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Synthesis and in vitro/in vivo Evaluation of the Antitrypanosomal Activity of 3-Bromoacivicin, a Potent CTP Synthetase Inhibitor

✍ Scribed by Prof. Paola Conti; Dr. Andrea Pinto; Dr. Pui E. Wong; Dr. Louise L. Major; Dr. Lucia Tamborini; Dr. Maria C. Iannuzzi; Prof. Carlo De Micheli; Prof. Michael P. Barrett; Dr. Terry K. Smith


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
288 KB
Volume
6
Category
Article
ISSN
1860-7179

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📜 SIMILAR VOLUMES


ChemInform Abstract: Design, Synthesis a
✍ Andrian Folkes; et al. et al. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Synthesis and in vi
✍ L. C. CREEMER; H. A. KIRST; C. J. VLAHOS; R. M. SCHULTZ 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

title esters, e.g. (Ib)-(Ie), are synthesized by deacetylation and subsequent reacylation of wortmannin (Ia). In comparison with the latter one, they show superior inhibition of phosphatidylinositol (PI) 3-kinase and increased cell cytotoxicity in vitro. Reduction of (Ib) to (IIa) slightly enhances

ChemInform Abstract: Synthesis and in vi
✍ Adrian Folkes; Michael B. Roe; Sukhjit Sohal; Julian Golec; Richard Faint; Teres 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Synthesis and in vitro and in vivo Antif
✍ Lieven Meerpoel; Jan Heeres; Leo J. J. Backx; Louis J. E. Van der Veken; Rob Hen 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 344 KB 👁 1 views

## Abstract __Herein we describe the scalable diastereoselective and enantioselective syntheses of eight enantiomers of hydroxy metabolites of saperconazole. The in vitro antifungal activity of the eight stereoisomers (compounds **1**–**8**) was compared against a broad panel of__ Candida__spp. (__