Results 191 to 200 of about 18,245 (244)

Molecular Encapsulation of Cinnamaldehyde within Cyclodextrin Inclusion Complex Electrospun Nanofibers: Fast-Dissolution, Enhanced Water Solubility, High Temperature Stability, and Antibacterial Activity of Cinnamaldehyde

open access: yesJournal of Agricultural and Food Chemistry, 2019
The electrospinning of nanofibers (NFs) of cinnamaldehyde inclusion complexes (ICs) with two different hydroxypropylated cyclodextrins (CDs), hydroxypropyl-β-cyclodextrin (HP-β-CD) and hydroxypropyl-γ-cyclodextrin (HP-γ-CD), was successfully performed in
Engin Durgun   +2 more
exaly   +4 more sources
Some of the next articles are maybe not open access.

Fragrance material review on cinnamaldehyde

Food and Chemical Toxicology, 2005
A toxicologic and dermatologic review of cinnamaldehyde when used as a fragrance ingredient is presented.
C S Letizia, J Lalko, J Cocchiara
exaly   +3 more sources

Cinnamaldehyde—A potential antidiabetic agent

Phytomedicine, 2007
Cinnamonum zeylanicum (cinnamon) is widely used in traditional system of medicine to treat diabetes in India. The present study was carried out to isolate and identify the putative antidiabetic compounds based on bioassay-guided fractionation; the compound identified decreased the plasma glucose levels. The active compound was purified by repeat column
S Ignacimuthu
exaly   +3 more sources

Cinnamaldehydes in Cancer Chemotherapy

Phytotherapy Research, 2016
Cinnamaldehyde and cinnamaldehyde‐derived compounds are candidates for the development of anticancer drugs that have received extensive research attention. In this review, we summarize recent findings detailing the positive and negative aspects of cinnamaldehyde and its derivatives as potential anticancer drug candidates.
Su-Hyung, Hong   +4 more
openaire   +2 more sources

Mechanism of cinnamaldehyde sensitization *

Contact Dermatitis, 1977
The skin sensitization of cinnamaldehyde is probably initialed by the reaction of cinnamaldehyde with ɛ‐amino groups on protein side chains. α‐Substituted cinnamaldehydes, which are known nottobe skin sensitizers, react very slowly or not at all with amines in comparison with cinnamaldehyde.
V A, Majeti, R R, Suskind
exaly   +3 more sources

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