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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:

Positional scanning of natural product hispidol’s ring-B: discovery of highly selective human monoamine oxidase-B inhibitor analogues downregulating neuroinflammation for management of neurodegenerative diseases
Ahmed H.E. Hassan, Hyeon Jeong Kim, Min Sung Gee, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 37, Iss. 1, pp. 768-780
Open Access | Times Cited: 15

Showing 15 citing articles:

Bestatin analogs-4-quinolinone hybrids as antileishmanial hits: Design, repurposing rational, synthesis, in vitro and in silico studies
Ahmed H.E. Hassan, Kazem Mahmoud, Trong-Nhat Phan, et al.
European Journal of Medicinal Chemistry (2023) Vol. 250, pp. 115211-115211
Closed Access | Times Cited: 13
Dual-Target Inhibitors Based on Acetylcholinesterase: Novel Agents for Alzheimer's Disease
Xingyi Zhao, Qiaoguan Hu, Xiaoqian Wang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 279, pp. 116810-116810
Closed Access | Times Cited: 4
Antimicrobial resistance: new insights and therapeutic implications
Bashir Ahmad Sheikh, Basharat Ahmad Bhat, Manzoor Ahmad Mir
Applied Microbiology and Biotechnology (2022) Vol. 106, Iss. 19-20, pp. 6427-6440
Closed Access | Times Cited: 19
Design, Rational Repurposing, Synthesis, In Vitro Evaluation, Homology Modeling and In Silico Study of Sulfuretin Analogs as Potential Antileishmanial Hit Compounds
Ahmed H.E. Hassan, Trong-Nhat Phan, Yeonwoo Choi, et al.
Pharmaceuticals (2022) Vol. 15, Iss. 9, pp. 1058-1058
Open Access | Times Cited: 13
A monoamine oxidase B inhibitor ethyl ferulate suppresses microglia-mediated neuroinflammation and alleviates ischemic brain injury
Xinxin Zou, Shenghan Gao, Jiangnan Li, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 12
Escaping ESKAPE resistance: in vitro and in silico studies of multifunctional carbamimidoyl-tethered indoles against antibiotic-resistant bacteria
Kanika Gulia, Ahmed H.E. Hassan, Justin R. Lenhard, et al.
Royal Society Open Science (2023) Vol. 10, Iss. 4
Open Access | Times Cited: 7
Synthesis and Biological Evaluation of O6-Aminoalkyl-Hispidol Analogs as Multifunctional Monoamine Oxidase-B Inhibitors towards Management of Neurodegenerative Diseases
Ahmed H.E. Hassan, Hyeon Jeong Kim, Keontae Park, et al.
Antioxidants (2023) Vol. 12, Iss. 5, pp. 1033-1033
Open Access | Times Cited: 5
In Silico and In Vitro Evaluation of Some Amidine Derivatives as Hit Compounds towards Development of Inhibitors against Coronavirus Diseases
Ahmed H.E. Hassan, Selwan M. El‐Sayed, Mizuki Yamamoto, et al.
Viruses (2023) Vol. 15, Iss. 5, pp. 1171-1171
Open Access | Times Cited: 5
Synthesis, In-Vitro, In-Vivo screening, and molecular docking of disubstituted aminothiazole derivatives and their selenium nanoparticles as potential antiparkinson agents
Lamiaa O. El-Halaby, Nada F. Abo El‐Magd, Samar J. Almehmadi, et al.
Journal of Molecular Structure (2024) Vol. 1315, pp. 138951-138951
Closed Access | Times Cited: 1
Synthesis and biological evaluation of O4′-benzyl-hispidol derivatives and analogs as dual monoamine oxidase-B inhibitors and anti-neuroinflammatory agents
Ahmed H.E. Hassan, Yeonwoo Choi, Rium Kim, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 110, pp. 117826-117826
Closed Access | Times Cited: 1
Design, synthesis, and evaluation of new anti-inflammatory natural products amide derivatives endowed with anti-blood cancer activity towards development of potential multifunctional agents against hematological cancers
Ahmed H.E. Hassan, Hye Jin Kim, Su‐Jin Jung, et al.
European Journal of Medicinal Chemistry (2023) Vol. 258, pp. 115566-115566
Closed Access | Times Cited: 4
Rational repurposing, synthesis, in vitro and in silico studies of chromone-peptidyl hybrids as potential agents against Leishmania donovani
Ahmed H.E. Hassan, Waleed A. Bayoumi, Selwan M. El‐Sayed, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 4
The mechanism of Renshen-Fuzi herb pair for treating heart failure—Integrating a cardiovascular pharmacological assessment with serum metabolomics
Xiaofei Chen, Yulong Chen, Shiyang Xie, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 6
Design, Synthesis, In Vitro, and In Silico Studies of New N5-Substituted-pyrazolo[3,4-d]pyrimidinone Derivatives as Anticancer CDK2 Inhibitors
Waheed A. Zaki, Selwan M. El‐Sayed, Mohamed Alswah, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 11, pp. 1593-1593
Open Access | Times Cited: 2
Repurposing Synthetic Congeners of a Natural Product Aurone Unveils a Lead Antitumor Agent Inhibiting Folded P-Loop Conformation of MET Receptor Tyrosine Kinase
Ahmed H.E. Hassan, Cai Yi Wang, Cheol Jung Lee, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 11, pp. 1597-1597
Open Access | Times Cited: 2
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