Design, Synthesis, and X-ray Crystallographic Studies of α-Aryl Substituted Fosmidomycin Analogues as Inhibitors ofMycobacterium tuberculosis1-Deoxy-d-xylulose 5-Phosphate Reductoisomerase-Reference-Cited by-同舟云学术

Design, Synthesis, and X-ray Crystallographic Studies of α-Aryl Substituted Fosmidomycin Analogues as Inhibitors ofMycobacterium tuberculosis1-Deoxy-d-xylulose 5-Phosphate Reductoisomerase

Published:2011-07-28 Issue:14 Volume:54 Page:4964-4976
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Andaloussi Mounir,Henriksson Lena M.,Wiȩckowska Anna,Lindh Martin,Björkelid Christofer,Larsson Anna M.,Suresh Surisetti,Iyer Harini,Srinivasa Bachally R.,Bergfors Terese,Unge Torsten,Mowbray Sherry L.,Larhed Mats,Jones T. Alwyn,Karlén Anders

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm2000085

Reference54 articles.

1. Creating Isoprenoid Diversity

2. THE 1-DEOXY-D-XYLULOSE-5-PHOSPHATE PATHWAY OF ISOPRENOID BIOSYNTHESIS IN PLANTS

3. The discovery of a mevalonate-independent pathway for isoprenoid biosynthesis in bacteria, algae and higher plants†

4. Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate

5. The role of lateral gene transfer in the evolution of isoprenoid biosynthesis pathways

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