Archive for April, 2008

Clavariadelphus ligula

Wednesday, April 30th, 2008

The medicinal mushroom Clavariadelphus ligula
The strap coral mushroom, Clavariadelphus ligula (Schaeff.) Donk.
  Credit: Bernd Gliwa
  Source: Wikipedia Commons, licensed under CCAS2.5

Synonym

Clavaria ligula Schaeff.
  Fung. Bavar. Palat. 4: 116 (1774)

Common names

Strap coral mushroom
Tongue mushroom

Description

Fruiting body: 3-10 cm tall, 0.5-1.5 cm wide (at apex), cylindrical to narrowly clavate, the apex appearing slightly flattened or blunt; surface roughened, cream to orange-buff to yellowish-brown, fine white tomentose base.
Flesh: spongy, not brittle, white;green in ferric sulphate solution.
Odor: none.
Taste: slightly bitter.
Spores: 8-18 x 3-6 µm, nonamyloid, ellipsoid, smooth, entire.
Spore print: white.
Edibility: inedible.
Habitat: gregarious, clustered or caespitose, under many different conifers. Widely distributed; summer-fall.

Biochemistry

Medicinal properties
Antitumor effects

An extract of the fruit bodies of C. ligula inhibited the growth of Sarcoma 180 and Ehrlich solid cancers in mice by 60% (Ohtsuka et al., 1973).

References

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
UK Patent 1331513, 26 September 1973.

 

Last updated: 30-Apr-2008

Ramaria botrytis

Saturday, April 26th, 2008

The medicinal mushroom Ramaria botrytis
The pink-tipped coral, Ramaria botrytis (Pers.) Ricken.
  Credit: Douglas Smith
  Source: Mushroom Observer, licensed under SSCA3.0

Synonyms

Clavaria botrytis Pers.
  Comment. Fungis Clavaeform: 42 (1797)
Clavaria botrytis var. alba A. Pearson
  Trans. Br. mycol. Soc. 29(4): 209 (1946)
Corallium botrytis (Pers.) Hahn
  Pilzsammler: 72 (1883)

Common names

Cauliflower coral
Clustered coral
Pink-tipped coral
Rosso coral
Clavaire chou-fleur (French)
Hahnenkamm (German)
Druvfingersvamp (Swedish)
Houkitake (Japanese)

Description

Fruiting body: 10-12 cm diameter, 7-12 cm high, forming fleshy round masses with a short, stout base, densely branched above, white to buff, the tips of the branches reddish.
Smell: slight.
Taste: pleasant.
Stem: short, stout, white, tapering below, branching irregular, the primary branches few and stout (2-3 cm), ultimate branches slender (2-3 mm), more or less dichotomous.
Flesh: solid, white, brittle.
Spore print: dull yellow.
Spores: ellipsoid, entire in outline but with fine longitudinal or oblique striations often anastomosing, 11-17 x 4-6 µm. See spores here.
Habitat: on ground among leaves in woods; late summer to late autumn.
Edibility: edible, and for some, choice - especially if you're a Katmandu native (Adhikari et al., 2005).

Description adapted from Burt, 1922.

Traditional use

Adhikari et al. (2005) report that in Kathmandu, this species is used medicinally to relieve muscle pain.

Bioactive compounds

A number of compounds have been isolated and identified from the fruiting bodies of Ramaria botrytis (Yaoita et al., 2007):

  • a novel ceramide, (2S,2'R,3R,4E,8E)- N2'-hydroxyoctadecanoyl- 2-amino-9-methyl- 4,8-heptade-cadiene-1,3-diol
  • 5α,6α-epoxy-3β-hydroxy-(22E)-ergosta-8(14),22-dien-7-one
  • ergosterol peroxide (3), cerevisterol (4)
  • 9α-hydroxycerevisterol

Ramaria botrytis was found to produce the unusual amino acid nicotianamine, an inhibitor of angiotensin I-converting enzyme (Izawa and Aoyagi, 2006).

