New borrelidin derivatives from an endophytic Streptomyces sp.

被引:10
作者
Zhang, Li [1 ]
Shi, Jing [1 ]
Liu, Cheng Li [1 ]
Xiang, Lang [1 ]
Ma, Shi Ying [1 ]
Li, Wei [1 ]
Jiao, Rui Hua [1 ]
Tan, Ren Xiang [1 ,2 ]
Ge, Hui Ming [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, Inst Funct Biomol, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, State Key Lab Cultivat Base TCM Qual & Efficacy, Nanjing 210023, Jiangsu, Peoples R China
关键词
Borrelidin; Endophyte; Streptomyces sp; Antibacterial activity; Structure elucidation; ANGIOGENESIS INHIBITOR; BIOSYNTHESIS;
D O I
10.1016/j.tetlet.2018.11.023
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Three new borrelidin-type macrolactones, designated as borrelidins J-L (4-6), together with borrelidin A (1), borrelidin E (2), and 12-desnitrile-12-carboxyl-borrelidin (3) were isolated from a plant endophytic Streptomyces sp. NA06554. Their structures were determined by extensive spectroscopic analysis including HRESIMS, 1D and 2D NMR data. The antibacterial activities for compounds 1-6 were examined. Borrelidins A (1) and L (6) showed potent and moderate antibacterial activity against Micrococcus luteus, respectively, whereas other derivatives (2-5) are almost inactive, which allows us to propose a plausible structure-activity relationship. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4517 / 4520
页数:4
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