The Role of Polyamine Architecture on the Pharmacological Activity of Open Lactone Camptothecin−Polyamine Conjugates-Reference-Cited by-同舟云学术

The Role of Polyamine Architecture on the Pharmacological Activity of Open Lactone Camptothecin−Polyamine Conjugates

Published:2008-10-08 Issue:11 Volume:19 Page:2270-2279
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Samor Cristian¹,Guerrini Andrea¹,Varchi Greta¹,Beretta Giovanni Luca¹,Fontana Gabriele¹,Bombardelli Ezio¹,Carenini Nives¹,Zunino Franco¹,Bertucci Carlo¹,Fiori Jessica¹,Battaglia Arturo¹

Affiliation:

1. Istituto CNR per la Sintesi Organica e Fotoreattività “I.S.O.F.”, Area della Ricerca di Bologna, Via Gobetti 101, 40129 Bologna, Italy, Dipartimento di Oncologia Sperimentale e Laboratori, Fondazione IRCCS Istituto Nazionale Tumori, 20133 Milano, Italy, Indena SPA, viale Ortles 12, 20139 Milano, Italy, and Dipartimento di Scienze Farmaceutiche, Università di Bologna, Via Belmeloro 6, 40126 Bologna, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc800033r

Reference74 articles.

1. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I.

2. DNA TOPOISOMERASES

3. Domains of Human Topoisomerase I and Associated Functions

4. Processing of topoisomerase I cleavable complexes into DNA damage by transcription

5. Crystal Structures of Human Topoisomerase I in Covalent and Noncovalent Complexes with DNA

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