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Glycosylated diazeniumdiolates: a novel class of enzyme-activated nitric oxide donors
✍ Scribed by Xuejun Wu; Xiaoping Tang; Ming Xian; Peng George Wang
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 101 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Synthetic procedures have been developed to attach the nitric oxide releasing diazeniumdiolate functional groups [N(O)NO] -to a carbohydrate unit. These glycosylated diazeniumdiolates exhibited significantly improved stability as compared to their parent diazeniumdiolate salts, yet they could readily release nitric oxide upon activation by glycosidases. Preliminary antitumor screen assay demonstrated that this class of compounds had antitumor activity.
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## Abstract So far, nitric oxide (NO) donors have been applied to various aspects of antitumor therapy. To selectively sensitize tumor cells and avoid unwanted side effects, we recently synthesized a β‐galactosidase‐activatable NO‐releasing compound, β‐galactosyl‐pyrrolidinyl diazeniumdiolate (β‐Ga
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Background: Several studies have shown that nitric oxide (no)-releasing agents can kill tumor cells. unfortunately, currently available no delivery molecules do not target tumor cells preferentially. to exploit the overexpression of glucose transport proteins and the high level of glucose transp