Ergosterol peroxide
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Names | |
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IUPAC name (3S,5S,8S,9R,10R,13R,14R,17R)-10,13-dimethyl-17-[(1R,2E,4R)-1,4,5-trimethylhex-2-en-1-yl]-1,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-2H-5,8-epidioxycyclopenta[a]phenanthren-3-ol | |
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3D model (JSmol) | |
ChEBI | |
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CompTox Dashboard (EPA) | |
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Properties | |
C28H44O3 | |
Molar mass | 428.647 |
Density | 1.08g/cm3 |
Boiling point | 499.7 °C (931.5 °F; 772.8 K) at 760mmHg |
Hazards | |
Flash point | 256 °C (493 °F; 529 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Ergosterol peroxide (5α,8α-epidioxy-22E-ergosta-6,22-dien-3β-ol) is a steroid derivative. It has been isolated from a variety of fungi, yeast, lichens and sponges,[1][2][3][4][5] and has been reported to exhibit immunosuppressive,[6] anti-inflammatory,[7] antiviral,[8] trypanocidal [9] and antitumor activities in vitro.[10][11]
References
[edit]- ^ Lobo AM, Abreu PM, Prabhakar S, Godhino LS, Jones R, Rzepa HS, Williams DJ (1988). "Triterpenoids of the fungus Pisolithus tinctorius". Phytochemistry. 27 (11): 3569–74. Bibcode:1988PChem..27.3569L. doi:10.1016/0031-9422(88)80770-2.
- ^ Jimenez C, Quinoa E, Rignera R, Vilalta R, Quintella JM (1989). "The dietary origin of epidioxy steroids in Actinia equina. A carbon14 incorporation experiment". Journal of Natural Products. 52 (3): 619–22. doi:10.1021/np50063a023.
- ^ Kahols K, Kangas L, Hiltunen R (1989). "Ergosterol peroxide, an active compound from Inonotus radiatus". Planta Medica. 55 (4): 389–90. doi:10.1055/s-2006-962036. PMID 2813575.
- ^ Tchouankeu JC, Nyasse B, Tsamo E, Sondengam B, Morin C (1992). "An ergostane derivative from the bark of Entandrophragma utile". Phytochemistry. 31 (2): 704–705. Bibcode:1992PChem..31..704T. doi:10.1016/0031-9422(92)90067-Z.
- ^ Fujimoto H, Nakayama Y, Yamazaki M (1994). "Isolation and characterization of immunosuppressive components of three mushrooms, Pisolithus tinctorius, Microporus flabelliformis and Lenzites betulina". Chem. Pharm. Bull. 42 (3): 694–97. doi:10.1248/cpb.42.694. PMID 8004718.
- ^ Yasukawa K, Akihisa T, Kanno H, Kaminaga T, Izumida M, Sakoh T, Tamura T, Takido M (1996). "Inhibitory effects of sterols isolated from Chlorella vulgaris on 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and tumor promotion in mouse skin". Biological and Pharmaceutical Bulletin. 19 (4): 573–576. doi:10.1248/bpb.19.573. PMID 8860961.
- ^ Lindequist U, Lesnau A, Teuscher E, Pilgrim H (1989). "Antiviral activity of ergosterol peroxide". Pharmazie. 44 (8): 579–80. PMID 2594833.
- ^ Nakanishi T, Murata H, Inatomi Y, Inada A, Murata J, Lang FA, Yamasaki K, Nakano M, Kawahata T, Mori H, Otake T (1998). "Screening of anti-HIV-1 activity of North American plants. Anti-HIV-1 activities of plant extracts, and active components of Lethalia vulpina (L.) Hue". Journal of Natural Medicines. 52: 521–26.
- ^ Ramos-Ligonio, Angel; López-Monteon, Aracely; Trigos, Ángel (2012-06-01). "Trypanocidal Activity of Ergosterol Peroxide from Pleurotus ostreatus". Phytotherapy Research. 26 (6): 938–943. doi:10.1002/ptr.3653. ISSN 1099-1573. PMID 22083593. S2CID 1858275.
- ^ Bok JW, Lermer L, Chilton J, Klingeman HG, Towers NG (1999). "Antitumor sterols from the mycelia of Cordyceps sinensis". Phytochemistry. 51 (7): 891–98. Bibcode:1999PChem..51..891B. CiteSeerX 10.1.1.565.2857. doi:10.1016/S0031-9422(99)00128-4. PMID 10423860.
- ^ Nam KS, Jo YS, Kim YH, Hyun JW, Kim HW (2001). "Cytotoxic activities of acetoxyscirpenediol and ergosterol peroxide from Paecilomyces tenuipes". Life Sciences. 69 (2): 229–37. doi:10.1016/s0024-3205(01)01125-0. PMID 11441913. S2CID 8970168.