Novel 7-Oxyiminomethyl Derivatives of Camptothecin with Potent in Vitro and in Vivo Antitumor Activity-Reference-Cited by-同舟云学术

Novel 7-Oxyiminomethyl Derivatives of Camptothecin with Potent in Vitro and in Vivo Antitumor Activity

Published:2001-09-01 Issue:20 Volume:44 Page:3264-3274
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Dallavalle Sabrina¹,Ferrari Anna¹,Biasotti Barbara¹,Merlini Lucio¹,Penco Sergio¹,Gallo Grazia¹,Marzi Mauro¹,Tinti Maria Ornella¹,Martinelli Roberta¹,Pisano Claudio¹,Carminati Paolo¹,Carenini Nives¹,Beretta Giovanni¹,Perego Paola¹,De Cesare Michelandrea¹,Pratesi Graziella¹,Zunino Franco¹

Affiliation:

1. Dipartimento di Scienze Molecolari Agroalimentari, Sezione di Chimica, Università di Milano, Via Celoria 2, 20133 Milano, Italy, R & D, Sigma-tau, Pomezia, Italy, and Dipartimento Oncologia Sperimentale, Istituto Nazionale per lo Studio e la Cura dei Tumori, Via Venezian 1, 20133 Milano, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0108092

Reference32 articles.

1. Bifunctional Reagents. Cross-Linking of Pancreatic Ribonuclease with a Diimido Ester1

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

3. (a)Camptothecins: New Anticancer Agents.Potmesil, H., Pinedo, H., Eds.; CRC: Boca Raton, FL, 1995.

Cited by 100 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The antimicrobial potential of adarotene derivatives against Staphylococcus aureus strains;Bioorganic Chemistry;2024-04

2. A Computational QSAR, Molecular Docking and In Vitro Cytotoxicity Study of Novel Thiouracil-Based Drugs with Anticancer Activity against Human-DNA Topoisomerase II;International Journal of Molecular Sciences;2022-10-05

3. A camptothecin-based, albumin-binding prodrug enhances efficacy and safety in vivo;European Journal of Medicinal Chemistry;2021-12

4. Addressing the Target Identification and Accelerating the Repositioning of Anti‐Inflammatory/Anti‐Cancer Organic Compounds by Computational Approaches;European Journal of Organic Chemistry;2021-06

5. Putative SARS-CoV-2 Mpro Inhibitors from an In-House Library of Natural and Nature-Inspired Products: A Virtual Screening and Molecular Docking Study;Molecules;2020-08-17