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:

Discovery of chalcone derivatives as potential α-glucosidase and cholinesterase inhibitors: Effect of hyperglycemia in paving a path to dementia
Hanan Al-Ghulikah, Ehsan Ullah Mughal, Eslam B. Elkaeed, et al.
Journal of Molecular Structure (2022) Vol. 1275, pp. 134658-134658
Closed Access | Times Cited: 18

Showing 18 citing articles:

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: 23

Exploring Fluorine-Substituted Piperidines as Potential Therapeutics for Diabetes Mellitus and Alzheimer’s Diseases
Ehsan Ullah Mughal, Mohammed B. Hawsawi, Nafeesa Naeem, et al.
European Journal of Medicinal Chemistry (2024) Vol. 273, pp. 116523-116523
Closed Access | Times Cited: 8

Current status ofN-,O-,S-heterocycles as potential alkaline phosphatase inhibitors: a medicinal chemistry overview
Rabab S. Jassas, Nafeesa Naeem, Amina Sadiq, et al.
RSC Advances (2023) Vol. 13, Iss. 24, pp. 16413-16452
Open Access | Times Cited: 16

Novel hydrazones derived from anthranilic acid as potent cholinesterases and α‐glycosidase inhibitors: Synthesis, characterization, and biological effects
Feyzi Sinan Tokalı, Parham Taslimi, Tuğba Taşkın‐Tok, et al.
Journal of Biochemical and Molecular Toxicology (2023) Vol. 38, Iss. 1
Closed Access | Times Cited: 12

Design and synthesis of 2-amino-4,6-diarylpyrimidine derivatives as potent α-glucosidase and α-amylase inhibitors: structure–activity relationship, in vitro , QSAR, molecular docking, MD simulations and drug-likeness studies
Ehsan Ullah Mughal, Samreen Amjid, Amina Sadiq, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 1, pp. 244-260
Closed Access | Times Cited: 11

Synthesis, biological evaluation and molecular modeling studies of modulated benzyloxychalcones as potential acetylcholinesterase inhibitors
Arman Abdalla Ali, Shakhawan Ahmad Mhamad, Aso Hameed Hasan, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 7, pp. 3604-3615
Closed Access | Times Cited: 11

Synthesis of thiadiazole derivatives as competitive inhibitors of α-glucosidase and tyrosinase
Usman Ghani, Ulviye Acar Çevik, Mithun Rudrapal, et al.
Journal of Molecular Structure (2024) Vol. 1307, pp. 138028-138028
Closed Access | Times Cited: 2

Synthesis of zinc phthalocyanine containing 1,2-phenylene bis(3-chloropropanoate) substituted groups and investigation of their metabolic enzyme inhibitory effects
Derya Güngördü Solğun, Nastaran Sadeghian, Parham Taslimi, et al.
Polyhedron (2024) Vol. 264, pp. 117251-117251
Closed Access | Times Cited: 2

Synthesis and Biological Activity of Some Bromophenols and Their Derivatives Including Natural Products
Çetin Bayrak, Parham Taslimi, Namık Kılınç, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 8
Closed Access | Times Cited: 6

13C NMR-based dereplication using MixONat software to decipher potent anti-cholinesterase compounds in Mesua lepidota bark
Sow Tein Leong, Sook Yee Liew, Kooi Yeong Khaw, et al.
Bioorganic Chemistry (2023) Vol. 141, pp. 106859-106859
Closed Access | Times Cited: 6

Synthesis, in vitro Α-Glucosidase, and acetylcholinesterase inhibitory activities of novel Indol-Fused Pyrano[2,3-D]Pyrimidine compounds
Nguyễn Hà Thành, Nguyen Tuan Anh, Tuyet Anh Dang Thi, et al.
Bioorganic & Medicinal Chemistry Letters (2023) Vol. 98, pp. 129566-129566
Closed Access | Times Cited: 6

Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking study of benzimidazole analogues
Hayat Ullah, Ayesha Nawaz, Fazal Rahim, et al.
Chemical Data Collections (2023) Vol. 44, pp. 100996-100996
Closed Access | Times Cited: 3

Synthesis, in-silico antiviral screening and in-vitro antibacterial screening of a novel chalcone derivatives
Akshat Uniyal, Bandana Kumari Thakur, Seema Singh, et al.
Journal of the Indian Chemical Society (2023) Vol. 100, Iss. 7, pp. 101038-101038
Closed Access | Times Cited: 2

Ameliorative activity of standardized Coccoloba uvifera leaves extract against streptozotocin-induced diabetic rats via activation of IRS-1/PI3K/AKT/GLUT2 pathway in liver
Fatma A. Mohamed, Rabab H. Sayed, Mohammed N. A. Khalil, et al.
Future Journal of Pharmaceutical Sciences (2024) Vol. 10, Iss. 1
Open Access

Discovery and synthesis of novel phenoxyacetate ester Schiff base α-glucosidase inhibitors
Zeng Fan, Wan Pang, Yan Yan Yu, et al.
Bioorganic Chemistry (2024) Vol. 154, pp. 107952-107952
Closed Access

Hydroxyl chalcone derivative DK02 as a multi‐target‐directed ligand for Alzheimer's disease: A preclinical study in zebrafish
Balasubramanian Haridevamuthu, Ankit Kumar Bharti, S.P. Ramya Ranjan Nayak, et al.
British Journal of Pharmacology (2024)
Closed Access

Pyrazole‐Imidazopyridine Hydrazones: Synthesis, α‐Glucosidase, α‐Amylase Inhibitory Activity and Computational Studies
D. Ganavi, Shashank M. Patil, Vasantha Kumar, et al.
ChemistrySelect (2023) Vol. 8, Iss. 30
Closed Access | Times Cited: 1

One Pot Synthesis of “3-(4,5-Diphenyl-1H-Imidazol-2-yl)-2-Phenoxyquinolines” and Their Potential as α-Glucosidase Inhibitors: Molecular Docking and MDS Investigation
Peruru Hemanth Kumar, Abbareddy Srikanth, Shree Kumari G R, et al.
Polycyclic aromatic compounds (2023) Vol. 44, Iss. 6, pp. 4239-4260
Closed Access | Times Cited: 1

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