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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:

Synthesis and anti-α-glucosidase activity evaluation of betulinic acid derivatives
Xiao-Zheng Wu, Wenjian Zhu, Li Lu, et al.
Arabian Journal of Chemistry (2023) Vol. 16, Iss. 5, pp. 104659-104659
Open Access | Times Cited: 58

Showing 1-25 of 58 citing articles:

Synthesis and biological evaluation of indole derivatives containing thiazolidine-2,4-dione as α-glucosidase inhibitors with antidiabetic activity
Chunmei Hu, Bingwen Liang, Jinping Sun, et al.
European Journal of Medicinal Chemistry (2023) Vol. 264, pp. 115957-115957
Closed Access | Times Cited: 44
Identification of 1,3,4-oxadiazolyl-containing β-carboline derivatives as novel α-glucosidase inhibitors with antidiabetic activity
Di Xiao, Li Lu, Bingwen Liang, et al.
European Journal of Medicinal Chemistry (2023) Vol. 261, pp. 115795-115795
Closed Access | Times Cited: 42
New β-carboline derivatives as potential α-glucosidase inhibitor: Synthesis and biological activity evaluation
Jing Lin, Di Xiao, Li Lu, et al.
Journal of Molecular Structure (2023) Vol. 1283, pp. 135279-135279
Closed Access | Times Cited: 37
Investigation on the inhibition mechanism and binding behavior of cryptolepine to α-glucosidase and its hypoglycemic activity by multi-spectroscopic method
Xiaofeng Min, Suqin Guo, Yu‐Jing Lu, et al.
Journal of Luminescence (2024) Vol. 269, pp. 120437-120437
Closed Access | Times Cited: 25
Thiazolidine-2,4-dione derivatives as potential α-glucosidase inhibitors: Synthesis, inhibitory activity, binding interaction and hypoglycemic activity
Mengyue Li, Jinping Sun, Bingwen Liang, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107177-107177
Closed Access | Times Cited: 24
Identification of 1,3,4-Thiadiazolyl-Containing Thiazolidine-2,4-dione Derivatives as Novel PTP1B Inhibitors with Antidiabetic Activity
Mengyue Li, Huiyun Li, Xiaofeng Min, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 10, pp. 8406-8419
Closed Access | Times Cited: 23
Novel thiosemicarbazide-based β-carboline derivatives as α-glucosidase inhibitors: Synthesis and biological evaluation
Bingwen Liang, Di Xiao, Shao‐Hua Wang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116595-116595
Closed Access | Times Cited: 22
Synthesis, anti-α-glucosidase activity, inhibition interaction, and anti-diabetic activity of novel cryptolepine derivatives
Mei Feng, Bingwen Liang, Jinping Sun, et al.
Journal of Molecular Structure (2024) Vol. 1310, pp. 138311-138311
Closed Access | Times Cited: 20
Synthesis, biological activities, and molecular docking studies of triazolo[4,3‐b]triazine derivatives as a novel class of α‐glucosidase and α‐amylase inhibitors
Soheila Seyfi, Somayeh Salarinejad, Setareh Moghimi, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 6
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
Synthesis, single crystal XRD, in vitro evaluation, molecular docking and ADMET studies of cuminaldehyde-thiazolidine-2,4-dione hybrids as potential α-glucosidase inhibitors
Abhik Paul, Sai Satyaprakash Mishra, Arnab Sarkar, et al.
Journal of Molecular Structure (2025), pp. 141510-141510
Closed Access
Dimethylallylated stilbenoids by chemo-selective prenyltransferases and their α-glucosidase inhibitory effects
Yang Min, Jun‐O Jin, Jingbo Yi, et al.
Bioorganic Chemistry (2025), pp. 108261-108261
Closed Access
Synthesis, Anti-Tyrosinase Activity, and Spectroscopic Inhibition Mechanism of Cinnamic Acid–Eugenol Esters
Jianping Li, Xiaofeng Min, Xi Zheng, et al.
Molecules (2023) Vol. 28, Iss. 16, pp. 5969-5969
Open Access | Times Cited: 15
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
Investigation on the inhibition mechanism and binding behavior of paeonol to tyrosinase and its anti-browning property by multi-spectroscopic and molecular docking methods
Xiaofeng Min, Li Lu, Xuetao Xu, et al.
International Journal of Biological Macromolecules (2023) Vol. 253, pp. 126962-126962
Closed Access | Times Cited: 15
α-Glucosidase Inhibition Research of Derivatives Based on 2β-Acetoxyferruginol Scaffold Excluding Acetic Acid Group
Simin Wu, Jiaxin Tang, Yujia Zhou, et al.
Chinese Journal of Organic Chemistry (2024) Vol. 44, Iss. 2, pp. 613-613
Open Access | Times Cited: 5
Anti-α-Glucosidase, SAR Analysis, and Mechanism Investigation of Indolo[1,2-b]isoquinoline Derivatives
Mengyue Li, Lin Li, Li Lu, et al.
Molecules (2023) Vol. 28, Iss. 13, pp. 5282-5282
Open Access | Times Cited: 13
Rapid screening of the novel bioactive peptides with notable α-glucosidase inhibitory activity by UF-LC-MS/MS combined with three-AI-tool from black beans
Yuancheng Li, Xinlei Wang, Xumeng Guo, et al.
International Journal of Biological Macromolecules (2024) Vol. 266, pp. 130982-130982
Closed Access | Times Cited: 3
1,2,3-Triazole-based betulinic acid derivatives as α-glucosidase inhibitors: Synthesis and in vitro and in vivo biological evaluation
Yufei Zhang, Jiangyi Li, Xiaofeng Min, et al.
Journal of Molecular Structure (2024) Vol. 1310, pp. 138294-138294
Closed Access | Times Cited: 3
Synthesis of the chromone‐thiosemicarbazone scaffold as promising α‐glucosidase inhibitors: An in vitro and in silico approach toward antidiabetic drug design
Rima D. Alharthy, Sana Khalid, Shamool Fatima, et al.
Archiv der Pharmazie (2024)
Closed Access | Times Cited: 3
Novel sulfonyl hydrazide based β-carboline derivatives as potential α-glucosidase inhibitors: design, synthesis, and biological evaluation
Jinping Sun, Di Xiao, Ming Lang, et al.
Molecular Diversity (2024)
Closed Access | Times Cited: 3
Synthesis and biological evaluation of chromone-thiazolidine-2,4-dione derivatives as potential α-glucosidase inhibitors
Yingying Zheng, Mengyu Li, Simin Wu, et al.
Arabian Journal of Chemistry (2023) Vol. 16, Iss. 11, pp. 105279-105279
Open Access | Times Cited: 8
In Vitro and In Vivo Biological Evaluation of Indole-thiazolidine-2,4-dione Derivatives as Tyrosinase Inhibitors
Li Lü, Chunmei Hu, Xiaofeng Min, et al.
Molecules (2023) Vol. 28, Iss. 22, pp. 7470-7470
Open Access | Times Cited: 8
Inhibition mechanism investigation of quercetagetin as a potential tyrosinase inhibitor
Faliang Liang
Frontiers in Chemistry (2024) Vol. 12
Open Access | Times Cited: 2
Design, synthesis and biological evaluation of novel betulinic acid derivatives containing 1,2,4-triazole-derived schiff bases as α-glucosidase inhibitors
Yufei Zhang, Xiaoyan Yu, Jiangyi Li, et al.
Journal of Molecular Structure (2024) Vol. 1315, pp. 138889-138889
Closed Access | Times Cited: 2
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