Aristoxazole Analogues. Conversion of 8-Nitro-1-naphthoic Acid to 2-Methylnaphtho[1,2-d]oxazole-9-carboxylic Acid: Comments on the Chemical Mechanism of Formation of DNA Adducts by the Aristolochic Acids-Reference-Cited by-同舟云学术

Aristoxazole Analogues. Conversion of 8-Nitro-1-naphthoic Acid to 2-Methylnaphtho[1,2-d]oxazole-9-carboxylic Acid: Comments on the Chemical Mechanism of Formation of DNA Adducts by the Aristolochic Acids

Published:2012-07-02 Issue:7 Volume:75 Page:1414-1418
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Priestap Horacio A.¹,Barbieri Manuel A.¹,Johnson Francis²

Affiliation:

1. Department of Biological Sciences, Florida International University, 11200 Southwest 8th Street, Miami, Florida 33199, United States

2. Department of Chemistry, Stony Brook University, Nichols Road, Stony Brook, New York 11794, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/np300137f

Reference7 articles.

1. Identification of a Reduction Product of Aristolochic Acid: Implications for the Metabolic Activation of Carcinogenic Aristolochic Acid

2. Zur Kenntniss der Naphtoësäuren

3. Mass Spectrometry of Aristolochic Acids

4. The structural basis for the mutagenicity of aristolochic acid

5. Allylic strain in six-membered rings

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