Results 61 to 70 of about 3,309 (181)
Actinomycetes are powerhouses of natural product biosynthesis. Full realization of this biosynthetic potential requires approaches for recognizing novel metabolites and determining mediators of metabolite production.
Jordan Carey +5 more
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Cyclodipeptide synthases (CDPSs) use as substrates two amino acids activated as aminoacyl-tRNAs to synthesize cyclodipeptides in secondary metabolites biosynthetic pathways.
Muriel Gondry +8 more
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The syntheses and structures of the dimethyl sulfoxide (DMSO) solvate of 3,6-bis(indol-3-yl)-1,4-dimethylpiperazine-2,5-dione, C11H10N2O (I), and of the dimethyl sulfoxide and tetrahydrofuran (THF) solvates of 1,4-dimethyl-3,6-bis(2-methylindol-3-yl ...
Clifford W. Padgett +3 more
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During an experiment where we were cultivating aflatoxigenic Aspergillus flavus on peanuts, we accidentally discovered that a bacterium adhering to the peanut strongly inhibited aflatoxin (AF) production by A. flavus.
Shohei Sakuda +8 more
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The simplest cyclo-peptides, also known as diketopiperazines (DKPs), are widespread in nature. The growing interest in these simplest cyclo-peptides is driven by their significant potential for therapeutic applications.
Dekun Kong, Xin Wang, Li Liu
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Aiming at restricting the conformational freedom of tryptophan-containing peptide ligands, we designed a THBC (tetrahydro-β-carboline)-DKP (diketopiperazine)-based peptidomimetic scaffold capable of arranging in an unusual α-turn conformation.
Francesco Airaghi +5 more
doaj +1 more source
The Mode of Action of Cyclo(l-Ala-l-Pro) in Inhibiting Aflatoxin Production of Aspergillus flavus
Cyclo(l-Ala-l-Pro) inhibits aflatoxin production in aflatoxigenic fungi without affecting fungal growth. The mode of action of cyclo(l-Ala-l-Pro) in inhibiting aflatoxin production of Aspergillus flavus was investigated. A glutathione S-transferase (GST)
Kurin Iimura +5 more
doaj +1 more source
A new bacterial strain, designated 452T, was isolated from the rhizosphere soil of the mangrove Avicennia marina in China. As determined, its cell wall peptidoglycan contained LL-diaminopimelic acid; MK-9(H8) and MK-9(H6) were the major isoprenoid ...
Can Chen +8 more
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Solid-Phase Synthesis of Methyl N-(pyrimidin-2-yl)glycinate
A versatile method for the preparation of N-heteroaryl substituted aminoacid derivatives is suggested. The method avoids facile diketopiperazine formation.
Eugene V. Babaev, Denis S. Ermolat'ev
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Synthesis and Neuroprotective Action of Optically Pure Neoechinulin A and Its Analogs
We developed an efficient, stereoselective synthetic method for the diketopiperazine moiety of neoechinulin A and its derivatives. The intramolecular cyclization at 80 ºC proceeded with minimal racemization of the stereogenic center at C-12 on ...
Toshiaki Aoki +10 more
doaj +1 more source

