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:

Design and synthesis of new benzylidene-quinazolinone hybrids as potential anti-diabetic agents: In vitro α-glucosidase inhibition, and docking studies
Mohamed M. Khalifa, Helmy Sakr, Albaraa Ibrahim, et al.
Journal of Molecular Structure (2021) Vol. 1250, pp. 131768-131768
Closed Access | Times Cited: 26

Showing 1-25 of 26 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

Inhibitory Mechanism of Prenylated Flavonoids Isolated from Mulberry Leaves on α-Glucosidase by Multi-Spectroscopy and Molecular Dynamics Simulation
Jinlong Tian, Min Zhao, Jingyi Xu, et al.
Journal of Agricultural and Food Chemistry (2023) Vol. 71, Iss. 23, pp. 9135-9147
Closed Access | Times Cited: 14

Identification of isobenzofuranone derivatives as promising antidiabetic agents: Synthesis, in vitro and in vivo inhibition of α-glucosidase and α-amylase, computational docking analysis and molecular dynamics simulations
Shabab Zahra, Sumera Zaib, Imtiaz Khan
International Journal of Biological Macromolecules (2024) Vol. 259, pp. 129241-129241
Closed Access | Times Cited: 5

Preparation, Agricultural Bioactivity Evaluation, Structure–Activity Relationships Estimation, and Molecular Docking of Some Quinazoline Compounds
Bahgat R. M. Hussein, Amr H. Moustafa, Aly Abdou, et al.
Journal of Agricultural and Food Chemistry (2024)
Closed Access | Times Cited: 4

Synthesis, biological evaluation and action mechanism of 7H-[1,2,4] triazolo [3,4-b] [1,3,4] thiadiazine-phenylhydrazone derivatives as α-glucosidase inhibitors
Qianqian Feng, Jinfeng Zhang, Shuang Luo, et al.
European Journal of Medicinal Chemistry (2023) Vol. 262, pp. 115920-115920
Closed Access | Times Cited: 12

Thiazolidinone‐Heterocycle Frameworks: A Concise Review of Their Pharmacological Significance
Pule Seboletswe, Nosipho Cele, Parvesh Singh
ChemMedChem (2023) Vol. 18, Iss. 7
Closed Access | Times Cited: 11

Synthesis, ADMT prediction, and in vitro and in silico α-glucosidase inhibition evaluations of new quinoline–quinazolinone–thioacetamides
Sajedeh Safapoor, Mohammad Halimi, Minoo Khalili Ghomi, et al.
RSC Advances (2023) Vol. 13, Iss. 28, pp. 19243-19256
Open Access | Times Cited: 7

Imidazo[1,2-c]quinazolines as a novel and potent scaffold of α-glucosidase inhibitors: design, synthesis, biological evaluations, and in silico studies
Fariba Peytam, Faezeh Sadat Hosseini, Malak Hekmati, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 6

Synthesis and bioactivities evaluation of quinazolin-4(3H)-one derivatives as α-glucosidase inhibitors
Mahshid Moheb, Aida Iraji, Navid Dastyafteh, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 10

Microwave accelerated green access to functionalized pyrazolo[5,1-b]quinazoline-3-carboxylate scaffold and their pharmacological screening
Reena C. Patel, Dhanji P. Rajani, Anju Kunjadiya, et al.
Journal of Molecular Structure (2024) Vol. 1310, pp. 138295-138295
Closed Access | Times Cited: 1

Design and Synthesis of Some New Oxadiazole Derivatives as Anticancer Agents
Mo’men Salem, Rezk R. Ayyad, Helmy Sakr
International Journal of Organic Chemistry (2022) Vol. 12, Iss. 02, pp. 64-74
Open Access | Times Cited: 8

Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
Fahimeh Taayoshi, Aida Iraji, Ali Moazzam, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 6

Design and Synthesis of New Compounds Derived from Phenyl Hydrazine and Different Aldehydes as Anticancer Agents
Mo’men Salem, Rezk R. Ayyad, Helmy Sakr, et al.
International Journal of Organic Chemistry (2022) Vol. 12, Iss. 01, pp. 28-39
Open Access | Times Cited: 5

An Insight into the Development of Potential Antidiabetic Agents along with their Therapeutic Targets
Siddhita Tiwari, Paranjeet Kaur, Deepali Gupta, et al.
Endocrine Metabolic & Immune Disorders - Drug Targets (2023) Vol. 24, Iss. 1, pp. 50-85
Closed Access | Times Cited: 2

Environmentally Friendly Approach to the Synthesis of 3‐[Benzylideneamino]‐2‐methylquinazolin‐4(3H)‐one Derivatives and Calculation of Their Toxicity
Maja Molnar, Tatjana Gazivoda Kraljević, Valentina Pavić, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 8
Closed Access | Times Cited: 2

A methodological approach for the synthesis of 4-aryl-8-arylidene-2-cyanoimino-1,2,3,4,5,6,7,8-octahydroquinazolines
Amr H. Moustafa, Bahgat R. M. Hussein
Synthetic Communications (2022) Vol. 52, Iss. 8, pp. 1131-1138
Closed Access | Times Cited: 4

Beta-1 Receptor (β1) in the Heart Specific Indicate to Stereoselectivity
Ayyad Rezk Rezk, Mansour Ahmed Mohamed, Nejm Ahmed Mohamed, et al.
Archives of Pharmacy and Pharmaceutical Sciences (2024) Vol. 8, Iss. 1, pp. 082-088
Open Access

Synthesis, In Silico, and In Vitro Evaluation of the Potential Antioxidant Activity of New Quinazoline Derivatives
Mohammed G. A. Al-Khuzaie, Lawand Hama karim kaka Hama, Suaad M. H. Al-Majidi
Russian Journal of Bioorganic Chemistry (2024) Vol. 50, Iss. 4, pp. 1476-1490
Closed Access

Quinoline-thiosemicarbazone-1,2,3-triazole-acetamide derivatives as new potent α-glucosidase inhibitors
Aynaz Khademian, Mohammad Halimi, Reza Azarbad, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access

N2,N6-Bis(6-iodo-2-methyl-4-oxoquinazolin-3(4H)-yl)pyridine-2,6-dicarboxamide
Maja Molnar, Mario Komar, Igor Jerković
Molbank (2022) Vol. 2022, Iss. 4, pp. M1500-M1500
Open Access | Times Cited: 1

[2,2'-Bipyrrolidine]-1,1'-disulfonic Acid as a Highly Active Catalyst for the Efficient Synthesis of Bis-triazoloquinazolinone Derivatives
Fatemeh Ehsaei, N. Montazeri, Masoud Mohammadi Zeydi
Russian Journal of Organic Chemistry (2023) Vol. 59, Iss. S1, pp. S155-S163
Closed Access

Page 1 - Next Page

Scroll to top