New borrelidin derivatives from an endophytic Streptomyces sp.

被引:6
|
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
下载
收藏
页码:4517 / 4520
页数:4
相关论文
共 50 条
  • [31] Julichrome derivatives and gliotoxin from a soil derived Streptomyces sp.
    Shen, Tong
    Li, Le-Mei
    Xu, Ze-Yu
    Wang, Yong-Dong
    Xie, Wei-Dong
    NATURAL PRODUCT RESEARCH, 2021, 35 (01) : 34 - 40
  • [32] New Metabolites from the Endophytic Fungus Mollisia sp.
    Fan, Nai Wen
    Chang, Hsun Shuo
    Cheng, Ming Jen
    Chan, Hing Yuen
    Hsieh, Sung Yuan
    Liu, Ta Wei
    Chen, Sheng Wen
    Yuan, Gwo Fang
    Chen, Ih Sheng
    CHEMISTRY OF NATURAL COMPOUNDS, 2016, 52 (04) : 585 - 590
  • [33] Identification of trichostatin derivatives from Streptomyces sp. CPCC 203909
    Chen, Minghua
    Wu, Yexiang
    He, Yi
    Xu, Yanni
    Li, Yongzhen
    Li, Dongsheng
    Feng, Tingting
    Yu, Liyan
    Hong, Bin
    Jiang, Wei
    Si, Shuyi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (03) : 562 - 565
  • [34] Colletodiol derivatives of the endophytic fungus Trichocladium sp.
    Simons, Viktor E.
    Mandi, Attila
    Frank, Marian
    van Geelen, Lasse
    Tran-Cong, Nam
    Albrecht, Dorothea
    Coort, Annika
    Gebhard, Christina
    Kurtan, Tibor
    Kalscheuer, Rainer
    FITOTERAPIA, 2024, 175
  • [35] A new sesquiterpene from endophytic fungus Aspergillus sp.
    Luo, Shao-Liu
    Li, Guo-Hong
    Liu, Fang-Fang
    Lei, Li-Ping
    Xia, Zhen-Yuan
    Zhang, Ke-Qin
    NATURAL PRODUCT RESEARCH, 2012, 26 (14) : 1334 - 1338
  • [36] Bioremediation of Copper with Endophytic Bacteria Bacillus sp. and Streptomyces griseus
    Ozkoc, Hulya Boke
    Aliustaoglu, Mirac Tansu
    Senturk, Ilknur
    JOURNAL OF ENVIRONMENTAL ENGINEERING, 2023, 149 (11)
  • [37] Exserolides A-F, new isocoumarin derivatives from the plant endophytic fungus Exserohilum sp.
    Li, Ruxin
    Chen, Shenxi
    Niu, Shubin
    Guo, Liangdong
    Yin, Jun
    Che, Yongsheng
    FITOTERAPIA, 2014, 96 : 88 - 94
  • [38] Verbalide A~F: new phthalide derivatives from the endophytic fungus Preussia sp. CPCC 400972
    Ran Zhang
    Yujia Wang
    Guowei Cai
    Juxian Wang
    Jianyuan Zhao
    Jinglin Bai
    Tao Zhang
    Shan Cen
    Wenni He
    Liyan Yu
    The Journal of Antibiotics, 2023, 76 : 613 - 617
  • [39] Verbalide A∼F: new phthalide derivatives from the endophytic fungus Preussia sp. CPCC 400972
    Zhang, Ran
    Wang, Yujia
    Cai, Guowei
    Wang, Juxian
    Zhao, Jianyuan
    Bai, Jinglin
    Zhang, Tao
    Cen, Shan
    He, Wenni
    Yu, Liyan
    JOURNAL OF ANTIBIOTICS, 2023, 76 (10): : 613 - 617
  • [40] A new daidzein derivative from endophytic Streptomyces sp YIM 65408
    Yang, Yabin
    Yang, Xueqiong
    Zhang, Yong
    Zhou, Hao
    Zhang, Jucheng
    Xu, Lihua
    Ding, Zhongtao
    NATURAL PRODUCT RESEARCH, 2013, 27 (19) : 1727 - 1731