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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:

Flavone-1,2,3-triazole derivatives as potential α-glucosidase inhibitors: Synthesis, enzyme inhibition, kinetic analysis and molecular docking study
Manoj Dhameja, Hariom Kumar, Sirisha Kurella, et al.
Bioorganic Chemistry (2022) Vol. 127, pp. 106028-106028
Closed Access | Times Cited: 21

Showing 21 citing articles:

Synthetic α-glucosidase inhibitors as promising anti-diabetic agents: Recent developments and future challenges
Alia Mushtaq, Uzma Azam, Saba Mehreen, et al.
European Journal of Medicinal Chemistry (2023) Vol. 249, pp. 115119-115119
Closed Access | Times Cited: 100
Synthesis, in-vitro α-glucosidase inhibition and molecular docking studies of 1,3,4-thiadiazole-5,6-diphenyl-1,2,4-triazine hybrids: Potential leads in the search of new antidiabetic drugs
Hariom Kumar, Manoj Dhameja, Sirisha Kurella, et al.
Journal of Molecular Structure (2022) Vol. 1273, pp. 134339-134339
Closed Access | Times Cited: 29
Design, synthesis, biological evaluation, and docking study of chromone-based phenylhydrazone and benzoylhydrazone derivatives as antidiabetic agents targeting α‐glucosidase
Meiyan Fan, Wei Yang, Lin Liu, et al.
Bioorganic Chemistry (2023) Vol. 132, pp. 106384-106384
Closed Access | Times Cited: 17
Design, synthesis, biological evaluation, and docking study of new triazole-phenylacetamide derivatives as α-glucosidase inhibitors
Shuang Luo, Wei Yang, Yong Huang, et al.
Bioorganic Chemistry (2023) Vol. 141, pp. 106844-106844
Closed Access | Times Cited: 15
Indolyl imine compounds as multi-target agents; synthesis, antidiabetic, anticholinesterase, antioxidant activities and molecular modeling
Sadık M. Ceyhan, İrem Nur Zengin, Murat Bingül, et al.
Journal of Molecular Structure (2024) Vol. 1309, pp. 138159-138159
Closed Access | Times Cited: 3
Synthesis and molecular modeling studies of naphthazarin derivatives as novel selective inhibitors of α-glucosidase and α-amylase
Şebnem Abadan, Mehmet F. Sağlam, Mehmet Serdar Koca, et al.
Journal of Molecular Structure (2023) Vol. 1278, pp. 134954-134954
Closed Access | Times Cited: 9
Recent Developments in 1,2,3‐Triazole Based α‐Glucosidase Inhibitors: Design Strategies, Structure‐Activity Relationship and Mechanistic Insights
Atamjit Singh, Karanvir Singh, Aman Sharma, et al.
Chemistry & Biodiversity (2024) Vol. 21, Iss. 9
Closed Access | Times Cited: 2
Microwave-assisted Click Synthesis, Characterisation, and In silico Studies of novel 2H-chromene-1,2,3-triazolyl glycoconjugates as Potent Anticancer and Antibacterial agents
Bhabani Shankar Panda, Mohammed Ansar Ahemad, Suhasini Mohapatra, et al.
Journal of Molecular Structure (2024) Vol. 1318, pp. 139323-139323
Closed Access | Times Cited: 2
Recent updates in click and computational chemistry for drug discovery and development
Jiang Hong Cai, Xuan Zhe Zhu, Peng Yue Guo, et al.
Frontiers in Chemistry (2023) Vol. 11
Open Access | Times Cited: 7
Utilizing bio-affinity ultrafiltration combined with UHPLC Q-Exactive Plus Orbitrap HRMS to detect potential α-glucosidase inhibitors in Oxalis corniculate L.
Qianqian Feng, Wei Yang, Zhiyun Peng, et al.
International Journal of Biological Macromolecules (2023) Vol. 252, pp. 126490-126490
Closed Access | Times Cited: 6
Synthesis, anticancer activity and molecular modeling study of novel substituted triazole linked tetrafluoronaphthalene hybrid derivatives
Musa Erdoğan, Ferah Cömert Önder
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 18, pp. 9767-9786
Open Access | Times Cited: 5
Inhibition of α-glucosidase Enzyme By ‘click'-inspired Pharmacophore Framework 1,3,4-thiadiazole–1,2,3-triazole Hybrids
Manoj Dhameja, Hariom Kumar, Sirisha Kurella, et al.
Future Medicinal Chemistry (2023) Vol. 15, Iss. 4, pp. 345-363
Closed Access | Times Cited: 4
Exploring the potential of isonicotinohydrazide derivatives in N80 steel corrosion control: An integrated approach through synthesis, modeling, and experimentation in acidic environments
Abdelkarim Ait Mansour, Mustapha R. Al-hadeethi, Hassane Lgaz, et al.
Colloids and Surfaces A Physicochemical and Engineering Aspects (2023) Vol. 679, pp. 132542-132542
Closed Access | Times Cited: 4
Synthesis of 1,2,3‐triazole‐1,3,4‐thiadiazole hybrids as novel α‐glucosidase inhibitors by in situ azidation/click assembly
Hariom Kumar, Manoj Dhameja, Sirisha Kurella, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 8
Closed Access | Times Cited: 2
Investigation of the binding behavior of bioactive 7-methoxyflavone to human serum albumin by coupling multi-spectroscopic with computational approaches
Qing He, Qi’er Mu, Zhongxun Wei, et al.
Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy (2022) Vol. 285, pp. 121920-121920
Closed Access | Times Cited: 4
Inhibitory effect of quercetin-3-O-α-rhamnoside, p-coumaric acid, phloridzin and 4-O-β-glucopyranosyl-cis-coumaric acid on rats liver microsomes cytochrome P450 enzyme activities
Changyang Ma, Cunyu Liu, Mengjie Ren, et al.
Food and Chemical Toxicology (2022) Vol. 172, pp. 113583-113583
Closed Access | Times Cited: 4
Wide-ranging Study on Synthesis and Biological Evaluation of 1, 2, 3-triazole
Anshu Chaudhary Dudhe, Rupesh Dudhe, Renuka Mahajan, et al.
Current Bioactive Compounds (2024) Vol. 20, Iss. 7
Closed Access
Synthesis of furo[2,3-c]carbazoles as potent α -glucosidase and α -amylase inhibitors
T. Uçar, Murat Bingul, Hasan Şahin, et al.
Synthetic Communications (2024), pp. 1-9
Closed Access
Novel Dibenzoazepine-Substituted Triazole Hybrids as Cholinesterase and Carbonic Anhydrase Inhibitors and Anticancer Agents: Synthesis, Characterization, Biological Evaluation, and In Silico Studies
Musa Erdoğan, Alper Önder, Yeliz Demir, et al.
ACS Omega (2024) Vol. 9, Iss. 47, pp. 46860-46878
Open Access
Synthesis, in vitro and in silico evaluation of indole linked carbohydrazides and 1,3,4-oxadiazoles as new α-glycosidase inhibitors
Kubra Kocaman, Murat Bingül, Sadık M. Ceyhan, et al.
Journal of Molecular Structure (2024) Vol. 1325, pp. 141057-141057
Closed Access
In Vitro and in Silico Studies of 3‐Hydroxyflavone‐Based Sulfonate Esters: Potent Acetylcholinesterase, Carbonic Anhydrase and α‐Glycosidase Inhibitors
Murat Güney, Ahmet Gökhan Ağgül, Adem Ertürk, et al.
ChemistrySelect (2023) Vol. 8, Iss. 40
Closed Access
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