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 …

Thiazole-containing compounds as therapeutic targets for cancer therapy

PC Sharma, KK Bansal, A Sharma, D Sharma… - European journal of …, 2020 - Elsevier
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 …

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 …

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 …

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 …

Cyclic tetrapeptides from nature and design: A review of synthetic methodologies, structure, and function

V Sarojini, AJ Cameron, KG Varnava… - Chemical …, 2019 - ACS Publications
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 …

New horizons in benzothiazole scaffold for cancer therapy: Advances in bioactivity, functionality, and chemistry

PC Sharma, D Sharma, A Sharma, KK Bansal… - Applied Materials …, 2020 - Elsevier
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 …

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 …

Docking based screening of curcumin derivatives: A novel approach in the inhibition of tubercular DHFR

S Mujwar, K Shah, JK Gupta… - International Journal of …, 2021 - inderscienceonline.com
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 …

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 …