The nutritional effects of alcohol extracts and acid hydrolysates of Ramaria botrytis were studied on the multiplication of tissue cells HeLa [human cervical carcinoma] cells; both the alcohol extracts and acid hydrolysate favorably infuenced maintenance of the normal form and monolayer of HeLa cells (Chung 1979).

Medicinal properties
Hepatoprotective effects

One study demonstrated that the methanol extract of R. botrytis had a protective effect on liver damage in benzo(a)pyrene-treated mice. The activities of marker liver enzymes serum aminotransferase, cytochrome P-450, aminopyrine N-demethylase, aniline hydroxylase and hepatic content of lipid peroxide after benzo(a)pyrene-treatment were increased relative to the control, but those levels were significantly decreased by the treatment of methanol extract, whereas the hepatic glutathione content and activities of glutathione S-transferase and r-glutamylcysteine synthetase were increased by the treatment of R. botrytis methanol extract. Also, the cytochrome P-450 1A1 isozyme protein level, increased by benzo(a)pyrene-treatment, was decreased by the treatment with methanol extract. The authors suggest that the protective effect of the R. botrytis methanol extract on liver injury may be due to reduction of oxygen free radicals (Kim and Lee, 2003).

Antitumor effects

An extract of the fruitbodies inhibited the growth of both Sarcoma 180 and Ehrlich solid cancers in mice by 60% (Ohtsuka et al., 1973).

Links

Mycoweb, Mushroom Expert have additional information. This website about the fungi of Thrace, Greece has an impressive photo gallery, as does the Swedish Stridvall site.

References

Adhikari MK, Devkota S, Tiwari RD.
Ethnomycological knowledge on uses of wild mushrooms in western and central Nepal.
Our Nature. 2005 3:13-19.
PDF available online

Burt EA.
The North American species of Clavaria with illustrations of the type specimens
Annals of the Missouri Botanical Garden. 1922 9(1):1-78.

Chung KS.
The effects of mushroom components on the proliferation of HELA cell line in vitro.
Arch Pharm Res. 1979 2(1):25-34.

Izawa H, Aoyagi Y.
Inhibition of angiotensin converting enzyme by mushroom.
J Jap Soc Food Sci Technol. 2006 53(9):459-65.

Jarvis MC, Miller AM, Sheahan J, Ploetz K, Ploetz J, Watson RR, Palma Ruiz M, Pascario Villapan C, Garcia Alvarado J, Lopez Ramirez A, Orr B.
Edible wild mushrooms of the Cofre de Perote region, Veracruz, Mexico: An ethnomycological study of common names and uses.
Econ Bot. 2004 58:S111-S115.

Kim HJ, Lee KR.
Effect of Ramaria botrytis methanol extract on antioxidant enzyme activities in benzo(α)pyrene-treated mice.
Korean J Food Sci Technol. 2003 354: 286-290.

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
UK Patent 1331513, 26 September 1973.

Yaoita Y, Satoh Y, Kikuchi M.
A new ceramide from Ramaria botrytis (Pers.) Ricken.
J Nat Med. 2007 61(2):205-7.

 

Last modified: 26-April-2008

 

Exidia glandulosa

Tuesday, April 22nd, 2008

The medicinal mushroom Exidia glandulosa
Black witches' butter, Exidia glandulosa (Bull.) Fr.
  Credit: Eric Steinert
  Source:
Wikipedia Commons

Synonyms

Exidia intumescens sensu auct.
  fide Checklist of Basidiomycota of Great Britain and Ireland (2005)
Exidia plana sensu auct.
  fide Checklist of Basidiomycota of Great Britain and Ireland (2005)
Exidia spiculosa (Pers.) Sommerf.
  Suppl. Fl. lapp. (Oslo) (1826)
Gyraria spiculosa (Pers.) Gray
  Nat. Arr. Brit. Pl. (London) 1: 594 (1821)
Tremella arborea sensu auct.
  fide Checklist of Basidiomycota of Great Britain and Ireland (2005)
Tremella atra Fr.
  Fl. Danic. 5: tab. 884 (1782)
Tremella glandulosa Bull.
  Herbier de la France 9: tab. 420, fig. 1 (1789)
Tremella intumescens sensu auct.
  fide Checklist of Basidiomycota of Great Britain and Ireland (2005)
Tremella spiculosa Pers.
  Observ. mycol. (Lipsiae) 1: 99 (1796)

Common names

Black witch's butter
Black jelly roll
Warty jelly fungus

Description

In a 150-year old treatise on English botany, (Sowerby et al.,  1846, p. 225) it is mentioned that according to Dillenius, this species earned its common name "witches' butter" because it was believed to be useful against witchcraft when thrown into a fire.

