Capillary electrophoresis-SELEX selection of aptamers with affinity for HIV-1 reverse transcriptase

RK Mosing, SD Mendonsa, MT Bowser - Analytical chemistry, 2005 - ACS Publications
Capillary electrophoresis-SELEX (CE-SELEX) was used to select ssDNA aptamers with
affinity for HIV reverse transcriptase (HIVRT). A library of ssDNA was incubated with HIVRT …

Synthesis of novel test compounds for antiviral chemotherapy of severe acute respiratory syndrome (SARS)

AJ Kesel - Current medicinal chemistry, 2005 - ingentaconnect.com
This contribution reviews the synthesis of a range of experimental drugs designed for and
aiming at antiviral chemotherapy of severe acute respiratory syndrome (SARS) coronavirus …

Control of HIV through the inhibition of HIV-1 integrase: a medicinal chemistry perspective

CP Gordon, R Griffith, PA Keller - Medicinal Chemistry, 2007 - ingentaconnect.com
This article reviews the current status of classes of HIV-1 integrase enzyme inhibitors. These
classes include peptide-based inhibitors, natural products, polyhydroxylated aromatics …

Spectroscopic, structural, DFT and molecular docking studies on novel cocrystal salt hydrate of chromotropic acid and its antibiofilm activity

SSA Abidi, U Garg, Y Azim, M Alam, AK Gupta… - Arabian Journal for …, 2021 - Springer
A novel organic cocrystal salt hydrate (CTPTH) of Chromotropic acid with 1, 10-
phenanthroline was successfully obtained using both traditional solution method and liquid …

Probing the antiamoebic and cytotoxicity potency of novel tetrazole and triazine derivatives

MY Wani, AR Bhat, A Azam, I Choi, F Athar - European journal of medicinal …, 2012 - Elsevier
A series of compounds bearing a Tetrazole and Triazine ring motif conjugated with a
SO2NH function were synthesized and investigated for their antiamoebic potency …

Steady-state kinetic studies with the polysulfonate U-9843, an HIV reverse transcriptase inhibitor

IW Althaus, JJ Chou, AJ Gonzales, RJ LeMay… - Experientia, 1994 - Springer
The tetramer of ethylenesulfonic acid (U-9843) is a potent inhibitor of HIV-1 RT* and
possesses excellent antiviral activity at nontoxic doses in HIV-1 infected lymphocytes grown …

Sulfonic acid: key drug design elements with potent, broad-ranging pharmacological activities

L Hu, H Jia, J Zhang, EF da Silva-Júnior… - Future Medicinal …, 2023 - Taylor & Francis
Conclusion Sulfonate groups can be used as hydrogen bond donors and acceptors in
drugs, improving their interactions with biological targets, thereby enhancing the affinity and …

Synthesis, Characterization, and Anti‐Amoebic Activity of N‐(Pyrimidin‐2‐yl)benzenesulfonamide Derivatives

A Roouf Bhat, M Arshad, E Ju Lee… - Chemistry & …, 2013 - Wiley Online Library
A new series of N‐(pyrimidin‐2‐yl) benzenesulfonamide derivatives, 3a–3i and 4a–4i, was
synthesized from pyrimidin‐2‐amines, 2a–2i, with the aim to explore their effects on in vitro …

Development of high throughput screening assays and pilot screen for inhibitors of metalloproteases meprin α and β

F Madoux, C Tredup, TP Spicer, L Scampavia… - Peptide …, 2014 - Wiley Online Library
Zinc metalloproteinases meprin α and meprin β are implicated in a variety of diseases, such
as fibrosis, inflammation and neurodegeneration, however, there are no selective small …

A novel mechanism for inhibition of HIV-1 reverse transcriptase

AG Skillman, KW Maurer, DC Roe, MJ Stauber… - Bioorganic …, 2002 - Elsevier
The human immunodeficiency virus (HIV) epidemic is an important medical problem.
Although combination drug regimens have produced dramatic decreases in viral load …