Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Probing 2-acetylbenzofuran hydrazones and their metal complexes as α-glucosidase inhibitors
Samra Khan, Muhammad Tariq, Muhammad Ashraf, et al.
Bioorganic Chemistry (2020) Vol. 102, pp. 104082-104082
Closed Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

A review on α-glucosidase inhibitory activity of first row transition metal complexes: a futuristic strategy for treatment of type 2 diabetes
Marzieh Sohrabi, Mohammad Reza Binaeizadeh, Aida Iraji, et al.
RSC Advances (2022) Vol. 12, Iss. 19, pp. 12011-12052
Open Access | Times Cited: 41
Synthesis, biological evaluation and molecular modelling of 3-Formyl-6-isopropylchromone derived thiosemicarbazones as α-glucosidase inhibitors
Rabia Basri, Saeed Ullah, Ajmal Khan, et al.
Bioorganic Chemistry (2023) Vol. 139, pp. 106739-106739
Closed Access | Times Cited: 22
Novel potential metabolic enzymes inhibitor, photosensitizer and antibacterial agents based on water-soluble phthalocyanine bearing imidazole derivative
Armağan Günsel, Parham Taslimi, Göknur Yaşa Atmaca, et al.
Journal of Molecular Structure (2021) Vol. 1237, pp. 130402-130402
Closed Access | Times Cited: 41
Design and synthesis of novel quinazolinone-pyrazole derivatives as potential α-glucosidase inhibitors: Structure-activity relationship, molecular modeling and kinetic study
Fateme Azimi, Homa Azizian, Mohammad Najafi, et al.
Bioorganic Chemistry (2021) Vol. 114, pp. 105127-105127
Closed Access | Times Cited: 40
Metal complexes of hydrazone–oxime derivative as promising in vitro antimicrobial agents against some fungal and bacterial strains
Essam Hassan, Mohamad M. Ebrahium, Adel M. Ebrahium
Applied Organometallic Chemistry (2022) Vol. 36, Iss. 5
Closed Access | Times Cited: 30
Design, synthesis, in-vitro and in-silico studies of novel N-heterocycle based hydrazones as α-glucosidase inhibitors
Rehmatullah Farooqi, Naeem Ullah, Ajmal Khan, et al.
Bioorganic Chemistry (2025) Vol. 156, pp. 108155-108155
Closed Access
A glance into Schiff-based α-glucosidase inhibitors in medicinal chemistry
Sakineh Dadashpour
Medicinal Chemistry Research (2025)
Closed Access
Isatin-hydrazide conjugates as potent α-amylase and α-glucosidase inhibitors: Synthesis, structure and in vitro evaluations
Inzamam Abbasi, Humaira Nadeem, Adil Saeed, et al.
Bioorganic Chemistry (2021) Vol. 116, pp. 105385-105385
Closed Access | Times Cited: 39
PEPPSI type Pd(II)NHC complexes bearing chloro-/fluorobenzyl group: Synthesis, characterization, crystal structures, α-glycosidase and acetylcholinesterase inhibitory properties
Selma Bal, Özlem Demirci, Betül Şen, et al.
Polyhedron (2021) Vol. 198, pp. 115060-115060
Closed Access | Times Cited: 38
Novel benzothiazole sulfonamides as potent α-glucosidase and cholinesterase inhibitors: Design, synthesis, structural properties, biological evaluation and docking studies
Syeda Khair-ul-Bariyah, Muhammad Sarfraz, Ahsan Sharif, et al.
Journal of Molecular Structure (2023) Vol. 1299, pp. 137118-137118
Closed Access | Times Cited: 14
Novel molecular hybrids of EGCG and quinoxaline: Potent multi-targeting antidiabetic agents that inhibit α-glucosidase, α-amylase, and oxidative stress
Manan Kothari, K. K. Kannan, Revathy Sahadevan, et al.
International Journal of Biological Macromolecules (2024) Vol. 263, pp. 130175-130175
Closed Access | Times Cited: 4
Buchwald coupling promoted benign synthesis of benzoxazine derivatives supported Cu complexes with their multipurpose potential in antimicrobial and catalytical fields
Sagar R. Sangani, Ranjitsinh C. Dabhi, Mukesh Kawad, et al.
