Mustafa,A. et al., Justus Liebigs Annalen der Chemie, 1966, vol. 692, p. 166 - 173
作者:Mustafa,A. et al.
DOI:——
日期:——
Aziz,G. et al., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1976, vol. 14, p. 286 - 291
作者:Aziz,G. et al.
DOI:——
日期:——
FURANOCHALCONES AS INHIBITORS OF CYP1A1, CYP1A2 AND CYP1B1 FOR CANCER CHEMOPREVENTION
申请人:Council of Scientific & Industrial Research
公开号:US20210284618A1
公开(公告)日:2021-09-16
The present invention relates to the furanochalcone class of compounds of general formula A. The present invention particularly relates to the synthesis of furanochalcones and their CYP1A1, CYP1A2 and CYP1B1 inhibitory activity. In addition, the invention relates to the prevention or treatment of cancer caused by polyaromatic hydrocarbons (PAHs), 4-nitroquinoline-1-oxide, and N-nitroso-N-methylurea, heterocyclic amines, estrogen and 17β-estradiol, resulting from the inhibition of CYP1A1, CYP1A2 and CYP1B1 enzymes.
A simple approach to fused pyrido[2,3-<i>d</i>]pyrimidines incorporating khellinone and trimethoxyphenyl moieties as new scaffolds for antibacterial and antifungal agents
作者:Khadiga M. Abu-Zied、Tahia K. Mohamed、Omar K. Al-Duiaj、Magdi E.A. Zaki
DOI:10.1515/hc-2013-0199
日期:2014.4.1
Abstract 2-Amino-3-cyanopyridine is a simple precursor for the synthesis of analogues of Egyptian natural products visnagin and khellin. Fused pyrido[2,3-d]pyrimidines were prepared under mild reaction conditions. The detailed syntheses and spectroscopic data of the synthesised compounds are reported. Some isolated compounds show antibacterial and antifungal activity.