Results 81 to 90 of about 19,944 (197)
Evaluation of chlorofusin, its seven chromophore diastereomers, and key analogues
Chlorofusin, its seven chromophore diastereomers, and key analogues were comparatively examined for inhibition of MDM2–p53 binding revealing that the chromophore, but not simple replacements, contributes significantly to the natural products properties ...
Lee, Sang Yeul +9 more
core +1 more source
An indirect approach for the determination of enantiomeric purity of chiral α-(benzyl)-carboxyethyl- and γ-methyl-substituted monomers of polyamide nucleic acids mimics (PANAM) is described.
Yu. G. Kirillova +6 more
doaj
Determining the Extent of Biodegradation of Fuels Using the Diastereomers of Acyclic Isoprenoids
Improved testing and remediation procedures for sites contaminated with petroleum hydrocarbons are a priority in remote cold regions such as Antarctica, where costs are higher and remediation times are longer. Isoprenoid/n-alkane ratios are commonly used
Susan H. Ferguson (2498431) +6 more
core +1 more source
In the present work, the neuroprotective effect stereospecificity of dimeric dipeptide mimetic of the 4th loop of BDNF-GSB-106 is studied. Activity of its diastereomers GT-106DL (hexamethylenediamide bis-monosuccinyl-D-seryl-L-lysine) and GT-106LD ...
I. O. Logvinov +3 more
doaj
Synthesis of a new type of antitumour agent panaxytriol: synthesis of its four diastereomers
Synthesis of four diastereomers of panaxytriol has been described. The basic objective is to create two acetylenic precursors followed by cuprous chloride mediated C-C coupling ...
Sylesh Kumar, V. +2 more
core +1 more source
Unified Total Synthesis of Pteriatoxins and Their Diastereomers
A unified total synthesis is reported to access all of the possible diastereomers of pteriatoxins A−C, with the use of an intramolecular Diels−Alder reaction as the key step to form the carbo-macrocyclic core structure. The C34/C35-diol protecting groups
Scott S. Harried (2025583) +5 more
core +1 more source
Synthetic oligonucleotides often contain chemically modified backbones to prevent degradation and improve bioactivity. Phosphorothioate (PS) linkage in place of phosphodiester is the most used one.
Luca Gherardi +5 more
doaj +1 more source
[reaction: see text] Stereo-controlled syntheses of two possible C1-C25 diastereomers of spirastrellolide A containing the cis-disubstituted tetrahydropyran and [6,6]-spiroacetal are reported, exploiting boron-mediated asymmetric aldol and allylation ...
Anderson, EA +4 more
core +1 more source
Separation of phosphinic pseudopeptide diastereomers by CZE and RP-HPLC
Capillary zone electrophoresis (CZE) and reverse phase high-performance liquid chromatography (RP-HPLC) were used for separation of diastereomers of phosphinic pseudopeptides.
Koval, Dušan
core
Multi-color luminescent crystals derived from dynamic diastereomers of a perylene-substituted binaphthol derivative [PDF]
Herein, we demonstrate a novel strategy for obtaining multi-color luminescent crystals. A perylene-substituted (S)-binaphthol derivative was designed, exhibiting dynamic conversion of diastereomers in solution.
Yano, Riko +3 more
core

