Results 141 to 150 of about 3,874 (203)

Cyclic peptide inhibitors function as molecular glues to stabilize Gq/11 heterotrimers. [PDF]

Proc Natl Acad Sci U S A
Mühle J, Alenfelder J, Rodrigues MJ, Jürgenliemke L, Guixà-González R, Grätz L, Andres F, Bacchin A, Hennig M, Schihada H, Crüsemann M, König GM, Schertler G, Kostenis E, Deupi X.   +14 more
europepmc   +1 more source

Antioxidant, Anti-Inflammatory and Anticancer Peptides from Extreme Marine Environments. [PDF]

Antioxidants (Basel)
Zakariya M, Montuori E, Kopp G, Coppola A, Giordano D, Bruno S, Lauritano C.   +6 more
europepmc   +1 more source

Identification of Hoiamide A as an Inducer of Oxidative and Endoplasmic Reticulum Secretory Pathway Stress. [PDF]

J Nat Prod
Bonar SE, Mattos DR, Yu X, Neuhaus GF, Youssef DTA, Shaala LA, Gerwick WH, McPhail KL, Ishmael JE.   +8 more
europepmc   +1 more source

Discovery, biosynthesis, and bioactivities of peptidic natural products from marine sponges and sponge-associated bacteria.

Nat Prod Rep
Zhong W, Lin Z, Schmidt EW, Agarwal V.
europepmc   +1 more source

Small depsipeptides as solvent gelators

Journal of the Chemical Society, Chemical Communications, 1993
The formation of very thermostable gels with several solvents is reported for two cyclic depsipeptides of comparatively low molecular mass.
DEVRIES, EJ, KELLOGG, RM
core   +4 more sources

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The cyclization of peptides and depsipeptides

Journal of Peptide Science, 2003
AbstractConstricting the peptide backbone into a more defined conformational form through cyclization is an activity evolved in nature and in synthetic work, the latter straddling only the most recent decades. The resulting conformational constraints increase the probability of an optimum response with bio‐receptors.
exaly   +3 more sources

Fungal cyclooligomer depsipeptides [PDF]

Natural Product Reports, 2011
This review surveys the biological activities and the iterative and recursive biosynthetic mechanisms of fungal cyclooligomer depsipeptides, and their structural diversification by various combinatorial biosynthetic methods.
Süssmuth, Roderich, Müller, Jane, Von Döhren, Hans, Molnár, István   +3 more
openaire   +2 more sources

The mycotoxin definition reconsidered towards fungal cyclic depsipeptides

Journal of Environmental Science and Health, Part C: Environmental Carcinogenesis and Ecotoxicology Reviews, 2016
Currently, next to the major classes, cyclic depsipeptides beauvericin and enniatins are also positioned as mycotoxins. However, as there are hundreds more fungal cyclic depsipeptides already identified, should these not be considered as mycotoxins as ...
Bart de Spiegeleer, Lien Taevernier, Christian Burvenich   +2 more
exaly   +2 more sources

Depsipeptide Dendrimers

Chemistry - A European Journal, 2000
The convergent synthesis of a new class of chiral dendrimers is described. Owing to their structural resemblance to depsipeptides they are called depsipeptide dendrimers. The ex-chiral pool synthesis starts from (R,R)-, (S,S)-, and meso-tartaric acid as branching units and dipeptides or tripeptides consisting of glycine, (L)-alanine, and (L)-leucine as
J, Kress, A, Rosner, A, Hirsch
openaire   +2 more sources