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:

Structure-directed expansion of biphenyl-pyridone derivatives as potent non-nucleoside reverse transcriptase inhibitors with significantly improved potency and safety
Limin Zhao, Christophe Pannecouque, Erik De Clercq, et al.
Chinese Chemical Letters (2023) Vol. 34, Iss. 12, pp. 108261-108261
Closed Access | Times Cited: 8

Showing 8 citing articles:

Structure-based discovery of novel piperidine-biphenyl-DAPY derivatives as non-nucleoside reverse transcriptase inhibitors featuring improved potency, safety, and selectivity: From piperazine-biphenyl-DAPYs to piperidine-biphenyl-DAPYs
Wenjuan Huang, Christophe Pannecouque, Erik De Clercq, et al.
European Journal of Medicinal Chemistry (2024) Vol. 276, pp. 116668-116668
Closed Access | Times Cited: 5

Structure-based discovery of novel diarylpyrimidines as potent and selective Non-Nucleoside reverse transcriptase inhibitors: From CH(CN)-Biphenyl-Diarylpyrimidines to C NNH2-Biphenyl-Diarylpyrimidines
Xiaomei Chen, Christophe Pannecouque, Erik De Clercq, et al.
European Journal of Medicinal Chemistry (2025) Vol. 285, pp. 117271-117271
Closed Access

Structure-based design of novel heterocycle-substituted ATDP analogs as non-nucleoside reverse transcriptase inhibitors with improved selectivity and solubility
Limin Zhao, Christophe Pannecouque, Erik De Clercq, et al.
Acta Pharmaceutica Sinica B (2023) Vol. 13, Iss. 12, pp. 4906-4917
Open Access | Times Cited: 7

Synthesis, evaluation, and computational chemistry of novel selenenyl sulfides as 3C protease inhibitors with strong cell-based antiviral activity
Jin‐Yin Tang, Shengwang Dai, Xiaofang Wang, et al.
Arabian Journal of Chemistry (2024) Vol. 17, Iss. 4, pp. 105713-105713
Open Access | Times Cited: 2

Synthetic approaches and application of clinically approved small-molecule Anti-HIV drugs: An update
Lu Sun, Peng Nie, Luan Li, et al.
European Journal of Medicinal Chemistry (2023) Vol. 261, pp. 115847-115847
Closed Access | Times Cited: 5

Advances in diarylpyrimidines and related analogues as HIV-1 nonnucleoside reverse transcriptase inhibitors (2019-2023)
M. Nie, Shuang‐Shuang Zhang, Shuang‐Xi Gu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 280, pp. 116973-116973
Closed Access | Times Cited: 1

Improving the anti-HIV-1 activity and solubility of poorly water-soluble DAPYs by heteroaromatic replacement strategy: From naphthalene-DAPYs to quinoline-DAPYs
Ruo-Lan Zhou, Chao Yu, Christophe Pannecouque, et al.
Bioorganic Chemistry (2023) Vol. 140, pp. 106821-106821
Closed Access | Times Cited: 3

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