Study on new biologically active substances isolated from Ascomycetous fungi

子囊菌新生物活性物质的研究

基本信息

  • 批准号:
    07672296
  • 负责人:
  • 金额:
    $ 1.41万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1995
  • 资助国家:
    日本
  • 起止时间:
    1995 至 1996
  • 项目状态:
    已结题

项目摘要

The following compounds were isolated from Emericella sp. From E.purpurea, two new sesterterpenes designated variecolol and variecolic acid and three new yellow 2,3-dicyano-1,4-diphenyl-1,3-butadiene derivatives, epurpurins A-C,were isolated along with the sesterterpene, variecolin, which has angiotensin II binding inhibitory activity. The dicyanide derivatives had the growth inhibitory activity for L1210 cells. Six new hydrogenated azaphilones, falconensin E-G and I-N,and two new pigments with a long conjugated system, EF-Y1 and EF-Y2, were isolated along with the azaphilones from the mycelium of E.falconensis and/or E.fruticulosa. These falconensins will be expected the inhibitory activity for tumor promotor. From the culture medium of E.heterothallica, new 18,22-cyclosterols, emesterols B and C,were isolated along with emesterol A,which had the strong antifungal activty against Aspergillus fumigatus. A new epitetrathiodioxopiperazine, secoemestrin C,was isolated from the early stage of the culture broth of E.foveolata.From the ascostromata of Talaromyces austrocalifornicus, an azaphilone and a hydrogenated anthraquinone dimer was isolated. A hydroganated azaphilone derivatives and an anthraquinone dimer, skyrin, were also isolated from T.wortmanni. From the ascostromata of Petromyces muricans, four new bisindolylbenzene derivatives, petromurin A-D,a bisindolylbenzoquine (asteriiquinone), Pm-53, and an indoloditerpene, petromindole, were isolated.
从 Emericella sp. 中分离出以下化合物。从 E.purpurea 中,分离出了两种新的二元萜烯(variecolol 和 variecolin)以及三种新的黄色 2,3-二氰基-1,4-二苯基-1,3-丁二烯衍生物 epurpurins A-C,以及二元萜烯 variecolin(具有血管紧张素 II 结合抑制活性)。二氰化物衍生物对L1210细胞具有生长抑制活性。从 E.falconensis 和/或 E.fruticulosa 的菌丝体中分离出了六种新的氢化氮杂酮类化合物:falconensin E-G 和 I-N,以及两种具有长共轭体系的新色素 EF-Y1 和 EF-Y2。这些鹰嘴菌素预计具有对肿瘤促进剂的抑制活性。从E.heterothallica培养基中分离得到新的18,22-环甾醇,即艾甾醇B和C,以及艾甾醇A,其对烟曲霉具有较强的抗真菌活性。从E.foveolata早期培养液中分离得到一个新的表四硫二氧代哌嗪,secoemestrin C。从Talaromyces austrocalifornicus的子盘中分离得到氮杂菲酮和氢化蒽醌二聚体。还从 T.wortmanni 中分离出氢化阿扎菲酮衍生物和蒽醌二聚体 Skyrin。从 Petroomyces muricans 的子囊中,分离出四种新的双吲哚基苯衍生物:petromurin A-D、双吲哚基苯喹(asteriiquinone)、Pm-53 和吲哚二萜 petromindole。

项目成果

期刊论文数量(9)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
H.Takahashi, K.Nozawa, K.Kawai: "Isolation and Structures of Dicyanide Derivatives, Epurpurins A to C,from Emericella purpurea." Chem.Pharm.Bull. 44 (12). 2227-2230 (1996)
H.Takahashi、K.Nozawa、K.Kawai:“Emericella purpurea 中二氰化物衍生物 Epurpurins A 至 C 的分离和结构。”
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    0
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T.Itabashi,N.Ogasawara,K.Nozawa,K.Kawai: "Isolation and Structures of New Azaphilone Derivatives,Falconensins E-G,from Emericella falconensis and Absolute Configuration of Ealconensins A-C" Chem.Pharm.Bull.44(12). 2213-2217 (1996)
T.Itabashi、N.Ogasawara、K.Nozawa、K.Kawai:“新 Azaphilone 衍生物 Falconensins E-G 的分离和结构,来自 Emericella falconensis 和 Ealconensins A-C 的绝对构型”Chem.Pharm.Bull.44(12)。
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    0
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T.Itabashi, N.Ogasawara, K.Nozawa, K.Kawai: "Isolation and Structures of New Azaphilone Derivatives, Falconensins E-G,from Emericella falconensis and Absolute Configurations of Falconensins A-G" Chem.Pharm.Bull. 44 (12). 2213-2217 (1996)
T.Itabashi、N.Ogasawara、K.Nozawa、K.Kawai:“新 Azaphilone 衍生物 Falconensins E-G 的分离和结构,来自 Emericella falconensis 和 Falconensins A-G 的绝对构型”Chem.Pharm.Bull。
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    0
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M.Ooike, K.Nozawa, S.Udagawa, K.Kawai: "Bisindolylbenzenoids from Petromyces muricatus" Can.J.Chem.(in press). (1997)
M.Ooike、K.Nozawa、S.Udakawa、K.Kawai:“来自 Petromyces muricatus 的 Bisindolylbenzenoids”Can.J.Chem.(印刷中)。
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    0
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T.Itabashi,N.Ogasawara,K.Nozawa,K.Kawai: "Isolation and Structures of New Azaphilone Derivatives,Falconensins E-G,from Emericella falconensis and Absolute Configurations of Falconensins A-G" Chemical and Pharmaceutical Bulletin. 44. 2213-2217 (1996)
T.Itabashi、N.Ogasawara、K.Nozawa、K.Kawai:“新 Azaphilone 衍生物 Falconensins E-G 的分离和结构,来自 Emericella falconensis 和 Falconensins A-G 的绝对构型”化学和制药通报。
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KAWAI Kenichi其他文献

KAWAI Kenichi的其他文献

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{{ truncateString('KAWAI Kenichi', 18)}}的其他基金

Development of new antifungal drugs isolated from fungal sources in order to overcome of deep-seated mycosis
开发从真菌来源分离的新型抗真菌药物以克服深部真菌病
  • 批准号:
    20590017
  • 财政年份:
    2008
  • 资助金额:
    $ 1.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Enhancement of chemosensitivity of the quiescent call populations in murine solid tumor by combination treatment with antitumor drugs and vasoactive agent
抗肿瘤药物与血管活性药物联合治疗增强小鼠实体瘤静止细胞群的化疗敏感性
  • 批准号:
    05807076
  • 财政年份:
    1993
  • 资助金额:
    $ 1.41万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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