Fumiquinazoline C

ID 2: 664

Toxin: n

Trivial name:

Spiro[9H-​imidazo[1,​2-​a]​indole-​9,​3′-​[1,​5]​(iminomethano)​[3H]​[1,​4]​oxazepino[3,​4-​b]​quinazoline]​-​3,​7′,​13′(1’H,​2H)​-​trione, 1,​4′,​5′,​9a-​tetrahydro-​1′,​2-​dimethyl-​, [1’R-​[1’α,​3’β(2S*,​9aS*)​,​5’α]​]​-; (-​)​-​Fumiquinazoline C; Fumiquinazoline C

Systematic name:

Spiro[9H-​imidazo[1,​2-​a]​indole-​9,​3′-​[1,​5]​(iminomethano)​[3H]​[1,​4]​oxazepino[3,​4-​b]​quinazoline]​-​3,​7′,​13′(1’H,​2H)​-​trione, 1,​4′,​5′,​9a-​tetrahydro-​1′,​2-​dimethyl-​, (1’R,​2S,​3’R,​5’S,​9aS)​-

Molecular formulae: 

C24H21N5O4

Molecular weight: 443.46

Chemical abstract number: 140924-01-2

Literature reference:

  • Structures of cytotoxic substances and new quinazoline derivatives produced by a fungus from a saltwater fish. Numata, Atsushi; Takahashi, Chika; Miyamoto, Tamie; Matsushita, Tomochika; Kawai, Kenzo; Usami, Yoshihide; Matsumura, Eiko; Inoue, Masatoshi; Ohishi, Hirofumi; Shingu, Tetsuro. Tennen Yuki Kagobutsu Toronkai Koen Yoshishu (1991), 33rd, 723-30.
    Fumiquinazolines A-​G, novel metabolites of a fungus separated from a Pseudolabrus marine fish. Takahashi, Chika; Matsushita, Tomochika; Doi, Mitsunobu; Minoura, Katsuhiko; Shingu, Tetsuro; Kumeda, Yuko; Numata, Atsushi. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1995), (18), 2345-53.
    Antitumor metabolites from fungus Aspergillus sydowi D 2-​6. Ren, Hong; Cao, Xueli; Wang, Qiaoe; Xu, Chunming. Zhongguo Yaoxue Zazhi (Beijing, China) (2011), 46(8), 569-575

References URL: 

Aspergillus Species known to produce this metabolite:

Structure image:  

Date uploaded: 2011-10-19 11:23:51

Mycotoxin & Metabolites

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