Fruiting body: wrinkled, gelatinous; beginning as a pallid or translucent blister but soon becoming cushion-shaped to irregularly lobed, appearing effused, undulate, brain-like in structure; usually dark black color, but sometimes reddish black to olive-black in younger specimens; 1-2 cm broad but often fusing with adjacent sporophores to form extensive patches; upper surface smooth to minutely roughened with scattered, erect, short spicules.
Flesh: gelatinous, black.
Taste, smell: indistinct.
Spore print: whitish; the spores are borne on the lobes, warts or wrinkles.
Spores: 10-16 x 3-5 µm, allantoid, smooth.
Edibility: unclear (different opinions depending on the source).
Habitat: found on dead wood of deciduous trees, especially birch, beech, alder, pine, hawthorn. It prefers cooler temperatures and is more likely to be found Sept to May.

The fruiting body will dehydrate to form a thin membrane, but will rehydrate when moistened. The fruiting bodies are somewhat translucent when young and fresh.

Lipid composition

The lipid composition of E. glandulosa is 37.5% total lipids (mg/g dry weight). Of this total, 60.5% is neutral lipids, 35.8% is phospholipids and 3.7% glycolipids (Dembitsky et al., 1992). Further details about the particulars of lipid composition in this species can be found in that reference and in Demibitsky et al., 1993.

Medicinal properties
Antitumor effects

An extract of the mycelial culture of black witches' butter inhibited the growth of Sarcoma 180 solid cancer in mice by 90% (Ohtsuka et al., 1973).

Links

California Fungi, the Fungi on Wood site, and Biolib all have more photos or descriptions.

References

Dembitsky VM, Rezanka T, Shubina EE.
Chemical composition of fatty acids from some fungi
Crypt Bot. 1993 3(4):383-6.

Dembitsky VM, Shubina EE, Kashin AG.
Phospholipid and fatty acid composition of some basidiomycetes.
Phytochem. 1992 31(3):845-9.

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
UK Patent 1331513, 26 September 1973.

 

Last modified: 23-Apr-2008

Lepista inversa

Sunday, April 20th, 2008

The medicinal mushroom Lepista inversa
The tawny funnel cap, Lepista inversa (Scop Pat.). The red-brown drop-like flecks on the cap suggest that this specimen grew under fairly humid conditions
  Source: Wikipedia Commons

Synonyms

Agaricus inversus Scop., Fl. carniol.
  Edn 2 (Vienna) 2: 445 (1772)
Clitocybe inversa (Scop.) Quél. [as 'inversus']
  Mém. Soc. Émul. Montbéliard, Sér. 2 5: 235 (1872)
Lepista flaccida var. inversa (Scop.) Chiari
  (2001) Recent record: see Index of Fungi

Common names

Tawny funnel cap
Roodbruine schijnridder (Dutch)
Clitocybe renversé (French)
Fuchsiger Trichterling (German)

Description

Cap: 5-10 cm diameter, broadly convex or centrally depressed with an inrolled  margin, becoming broadly depressed or even infundibuloform in age; surface dry, glabrous; color initially ochraceous-buff, later tawny, paler color when dry.
Gills: decurrent, close to crowded, narrow (3-4 mm), sometimes forked, white to buff to light pinkish-cinnamon or concolorous with cap
Stem: 2-5 cm long x 0.5- 1 cm diameter; concolorous (or paler) with cap, smooth at the apex, tomentose at base.
Sporeprint: almost whitish, very pale cream to pale-orange cream.
Spores: hyaline, verruculose, globose or subglobose to ellipsoid, non-amyloid, 4-5 x 3-4 µm.
Habitat: solitary or in small troops on soil in woods, especially in nitrogen-enriched areas; common; late July-Oct.
Odor and taste: not distinctive.
Edibility: edible.

