Design and synthesis of trans-2-substituted-cyclopropane-1-carboxylic acids as the first non-natural small molecule inhibitors of O-acetylserine sulfhydrylase-Reference-Cited by-同舟云学术

Design and synthesis of trans-2-substituted-cyclopropane-1-carboxylic acids as the first non-natural small molecule inhibitors of O-acetylserine sulfhydrylase

Published:2012 Issue:9 Volume:3 Page:1111
ISSN:2040-2503
Container-title:MedChemComm
language:en
Short-container-title:Med. Chem. Commun.

Author:

Amori Laura,Katkevica Sarmite,Bruno Agostino,Campanini Barbara,Felici Paolo,Mozzarelli Andrea,Costantino Gabriele

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/MD/C2MD20100C

Reference32 articles.

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2. Oxazolidinone Structure–Activity Relationships Leading to Linezolid

3. Trends in Antimicrobial Drug Development: Implications for the Future

4. Where are all the new antibiotics? The new antibiotic paradox

5. Daptomycin: first in a new class of antibiotics for complicated skin and soft-tissue infections

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