New Caloporoside Derivatives and their Inhibition of Fungal Spore Germination

被引：0
作者：
Schueffler, Anja [3 ]
Liermann, Johannes C. [2 ]
Kolshorn, Heinz [4 ]
Opatz, Till [2 ]
Anke, Timm [1 ]
机构：
[1] Inst Biotechnol & Drug Res, D-67663 Kaiserslautern, Germany
[2] Univ Hamburg, Inst Organ Chem, D-20146 Hamburg, Germany
[3] Univ Kaiserslautern, D-67663 Kaiserslautern, Germany
[4] Johannes Gutenberg Univ Mainz, Inst Organ Chem, D-55128 Mainz, Germany
来源：
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES | 2009年 / 64卷 / 7-8期
关键词：
Caloporoside; Spore Germination Inhibition; Gloeoporus dichrous; BIOLOGICAL-ACTIVITIES; BINDING INHIBITORS; HYALURONIC-ACID; FERMENTATION; F-16438S; ORGANISM; CD44;
D O I：
暂无
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：
In our ongoing screening culture fluid extracts of Gloeoporus (Caloporus) dichrous strain 83065 inhibited the germination of Magnaporthe grisea and Fusarium graminearum spores. While isolating the active metabolites two new caloporosides, caloporoside G and caloporoside H, in addition to the known caloporoside derivatives F-16438G, caloporoside A, and 2-hydroxy-6-(16-hydroxyheptadecyl)benzoic acid were obtained.
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收藏
页码：521 / 525
页数：5
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