HALICHONADINS M-Q, SESQUITERPENES FROM AN OKINAWAN MARINE SPONGE HALICHONDRIA SP.

被引:11
|
作者
Tanaka, Naonobu [1 ]
Suto, Shohei [1 ]
Asai, Miki [1 ]
Kusama, Taishi [1 ]
Takahashi-Nakaguchi, Azusa [2 ]
Gonoi, Tohru [2 ]
Fromont, Jane [3 ]
Kobayashi, Jun'ichi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
[2] Chiba Univ, Med Mycol Res Ctr, Chiba 2608673, Japan
[3] Western Australian Museum, Welshpool Dc, WA 6986, Australia
关键词
Marine Sponge; Helichondria sp; Sesquiterpene; Halichonadins M-Q; NATURAL-PRODUCTS;
D O I
10.3987/COM-14-S(K)2
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Four new dimeric sesquiterpenes, halichonadins M-P (1-4), and one new sesquiterpene, halichonadin Q (5), were isolated from an Okinawan marine sponge Halichondria sp. The sesquiterpenes have eudesmane skeleton in common Halichonadin M (1) is a symmetrical dimer linked to a nitrilotriacetic acid fragment through amide bonds. Halichonadin N (2) is a structurally unique dimeric sesquiterpene connected via a pyrrolidine unit, while halichonadins 0 (3) and P (4) have linker moieties consisting of a piperidine unit. Halichonadin Q (5) is a sesquiterpene possessing a pyrrolidine unit. The structures of 1-5 were elucidated by spectroscopic analysis. Halichonadin 0 (3) showed antimicrobial activity against Staphylococcus aureus, Micrococcus luteus, and Trichophyton mentagrophytes.
引用
收藏
页码:173 / 185
页数:13
相关论文
共 50 条
  • [21] New formamidobisabolene-type sesquiterpenoids from a Hainan Sponge Halichondria sp.
    Chen, Bao
    Li, Wang-Sheng
    Gu, Yu-Cheng
    Zhang, Hai-Yan
    Luo, Hui
    Wang, Chang-Yun
    Guo, Yue-Wei
    Li, Xu-Wen
    TETRAHEDRON, 2021, 96
  • [22] Four homoverrucosane-type diterpenes from the marine sponge Halichondria sp
    Tian, Yong-Qi
    Gu, Bin-Bin
    Jiao, Wei-Hua
    Lin, Hou-Wen
    TETRAHEDRON, 2020, 76 (50)
  • [23] Norisoprenoids from the marine sponge Spheciospongia sp.
    Liu, Dong
    Xu, Min-Juang
    Wu, Li-Jun
    Deng, Zhi-Wei
    Lin, Wen-Han
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2009, 11 (09) : 811 - 816
  • [24] Diketopiperazines from the Marine Sponge Axinella sp.
    Riming Huang
    Tao Yan
    Yan Peng
    Xuefeng Zhou
    Xianwen Yang
    Yonghong Liu
    Chemistry of Natural Compounds, 2014, 50 : 191 - 193
  • [25] New bromopyrrole alkaloids from the marine sponge Agelas sp.
    Sun, Ya-Ting
    Lin, Bin
    Li, Sheng-Ge
    Liu, Man
    Zhou, Yong Jun
    Xu, Ying
    Hua, Hui-Ming
    Lin, Hou-Wen
    TETRAHEDRON, 2017, 73 (19) : 2786 - 2792
  • [26] Six New Polyacetylenic Alcohols from the Marine Sponges Petrosia sp and Halichondria sp.
    Gabriel, Adeyemi Francis
    Li, Zhen
    Kusuda, Ryouhei
    Tanaka, Chiaki
    Miyamoto, Tomofumi
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2015, 63 (06) : 469 - 475
  • [27] Monoindole alkaloids from a marine sponge Spongosorites sp.
    Bao, Baoquan
    Zhang, Ping
    Lee, Yoonmi
    Hong, Jongki
    Lee, Chong-O.
    Jung, Jee H.
    MARINE DRUGS, 2007, 5 (02) : 31 - 39
  • [28] Discorhabdins from the Korean Marine Sponge Sceptrella sp.
    Jeon, Ju-eun
    Na, Zeyei
    Lung, Misong
    Lee, Hyi-Seung
    Sim, Chung J.
    Nahm, Keepyung
    Oh, Ki-Bong
    Shin, Jongheon
    JOURNAL OF NATURAL PRODUCTS, 2010, 73 (02): : 258 - 262
  • [29] New cerebrosides from the marine sponge Oceanapia sp.
    Guzii, A. G.
    Makarieva, T. N.
    Denisenko, V. A.
    Svetashev, V. I.
    Rodkina, S. A.
    Dmitrenok, P. S.
    Anastyuk, S. D.
    Stonik, V. A.
    RUSSIAN CHEMICAL BULLETIN, 2006, 55 (05) : 928 - 933
  • [30] New cerebrosides from the marine sponge Oceanapia sp.
    A. G. Guzii
    T. N. Makarieva
    V. A. Denisenko
    V. I. Svetashev
    S. A. Rodkina
    P. S. Dmitrenok
    S. D. Anastyuk
    V. A. Stonik
    Russian Chemical Bulletin, 2006, 55 : 928 - 933