Results 101 to 110 of about 1,844 (163)

Paenidepsins are a Family of Lipopeptides from <i>Paenibacillus</i>. [PDF]

open access: yesJ Nat Prod
Torres-Püschel D   +7 more
europepmc   +1 more source

The thiazolidinedione drug troglitazone inhibits Gq signaling through direct binding to the Gq alpha subunit through inhibition of GDP release. [PDF]

open access: yesMol Pharmacol
Issa NT   +10 more
europepmc   +1 more source

Paraisariamides: Cycloheptapeptide Toxins from Entomopathogenic Fungi (Paraisaria spp.) That Inhibit Total Protein Synthesis. [PDF]

open access: yesJ Nat Prod
Tehan RM   +12 more
europepmc   +1 more source

Isolation, total synthesis and structure determination of antifungal macrocyclic depsipeptide, tetraselide. [PDF]

open access: yesChem Sci
Nakahara H   +9 more
europepmc   +1 more source

From Catalysis of Evolution to Evolution of Catalysis. [PDF]

open access: yesAcc Chem Res
Edri R, Williams LD, Frenkel-Pinter M.
europepmc   +1 more source

Cyclic depsipeptides as potential cancer therapeutics

Anti-Cancer Drugs, 2015
Cyclic depsipeptides are polypeptides in which one or more amino acid is replaced by a hydroxy acid, resulting in the formation of at least one ester bond in the core ring structure. Many natural cyclic depsipeptides possessing intriguing structural and biological properties, including antitumor, antifungal, antiviral, antibacterial, anthelmintic, and ...
Jirouta Kitagaki   +2 more
exaly   +3 more sources

Cyclic Peptides and Depsipeptides from Fungi

2009
This chapter describes the occurrence of cyclic peptides and cyclic depsipeptides within the kingdom Eumycota (true fungi), the diversity of structures and their chemical building blocks, their ecological roles and their different biological activities.
Heidrun Anke, Luis Antelo
exaly   +2 more sources

The Cyclic Depsipeptide Backbone of the Didemnins

Acta Crystallographica Section C Crystal Structure Communications, 1995
An X-ray crystal analysis of phi-lactone N-¿1-¿N-¿4-¿[3- hydroxy-5-methyl-1-oxo-4-(N-L-threonylamino)heptyl]- oxy¿-2,5-dimethyl-1,3-dioxohexyl¿-L-leucyl¿-L-prolyl¿- N,O-dimethyl-L-tyrosine hydrobromide hydrate (1a), C42H66N5O11+.Br-.H2O, was obtained in order to determine the backbone folding of the macrocycle and to compare the results obtained with ...
S C, Mayer, P J, Carroll, M M, Joullié
openaire   +2 more sources

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