Coumarin-derived Hydroxamic Acids as Histone Deacetylase Inhibitors: A Review of Anti-cancer Activities
NQ Khai, TK Vu - Anti-Cancer Agents in Medicinal Chemistry …, 2024 - ingentaconnect.com
Since coumarin and hydroxamic acid compounds are well-known in medicinal chemistry, a
variety of their derivatives have been highlighted due to their potential uses for plentiful …
variety of their derivatives have been highlighted due to their potential uses for plentiful …
Thiazole-containing compounds as therapeutic targets for cancer therapy
In the last few decades, considerable progress has been made in anticancer agents
development, and several new anticancer agents of natural and synthetic origin have been …
development, and several new anticancer agents of natural and synthetic origin have been …
HDAC inhibitors in acute myeloid leukemia
E San José-Enériz, N Gimenez-Camino, X Agirre… - Cancers, 2019 - mdpi.com
Acute myeloid leukemia (AML) is a hematological malignancy characterized by uncontrolled
proliferation, differentiation arrest, and accumulation of immature myeloid progenitors …
proliferation, differentiation arrest, and accumulation of immature myeloid progenitors …
Inhibitors of histone deacetylase as antitumor agents: A critical review
M Manal, MJN Chandrasekar, JG Priya, MJ Nanjan - Bioorganic chemistry, 2016 - Elsevier
Abstract Histone deacetylase (EC 3.5. 1.98–HDAC) is an amidohydrolase involved in
deacetylating the histone lysine residues for chromatin remodeling and thus plays a vital …
deacetylating the histone lysine residues for chromatin remodeling and thus plays a vital …
The search for potent, small‐molecule HDACIs in cancer treatment: a decade after vorinostat
C Zagni, G Floresta, G Monciino… - Medicinal research …, 2017 - Wiley Online Library
Histone deacetylases (HDACs) play a crucial role in the remodeling of chromatin, and are
involved in the epigenetic regulation of gene expression. In the last decade, inhibition of …
involved in the epigenetic regulation of gene expression. In the last decade, inhibition of …
Cyclic tetrapeptides from nature and design: A review of synthetic methodologies, structure, and function
Small cyclic peptides possess a wide range of biological properties and unique structures
that make them attractive to scientists working in a range of areas from medicinal to …
that make them attractive to scientists working in a range of areas from medicinal to …
New horizons in benzothiazole scaffold for cancer therapy: Advances in bioactivity, functionality, and chemistry
In the pasture of oncology, anticancer agents having advanced modes of action are of great
interest because of increasing chronicity of resistance against anticancer drugs. Heterocyclic …
interest because of increasing chronicity of resistance against anticancer drugs. Heterocyclic …
Multi-targeted HDAC inhibitors as anticancer agents: current status and future prospective
VK Patel, E Shirbhate, P Tiwari, R Kore… - Current Medicinal …, 2023 - ingentaconnect.com
Multi-targeted agents can interact with multiple targets sequentially, resulting in synergistic
and more effective therapies for several complicated disorders, including cancer, even with …
and more effective therapies for several complicated disorders, including cancer, even with …
Docking based screening of curcumin derivatives: A novel approach in the inhibition of tubercular DHFR
Tuberculosis is one of the main causes of morbidity and mortality across the globe.
Mycobacterium tuberculosis can attack any part of the human body and can cause …
Mycobacterium tuberculosis can attack any part of the human body and can cause …
Design, synthesis and biological evaluation of novel coumarin-based hydroxamate derivatives as histone deacetylase (hdac) inhibitors with antitumor activities
F Yang, N Zhao, J Song, K Zhu, C Jiang, P Shan… - Molecules, 2019 - mdpi.com
A series of novel coumarin-based hydroxamate derivatives were designed and synthesized
as histone deacetylase inhibitors (HDACis). Selective compounds showed a potent HDAC …
as histone deacetylase inhibitors (HDACis). Selective compounds showed a potent HDAC …