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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:

Utilization of the common functional groups in bioactive molecules: Exploring dual inhibitory potential and computational analysis of keto esters against α-glucosidase and carbonic anhydrase-II enzymes
Imtiaz Khan, Ajmal Khan, Sobia Ahsan Halim, et al.
International Journal of Biological Macromolecules (2020) Vol. 167, pp. 233-244
Closed Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Bio-Oriented Synthesis of Novel Polyhydroquinoline Derivatives as α-Glucosidase Inhibitor for Management of Diabetes
Faiz Talab, Saeed Ullah, Aftab Alam, et al.
ACS Omega (2023) Vol. 8, Iss. 7, pp. 6234-6243
Open Access | Times Cited: 32
Synthesis of new bis(dimethylamino)benzophenone hydrazone for diabetic management: In-vitro and in-silico approach
Momin Khan, Ghulam Ahad, Aftab Alam, et al.
Heliyon (2023) Vol. 10, Iss. 1, pp. e23323-e23323
Open Access | Times Cited: 24
Recent Advances of α-Glucosidase Inhibitors: A Comprehensive Review
Neetu Agrawal, Manisha Sharma, Shikha Singh, et al.
Current Topics in Medicinal Chemistry (2022) Vol. 22, Iss. 25, pp. 2069-2086
Closed Access | Times Cited: 35
Novel polyhydroquinoline Schiff’s base derivatives: synthesis, characterization, in vitro α-glucosidase inhibitory, and molecular docking studies
Nazish Shahab, Duanyang Kong, Mumtaz Ali, et al.
Research on Chemical Intermediates (2023) Vol. 49, Iss. 7, pp. 3005-3028
Closed Access | Times Cited: 20
Polyhydroquinoline Derivatives for Diabetic Management: Synthesis, in Vitro and in Silico Approaches
Faiz Talab, Zainab Zainab, Aftab Alam, et al.
Future Medicinal Chemistry (2023) Vol. 15, Iss. 23, pp. 2195-2208
Closed Access | Times Cited: 17
Probing benzenesulfonamide–thiazolidinone hybrids as multitarget directed ligands for efficient control of type 2 diabetes mellitus through targeting the enzymes: α-glucosidase and carbonic anhydrase II
Mona A. Gamal, Samar H. Fahim, Simone Giovannuzzi, et al.
European Journal of Medicinal Chemistry (2024) Vol. 271, pp. 116434-116434
Closed Access | Times Cited: 6
Synthesis of new diphenyl urea-clubbed imine analogs and its Implications in diabetic management through in vitro and in silico approaches
Anam Rubbab Pasha, Ajmal Khan, Saeed Ullah, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 14
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
Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer’s Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis
Sumera Zaib, Rubina Munir, Muhammad Tayyab Younas, et al.
Molecules (2021) Vol. 26, Iss. 21, pp. 6573-6573
Open Access | Times Cited: 31
Novel tetrahydrobenzo[b]thiophen-2-yl)urea derivatives as novel α-glucosidase inhibitors: Synthesis, kinetics study, molecular docking, and in vivo anti-hyperglycemic evaluation
Hong-Xu Xie, Juan Zhang, Yue Li, et al.
Bioorganic Chemistry (2021) Vol. 115, pp. 105236-105236
Closed Access | Times Cited: 26
New acetylphenol-based acyl thioureas broaden the scope of drug candidates for urease inhibition: synthesis, in vitro screening and in silico analysis
Urage Zahra, Sumera Zaib, Aamer Saeed, et al.
International Journal of Biological Macromolecules (2021) Vol. 198, pp. 157-167
Closed Access | Times Cited: 25
Personal Glucose Meter for α-Glucosidase Inhibitor Screening Based on the Hydrolysis of Maltose
Tao Tian, Guoying Chen, Hao Zhang, et al.
