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Synthesis of 1-indole substituted beta-carboline alkaloid and its derivatives and evaluation of their preliminary antitumor activities / 药学学报
Acta Pharmaceutica Sinica ; (12): 259-262, 2004.
Article in Chinese | WPRIM | ID: wpr-301101
ABSTRACT
<p><b>AIM</b>To synthesize eudistomin U and its 6-OCH3/Br derivatives and 5'-Br derivatives as antitumor agents.</p><p><b>METHODS</b>Using tryptamine and indole-3-aldehyde as starting materials, through condensation, Pictet-Spengler cyclization and dehydrogenation three steps, the alkaloids and its derivatives were prepared.</p><p><b>RESULTS</b>The structures of the compounds were determined by 1HNMR, MS and HRMS. Antitumor activity in vitro was tested.</p><p><b>CONCLUSION</b>Eudistomin U and its derivatives were synthesized. The results showed that they all showed antitumor activities against mouse P388 strain.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Carbolines / Molecular Structure / Leukemia P388 / Tryptamines / Cell Division / Chemistry / Cell Line, Tumor / Alkaloids Limits: Animals Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2004 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Carbolines / Molecular Structure / Leukemia P388 / Tryptamines / Cell Division / Chemistry / Cell Line, Tumor / Alkaloids Limits: Animals Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2004 Type: Article