Novel benzohydroxamate-based potent and selective histone deacetylase 6 (HDAC6) inhibitors bearing a pentaheterocyclic scaffold: design, synthesis, and biological …

B Vergani, G Sandrone, M Marchini… - Journal of Medicinal …, 2019 - ACS Publications
Histone deacetylase 6 (HDAC6) is a peculiar HDAC isoform whose expression and
functional alterations have been correlated with a variety of pathologies such as …

[HTML][HTML] HIV Infection: Shaping the Complex, Dynamic, and Interconnected Network of the Cytoskeleton

R Cabrera-Rodríguez, S Pérez-Yanes… - International journal of …, 2023 - mdpi.com
HIV-1 has evolved a plethora of strategies to overcome the cytoskeletal barrier (ie, actin and
intermediate filaments (AFs and IFs) and microtubules (MTs)) to achieve the viral cycle. HIV …

Structural determinants of affinity and selectivity in the binding of inhibitors to histone deacetylase 6

JD Osko, DW Christianson - Bioorganic & medicinal chemistry letters, 2020 - Elsevier
Abstract Histone deacetylase 6 (HDAC6) is associated with multiple neurological disorders
as well as aggressive cancers, making its selective inhibition highly desirable for therapeutic …

Identification and structure–activity relationship of HDAC6 zinc-finger ubiquitin binding domain inhibitors

R Ferreira de Freitas, RJ Harding… - Journal of Medicinal …, 2018 - ACS Publications
HDAC6 plays a central role in the recruitment of protein aggregates for lysosomal
degradation and is a promising target for combination therapy with proteasome inhibitors in …

[HTML][HTML] Emerging roles of prominin-1 (CD133) in the dynamics of plasma membrane architecture and cell signaling pathways in health and disease

P Pleskač, CA Fargeas, R Veselska, D Corbeil… - Cellular & Molecular …, 2024 - Springer
Abstract Prominin-1 (CD133) is a cholesterol-binding membrane glycoprotein selectively
associated with highly curved and prominent membrane structures. It is widely recognized …

Design, Synthesis, and Pharmacological Evaluation of First‐in‐Class Multitarget N‐Acylhydrazone Derivatives as Selective HDAC6/8 and PI3Kα Inhibitors

DA Rodrigues, FS Guerra, FS Sagrillo… - …, 2020 - Wiley Online Library
Targeting histone deacetylases (HDACs) and phosphatidylinositol 3‐kinases (PI3Ks) is a
very promising approach for cancer treatment. This manuscript describes the design …

Tubulin mutations in neurodevelopmental disorders as a tool to decipher microtubule function

G Fourel, C Boscheron - FEBS letters, 2020 - Wiley Online Library
Malformations of cortical development (MCDs) are a group of severe brain malformations
associated with intellectual disability and refractory childhood epilepsy. Human missense …

Entropy as a driver of selectivity for inhibitor binding to histone deacetylase 6

NJ Porter, FF Wagner, DW Christianson - Biochemistry, 2018 - ACS Publications
Among the metal-dependent histone deacetylases, the class IIb isozyme HDAC6 is
remarkable because of its role in the regulation of microtubule dynamics in the cytosol …

Influenza A virus uncoating

Y Yamauchi - Advances in virus research, 2020 - Elsevier
Influenza A virus (IAV) is an enveloped virus of the Orthomyxoviridae with a negative-sense
single-stranded RNA genome. During virus cell entry, viral and cellular cues are delivered in …

Research Strategies of Small Molecules as Chemotherapeutics to Overcome Multiple Myeloma Resistance

J Yang, YC Yu, ZX Wang, QQ Li, N Ding… - European Journal of …, 2024 - Elsevier
Multiple myeloma (MM), a cancer of plasma cells, is the second most common
hematological malignancy which is characterized by aberrant plasma cells infiltration in the …