Synthesis and antiviral activity of diverse heterocyclic scaffolds

S Sharma, D Utreja - Chemical Biology & Drug Design, 2022 - Wiley Online Library
Heterocyclic moieties form a major part of organic chemistry as they are widely distributed in
nature and have wide scale practical applications ranging from extensive clinical use to …

PEGylated liposomes loaded with carbamate inhibitor ANP0903 trigger apoptosis by enhancing ER stress in Hepg2 cancer cells

C Caddeo, R Miglionico, R Rinaldi, I Nigro… - International journal of …, 2023 - mdpi.com
Liver cancer is one of the most common causes of cancer death worldwide. In recent years,
substantial progress has been made in the development of systemic therapies, but there is …

Two novel precursors of the hiv-1 protease inhibitor darunavir target the upr/proteasome system in human hepatocellular carcinoma cell line hepg2

R Rinaldi, R Miglionico, I Nigro, R D'Orsi… - Cells, 2021 - mdpi.com
Background: Several pre-clinical and clinical reports suggest that HIV-1 protease inhibitors,
in addition to the antiretroviral properties, possess pleiotropic pharmacological effects …

[HTML][HTML] Design, synthesis and in vitro biological evaluation of a novel class of anti-adenovirus agents based on 3-amino-1, 2-propanediol

S Mazzotta, J Berastegui-Cabrera, M Vega-Holm… - Bioorganic …, 2021 - Elsevier
Nowadays there is not an effective drug for the treatment of infections caused by human
adenovirus (HAdV) which supposes a clinical challenge, especially for paediatric and …

Serinol-Based Benzoic Acid Esters as New Scaffolds for the Development of Adenovirus Infection Inhibitors: Design, Synthesis, and In Vitro Biological Evaluation

S Mazzotta, J Berastegui-Cabrera… - ACS Infectious …, 2020 - ACS Publications
Over the years, human adenovirus (HAdV) has progressively been recognized as a
significant viral pathogen. Traditionally associated with self-limited respiratory …

The Pseudo-Symmetric N-benzyl Hydroxyethylamine Core in a New Series of Heteroarylcarboxyamide HIV-1 Pr Inhibitors: Synthesis, Molecular Modeling and …

R D'Orsi, M Funicello, T Laurita, P Lupattelli, F Berti… - Biomolecules, 2021 - mdpi.com
Here, we report the synthesis, enzyme inhibition and structure–activity relationship studies of
a new potent class of HIV-1 protease inhibitors, which contain a pseudo-symmetric …

[HTML][HTML] Novel wild type and mutate HIV-1 protease inhibitors containing heteroaryl carboxamides in P2: Synthesis, biological evaluations and in silico ADME …

MF Armentano, P Lupattelli, F Bisaccia, R D'Orsi… - Results in …, 2023 - Elsevier
The Virus HIV-1 infection still represents a serious disease even if actually it is transformed
in chronic pathology. Considering the crucial role of the enzyme Protease in life cycle of HIV …

Total synthesis of naturally occurring moracinflavan E and related compounds

TY Lin, CY Chou, YH Chen, CK Ku, MJ Don - Phytochemistry Letters, 2022 - Elsevier
A total synthesis of four flavans with a furan ring in different positions (1–4) was achieved
successfully. The flavan was synthesized from flavanone by reduction and followed by …

Novel Wild Type and Mutate HIV-1 Protease Inhibitors Containing Heteroaryl Carboxamides in P2: Synthesis, Biological and ADME Evaluations

MF Armentano, P Lupattelli, F Bisaccia, R D'Orsi… - 2023 - preprints.org
The Virus HIV-1 infection still represents a serious disease even if actually it is transformed
in chronic pathology. Considering the crucial role of the enzyme Protease in life cycle of HIV …

[引用][C] Novel anti-adenovirus agents based on aminoglycerol and piperazine scaffolds: design, synthesis and in vitro biological evaluation

S Mazzotta - 2020