475-54-7
Chemical Structure
Oosporein
- CAS No.: 475-54-7
- Formula:C14H10O8
- Molecular Weight:306.22
IUPAC Name: 3,3',6,6'-tetrahydroxy-4,4'-dimethyl-[1,1'-bi(cyclohexane)]-3,3',6,6'-tetraene-2,2',5,5'-tetraone
InChIKey: DHMPJEGFPQTNFX-UHFFFAOYSA-N
SMILES: O=C(C(C)=C1O)C(O)=C(C2=C(O)C(C(C)=C(O)C2=O)=O)C1=O
Biological Activity: Oosporein is a microbial metabolite and a red crystalline toxin produced by various fungi. Oosporein can promote the reproduction of fungi in host bodies by inhibiting insect immunity, and possesses multiple activities such as antibacterial, antiviral (HSV), and insecticidal effects. Oosporein can inhibit plant growth. In addition, Oosporein can also induce apoptosis, cell membrane damage, oxidative stress, and mitochondrial damage. Oosporein has certain antitumor activity[1][2][3][4][5].
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Oosporein | 99.16% | Oosporein is a microbial metabolite and a red crystalline toxin produced by various fungi. Oosporein can promote the reproduction of fungi in host bodies by inhibiting insect immunity, and possesses multiple activities such as antibacterial, antiviral (HSV), and insecticidal effects. Oosporein can inhibit plant growth. In addition, Oosporein can also induce apoptosis, cell membrane damage, oxidative stress, and mitochondrial damage. Oosporein has certain antitumor activity. | ||||||||||||||||||||
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Oosporein (Standard) | ≥98% | Oosporein (Standard) is the analytical standard of Oosporein (HY-N7719). This product is intended for research and analytical applications. Oosporein is a microbial metabolite and a red crystalline toxin produced by various fungi. Oosporein can promote the reproduction of fungi in host bodies by inhibiting insect immunity, and possesses multiple activities such as antibacterial, antiviral (HSV), and insecticidal effects. Oosporein can inhibit plant growth. In addition, Oosporein can also induce apoptosis, cell membrane damage, oxidative stress, and mitochondrial damage. Oosporein has certain antitumor activity. | ||||||||||||||||||||
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- [1]. Mao B Z, et al. Separation and determination of the bioactivity of oosporein from Chaetomium cupreum. African Journal of Biotechnology, 2010, 9(36).
- [2]. Taniguchi M, et al. Antimicrobial and Respirationinhibitory Activities of Oosporein. Agricultural and biological chemistry, 1984, 48(4): 1065-1067.
- [3]. Cole RJ, et al. Toxic effects of oosporein from Chaetomium trilaterale. J Agric Food Chem. 1974;22(3):517-520. [Content Brief]
- [4]. Ramesha A, et al. Cytotoxic effects of oosporein isolated from endophytic fungus Cochliobolus kusanoi. Front Microbiol. 2015 Sep 1;6:870. [Content Brief]
- [5]. Feng P, et al. C. Fungal biosynthesis of the bibenzoquinone oosporein to evade insect immunity. Proc Natl Acad Sci U S A. 2015 Sep 8;112(36):11365-70. [Content Brief]
Keywords
