Lysine deacetylase inhibitors in parasites: past, present, and future perspectives

GS Hailu, D Robaa, M Forgione, W Sippl… - Journal of Medicinal …, 2017 - ACS Publications
Current therapies for human parasite infections rely on a few drugs, most of which have
severe side effects, and their helpfulness is being seriously compromised by the drug …

Structure-activity relationships of HDAC8 inhibitors: Non-hydroxamates as anticancer agents

SA Amin, N Adhikari, T Jha - Pharmacological Research, 2018 - Elsevier
Histone deacetylase inhibitors (HDACIs) have a paramount importance in the acetylation
process of histone and non-histone proteins that are crucial players in the cellular epigenetic …

[HTML][HTML] HDAC inhibitors Tubastatin A and SAHA affect parasite cell division and are potential anti-Toxoplasma gondii chemotherapeutics

CA Araujo-Silva, W De Souza… - International Journal for …, 2021 - Elsevier
The redirectioning of drugs in the pharmaceutical market is a well-known practice to identify
new therapies for parasitic diseases. The histone deacetylase inhibitors Tubastatin A (TST) …

Post-translational Modifications of Trypanosoma cruzi Canonical and Variant Histones

GFA Picchi, V Zulkievicz, MA Krieger… - Journal of proteome …, 2017 - ACS Publications
Chagas disease, caused by Trypanosoma cruzi, still affects millions of people around the
world. No vaccines nor treatment for chronic Chagas disease are available, and …

Homology modeling of parasite histone deacetylases to guide the structure-based design of selective inhibitors

J Melesina, D Robaa, RJ Pierce, C Romier… - Journal of Molecular …, 2015 - Elsevier
Histone deacetylases (HDACs) are promising epigenetic targets for the treatment of various
diseases, including cancer and neurodegenerative disorders. There is evidence that they …

Going ballistic: Leishmania nuclear subversion of host cell plasticity

H Lecoeur, E Prina, M Gutiérrez-Sanchez… - Trends in …, 2022 - cell.com
Intracellular parasites have evolved intricate strategies to subvert host cell functions for their
own survival. These strategies are particularly damaging to the host if the infection involves …

Hydroxamic acid based histone deacetylase inhibitors with confirmed activity against the malaria parasite

G Giannini, G Battistuzzi, D Vignola - Bioorganic & medicinal chemistry …, 2015 - Elsevier
Recent studies have highlighted a key role in regulating gene transcription, in both
eukaryotes and prokaryotes, by enzymes that control the acetylation and deacetylation of …

A nanodelivered Vorinostat derivative is a promising oral compound for the treatment of visceral leishmaniasis

V Corpas-López, M Díaz-Gavilán… - Pharmacological …, 2019 - Elsevier
There is currently no satisfactory treatment for visceral leishmaniasis; the disease is thus in
desperate need of novel drugs. The ideal candidate should be effective, safe, affordable …

Antimicrobial and antileishmanial activities of diterpenoids isolated from the roots of Salvia deserta

J Búfalo, CL Cantrell, MR Jacob, KK Schrader… - Planta …, 2016 - thieme-connect.com
Four diterpenes with biological activity were isolated from Salvia deserta roots. Taxodione
was considered leishmanicidal with an IC 50 value of 1.46 µM (0.46 mg/L) against …

Histone deacetylases as targets for antitrypanosomal drugs

AA Zuma, W Souza - Future Science OA, 2018 - Taylor & Francis
Parasitic protozoa comprise several species that are causative agents of important diseases.
These diseases are distributed throughout the world and include leishmaniasis, Chagas …