Issue 15, 1996

Design of chelate ring-opening platinum anticancer complexes: reversible binding to guanine

Abstract

Chelate ring-opening in bis(aminophosphine) complexes of platinum(II) can be controlled by the substituents on N and P under biologically relevant conditions of pH and Cl concentration; selective and reversible binding to the DNA base guanine can be achieved as well as cytotoxicity towards cancer cell lines.

Article information

Article type
Paper

Chem. Commun., 1996, 1785-1786

Design of chelate ring-opening platinum anticancer complexes: reversible binding to guanine

A. Habtemariam and P. J. Sadler, Chem. Commun., 1996, 1785 DOI: 10.1039/CC9960001785

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements