Synthesis and Structure–Activity Relationships of Lapacho Analogues. 2. Modification of the Basic Naphtho[2,3-b]furan-4,9-dione, Redox Activation, and Suppression of Human Keratinocyte Hyperproliferation by 8-Hydroxynaphtho[2,3-b]thiophene-4,9-diones-Reference-Cited by-同舟云学术

Synthesis and Structure–Activity Relationships of Lapacho Analogues. 2. Modification of the Basic Naphtho[2,3-b]furan-4,9-dione, Redox Activation, and Suppression of Human Keratinocyte Hyperproliferation by 8-Hydroxynaphtho[2,3-b]thiophene-4,9-diones

Published:2014-07-07 Issue:14 Volume:57 Page:6226-6239
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Bannwitz Sven¹,Krane Dirk¹,Vortherms Silke¹,Kalin Tobias¹,Lindenschmidt Cathrin¹,Zahedi Golpayegani Nader¹,Tentrop Jan¹,Prinz Helge¹,Müller Klaus¹

Affiliation:

1. Institute of Pharmaceutical and Medicinal Chemistry, PharmaCampus, Westphalian Wilhelms University, Corrensstrasse 48, D-48149 Münster, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm500754d

Reference75 articles.

1. Naturally occurring quinones. Part X. The quinonoid constituents of Tabebuia avellanedae(Bignoniaceae)

2. Plant Anticancer Agents. XII. Isolation and Structure Elucidation of New Cytotoxic Quinones From Tabebuia cassinoides

3. Lapachol and its congeners as anticancer agents: a review

4. Red Lapacho (Tabebuia impetiginosa)—A global ethnopharmacological commodity?

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