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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Discovery of imidazopyridine derived oxadiazole-based thiourea derivatives as potential anti-diabetic agents: Synthesis, in vitro antioxidant screening and in silico molecular modeling approaches
Rafaqat Hussain, Wajid Rehman, Fazal Rahim, et al.
Journal of Molecular Structure (2023) Vol. 1293, pp. 136185-136185
Closed Access | Times Cited: 37

Showing 1-25 of 37 citing articles:

A promising acetylcholinesterase and butyrylcholinesterase inhibitors: In vitro enzymatic and in silico molecular docking studies of benzothiazole-based oxadiazole containing imidazopyridine hybrid derivatives
Rafaqat Hussain, Hayat Ullah, Shoaib Khan, et al.
Results in Chemistry (2024) Vol. 7, pp. 101503-101503
Open Access | Times Cited: 15
Novel bis-thiazole-thiazolidinone hybrid derivatives: Synthesis, structural properties and anticholinesterase bioactive potential as drug competitor based on docking studies
Shoaib Khan, Rafaqat Hussain, Yousaf Khan, et al.
Journal of Molecular Structure (2024) Vol. 1303, pp. 137417-137417
Closed Access | Times Cited: 14
In vitro and in silico correlation of bis-thiazole based Schiff base hybrids analogues: A computational approach develop to promising acetylcholinesterase and butyrylcholinesterase inhibitors
Uzma Jehangir, Shoaib Khan, Rafaqat Hussain, et al.
Journal of Molecular Structure (2024) Vol. 1303, pp. 137585-137585
Closed Access | Times Cited: 10
Investigation of novel benzimidazole-based indole/thiazole hybrids derivatives as effective anti-diabetics and anti-alzheimer's agents: Structure-activity relationship insight, in vitro and in silico approaches
Haseena Naz, Mohamed S. Othman, Fazal Rahim, et al.
Journal of Molecular Structure (2024) Vol. 1312, pp. 138592-138592
Closed Access | Times Cited: 9
Correlation between in vitro anti-urease activity and in silico molecular modeling approach of novel imidazopyridine–oxadiazole hybrids derivatives
Shoaib Khan, Rafaqat Hussain, Yousaf Khan, et al.
Open Chemistry (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 8
Design, synthesis, in vitro biological assessment and in silico molecular modeling study of thiazole-thiazolidinone derivatives as potent anti-cancer agents
Shoaib Khan, Hayat Ullah, Rafaqat Hussain, et al.
Results in Chemistry (2024) Vol. 7, pp. 101507-101507
Open Access | Times Cited: 8
Biological Characterization of One Oxadiazole Derivative (5(4‐Hydroxyphenyl)‐2‐(N‐Phenyl Amino)‐1,3,4‐Oxadiazole): In Vitro, In Silico, and Network Pharmacological Approaches
Tuğçe Duran, Irem Balikci, Busra Buyukkosucu, et al.
Chemical Biology & Drug Design (2025) Vol. 105, Iss. 1
Closed Access
Design, 3D-QSAR, molecular docking, MD simulations, ADME/Tox properties and DFT study of benzimidazole derivatives as promising α-glucosidase inhibitors
Ayoub Khaldan, Soukaina Bouamrane, Mohamed Ouabane, et al.
Journal of Molecular Structure (2025) Vol. 1328, pp. 141351-141351
Closed Access
Unveiling the structural and theoretical properties of 6-(2-fluoro-3-methylpyridin-4-yl)-2-(4-methoxyphenyl)-N-phenylquinoline-4-carboxamide compound as Sonic Hedgehog protein inhibitor: Synthesis, SCXRD, HSA, DFT, Docking and ADMET studies
Veeresha Gowda Shalini, Dheeraj Kumar, Darshini Gowda, et al.
Journal of Molecular Structure (2025), pp. 141495-141495
Closed Access
Synthesis and Anti-acute Myeloid Leukemia Activity of Cyclopropane-1,1-diamide Derivatives Containing Imidazo[1,2-a]pyridine
L. Eduardo Wu, Jiangdong Li, Zhonghua Shi, et al.
Chinese Journal of Organic Chemistry (2025) Vol. 45, Iss. 1, pp. 286-286
Closed Access
Insight into in vitro thymidine phosphorylase and in silico molecular docking studies: identification of hybrid thiazole bearing Schiff base derivatives
Sundas Mumtaz, Fakher Rahim, Rafaqat Hussain, et al.
Zeitschrift für Naturforschung C (2025)
Closed Access
Synthesis, in Vitro Bio-Evaluation and in Silico Molecular Docking Studies of Thiadiazole-Based Schiff Base Derivatives
Yousaf Khan, Aneela Maalik, Wajid Rehman, et al.
