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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, molecular docking study of thiazole derivatives and exploring their dual inhibitor potentials against α-amylase and α-glucosidase
Hayat Ullah, Nisar Ahmad, Fazal Rahim, et al.
Chemical Data Collections (2022) Vol. 41, pp. 100932-100932
Closed Access | Times Cited: 18

Showing 18 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
Investigating Novel Thiophene Carbaldehyde Based Thiazole Derivatives as Potential Hits for Diabetic Management: Synthesis, In Vitro and In Silico Approach
Najeeb Ullah, Aftab Alam, Zainab Zainab, et al.
ChemistrySelect (2024) Vol. 9, Iss. 8
Closed Access | Times Cited: 8
Recent Studies of Nitrogen and Sulfur Containing Heterocyclic Analogues as Novel Antidiabetic Agents: A Review
Shankar Gharge, Shankar G. Alegaon
Chemistry & Biodiversity (2023) Vol. 21, Iss. 2
Closed Access | Times Cited: 15
Synthesis of Indole Based Sulfonamide Derivatives as potent inhibitors of α-glucosidase and α-amylase in management of type-II diabetes
Wasi Ullah, Fazal Rahim, Shawkat Hayat, et al.
Chemical Data Collections (2024) Vol. 50, pp. 101122-101122
Closed Access | Times Cited: 4
Synthesis, in vitro urease inhibitory potential and molecular docking study of bis-indole bearing sulfonamide analogues
Hayat Ullah, Ghazala Arshad, Fazal Rahim, et al.
Chemical Data Collections (2023) Vol. 44, pp. 100999-100999
Closed Access | Times Cited: 10
Synthesis, in vitro α-glucosidase and α-amylase activities, and an in silico molecular docking study of triazinoindole-thiazolidinone hybrid derivatives
Aftab Ahmad Khan, Hayat Ullah, Fazal Rahim, et al.
Chemical Data Collections (2023) Vol. 45, pp. 101035-101035
Closed Access | Times Cited: 10
Synthesis, in vitro α-glucosidase, α-amylase inhibitory potentials and molecular docking study of benzimidazole bearing sulfonamide analogues
Hayat Ullah, Tayyaba Batool, Ayesha Nawaz, et al.
Chemical Data Collections (2023) Vol. 47, pp. 101070-101070
Closed Access | Times Cited: 10
Synthesis of amantadine clubbed N-aryl amino thiazoles as potent urease, α-amylase & α-glucosidase inhibitors, kinetic and molecular docking studies
Fatima Tuz Zahra, Aamer Saeed, Atteeque Ahmed, et al.
RSC Advances (2023) Vol. 13, Iss. 36, pp. 24988-25001
Open Access | Times Cited: 9
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, in vitro α-glucosidase and α-amylase activities and molecular docking study of oxadiazole-sulphonamide hybrid analogues
Hayat Ullah, Muhammad Waseem Aslam, Fazal Rahim, et al.
Chemical Data Collections (2023) Vol. 45, pp. 101031-101031
Closed Access | Times Cited: 4
Design, synthesis, in vitro urease inhibitory potential and in silico molecular docking study of substituted thiazole bearing thiourea hybrid analogues
Hayat Ullah, Aisha Rab Nawaz, Muhammad Nabi, et al.
Chemical Data Collections (2023) Vol. 48, pp. 101086-101086
Closed Access | Times Cited: 4
Designing and Exploration of the Biological Potentials of Novel Centrosymmetric Heteroleptic Copper(II) Carboxylates
Viola, Niaz Muhammad, Awal Noor, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 10, pp. 1462-1462
Open Access | Times Cited: 4
Synthesis of benzimidazole-thiosemicarbazone hybrid derivatives, in vitro ..-glucosidase and ..-amylase activities, and an in silico molecular docking study
Hayat Ullah, Anosh Majeed, Fazal Rahim, et al.
Chemical Data Collections (2023) Vol. 45, pp. 101027-101027
Closed Access | Times Cited: 3
Design, synthesis, in vitro urease inhibitory potentials and in silico molecular docking study of benzimidazole bearing thiosemicarbazides/sulfonamide Analogues
Abdullah Yahya Abdullah Alzahrani, Bushra Adalat, Hayat Ullah, et al.
Journal of Molecular Structure (2023) Vol. 1296, pp. 136850-136850
Closed Access | Times Cited: 2
Synthesis of small size adamantane-linked aminothiazoles as potent inhibitors of urease, α-glucosidase and carbonic anhydrase and their molecular docking studies
Atteeque Ahmed, Pervaiz Ali Channar, Syeda Abida Ejaz, et al.
Chemical Papers (2024) Vol. 78, Iss. 11, pp. 6747-6770
Closed Access
Synthesis and Molecular Docking of Curcumin‐Derived Pyrazole‐Thiazole Hybrids as Potent α‐Glucosidase Inhibitors
Jehan Y. Al‐Humaidi, Lamia A. Albedair, Deepika Maliwal, et al.
Chemistry & Biodiversity (2024)
Closed Access
Synthesis, in vitro α-glucosidase, anti-bacterial, anti-fungal activities and in silico molecular docking studies of benzohydrazide derivatives
Muhammad Mujeeb Ali, Shoaib Khan, Hayat Ullah, et al.
Chemical Data Collections (2023) Vol. 48, pp. 101088-101088
Closed Access
A simple sequential one-pot synthesis of 4-aryl thiazole-based Schiff bases
Preethi Dhanapal, S. L. Manju
Synthetic Communications (2023) Vol. 54, Iss. 2, pp. 111-120
Closed Access
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