Marine natural products

JW Blunt, BR Copp, WP Hu, MHG Munro… - Natural product …, 2007 - pubs.rsc.org
Covering: 2005. Previous review: Nat. Prod. Rep., 2006, 23, 26 This review covers the
literature published in 2005 for marine natural products, with 704 citations (493 for the …

Marine natural product peptides with therapeutic potential: Chemistry, biosynthesis, and pharmacology

V Gogineni, MT Hamann - Biochimica et Biophysica Acta (BBA)-General …, 2018 - Elsevier
The oceans are a uniquely rich source of bioactive metabolites, of which sponges have
been shown to be among the most prolific producers of diverse bioactive secondary …

Cyclodepsipeptides from marine sponges: Natural agents for drug research

GSB Andavan, R Lemmens-Gruber - Marine drugs, 2010 - mdpi.com
A number of natural products from marine sponges, such as cyclodepsipeptides, have been
identified. The structural characteristics of this family of cyclic peptides include various …

Mirabamides A–D, Depsipeptides from the Sponge Siliquariaspongia mirabilis That Inhibit HIV-1 Fusion

A Plaza, E Gustchina, HL Baker, M Kelly… - Journal of natural …, 2007 - ACS Publications
Four new cyclic depsipeptides termed mirabamides A–D (1–4) have been isolated from the
marine sponge Siliquariaspongia mirabilis and shown to potently inhibit HIV-1 fusion. Their …

Homophymine A, an Anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp.

A Zampella, V Sepe, P Luciano, F Bellotta… - The Journal of …, 2008 - ACS Publications
A new anti-HIV cyclodepsipeptide, homophymine A, was isolated from a New Caledonian
collection of the marine sponge Homophymia sp. The structure of homophymine A was …

Mirabamides E−H, HIV-Inhibitory Depsipeptides from the Sponge Stelletta clavosa

Z Lu, RM Van Wagoner, MK Harper… - Journal of natural …, 2011 - ACS Publications
Four new depsipeptides, mirabamides E− H (1− 4), and the known depsipeptide
mirabamide C (5) have been isolated from the sponge Stelletta clavosa, collected from the …

Histone deacetylase inhibitor induced the production of three novel prenylated tryptophan analogs in the entomopathogenic fungus, Torrubiella luteorostrata

T Asai, T Yamamoto, Y Oshima - Tetrahedron letters, 2011 - Elsevier
Suberoyl bis-hydroxamic acid (SBHA), a histone deacetylase (HDAC) inhibitor, led to
significant changes in the secondary metabolism of an entomopathogenic fungus …

“Head-to-side-chain” cyclodepsipeptides of marine origin

M Pelay-Gimeno, J Tulla-Puche, F Albericio - Marine drugs, 2013 - mdpi.com
Since the late 1980s, a large number of depsipeptides that contain a new topography,
referred to as “head-to-side-chain” cyclodepsipeptides, have been isolated and …

The chemistry and biology of organic guanidine derivatives

RGS Berlinck, ACB Burtoloso, MH Kossuga - Natural Product Reports, 2008 - pubs.rsc.org
Covering: 2005 to 2007. Previous review: Nat. Prod. Rep., 2005, 22, 516. Organic guanidine
compounds are reviewed, with emphasis on natural products isolation, identification …

Recent progress of synthetic studies to peptide and peptidomimetic cyclization

S Jiang, Z Li, K Ding, PP Roller - Current Organic Chemistry, 2008 - ingentaconnect.com
A large number of cyclic peptides, which exhibit a range of biological activities, have been
found in nature. The reason of cyclic peptides that attracted world wide attention and made …