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Bioorganic Chemistry
|
January 13, 2026
Design and evaluation of DNA aptamers with "stem-loop-chain" structures for spectrum neutralization of ricin and abrin
Zhenfang Xu, Jiawei Zhang, Shuangshuang Liu, et al.
International Journal of Molecular Sciences
|
September 13, 2025
A Bifunctional SARS-CoV-2 Entry Inhibitor Targeting the Host Protease TMPRSS2 and Viral Spike Protein HR1 Region
Huan Wang, Qing Li, Zhe Yin, et al.
The Journal of Antimicrobial Chemotherapy
|
February 7, 2014
Artificial peptides conjugated with cholesterol and pocket-specific small molecules potently inhibit infection by laboratory-adapted and primary HIV-1 isolates and enfuvirtide-resistant HIV-1 strains
Chao Wang, Weiguo Shi, Lifeng Cai, et al.
Pharmaceuticals (Basel, Switzerland)
|
December 31, 2025
Synthesis and Evaluation of AS1411-Lenalidomide-Targeted Degradation Chimera in Antitumor Therapy
Xueling Ma, Shuangshuang Liu, Xiao Dong, et al.
Chemical Communications (Cambridge, England)
|
October 25, 2012
Design of highly potent HIV fusion inhibitors based on artificial peptide sequences
Weiguo Shi, Lifeng Cai, Lu Lu, et al.
Journal of Medicinal Chemistry
|
March 6, 2013
Design, synthesis, and biological evaluation of highly potent small molecule-peptide conjugates as new HIV-1 fusion inhibitors
Chao Wang, Weiguo Shi, Lifeng Cai, et al.
Journal of Medicinal Chemistry
|
September 8, 2018
De Novo Design of α-Helical Lipopeptides Targeting Viral Fusion Proteins: A Promising Strategy for Relatively Broad-Spectrum Antiviral Drug Discovery
Chao Wang, Lei Zhao, Shuai Xia, et al.
Journal of Medicinal Chemistry
|
August 22, 2025
Potent Inhibition of Human Betacoronaviruses by a Short Double-Stapled Peptide Mimicking the HR2 Core Region in Viral Spike Protein
Chao Wang, Qing Li, Yuanzhou Wang, et al.
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Search research articles
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Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Bioorganic Chemistry
|
January 13, 2026
Design and evaluation of DNA aptamers with "stem-loop-chain" structures for spectrum neutralization of ricin and abrin
Zhenfang Xu, Jiawei Zhang, Shuangshuang Liu, et al.
International Journal of Molecular Sciences
|
September 13, 2025
A Bifunctional SARS-CoV-2 Entry Inhibitor Targeting the Host Protease TMPRSS2 and Viral Spike Protein HR1 Region
Huan Wang, Qing Li, Zhe Yin, et al.
The Journal of Antimicrobial Chemotherapy
|
February 7, 2014
Artificial peptides conjugated with cholesterol and pocket-specific small molecules potently inhibit infection by laboratory-adapted and primary HIV-1 isolates and enfuvirtide-resistant HIV-1 strains
Chao Wang, Weiguo Shi, Lifeng Cai, et al.
Pharmaceuticals (Basel, Switzerland)
|
December 31, 2025
Synthesis and Evaluation of AS1411-Lenalidomide-Targeted Degradation Chimera in Antitumor Therapy
Xueling Ma, Shuangshuang Liu, Xiao Dong, et al.
Chemical Communications (Cambridge, England)
|
October 25, 2012
Design of highly potent HIV fusion inhibitors based on artificial peptide sequences
Weiguo Shi, Lifeng Cai, Lu Lu, et al.
Journal of Medicinal Chemistry
|
March 6, 2013
Design, synthesis, and biological evaluation of highly potent small molecule-peptide conjugates as new HIV-1 fusion inhibitors
Chao Wang, Weiguo Shi, Lifeng Cai, et al.
Journal of Medicinal Chemistry
|
September 8, 2018
De Novo Design of α-Helical Lipopeptides Targeting Viral Fusion Proteins: A Promising Strategy for Relatively Broad-Spectrum Antiviral Drug Discovery
Chao Wang, Lei Zhao, Shuai Xia, et al.
Journal of Medicinal Chemistry
|
August 22, 2025
Potent Inhibition of Human Betacoronaviruses by a Short Double-Stapled Peptide Mimicking the HR2 Core Region in Viral Spike Protein
Chao Wang, Qing Li, Yuanzhou Wang, et al.
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