Design, Synthesis, and Evaluation of Acyclic C-Nucleoside and N-Methylated Derivatives of the Ribitylaminopyrimidine Substrate of Lumazine Synthase as Potential Enzyme Inhibitors and Mechanistic Probes-Reference-Cited by-同舟云学术

Design, Synthesis, and Evaluation of Acyclic C-Nucleoside and N-Methylated Derivatives of the Ribitylaminopyrimidine Substrate of Lumazine Synthase as Potential Enzyme Inhibitors and Mechanistic Probes

Published:2004-09-10 Issue:21 Volume:69 Page:6996-7003
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Jinhua¹,Sambaiah Thota¹,Illarionov Boris¹,Fischer Markus¹,Bacher Adelbert¹,Cushman Mark¹

Affiliation:

1. Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, Indiana 47907, and Lehrstuhl für Organische Chemie und Biochemie, Technische Universität München, D-85747 Garching, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048975f

Reference31 articles.

1. Biosynthesis of Riboflavin: Structure and mechanism of lumazine synthase

2. Stereospecificity of the enzymic synthesis of the o-xylene ring of riboflavin

3. Biosynthesis of riboflavin. The structure of the four-carbon precursor

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