Molecules (2021) Vol. 26, Iss. 15, pp. 4638-4638
Open Access | Times Cited: 18
Bis-pharmacophore of cinnamaldehyde-clubbed thiosemicarbazones as potent carbonic anhydrase-II inhibitors
Asif Rasool, Zahra Batool, Majid Khan, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 13
Synthesis, biological evaluation, and molecular docking study of chromen‐linked hydrazine carbothioamides as potent α‐glucosidase inhibitors
Rabia Basri, Saeed Ullah, Sobia Ahsan Halim, et al.
Drug Development Research (2023) Vol. 84, Iss. 5, pp. 962-974
Closed Access | Times Cited: 6
Rhodanine-3-acetamide derivatives as aldose and aldehyde reductase inhibitors to treat diabetic complications: synthesis, biological evaluation, molecular docking and simulation studies
Mohsinul Mulk Bacha, Humaira Nadeem, Sumera Zaib, et al.
BMC Chemistry (2021) Vol. 15, Iss. 1
Open Access | Times Cited: 14
Discovery of urease inhibitory effect of sulfamate derivatives: Biological and computational studies
Sumera Zaib, Muhammad Tayyab Younas, Seyed–Omar Zaraei, et al.
Bioorganic Chemistry (2021) Vol. 119, pp. 105545-105545
Closed Access | Times Cited: 14
Two Myricetin-Derived Flavonols from Morella rubra Leaves as Potent α-Glucosidase Inhibitors and Structure-Activity Relationship Study by Computational Chemistry
Yilong Liu, Ruoqi Wang, Chuanhong Ren, et al.
Oxidative Medicine and Cellular Longevity (2022) Vol. 2022, pp. 1-16
Open Access | Times Cited: 10
Synthesis, Biological Evaluation, and In Silico Studies of Novel Coumarin-Based 4H,5H-pyrano[3,2-c]chromenes as Potent β-Glucuronidase and Carbonic Anhydrase Inhibitors
Nadia Arif, Zahid Shafiq, Khalid Mahmood, et al.
ACS Omega (2022) Vol. 7, Iss. 32, pp. 28605-28617
Open Access | Times Cited: 10
Synthesis of novel substituted quinoline derivatives as diabetics II inhibitors and along with their in-silico studies
Satya Kumar Avula, Saeed Ullah, Sobia Ahsan Halim, et al.
Journal of Molecular Structure (2022) Vol. 1274, pp. 134560-134560
Closed Access | Times Cited: 9
Biochemical and computational inhibition of α-glucosidase by novel metronidazole-linked 1 H -1,2,3-triazole and carboxylate moieties: kinetics and dynamic investigations
Saeed Ullah, Sobia Ahsan Halim, Muhammad Waqas, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-21
Closed Access | Times Cited: 1
Molecular Architecture, Computational Exploration and Synthesis of PCL-PEG-PCL Triblock Copolymer-Based Reverse Nanomicelles: A Promising Method for Enhancing Macromolecular Delivery by Using Infliximab as a Model Protein
Dildar Khan, Naveed Ahmed, Maimoona Qindeel, et al.
BioNanoScience (2024) Vol. 14, Iss. 5, pp. 4968-4984
Closed Access | Times Cited: 1
Experimental and Computational Analysis of Newly Synthesized Benzotriazinone Sulfonamides as Alpha-Glucosidase Inhibitors
Zunera Khalid, Maha Abdallah Alnuwaiser, Hafiz Adnan Ahmad, et al.
Molecules (2022) Vol. 27, Iss. 20, pp. 6783-6783
Open Access | Times Cited: 8
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
Eupholaricanone, a potent α-glucosidase anthracene derivative from Euphorbia larica Boiss
Najeeb Ur Rehman, Rabia Maqsood, Saeed Ullah, et al.
South African Journal of Botany (2022) Vol. 148, pp. 88-92
Open Access | Times Cited: 7
Discovery of Hydrazone Scaffolds as Potent and Selective Multitarget‐Directed Ligands for the Treatment of Neurodegenerative Disorders
Muhammad Tayyab Younas, Sumera Zaib, Imtiaz Khan
ChemistrySelect (2023) Vol. 8, Iss. 47
Closed Access | Times Cited: 3
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