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Synthesis and antitumor activity of the derivatives of cephalotaxine and drupacine / 药学学报
Acta Pharmaceutica Sinica ; (12): 919-923, 2003.
Article in Chinese | WPRIM | ID: wpr-301175
ABSTRACT
<p><b>AIM</b>To make full use of cephalotaxus plant resources and search for antitumor agents with higher activities and lower side effects.</p><p><b>METHODS</b>The C3 hydroxy groups of the cephlotaxine and drupacine were acylated by taxol side chain and its isomers to give a series of derivatives of cephlotaxine and drupacine.</p><p><b>RESULTS</b>Six novel alkaloid esters were designed and synthesized. The pharmacological screening results showed that VIIIa, VIIIb, IXa and IXc exhibited significant activities on KB, HCT and Bel in vitro.</p><p><b>CONCLUSION</b>Novel alkaloid esters are worthy to be intensively studied.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Tumor Cells, Cultured / KB Cells / Chemistry / Colonic Neoplasms / Carcinoma, Hepatocellular / Harringtonines / Liver Neoplasms / Antineoplastic Agents, Phytogenic Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Tumor Cells, Cultured / KB Cells / Chemistry / Colonic Neoplasms / Carcinoma, Hepatocellular / Harringtonines / Liver Neoplasms / Antineoplastic Agents, Phytogenic Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2003 Type: Article