Results 111 to 120 of about 7,439 (222)
Total Synthesis and Stereochemical Assignment of Burkholdac B, a Depsipeptide HDAC Inhibitor
Three diastereomers of burkholdac B were prepared by total synthesis, enabling the full stereochemical assignment of the natural product. It is proposed that burkholdac B is identical to thailandepsin A independently isolated by Cheng from the same ...
Graham Packham (1277634) +3 more
core +1 more source
The process by which the first peptides were formed is still unclear. A few hypotheses have been proposed, but still there are doubts on whether they were possible during the prebiotic era.
Toro Arévalo, Kathyria M.
core +1 more source
Isolation and Total Synthesis of PM170453, a New Cyclic Depsipeptide Isolated from Lyngbya sp.
In our continuing search for biologically active new chemical entities from marine organisms, we have isolated a new cyclic depsipeptide, PM170453 (1), from a cyanobacterium of the genus Lyngbya sp., collected in the Indo-Pacific Ocean.
Rogelio Fernández +8 more
doaj +1 more source
Acyl depsipeptide (ADEP) resistance in Streptomyces
ADEP, a molecule of the acyl depsipeptide family, has an antibiotic activity with a unique mode of action. ADEP binding to the ubiquitous protease ClpP alters the structure of the enzyme.
Philippe Mazodier +2 more
core +1 more source
Isopenicillin N synthase (IPNS) is a non-heme iron(II) oxidase, which catalyses the biosynthesis of isopenicillin N (IPN) from the tripeptide δ-L-α-aminoadipoyl-L-cysteinyl-D-valine (LLD-ACV) in a remarkable oxidative bicyclisation reaction.
Ge, Wei +12 more
core +1 more source
Tryptophan‐Selective Chemical Modification of Peptides by Thioether‐Mediated Sulfenylation
Chemical modification of biomolecules such as peptides and proteins is an important technology for the development of new functional molecules. Herein, a thioether‐mediated sulfenylation for tryptophan (Trp)‐selective chemical modification under mild ...
Hayate Shida +11 more
doaj +1 more source
Total synthesis and stereochemical assignment of burkholdac B, a depsipeptide HDAC inhibitor
Three diastereomers of burkholdac B were prepared by total synthesis, enabling the full stereochemical assignment of the natural product. It is proposed that burkholdac B is identical to thailandepsin A independently isolated by Cheng from the same ...
Packham, Graham +7 more
core +1 more source
Understanding the Role of Macrocycle Size and Amide Linkage in Teixobactin Analogues. [PDF]
Malkawi R +9 more
europepmc +1 more source
Depsipeptide Analogues of Gly-Ala-Gly: Proton Localization and Effects on Collision-Induced Dissociation. [PDF]
Shira BA +4 more
europepmc +1 more source
Characterization of Dapalides D and E and Genomic Comparison of the Two Co-Occurring Dapalide-Producing Dapis spp. [PDF]
Ellis EK +8 more
europepmc +1 more source