Journal of Molecular Structure (2023) Vol. 1285, pp. 135380-135380
Closed Access | Times Cited: 11
Novel phenylpyrimidine derivatives containing a hydrazone moiety protect rice seedlings from injury by metolachlor
Xile Deng, Wenna Zheng, Can Jin, et al.
Bioorganic Chemistry (2021) Vol. 108, pp. 104645-104645
Closed Access | Times Cited: 25
Exploration of nonlinear optical enhancement and interesting optical behavior with pyrene moiety as the conjugated donor and efficient modification in acceptor moieties
Muhammad Khalid, Muhammad Usman Khan, Nimra Azhar, et al.
Optical and Quantum Electronics (2022) Vol. 54, Iss. 7
Closed Access | Times Cited: 17
Silver N‐heterocyclic carbene complexes bearing fluorinated benzyl group: Synthesis, characterization, crystal structure, computational studies, and inhibitory properties against some metabolic enzymes
Selma Bal, Özlem Demirci, Betül Şen, et al.
Applied Organometallic Chemistry (2021) Vol. 35, Iss. 9
Closed Access | Times Cited: 21
Novel amino acid Schiff base Zn(II) complexes as new therapeutic approaches in diabetes and Alzheimer's disease: Synthesis, characterization, biological evaluation, and molecular docking studies
Ayşegül Şenocak, Nilay Taş, Parham Taslimi, et al.
Journal of Biochemical and Molecular Toxicology (2021) Vol. 36, Iss. 3
Closed Access | Times Cited: 21
Benzimidazolium salts bearing the trifluoromethyl group as organofluorine compounds: Synthesis, characterization, crystal structure, in silico study, and inhibitory profiles against acetylcholinesterase and α‐glycosidase
Burcu Tezcan, Yetkın Gök, Resul Sevinçek, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 4
Closed Access | Times Cited: 14
Anti-enzymatic and DNA docking studies of montelukast: A multifaceted molecular scaffold with in vitro investigations, molecular expression analysis and molecular dynamics simulations
Shawana Abdullah, Ambar Iqbal, Avinash Karkada Ashok, et al.
Heliyon (2024) Vol. 10, Iss. 2, pp. e24470-e24470
Open Access | Times Cited: 2
Synthesis, in vitro α‐Glucosidase Inhibition, DFT Calculations, and Molecular Docking Studies of Some New Substituted 2,5‐Bis(pyrazolyl)‐1,3,4‐oxadiazoles
Faryal Chaudhry, Shawana Abdullah, Mehr un‐Nisa, et al.
ChemistrySelect (2024) Vol. 9, Iss. 9
Closed Access | Times Cited: 2
Non-aggregated and water soluble non-peripherally octa substituted Co(II) and Cu(II) phthalocyanines: Synthesis and α-glucosidase inhibitory effects
Zekeriya Bıyıklıoğlu, Hüseyin Baş, Gökçe Seyhan, et al.
Journal of Inorganic Biochemistry (2024) Vol. 257, pp. 112581-112581
Closed Access | Times Cited: 2
Synthesis and characterization of 1-amidino-O-alkylureas metal complexes as α- glucosidase Inhibitors: Structure-activity relationship, molecular docking, and kinetic studies
Firouz Matloubi Moghaddam, Maryam Daneshfar, Zahra Daneshfar, et al.
Journal of Molecular Structure (2021) Vol. 1250, pp. 131726-131726
Closed Access | Times Cited: 18
Novel N′-substituted benzylidene benzohydrazides linked to 1,2,3-triazoles: potent α-glucosidase inhibitors
Mina Saeedi, Roshanak Hariri, Aida Iraji, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 7
Synthesis of novel coumarin-based thiosemicarbazones and their implications in diabetic management via in-vitro and in-silico approaches
Syeda Bakhtawar Zahra, Saeed Ullah, Sobia Ahsan Halim, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 7
New quinoxalin‐1,3,4‐oxadiazole derivatives: Synthesis, characterization, in vitro biological evaluations, and molecular modeling studies
Roghieh Mirzazadeh, Mohammad Asgari, Ebrahim Barzegari, et al.
Archiv der Pharmazie (2021) Vol. 354, Iss. 9
Closed Access | Times Cited: 17
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
Page 1 - Next Page

Scroll to top