d(TGGGAG) with 5′-nucleobase-attached large hydrophobic groups as potent inhibitors for HIV-1 envelop proteins mediated cell–cell fusion-Reference-Cited by-同舟云学术

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

Published:2011-10 Issue:19 Volume:21 Page:5762-5764
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Chen Wei,Xu Liang,Cai Lifeng,Zheng Baohua,Wang Kun,He Junlin,Liu Keliang

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference30 articles.

1. Prevalence of quadruplexes in the human genome

2. Gene function correlates with potential for G4 DNA formation in the human genome

3. Human telomere, oncogenic promoter and 5'-UTR G-quadruplexes: diverse higher order DNA and RNA targets for cancer therapeutics

4. A G-quadruplex structure within the 5′-UTR of TRF2 mRNA represses translation in human cells

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1. Synthesis, Biophysical Characterization, and Anti-HIV-1 Fusion Activity of DNA Quadruplex-based Inhibitors with Dipeptide MT Hook Conjugation;Current HIV Research;2021-08-30

2. Novel monomolecular derivatives of the anti-HIV-1 G-quadruplex-forming Hotoda’s aptamer containing inversion of polarity sites;European Journal of Medicinal Chemistry;2020-12

3. DNA Quadruplex–Based Inhibitor With Flexible Fragments at the 3′ Terminal Shows Enhanced Anti–HIV-1 Fusion Activity;Journal of Pharmaceutical Sciences;2019-07

4. Hotoda’s Sequence and Anti-HIV Activity: Where Are We Now?;Molecules;2019-04-10

5. A novel multivalent DNA helix–based inhibitor showed enhanced anti–HIV-1 fusion activity;European Journal of Pharmaceutical Sciences;2018-12

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