Marine Drugs | |
6″-Debromohamacanthin A, a Bis (Indole) Alkaloid, Inhibits Angiogenesis by Targeting the VEGFR2-Mediated PI3K/AKT/mTOR Signaling Pathways | |
Gi Dae Kim2  Oug Jae Cheong1  Song Yi Bae2  Jongheon Shin2  | |
[1]Department of Chemistry, McGill University, Montreal, Quebec, H3A 2K6, Canada | |
[2] E-Mail: | |
[3]Natural Products Research Institute, College of Pharmacy, Seoul National University, San 56-1 Sillim-dong, Gwanak-gu, Seoul 151-742, Korea | |
[4] E-Mails: | |
关键词: 6″-debromohamacanthin A; anti-angiogenesis; PI3K/AKT/mTOR; HUVEC; mouse embryonic stem cells; | |
DOI : 10.3390/md11041087 | |
来源: mdpi | |
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【 摘 要 】
Hamacanthins, bis (indole) alkaloids, are found in a few marine sponges, including
【 授权许可】
CC BY
© 2013 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
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RO202003190037436ZK.pdf | 794KB | ![]() |