12-Amino-andrographolide analogues: synthesis and cytotoxic activity

• Published in: Archives of pharmacal research Vol. 36; no. 12; pp. 1454 - 1464
• Main Authors: Kasemsuk, Sakkasem, Sirion, Uthaiwan, Suksen, Kanoknetr, Piyachaturawat, Pawinee, Suksamrarn, Apichart, Saeeng, Rungnapha
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.12.2013; 대한약학회
• Subjects: Andrographis; Animals; Antineoplastic Agents - chemical synthesis; Antineoplastic Agents - isolation & purification; Antineoplastic Agents - pharmacology; Cell Line, Tumor; Cytotoxins - chemical synthesis; Cytotoxins - isolation & purification; Cytotoxins - pharmacology; Diterpenes - chemical synthesis; Diterpenes - isolation & purification; Diterpenes - pharmacology; Drug Screening Assays, Antitumor - methods; Humans; MCF-7 Cells; Medicine; Mice; Pharmacology/Toxicology; Pharmacy; Plant Components, Aerial; Rats; Research Article; Structure-Activity Relationship; 약학; 12-Amino-andrographolide; Tandem aza-conjugate addition–elimination; Cytotoxic activity
• ISSN: 0253-6269; 1976-3786
• DOI: 10.1007/s12272-013-0152-0

Andrographolide, a diterpenoid lactone of the plant Andrographis paniculata , has been shown to be cytotoxic against various cancer cells in vitro. In the present study, a series of β -amino- γ -butyrolactone analogues has been synthesized from naturally occurring andrographolide via one pot tandem aza-conjugate addition–elimination reaction. By using economic procedure without any base or catalyst at room temperature, the products obtained were in fair to excellent yields with high stereoselectivity. The cytotoxicity of all new amino analogues were evaluated against six cancer cell lines and revealed their potential for being developed as promising anti-cancer agents.