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OpenAlex Citation Counts

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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:

α-Glucosidase inhibitory activity and cytotoxic effects of some cyclic urea and carbamate derivatives
Jelena Popović‐Djordjević, Ivana Jevtić, Nađa Grozdanić, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2017) Vol. 32, Iss. 1, pp. 298-303
Open Access | Times Cited: 16

Showing 16 citing articles:

Design, synthesis, molecular docking, and in vitro α-glucosidase inhibitory activities of novel 3-amino-2,4-diarylbenzo[4,5]imidazo[1,2-a]pyrimidines against yeast and rat α-glucosidase
Fariba Peytam, Ghazaleh Takalloobanafshi, Toktam Saadattalab, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 41
Artificial intelligence in antidiabetic drug discovery: The advances in QSAR and the prediction of α-glucosidase inhibitors
Adeshina I. Odugbemi, Clement N. Nyirenda, Alan Christoffels, et al.
Computational and Structural Biotechnology Journal (2024) Vol. 23, pp. 2964-2977
Open Access | Times Cited: 8
Repurposing metabolic regulators: antidiabetic drugs as anticancer agents
Yogita Dhas, Nupur Biswas, M R Divyalakshmi, et al.
Molecular Biomedicine (2024) Vol. 5, Iss. 1
Open Access | Times Cited: 6
Synthesis of 4-alkylaminoimidazo[1,2-a]pyridines linked to carbamate moiety as potent α-glucosidase inhibitors
Mina Saeedi, Maryam Raeisi-Nafchi, Sepideh Sobhani, et al.
Molecular Diversity (2020) Vol. 25, Iss. 4, pp. 2399-2409
Closed Access | Times Cited: 28
Urea and Polyurea Production: An Innovative Solvent- and Catalyst-Free Approach through Catechol Carbonate
Michelina Soccio, Rita Mazzoni, Carlo Lucarelli, et al.
ACS Sustainable Chemistry & Engineering (2020) Vol. 8, Iss. 41, pp. 15640-15650
Open Access | Times Cited: 22
Exploring gabosine and chlorogentisyl alcohol derivatives from a marine-derived fungus as EcGUS inhibitors with informatic assisted approaches
Yichao Ge, Yihan Ma, Meilu Zhao, et al.
European Journal of Medicinal Chemistry (2022) Vol. 242, pp. 114699-114699
Closed Access | Times Cited: 10
A click chemistry approach for the synthesis of cyclic ureido tethered coumarinyl and 1-aza coumarinyl 1,2,3-triazoles as inhibitors of Mycobacterium tuberculosis H37Rv and their in silico studies
Netravati Khanapurmath, Manohar V. Kulkarni, Shrinivas D. Joshi, et al.
Bioorganic & Medicinal Chemistry (2019) Vol. 27, Iss. 20, pp. 115054-115054
Closed Access | Times Cited: 15
N‐CF3 Imidazolidin‐2‐one Derivatives via Photocatalytic and Silver‐Catalyzed Cyclizations
Abdurrahman Türksoy, Samir Bouayad‐Gervais, Franziska Schoenebeck
Chemistry - A European Journal (2022) Vol. 28, Iss. 46
Open Access | Times Cited: 8
A Combined Experimental and Computational Study of Novel Benzotriazinone Carboxamides as Alpha-Glucosidase Inhibitors
Zunera Khalid, Syed Salman Shafqat, Hafiz Adnan Ahmad, et al.
Molecules (2023) Vol. 28, Iss. 18, pp. 6623-6623
Open Access | Times Cited: 4
Design, synthesis, biological evaluation, and molecular modeling studies of some quinazolin-4(3 H )-one-benzenesulfonamide hybrids as potential α-glucosidase inhibitors
Emre Kadir Ayan, Güneş Çoban, Zeynep Soyer
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-21
Closed Access | Times Cited: 1
Aqueous Ethanolic Extract of Adiantum incisum Forssk. Protects against Type 2 Diabetes Mellitus via Attenuation of α-Amylase and Oxidative Stress
Hafiz Muhammad Bilal, Ali Sharif, Muhammad Nasir Hayat Malik, et al.
ACS Omega (2022) Vol. 7, Iss. 42, pp. 37724-37735
Open Access | Times Cited: 6
Arylsulfonyl histamine derivatives as powerful and selective α-glucosidase inhibitors
M. I. Osella, Mario O. Salazar, Marcelo D. Gamarra, et al.
RSC Medicinal Chemistry (2020) Vol. 11, Iss. 4, pp. 518-527
Open Access | Times Cited: 8
Naturally bioactive compounds from Hemimycale aff arabica: antimicrobial, antiglycation, cytotoxicity, and molecular docking studies
Mohamed Shaaban, A. Hassan, Maha M. Soltan, et al.
Medicinal Chemistry Research (2018) Vol. 27, Iss. 9, pp. 2079-2088
Closed Access | Times Cited: 7
The 4-(dimethylaminoalkyl)piperazine inhibitors of α-glucosidase: allosteric enzyme inhibition and identification of interacting chemical groups
Usman Ghani, SAJDA ASHRAF, ZAHEER UL HAQ, et al.
TURKISH JOURNAL OF CHEMISTRY (2022) Vol. 46, Iss. 5, pp. 1484-1492
Open Access | Times Cited: 3
Thionization Method of Glycosyl Urea and Carbamide Sugars
Baktygul Ernazarova, Aida Bakirova, A. Z. Dzhumanazarova, et al.
International Journal of Organic Chemistry (2020) Vol. 10, Iss. 03, pp. 111-122
Open Access | Times Cited: 2
Antidiabetic potential of simple carbamate derivatives: Comparative experimental and computational study
Relja Suručić, Ivana Jevtić, Tatjana Stanojković, et al.
Journal of the Serbian Chemical Society (2023) Vol. 88, Iss. 11, pp. 1089-1102
Open Access
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