Results 121 to 130 of about 9,955 (253)
Clovibactin and Staphylococcus aureus: a new weapon against resistant strains
Clovibactin is a new depsipeptide and highly efficacious against () , including methicillin-resistant and vancomycin-resistant , with no apparent resistance. Clovibactutclasses current antibiotics such as vancomycin.
Adeiza, Shuaibu Suleiman
doaj +1 more source
Konformationsanalyse und Kinetik der Konformationsänderungen von membranaktiven Antibiotika
Molecular properties of the membrane active antibiotics enniatin B, valinomycin and gramicidin A were investigated in various solvents. The conformational rearrangements of these antibiotics have been studied as a function of solvent polarity by ...
E. Grell, F. Eggers, Th. Funck
doaj +1 more source
Total Synthesis of Cyclodepsipeptide Xylaroamide A
Cyclodepsipeptides constitute a structurally diverse class of natural products composed of amino acid and hydroxy acid residues interconnected through both amide and ester bonds.
Rongping Wu +8 more
doaj +1 more source
Kulokekahilide-2, a Cytotoxic Depsipeptide from a Cephalaspidean Mollusk Philinopsis speciosa†
A cytotoxic depsipeptide, kulokekahilide-2 (1), was isolated from a cephalaspidean mollusk, Philinopsis speciosa. The structure elucidation of kulokekahilide-2 was carried out by spectroscopic analysis and chemical degradation.
Wesley Y. Yoshida (1265682) +6 more
core +1 more source
Teixobactin is a highly potent cyclic depsipeptide which kills a broad range of multi-drug resistant, Gram-positive bacteria, such as Methicillin-resistant Staphylococcus aureus (MRSA) without detectable resistance.
Ruba Malkawi +9 more
doaj +1 more source
The depsipeptide technique is a recently developed method for peptide synthesis which is applicable to difficult sequences when the synthetic difficulty arises because of aggregation phenomena.
Michael Bienert (2355265) +6 more
core +1 more source
A cyclic depsipeptide, georgamide (1), was isolated from an Australian cyanobacterium and characterized by spectroscopic means. The constituent units were five amino acid residues, one each of l-Thr, l-Pro, l-Val, N-Me-l-Val, and N-Me-l-Phe, and two ...
Karen L. Erickson (2254336) +1 more
core +1 more source
Histone deacetylase inhibitors (HDACIs): multitargeted anticancer agents
Katherine Ververis,1 Alison Hiong,1 Tom C Karagiannis,1,* Paul V Licciardi2,*1Epigenomic Medicine, Alfred Medical Research and Education Precinct, 2Allergy and Immune Disorders, Murdoch Childrens Research Institute, Melbourne, VIC, Australia*These ...
Ververis K +3 more
doaj
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
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

