Streptopyrrolidine, an angiogenesis inhibitor from a marine-derived Streptomyces sp KORDI-3973

被引:58
作者
Shin, Hee Jae [1 ]
Kim, Tae Sik [1 ]
Lee, Hyi-Seung [1 ]
Park, Jung Youl [2 ]
Choi, In-Kwon [3 ]
Kwon, Ho Jeong [3 ]
机构
[1] Korea Ocean Res & Dev Inst, Marine Nat Prod Lab, Seoul 425600, South Korea
[2] C&C Res Labs, Hwasung Si 445976, Kyunggi Do, South Korea
[3] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Chem Genom Lab, Seoul 120749, South Korea
关键词
Streptomyces sp KORDI-3973; angiogenesis inhibitors; streptopyrrolidine; 5-benzyl-4-hydroxypyrrolidin-2-one; bioactive natural products;
D O I
10.1016/j.phytochem.2008.05.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Streptopyrrolidine, a benzyl pyrrolidine derivative, was isolated as an angiogenesis inhibitor from the fermentation broth of a marine Streptomyces sp. isolated from the deep sea sediment. its structure was elucidated by extensive 2D NMR and mass spectroscopic analyses. Streptopyrrolidine exhibited significant anti-angiogenesis activity. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2363 / 2366
页数:4
相关论文
共 12 条
[1]  
Atlas R. M., 1993, HDB MICROBIOLOGICAL
[2]   Combining agents that target the tumor microenvironment improves the efficacy of anticancer therapy [J].
Blansfield, Joseph A. ;
Caragacianu, Diana ;
Alexander, H. Richard, III ;
Tangrea, Michael A. ;
Morita, Shane Y. ;
Lorang, Dominique ;
Schafer, Peter ;
Muller, George ;
Stirling, David ;
Royal, Richard E. ;
Libutti, Steven K. .
CLINICAL CANCER RESEARCH, 2008, 14 (01) :270-280
[3]   A review on pro- and anti-angiogenic factors as targets of clinical intervention [J].
Bouïs, D ;
Kusumanto, Y ;
Meijer, C ;
Mulder, NH ;
Hospers, GAP .
PHARMACOLOGICAL RESEARCH, 2006, 53 (02) :89-103
[4]   The clinical toxicity profile of vascular endothelial growth factor (VEGF) and vascular endothelial growth factor receptor (VEGFR) targeting angiogenesis inhibitors; A review [J].
Eskens, Ferry A. L. M. ;
Verweij, Jaap .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (18) :3127-3139
[5]   Signaling vascular morphogenesis and maintenance [J].
Hanahan, D .
SCIENCE, 1997, 277 (5322) :48-50
[6]   A new approach to (S)-4-hydroxy-2-pyrrolidinone and its 3-substituted analogues [J].
Huang, PQ ;
Zheng, XA ;
Wang, SL ;
Ye, JL ;
Jin, LR ;
Chen, Z .
TETRAHEDRON-ASYMMETRY, 1999, 10 (17) :3309-3317
[7]   Antiangiogenic activity of 4-0-methylgallic acid from Canavalia gladiata, a dietary legume [J].
Jeon, KS ;
Na, HJ ;
Kim, YM ;
Kwon, HJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 330 (04) :1268-1274
[8]   Application of the asymmetric aminohydroxylation reaction for the syntheses of HIV-protease inhibitor, hydroxyethylene dipeptide isostere and γ-amino acid derivative [J].
Kondekar, NB ;
Kandula, SRV ;
Kumar, P .
TETRAHEDRON LETTERS, 2004, 45 (28) :5477-5479
[9]   Biological evaluation of multi-targeted small molecule inhibitor of tumor-induced angiogenesis [J].
McDermott, LA ;
Higgins, B ;
Simcox, M ;
Luk, KC ;
Nevins, T ;
Kolinsky, K ;
Smith, M ;
Yang, H ;
Li, JK ;
Chen, YS ;
Ke, J ;
Mallalleu, N ;
Egan, T ;
Kolls, S ;
Railkar, A ;
Gerber, L ;
Liu, JJ ;
Konzelmann, F ;
Zhang, ZM ;
Flynn, T ;
Morales, O ;
Chen, Y .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (07) :1950-1953
[10]  
Park TH, 2003, B KOREAN CHEM SOC, V24, P1227