Structural modification of sanguinarine and chelerythrine and their in vitro acaricidal activity against Psoroptes cuniculi
F Miao, XJ Yang, YN Ma, F Zheng, XP Song…
Index: Miao, Fang; Yang, Xin-Juan; Ma, Yan-Ni; Zheng, Feng; Song, Xiao-Ping; Zhou, Le Chemical and Pharmaceutical Bulletin, 2012 , vol. 60, # 12 p. 1508 - 1513
Full Text: HTML
Citation Number: 19
Abstract
Sanguinarine (1) and chelerythrine (2) are two quaternary benzo [c] phenanthridine alkaloids (QBAs). Eighteen derivatives of 1 and 2 were synthesized by modification of C= N+ bond and evaluated for their in vitro acaricidal activity against Psoroptes cuniculi, a mange mite. A new method was developed to prepare 6-alkoxy dihydro derivatives of 1 and 2 (1a– e, 2a–e). Among all the compounds, only 6-alkoxy dihydrosanguinarines (1a–e) showed ...
Related Articles:
Structural modification of sanguinarine and chelerythrine and their antibacterial activity
[Miao, Fang; Yang, Xin-Juan; Zhou, Le; Hu, Hai-Jun; Zheng, Feng; Ding, Xu-Dong; Sun, Dong-Mei; Zhou, Chun-Dong; Sun, Wei Natural Product Research, 2011 , vol. 25, # 9 p. 863 - 875]