Unknown

Dataset Information

0

Antineoplastic agents. 592. Highly effective cancer cell growth inhibitory structural modifications of dolastatin 10.


ABSTRACT: 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 (GI50 10(-2)-10(-4) ?g/mL), auristatin 2-AQ (4, GI50 10(-2)-10(-3) ?g/mL), and auristatin 6-AQ (5, GI50 10(-4) ?g/mL), exhibited superior cancer cell growth inhibitory properties.

SUBMITTER: Pettit GR 

PROVIDER: S-EPMC3116808 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Antineoplastic agents. 592. Highly effective cancer cell growth inhibitory structural modifications of dolastatin 10.

Pettit George R GR   Hogan Fiona F   Toms Steven S  

Journal of natural products 20110502 5


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 objec  ...[more]

Similar Datasets

| S-EPMC6045487 | biostudies-literature
| S-EPMC3111978 | biostudies-literature
| S-EPMC4010298 | biostudies-literature
| S-EPMC7256948 | biostudies-literature
| S-EPMC3251507 | biostudies-literature
| S-EPMC2837129 | biostudies-literature
| S-EPMC2782413 | biostudies-literature
| S-EPMC5319972 | biostudies-literature
| S-EPMC7225676 | biostudies-literature
| S-EPMC6856148 | biostudies-literature