4.7 Article

Antineoplastic Agents. 592. Highly Effective Cancer Cell Growth Inhibitory Structural Modifications of Dolastatin 10

期刊

JOURNAL OF NATURAL PRODUCTS
卷 74, 期 5, 页码 962-968

出版社

AMER CHEMICAL SOC
DOI: 10.1021/np1007334

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资金

  1. Division of Cancer Treatment and Diagnosis, NCI, DHHS [R01 CA 90441-01-05, 2R56 CA 090441-06A1, 5-R01 CA 90441-07-08]
  2. Arizona Disease Control Research Commission
  3. Fannie E. Rippel Foundation
  4. Robert B. Dalton Endowment Fund

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The dolastatin series of unique peptides, originally discovered as constituents of the sea hare Dolabella auricularia, is of increasing importance in providing biological leads, especially to new and useful anticancer drugs. Dolastatin 10 and three analogues, minor structural modifications designated auristatins, are currently in human cancer clinical trials. The present study was undertaken to explore delivery to the cancer sites by way of phosphate or quinoline modifications. The initial objectives, auristatin TP as sodium phosphate 3b (GI(50) 10(-2)-10(-4) mu g/mL), auristatin 2-AQ (4, GI(50) 10(-2)-10(-3) mu g/mL), and auristatin 6-AQ(5, GI(50) 10(-4) mu g/mL), exhibited superior cancer cell growth inhibitory properties.

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