In vitro antitumor activity of N-glycosyl sulfonamides
β Scribed by Rosana Crespo; Margarita G. de Bravo; Pedro A. Colinas; Rodolfo D. Bravo
- Book ID
- 104004899
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 171 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-894X
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β¦ Synopsis
A series of a-D-hex-2-enopyranosyl sulfonamides was evaluated for their antiproliferative activity against human hepatocellular liver carcinoma (HepG2) and human lung adenocarcinoma (A549) cell lines. The most potent compound (2,4,6-tri-O-acetyl-3-deoxy-a-D-erythro-hex-2-enopyranosyl ethanesulfonamide) showed antiproliferative properties in the micromolar range. The SARs of these sulfonamidoglycoside which includes the influence of carbohydrate rings and sulfonamide class are described.
π SIMILAR VOLUMES
Triarylantimony(V) di(N-phenylglycinates) (PhNHCH 2 COO) 2 SbAr 3 (Ar = Ph, p-CH 3 C 6 H 4 , p-ClC 6 H 4 , and p-FC 6 H 4 ) have been synthesized and characterized by elemental analysis, IR, 1 H NMR, and mass spectra. The crystal structure of (PhNHCH 2 COO) 2 Sb(C 6 H 4 F-p) 3 has been determined by
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