Prostaglandin fluorides in synthesis of natural prostaglandin derivatives at carboxyl group
摘要:
Methods of synthesis of prostaglandin fluorides were developed and their properties were investigated. These compounds were shown to be convenient synthetic precursors for obtaining esters and amides of natural prostaglandins and their fluorodeoxy analogues.
Synthesis and biological activity of carboxyl-terminus modified prostaglandin analogs
作者:Thomas K. Schaaf、Hans Juergen Hess
DOI:10.1021/jm00197a012
日期:1979.11
of PGE2, 16,16-dimethyl-PGE2, and PGF2 alpha analoguesmodified at the carboxyl terminus with tetrazole, amide, acylurea, imide, and sulfonimide functionalities was evaluated for uterine stimulant, bronchodilator, hypotensive, gastric antisecretory, and diarrheal activity. These compounds were prepared by modification of the Corey prostaglandin synthesis utilizing as a key step condensation of known
NOVEL PROSTAMIDES FOR THE TREATMENT OF GLAUCOMA AND RELATED DISEASES
申请人:Allergan, Inc.
公开号:US20140107124A1
公开(公告)日:2014-04-17
Disclosed herein are compositions comprising an amide related to a prostaglandin and a biogenic amine. Other aspects relate to certain chemical compounds, pharmaceutical compositions, and methods of treating glaucoma.