Genistein Derivatives Regioisomerically Substituted at 7-O- and 4′-O- Have Different Effect on the Cell Cycle
Our previous studies on antiproliferative properties of genistein derivatives substituted at C7 hydroxyl group of the ring A revealed some compounds with antimitotic properties. The aim of this work was to synthesize their analogues substituted at the 4′-position of the ring B in genistein and to de...
Main Authors: | A. Byczek, J. Zawisza-Puchalka, A. Gruca, K. Papaj, G. Grynkiewicz, M. Rusin, W. Szeja, A. Rusin |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2013-01-01
|
Series: | Journal of Chemistry |
Online Access: | http://dx.doi.org/10.1155/2013/191563 |
Similar Items
-
C-Glycosidic Genistein Conjugates and Their Antiproliferative Activity
by: Aleksandra Rusin, et al.
Published: (2013-01-01) -
Synthesis and Cytotoxicity of 2,3-Enopyranosyl C-Linked Conjugates of Genistein
by: Wieslaw Szeja, et al.
Published: (2014-05-01) -
Synthetic Genistein Glycosides Inhibiting EGFR Phosphorylation Enhance the Effect of Radiation in HCT 116 Colon Cancer Cells
by: Aleksandra Gruca, et al.
Published: (2014-11-01) -
Synthetic genistein derivatives as modulators of glycosaminoglycan storage
by: Kloska Anna, et al.
Published: (2012-07-01) -
The Study on Curcuminoids in Chromatography, Spectroscopy and Regioisomerism
by: Abdul Zahar, Z., et al.
Published: (2020)