Future Medicinal Chemistry (2024) Vol. 16, Iss. 4, pp. 335-348
Closed Access | Times Cited: 5
Novel carbazole-oxadiazole derivatives as anti-α-glucosidase and anti-α-amylase agents: Design, synthesis, molecular docking, and biological evaluation
Shuang Luo, Li Zhao, Huining Peng, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116600-116600
Closed Access | Times Cited: 4
The Synthesis, In Vitro Bio-Evaluation, and In Silico Molecular Docking Studies of Pyrazoline–Thiazole Hybrid Analogues as Promising Anti-α-Glucosidase and Anti-Urease Agents
Yousaf Khan, Shoaib Khan, Rafaqat Hussain, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 12, pp. 1650-1650
Open Access | Times Cited: 13
Synthesis of oxadiazole derivatives: Anti-bacterial, DNA binding and in silico molecular modelling approaches
Razia Sultana, Asghar Ali, Manish Rana, et al.
Journal of Molecular Structure (2024) Vol. 1318, pp. 139350-139350
Closed Access | Times Cited: 3
Advances in synthesis, medicinal properties and biomedical applications of Pyridine Derivatives: A Comprehensive Review
Duryodhan Sahu, P.S. Rama Sreekanth, Prasanta Kumar Behera, et al.
European Journal of Medicinal Chemistry Reports (2024) Vol. 12, pp. 100210-100210
Open Access | Times Cited: 3
Facile benzothiazole-triazole based thiazole derivatives as novel thymidine phosphorylase and α-glucosidase inhibitors: Experimental and computational approaches
Shoaib Khan, Rafaqat Hussain, Yousaf Khan, et al.
Enzyme and Microbial Technology (2024) Vol. 179, pp. 110470-110470
Closed Access | Times Cited: 2
Identification of novel benzothiazole–thiadiazole-based thiazolidinone derivative: in vitro and in silico approaches to develop promising anti-Alzheimer’s agents
Shoaib Khan, Rafaqat Hussain, Tayyiaba Iqbal, et al.
Future Medicinal Chemistry (2024) Vol. 16, Iss. 16, pp. 1601-1613
Closed Access | Times Cited: 1
A combined in vitro and in silico approach of thiadiazole based Schiff base derivatives as multipotent inhibitor: Synthesis, spectral analysis, antidiabetic and antimicrobial activity
Tayyaba Zahoor, Shoaib Khan, Sampath Chinnam, et al.
Results in Chemistry (2024) Vol. 9, pp. 101671-101671
Open Access | Times Cited: 1
Investigating the Efficacy of Naphthalene-Thiazole Hybrid hydrazones as α-Glucosidase Inhibitors
Jehan Y. Al‐Humaidi, Amr S. Abouzied, Magdi E. A. Zaki, et al.
Journal of Molecular Structure (2024) Vol. 1322, pp. 140288-140288
Closed Access | Times Cited: 1
Synthesis, α-Glucosidase, α-Amylase, and Aldol Reductase Inhibitory Activity with Molecular Docking Study of Novel Imidazo[1,2-a]pyridine Derivatives
Betül Kaya, Ulviye Acar Çevik, Bilge Çi̇ftci̇, et al.
ACS Omega (2024) Vol. 9, Iss. 42, pp. 42905-42914
Closed Access | Times Cited: 1
Design, Synthesis, Anticholinesterase and Antioxidant Activity of Indole, Benzothiophene and Thiophen-Based 1,3,4-Oxadiazole Derivatives
Zühal Kılıç-Kurt, Dilan Konyar, Hayati OKUR, et al.
(2024)
Closed Access
Synthesis, characterization, antimicrobial and antioxidant activity of 2- (2′-hydroxyphenyl) -1,3,4-oxadiazolyl-5-amino acid derivatives
Mouna Souad Abbassi, Talal Lahreche, Khaled Briki, et al.
Journal of Saudi Chemical Society (2024) Vol. 28, Iss. 3, pp. 101866-101866
Open Access
Pharmacophore Modeling of Indole Based Thiadiazole and Oxadiazole as Diabetic Therapeutic: A Multi-Routed Approach of Current Status and Future Directions
Shoaib Khan, Tayyiaba Iqbal, Rafaqat Hussain, et al.
(2024)
Closed Access
Luminescent Triazolo-fused Pyrido[3,4-b]pyrazines as Novel Fluorophores
Deepak Kumar, Nidhi Nidhi, Bharti Khungar, et al.
Dyes and Pigments (2024) Vol. 231, pp. 112365-112365
Closed Access
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