Kun Wang

发表

d(TGGGAG) with 5'-nucleobase-attached large hydrophobic groups as potent inhibitors for HIV-1 envelop proteins mediated cell-cell fusion.

Liang Xu, Keliang Liu, Junlin He, 2011, Bioorganic & medicinal chemistry letters.

and Cell Membranes Modifications Inhibit Fusion between HIV-1 DNA Duplexes with Hydrophobic

M. Cheng, Lifeng Cai, Wei Chen, 2014 .

DNA Duplexes with Hydrophobic Modifications Inhibit Fusion between HIV-1 and Cell Membranes

Wei Chen, Liang Xu, Keliang Liu, 2013, Antimicrobial Agents and Chemotherapy.

Covalent fusion inhibitors targeting HIV-1 gp41 deep pocket

L. Lai, Shuangyu Bi, Keliang Liu, 2012, Amino Acids.

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.

Liang Xu, Lu Lu, Shibo Jiang, 2014, The Journal of antimicrobial chemotherapy.

Design of highly potent HIV fusion inhibitors based on artificial peptide sequences.

Liang Xu, Lu Lu, Shibo Jiang, 2012, Chemical communications.

Covalent fusion inhibitors targeting HIV-1 gp41 deep pocket

L. Lai, Shuangyu Bi, Keliang Liu, 2013, Amino Acids.

Design, synthesis, and biological evaluation of highly potent small molecule-peptide conjugates as new HIV-1 fusion inhibitors.

Liang Xu, Jinglai Li, Lu Lu, 2013, Journal of medicinal chemistry.

Hydrophobic mutations in buried polar residues enhance HIV-1 gp41 N-terminal heptad repeat–C-terminal heptad repeat interactions and C-peptides’ anti-HIV activity

Lu Lu, Shibo Jiang, Keliang Liu, 2014, AIDS.

Multiple Bcl-2 family members demonstrate selective dimerizations with Bax.

Z. Oltvai, S. Korsmeyer, C. Thompson, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Hydrophobic mutations in buried polar residues enhance HIV-1 gp41 N-terminal heptad repeat–C-terminal heptad repeat interactions and C-peptides’ anti-HIV activity

Lu Lu, Shibo Jiang, Keliang Liu, 2014, AIDS.

d(TGGGAG) with 5'-nucleobase-attached large hydrophobic groups as potent inhibitors for HIV-1 envelop proteins mediated cell-cell fusion.

Liang Xu, Keliang Liu, Junlin He, 2011, Bioorganic & medicinal chemistry letters.