Syntheses and bio-activities of the l-enantiomers of two potent transition state analogue inhibitors of purine nucleoside phosphorylases-Reference-Cited by-同舟云学术

Syntheses and bio-activities of the l-enantiomers of two potent transition state analogue inhibitors of purine nucleoside phosphorylases

Published:2006 Issue:6 Volume:4 Page:1131
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Clinch Keith,Evans Gary B.,Fleet George W. J.,Furneaux Richard H.,Johnson Stephen W.,Lenz Dirk H.,Mee Simon P. H.,Rands Peter R.,Schramm Vern L.,Taylor Ringia Erika A.,Tyler Peter C.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2006/OB/B517883E

Reference41 articles.

1. L - Nucleosides: Antiviral Activity and Molecular Mechanism

2. Antiviral l -Nucleosides Specific for Hepatitis B Virus Infection

3. Hepatitis C Virus Therapies: Current Treatments, Targets and Future Perspectives

4. Pentopyranosyl Oligonucleotide Systems. Communication No. 13

5. Looking glass inhibitors:l-DMDP, a more potent and specific inhibitor of α-glucosidases than the enantiomeric natural product DMDP

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