Abstract
The structure of penicillazine has been revised on the basis of hydrolysis reaction. Its absolute stereochemistry has been confirmed by X-ray diffraction using copper radiation. Eight new penicillazine derivatives (1-8) were prepared and some of them showed higher levels of activity than penicillazine against α-glucosidase and Human DNA topoisomerase I.
Keywords: Penicillazine, derivatives, structure revision, biological activities, α-glucosidase, Human DNA topoisomerase I
Letters in Organic Chemistry
Title: Revised Structure of Penicillazine and Preparation, Bioactivities of Penicillazine Derivatives
Volume: 6 Issue: 5
Author(s): Chang-Lun Shao, Chang-Yun Wang, Yu-Cheng Gu, Ji-Wen Cai, Dong-Sheng Deng, Zhi-Gang She and Yong-Cheng Lin
Affiliation:
Keywords: Penicillazine, derivatives, structure revision, biological activities, α-glucosidase, Human DNA topoisomerase I
Abstract: The structure of penicillazine has been revised on the basis of hydrolysis reaction. Its absolute stereochemistry has been confirmed by X-ray diffraction using copper radiation. Eight new penicillazine derivatives (1-8) were prepared and some of them showed higher levels of activity than penicillazine against α-glucosidase and Human DNA topoisomerase I.
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Cite this article as:
Shao Chang-Lun, Wang Chang-Yun, Gu Yu-Cheng, Cai Ji-Wen, Deng Dong-Sheng, She Zhi-Gang and Lin Yong-Cheng, Revised Structure of Penicillazine and Preparation, Bioactivities of Penicillazine Derivatives, Letters in Organic Chemistry 2009; 6 (5) . https://dx.doi.org/10.2174/157017809788681301
DOI https://dx.doi.org/10.2174/157017809788681301 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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