2024). New piperidinyl heterocyclic azoles acquired through Li(I)-catalyzed reactions: Anti-enzymatic, ADME and computational studies. Journal of Molecular Structure. 1302. 137493–137493. 3 indexed citations
6.
Riaz, Naheed, Muhammad Saleem, Syeda Abida Ejaz, et al.. (2023). Molecular hybrids of substituted phenylcarbamoylpiperidine and 1,2,4-triazole methylacetamide as potent 15-LOX inhibitors: Design, synthesis, DFT calculations and molecular docking studies. Bioorganic Chemistry. 143. 106984–106984. 7 indexed citations
7.
Ashraf, Muhammad, Rafaqat Hussain, Shoaib Khan, et al.. (2023). In vitro and in silico correlation of benzoxazole-based thiazolidinone hybrids derivatives: A promising acetylcholinesterase and butyrylcholinesterase inhibitors. Journal of Molecular Structure. 1301. 137317–137317. 10 indexed citations
9.
Yasin, Muhammad, Muhammad Ashraf, Muhammad Saleem, et al.. (2022). 4-Chlorophenyl-N-furfuryl-1,2,4-triazole Methylacetamides as Significant 15-Lipoxygenase Inhibitors: an Efficient Approach for Finding Lead Anti-inflammatory Compounds. ACS Omega. 7(23). 19721–19734. 13 indexed citations
10.
Rehman, Azizur, et al.. (2020). Comparative conventional and microwave assisted synthesis of heterocyclic oxadiazole analogues having enzymatic inhibition potential. Journal of Heterocyclic Chemistry. 58(1). 93–110. 4 indexed citations
11.
Siddiqui, Sabahat Zahra, Mohammad Arfan, Muhammad Athar Abbasi, et al.. (2020). Discovery of Dual Inhibitors of Acetyl and Butrylcholinesterase and Antiproliferative Activity of 1,2,4‐Triazole‐3‐thiol: Synthesis and In Silico Molecular Study. ChemistrySelect. 5(21). 6430–6439. 14 indexed citations
12.
Muzaffar, Saima, Muhammad Saleem, Muhammad Ashraf, et al.. (2020). Evaluation of Ethylated Phenylcarbamoylazinane‐1,2,4‐Triazole Amides Derivatives as 15‐Lipoxygenase Inhibitors Together with Cytotoxic, ADME and Molecular Modeling Studies. ChemistrySelect. 5(44). 14210–14216. 7 indexed citations
13.
Mehmood, Rashad, Muhammad Tahir Khan, Zaheer-ud-din Khan, et al.. (2019). Bioassay Directed Isolation, Biological Evaluation and in Silico Studies of New Isolates from Pteris cretica L.. Antioxidants. 8(7). 231–231. 5 indexed citations
14.
White, Jonathan M., et al.. (2019). Biologically active scaffolds: Synthesis, characterization and studies of oxino bis-pyrazoles by environmental friendly method.. PubMed. 32(2 (Supplementary)). 831–837. 1 indexed citations
15.
16.
Ali, Basharat, Khalid Mohammed Khan, Uzma Salar, et al.. (2018). 1-[(4′-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies. Bioorganic Chemistry. 79. 363–371. 21 indexed citations
18.
Ahmad, Iftikhar, et al.. (2011). Urease inhibitors and antioxidants from vernonia cinerascens. Journal of the chemical society of pakistan. 33. 7 indexed citations
19.
Nazir, Mamona, Misbah Sultan, Naheed Riaz, et al.. (2011). Depsitinuside: a new depside galactoside from an endophytic fungus isolated fromViburnum tinus. Journal of Asian Natural Products Research. 13(11). 1056–1060. 3 indexed citations
20.
Hussain, Syed A., Ejaz Ahmed, Ahmed M. Malik, et al.. (2006). Recursterols A and B, chymotrypsin inhibiting sterols from Haloxylon recurvum. Polish Journal of Chemistry. 80(3). 409–415. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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