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Configurational requirements of the sugar moiety for the pharmacological activity of anthracycline disaccharides

✍ Scribed by Federico Arcamone; Fabio Animati; Mario Bigioni; Giovanni Capranico; Claudia Caserini; Amalia Cipollone; Michelandrea De Cesare; Alessandro Ettorre; Fulvio Guano; Stefano Manzini; Edith Monteagudo; Graziella Pratesi; Carmela Salvatore; Rosanna Supino; Franco Zunino


Book ID
113994370
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
263 KB
Volume
57
Category
Article
ISSN
0006-2952

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πŸ“œ SIMILAR VOLUMES


Stereochemical studies on esperamicins:
✍ J. Golik; H. Wong; D.M. Vyas; T.W. Doyle πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 201 KB

The absolute stereochmistry of the isopropylamino sugar moiety of esperamicin A1 was determined as the g-&-threo-pentopyranosyl by comparing the CD spectra of derivatized methanolysis product 4 with those of two synthesized antipodal glycosides 2 and Is.