Cryptotanshinone but not tanshinone IIA inhibits angiogenesis in vitro

被引:0
|
作者
Jong Moon Hur
Joong Sup Shim
Hye Jin Jung
Ho Jeong Kwon
机构
[1] Institute of Bioscience,Chemical Genomics National Research Laboratory, Department of Bioscience and Biotechnology
[2] Sejong University,undefined
来源
关键词
abietane; angiogenesis; cryptotanshinone; Salvia miltiorrhiza; tanshinone;
D O I
暂无
中图分类号
学科分类号
摘要
In the course of screening of angiogenesis inhibitor from natural products, cryptotanshinone from Salvia miltiorrhiza was isolated as a potent small molecule inhibitor of angiogenesis. Cryptotanshinone inhibits bFGF-induced angiogenesis of BAECs at ten micromolar ranges in vitro without cytotoxicity. Tanshinone IIA, another tanshinone isolated from S. miltiorrhiza, which is structurally very similar to cryptotanshinone except C-15 position of dihydrofuran ring does not inhibit angiogenesis induced by bFGF. These results demonstrate that cryptotanshinone is a new anti-angiogenic agent and double bond at C-15 position of the dihydrofuran ring plays a crucial role in the activity.
引用
收藏
页码:133 / 137
页数:4
相关论文
共 50 条
  • [1] Cryptotanshinone but not tanshinone IIA inhibits angiogenesis in vitro
    Hur, JM
    Shim, JS
    Jung, HJ
    Kwon, HJ
    EXPERIMENTAL AND MOLECULAR MEDICINE, 2005, 37 (02): : 133 - 137
  • [2] Tanshinone IIA inhibits angiogenesis in human endothelial progenitor cells in vitro and in vivo
    Lee, Hsiang-Ping
    Liu, Yueh-Ching
    Chen, Po-Chun
    Tai, Huai-Ching
    Li, Te-Mao
    Fong, Yi-Chin
    Chang, Chih-Shiang
    Wu, Min-Huan
    Chiu, Li-Pin
    Wang, Chia-Jung
    Chen, Yi-Hsuan
    Wu, Yih-Jer
    Tang, Chih-Hsin
    Wang, Shih-Wei
    ONCOTARGET, 2017, 8 (65): : 109217 - 109227
  • [3] Chemical Stability and Bioactivity of tanshinone I, tanshinone IIA, cryptotanshinone and dihydrotanshinone in in vitro test systems
    Roth, Annika
    Zhao, Piwen
    Soukup, Sebastian T.
    Guigas, Claudia
    Starke, Joachim
    Kulling, Sabine E.
    Diel, Patrick
    TOXICOLOGY LETTERS, 2023, 375 : 21 - 28
  • [4] Studies on the spectroscopic behavior of cryptotanshinone, tanshinone IIA, and tanshinone I
    Li, JF
    Wei, YX
    Xu, ZC
    Dong, C
    Shuang, SM
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2004, 60 (04) : 751 - 756
  • [5] Facile and efficient total synthesis of (±)-cryptotanshinone and tanshinone IIA
    Jiang, YY
    Li, Q
    Lu, W
    Cai, JC
    TETRAHEDRON LETTERS, 2003, 44 (10) : 2073 - 2075
  • [6] Determination of dihydrotanshinone I, cryptotanshinone, tanshinone I and tanshinone IIA in tanshinone ear drops by HPLC
    Liu, Gang
    Zhang, Qi-Ming
    Zhang, Jie
    Gao, Wen-Juan
    Chang, Hua
    Tan, Sheng-Jian
    Chinese Pharmaceutical Journal, 2004, 39 (03) : 218 - 220
  • [7] Potential intermediates for diterpenoid quinones:: Cryptotanshinone, tanshinone IIA, and miltirone
    Banerjee, AK
    Azócar, JA
    de Carrasco, MCS
    Mimó, ML
    SYNTHETIC COMMUNICATIONS, 2001, 31 (16) : 2471 - 2478
  • [8] Metabolism of Tanshinone IIA, Cryptotanshinone and Tanshinone I from Radix Salvia Miltiorrhiza in Zebrafish
    Wei, Yingjie
    Li, Ping
    Wang, Changmei
    Peng, Yunru
    Shu, Luan
    Jia, Xiaobin
    Ma, Wenquan
    Wang, Bing
    MOLECULES, 2012, 17 (07): : 8617 - 8632
  • [9] DETERMINATION OF TANSHINONE I, TANSHINONE IIA, AND CRYPTOTANSHINONE IN Salvia miltiorrhiza bunge AND URINE SAMPLE BY HPLC
    Tian, Minglei
    Row, Kyung Ho
    CANADIAN JOURNAL OF CHEMICAL ENGINEERING, 2010, 88 (05): : 818 - 821
  • [10] Determination of Cryptotanshinone, Tanshinone I, and Tanshinone IIA in Salvia Miltiorrhiza by Micro HPLC with Amperometric Detection
    Chen, Xianchun
    Kotani, Akira
    Hakamata, Hideki
    Du, Shouying
    Wang, Jie
    Kusu, Fumiyo
    ANALYTICAL LETTERS, 2013, 46 (04) : 605 - 614