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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:

Semi-Synthesis of N-Aryl Amide Analogs of Piperine from Piper nigrum and Evaluation of Their Antitrypanosomal, Antimalarial, and Anti-SARS-CoV-2 Main Protease Activities
Rattanaporn Wansri, Aye Chan Khine Lin, Jutharat Pengon, et al.
Molecules (2022) Vol. 27, Iss. 9, pp. 2841-2841
Open Access | Times Cited: 17

Showing 17 citing articles:

Evaluation of Antimicrobial Activity and Cytotoxicity Effects of Extracts of Piper nigrum L. and Piperine
Fabrine Silva Alves, Jorddy Neves Cruz, Ingryd Nayara de Farias Ramos, et al.
Separations (2022) Vol. 10, Iss. 1, pp. 21-21
Open Access | Times Cited: 49
Promising SARS-CoV-2 main protease inhibitor ligand-binding modes evaluated using LB-PaCS-MD/FMO
Kowit Hengphasatporn, Ryuhei Harada, Patcharin Wilasluck, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 30
Design, Synthesis, and Antiviral Activity of Fragmented-Lapatinib Aminoquinazoline Analogs towards SARS-CoV-2 Inhibition
Ayomide Olamide Adediji, Akeanan Sroithongmoon, Aphinya Suroengrit, et al.
European Journal of Medicinal Chemistry (2025), pp. 117303-117303
Closed Access
A Comprehensive Update of Anti-COVID-19 Activity of Heterocyclic Compounds
M. Tariq Nazir, Matloob Ahmad, Sana Aslam, et al.
Drug Design Development and Therapy (2024) Vol. Volume 18, pp. 1547-1571
Open Access | Times Cited: 3
Piperine: Chemistry and Biology
Jin Han, Shaoyong Zhang, Jun He, et al.
Toxins (2023) Vol. 15, Iss. 12, pp. 696-696
Open Access | Times Cited: 8
Synthesis of Piperine-Based Ester Derivatives with Diverse Aromatic Rings and Their Agricultural Bioactivities against Tetranychus cinnabarinus Boisduval, Aphis citricola Van der Goot, and Eriosoma lanigerum Hausmann
Tian-Ze Li, Min Lv, Houpeng Wen, et al.
Insects (2022) Vol. 14, Iss. 1, pp. 40-40
Open Access | Times Cited: 10
Identification of Promising Sulfonamide Chalcones as Inhibitors of SARS-CoV-2 3CLpro through Structure-Based Virtual Screening and Experimental Approaches
Piyatida Pojtanadithee, Kowit Hengphasatporn, Aphinya Suroengrit, et al.
Journal of Chemical Information and Modeling (2023) Vol. 63, Iss. 16, pp. 5244-5258
Closed Access | Times Cited: 5
Synthesis and structure-activity-toxicity relationships of DABCO-containing ammonium amphiphiles based on natural isatin scaffold
Tatiana N. Pashirova, Zukhra Shaihutdinova, A.E. Vandyukov, et al.
Journal of Molecular Liquids (2022) Vol. 365, pp. 120217-120217
Closed Access | Times Cited: 7
N-Containing α-Mangostin Analogs via Smiles Rearrangement as the Promising Cytotoxic, Antitrypanosomal, and SARS-CoV-2 Main Protease Inhibitory Agents
Nan Yadanar Lin Pyae, Arnatchai Maiuthed, Wongsakorn Phongsopitanun, et al.
Molecules (2023) Vol. 28, Iss. 3, pp. 1104-1104
Open Access | Times Cited: 3
A combination of structure-based virtual screening and experimental strategies to identify the potency of caffeic acid ester derivatives as SARS-CoV-2 3CLpro inhibitor from an in-house database
Piyatida Pojtanadithee, Kulpornsorn Isswanich, Koonchira Buaban, et al.
Biophysical Chemistry (2023) Vol. 304, pp. 107125-107125
Open Access | Times Cited: 3
Developing semisynthesis methods for neglected tropical diseases
Sasadhar Majhi, M. Sivakumar
Elsevier eBooks (2024), pp. 439-458
Closed Access
Structure-based Drug Design of New Cinnamic Acid Derivatives as Tyrosinase Inhibitors
Fayezeh Yousefnejad, Mohammad Hosein Sayahi, Ali Moazzam, et al.
Letters in Organic Chemistry (2024) Vol. 21, Iss. 8, pp. 647-654
Closed Access
Alpha and gamma mangostins inhibit wild-type B SARS-CoV-2 more effectively than the SARS-CoV-2 variants and the major target is unlikely the 3C-like protease
Aphinya Suroengrit, Van Cao, Patcharin Wilasluck, et al.
Heliyon (2024) Vol. 10, Iss. 11, pp. e31987-e31987
Open Access
Design, Synthesis, and Biological Evaluation of Darunavir Analogs as HIV-1 Protease Inhibitors
Muhammad Asad Ur Rehman, Hathaichanok Chuntakaruk, Soraat Amphan, et al.
ACS Bio & Med Chem Au (2024) Vol. 4, Iss. 5, pp. 242-256
Open Access
A Combination of Structure-based Virtual Screening and Experimental Strategies to Identify the Potency of Caffeic Acid Ester Derivatives as SARS-CoV-2 3CLpro Inhibitor from an In-house Database
Piyatida Pojtanadithee, Kulpornsorn Isswanich, Koonchira Buaban, et al.
Research Square (Research Square) (2023)
Open Access
ETHNOBOTANY, PHARMACOLOGICAL APPLICATION, PHYTOCHEMISTRY AND THERAPEUTIC POTENTIAL OF BLACK PEPPER (PIPER NIGRUM L.): AN UPDATED REVIEW
Shabnam Anjum Ara, Shaheen Akhlaq, Merajul Haque, et al.
Indian Journal of Unani Medicine (2023) Vol. 16, Iss. 01, pp. 35-46
Open Access
Computational approaches for identifying bioactive compounds inhibiting SARS-CoV-2 main protease
Piyatida Pojtanadithee
(2022)
Open Access
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