Beta-Cyclodextrin Duplexes That Are Connected through Two Disulfide Bonds: Potent Hosts for the Complexation of Organic Molecules
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F12%3A00383761" target="_blank" >RIV/68378271:_____/12:00383761 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/12:00383761
Result on the web
<a href="http://dx.doi.org/10.1002/chem.201201239" target="_blank" >http://dx.doi.org/10.1002/chem.201201239</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/chem.201201239" target="_blank" >10.1002/chem.201201239</a>
Alternative languages
Result language
angličtina
Original language name
Beta-Cyclodextrin Duplexes That Are Connected through Two Disulfide Bonds: Potent Hosts for the Complexation of Organic Molecules
Original language description
New tubular host molecules, which are composed of two beta-cyclodextrin macrocycles that are connected through two disulfide bonds, have been prepared by the air-promoted oxidation of 6I,6IV-dideoxy-6I,6IV-disulfanyl-beta-cyclodextrin in aqueous solution. This reaction leads to three products: monomeric intramolecular disulfide and two dimeric species, which are termed as non-eclipsed and eclipsed cyclodextrin duplexes. Oxidation at a concentration of the starting thiol of 0.1 mM gave the intramoleculardisulfide as the major product whereas a concentration in the millimolar range afforded the dimeric species as the dominant products. The tubular structure of the non-eclipsed isomer was unequivocally determined by X-ray analysis. The binding affinitiesof the duplexes to a wide range of compounds, including fluorescent dyes and clinically used drugs Imatinib and Esomeprazol, were studied in water by ITC. For most guest compounds, the experimentally determined Ka values were in the rang
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CF - Physical chemistry and theoretical chemistry
OECD FORD branch
—
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Chemistry - A European Journal
ISSN
0947-6539
e-ISSN
—
Volume of the periodical
18
Issue of the periodical within the volume
39
Country of publishing house
DE - GERMANY
Number of pages
13
Pages from-to
12292-12304
UT code for WoS article
000308879000018
EID of the result in the Scopus database
—