PUBLICATION

Supramolecular Encapsulation and Bioactivity Modulation of a Halonium Ion by Cucurbit[ n]uril ( n = 7, 8)

Authors
Yin, H., Huang, Q., Zhao, W., Bardelang, D., Siri, D., Chen, X., Lee, S.M.Y., Wang, R.
ID
ZDB-PUB-180703-10
Date
2018
Source
The Journal of organic chemistry   83: 4882-4887 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Animals
  • Bridged-Ring Compounds/chemistry*
  • Bridged-Ring Compounds/pharmacology*
  • Capsules
  • Cardiotonic Agents/chemistry*
  • Cardiotonic Agents/pharmacology*
  • Dose-Response Relationship, Drug
  • Halogens/chemistry*
  • Heart/drug effects
  • Imidazoles/chemistry*
  • Imidazoles/pharmacology*
  • Mice
  • RAW 264.7 Cells
  • Structure-Activity Relationship
  • Zebrafish
PubMed
29616817 Full text @ J. Org. Chem.
Abstract
This is the first time that cucurbit[7]uril and cucurbit[8]uril have been demonstrated to serve as synthetic receptors for a halonium guest species, diphenyleneiodonium, modulating its bioactivities and alleviating its cardiotoxicity, which further expands the onium family of guest molecules for the cucurbit[ n]uril family and provides new insights for halonium-cucurbit[ n]uril host-guest chemistry and its potential applications in pharmaceutical chemistry.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping