Marine natural products

JW Blunt, BR Copp, MHG Munro, PT Northcote… - Natural product …, 2006 - pubs.rsc.org
Covering: 2004. Previous review: Nat. Prod. Rep., 2005, 22, 15This review covers the
literature published in 2004 for marine natural products, with 693 citations (491 for the …

Histone deacetylase inhibitors: from bench to clinic

M Paris, M Porcelloni, M Binaschi… - Journal of medicinal …, 2008 - ACS Publications
The interest in histone deacetylase (HDACa) inhibitors began almost 30 years ago during
some studies designed to understand why dimethyl sulfoxide (DMSO) caused terminal …

HDAC as onco target: Reviewing the synthetic approaches with SAR study of their inhibitors

R Sangwan, R Rajan, PK Mandal - European journal of medicinal chemistry, 2018 - Elsevier
Even though one is moving towards the success in the discovery of efficient anti-cancer
molecules, the drugs used in the treatment of various malignancies are found to possess …

Marine pharmacology in 2003–2004: anti-tumour and cytotoxic compounds

AMS Mayer, KR Gustafson - European Journal of Cancer, 2006 - Elsevier
During 2003 and 2004, marine pharmacology research directed towards the discovery and
development of novel anti-tumour agents was published in 163 peer-reviewed articles. The …

Feijoa sellowiana derived natural Flavone exerts anti-cancer action displaying HDAC inhibitory activities

P Bontempo, L Mita, M Miceli, A Doto… - The international journal …, 2007 - Elsevier
Curative properties of some medicinal plants such as the Feijoa sellowiana
Bert.(Myrtaceae), have been often claimed, although the corresponding molecular …

A comprehensive review of marine sponge metabolites, with emphasis on Neopetrosia sp.

N Barzkar, S Sukhikh, O Babich - International Journal of Biological …, 2024 - Elsevier
The secondary metabolites that marine sponges create are essential to the advancement of
contemporary medicine and are often employed in clinical settings. Over the past five years …

Non-hydroxamate histone deacetylase inhibitors

T Suzuki, N Miyata - Frontiers in Medicinal Chemistry: Volume 4, 2009 - benthamdirect.com
A number of histone deacetylase (HDAC) inhibitors have been developed as anticancer
agents and most of them are hydroxamic acid derivatives, typified by suberoylanilide …

Macrocyclic histone deacetylase inhibitors

SC Mwakwari, V Patil, W Guerrant… - Current topics in …, 2010 - ingentaconnect.com
Histone deacetylase inhibitors (HDACi) are an emerging class of novel anti-cancer drugs
that cause growth arrest, differentiation, and apoptosis of tumor cells. In addition, they have …

Potential of synthetic and natural compounds as novel histone deacetylase inhibitors for the treatment of hematological malignancies

D Pal, K Raj, SS Nandi, S Sinha, A Mishra, A Mondal… - Cancers, 2023 - mdpi.com
Simple Summary Histone deacetylases (HDACs) are epigenetic regulators that influence
chromatin structure and gene transcription, but also the function of non-histone targets like …

Azumamides A–E: Histone Deacetylase Inhibitory Cyclic Tetrapeptides from the Marine Sponge Mycale izuensis

Y Nakao, S Yoshida, S Matsunaga… - Angewandte Chemie …, 2006 - Wiley Online Library
Histone acetylation and deacetylation, which are catalyzed by histone acetyltransferases
(HATs) and histone deacetylases (HDACs), respectively, play important roles in …