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Depsipeptides

Known as: Depsipeptides [Chemical/Ingredient] 
Compounds consisting of chains of AMINO ACIDS alternating with CARBOXYLIC ACIDS via ester and amide linkages. They are commonly cyclized.
National Institutes of Health

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MBJ-0086MK 1688NW-G01alternaramide
Process of secretionantagonists & inhibitorschemical synthesis

Papers overview

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2009
2009
Halogenated fatty acid amides and cyclic depsipeptides from an eastern Caribbean collection of the cyanobacterium Lyngbya majuscula.
A lipophilic extract of an eastern Caribbean collection of Lyngbya majuscula yielded two new halogenated fatty acid amides… 
2008
2008
Concise route to defined stereoisomers of the hydroxy acid of the chondramides.
2007
2007
Two new depsipeptides from the marine fungus Spicellum roseum.
Investigation of the secondary metabolites of the marine-derived fungus Spicellum roseum yielded two new cyclohexadepsipeptides… 
2001
2001
Anti-leukemia selectivity in actinomycin analogues.
Highly Cited
2000
Highly Cited
2000
Genes encoding synthetases of cyclic depsipeptides, anabaenopeptilides, in Anabaena strain 90
Anabaena strain 90 produces three hepatotoxic heptapeptides (microcystins), two seven‐residue depsipeptides called… 
Highly Cited
1999
Highly Cited
1999
A nomenclature system for labeling cyclic peptide fragments
Highly Cited
1999
Highly Cited
1999
A General Methodology for Automated Solid-Phase Synthesis of Depsides and Depsipeptides. Preparation of a Valinomycin Analogue.
A general methodology is described that allows the solid-phase synthesis of depsides and depsipeptides from chiral alpha-hydroxy… 
1987
1987
A comparative 1H-n.m.r. study of MurNAc-L-Ala-D-iGln (MDP) and its analogue murabutide: evidence for a structure involving two successive beta-turns in MDP.
1984
1984
beta-Lactamase-catalyzed hydrolysis of acyclic depsipeptides and acyl transfer to specific amino acid acceptors.
beta-Lactamases from all three classes, A, B, and C, catalyze the hydrolysis of specific acyclic depsipeptide… 
Highly Cited
1965
Highly Cited
1965
Activation of the amide group by acylation hydroxy- and aminoacyl incorporation in peptide systems.
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