Results 31 to 40 of about 2,772 (159)

Total Syntheses of Cathepsin D Inhibitory Izenamides A, B, and C and Structural Confirmation of Izenamide B

open access: yesMolecules, 2019
The first total syntheses of izenamides A, B, and C, which are depsipeptides inhibitor of cathepsin D, were accomplished. In addition, the stereochemistry of izenamide B was confirmed by our syntheses.
Changjin Lim
doaj   +1 more source

Bright Side of Fusarium oxysporum: Secondary Metabolites Bioactivities and Industrial Relevance in Biotechnology and Nanotechnology

open access: yesJournal of Fungi, 2021
Fungi have been assured to be one of the wealthiest pools of bio-metabolites with remarkable potential for discovering new drugs. The pathogenic fungi, Fusarium oxysporum affects many valuable trees and crops all over the world, producing wilt.
Sabrin R. M. Ibrahim   +4 more
doaj   +1 more source

High‐Throughput Engineering and Modification of Non‐Ribosomal Peptide Synthetases Based on Golden Gate Assembly

open access: yesAngewandte Chemie, Volume 137, Issue 49, December 1, 2025.
A Golden Gate Assembly (GGA)‐based method was developed for the efficient assembly of natural and engineered non‐ribosomal peptide synthetases (NRPS). This method has enabled the creation of NRPS libraries to generate novel peptides in high‐throughput as well as the targeted derivatisation of natural products (NPs).
Adrian Podolski   +7 more
wiley   +2 more sources

Cyclic Octamer Peptoids: Simplified Isosters of Bioactive Fungal Cyclodepsipeptides

open access: yesMolecules, 2018
Cyclic peptoids have recently emerged as an important class of bioactive scaffolds with unique conformational properties and excellent metabolic stabilities.
Assunta D’Amato   +5 more
doaj   +1 more source

Structure-affinity and structure-residence time relationships of macrocyclic Gαq protein inhibitors

open access: yesiScience, 2023
Summary: The macrocyclic depsipeptides YM-254890 (YM) and FR900359 (FR) are potent inhibitors of Gαq/11 proteins. They are important pharmacological tools and have potential as therapeutic drugs.
Jan H. Voss   +7 more
doaj   +1 more source

Multicomponent synthesis of hydrazino depsipeptides [PDF]

open access: yesRSC Advances, 2016
Multicomponent reactions (MCRs) offer numerous advantages over traditional sequential reactions for the synthesis of diverse structurally demanding compounds. Isocynide-based MCRs, particularly Passerini and Ugi reactions, are of special importance, because they provide peptide-like compounds able to mimic structure and/or function of natural peptides ...
Barić, Danijela, Jerić, Ivanka
openaire   +3 more sources

Synthetic Strategies for Activity‐Based Probes to Decode Ubiquitin‐Like Modifiers

open access: yesChemistry – A European Journal, EarlyView.
ABSTRACT Ubiquitin‐like proteins (Ubls) such as SUMO, NEDD8, ISG15, URM1, UFM1, FAT10, ATG8/ATG12, and FUBI are essential regulators of cellular homeostasis, controlling processes from protein stability and trafficking to immune signaling and autophagy.
Saibal Chanda   +5 more
wiley   +1 more source

In situ natural product discovery via an artificial marine sponge. [PDF]

open access: yesPLoS ONE, 2014
There is continuing international interest in exploring and developing the therapeutic potential of marine-derived small molecules. Balancing the strategies for ocean based sampling of source organisms versus the potential to endanger fragile ecosystems ...
James J La Clair   +5 more
doaj   +1 more source

Application of feature-based molecular networking and MassQL for the MS/MS fragmentation study of depsipeptides

open access: yesFrontiers in Molecular Biosciences, 2023
The Feature-based Molecular Networking (FBMN) is a well-known approach for mapping and identifying structures and analogues. However, in the absence of prior knowledge about the molecular class, assessing specific fragments and clusters requires time ...
Denise M. Selegato   +4 more
doaj   +1 more source

Total Synthesis of the Depsipeptide FR‐901375. [PDF]

open access: yesChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Yanping, Chen   +4 more
openaire   +2 more sources

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