Description based on Bigelow and Smith, 1969.

This species is similar in appearance to L. flaccida. Some research has been put into determining if there are differences in the makeup of the volatile chemical profile that might be used to chemotaxonomically distinguish between these two species; there may be certain chlorinated compounds present only in L. inversa that might distinguish it from L. flaccida (Boustie et al., 2005).

As a note of warning, this species has been reported to have been mistaken with Clitocybe amoenolens, a poisonous mushroom that can cause erythromelalgia, a painful disorder resulting from blocked blood vessels in the lower extremities (Saviuc et al., 2002). Furthermore, significant bioaccumulation of arsenic and cadmium has been reported in L. inversa (Vetter, 1994). Avoid consuming mushrooms grown near contaminated sites!

Bioactive compounds

Clitocine (6-amino-5-nitro-4-(β-D-ribo-furanosylamino)pyrimidine, shown below) is an exocyclic amino nucleoside that was first isolated from C. inversa (Kubo and Kim, 1986). The total synthesis of clitocine has also been reported (Moss et al., 1988), as well as the solid-phase synthesis of a variety of chemical analogues (Varaprasad et al., 2006).

Clitocine, the anti-cancer metabolite from the medicinal mushroom Lepista inversa

Medicinal properties
Antitumor activity

The cytotoxic activity of methanol extracts of fresh fruiting bodies of L. inversa was evaluated with two mouse cancer cell lines, L1210 (lymphocytic leukemia) and 3LL (Lewis lung carcinoma), and was shown to be active against both lines. The extract was also shown to have significant activity (IC50 ≤ 20 µg/ml) with 4 human cancer cell lines (K-562, U251, DU145, MCF7). This activity was even equal to or greater than a bark extract from Taxus baccata L., used as positive control (Bezivin et al., 2002).

In another study, a crude extract was studied against intraperitoneally transplanted lymphocytic leukemia (L1210) and intramuscularly transplanted Lewis lung carcinoma (3LL) in mice. The IC50 was determined to be about 500 mg/kg for an intraperitoneal administration (i.p.) of the extract; compared to the control group, i.p. administration of 75 mg/kg of body weight/day of the extract increased the lifespan of L1210 and 3LL tumor-bearing mice by 50% and 14%, respectively. The antileukemic activity against the L1210 model in mice was considered to be significant (Bevizin et al., 2003).

The purified compound clitocine, mentioned above, was also shown to have strong antitumor activity, with IC50 values ranging from 20.5 to 42 nm against murine 3LL and L1210, and from 185 to 578 nm in the human cancer cell lines DU145, K-562, MCF7, and U251. The authors suggest that the anti-tumor mechanism of clitocine may be due to apoptosis induction (Fortin et al., 2006).

Antibacterial activity

The mycelia and culture filtrate of L. inversa was shown to have antibiotic activity against the pathogenic bacteria Bacillus cereus and Staphylococcus aureus (Coletto et al., 1995).

Antiviral activity

In a study on the antiviral activity of 121 Homobasidiomycetes species, a crude extract from L. inversa showed the highest antiviral activity against the RNA viruses tested (poliovirus and VSV), and showed low cytotoxicity against the established Vero cell line (Amoros et al., 1997). These result corroborate an earlier study (Autrou et al., 1994) which revealed antiviral activity against HSV-1 and HSV-2, poliovirus and VSV.

Links

Photo and description at California Fungi

References

Amoros M, Boustie J, Py M-L, Hervé V, Robin V, Girre L.
Antiviral activity of homobasidiomycetes: Evaluation of 121 basidiomycetes extracts on four viruses.
Int J Pharmacog. 1997 35:255–60.

Autrou I, Amoros M., Boustie J, Girre L.
In vitro study of antiviral activity of Macromycetes.
Plantes Medicinales et Phytotherapie. 1994 26(4):347-55.

Bezivin C, Lohezic F, Sauleau P, Amoros M, Boustie J.
Cytotoxic activity of Tricholomatales determined with murine and human cancer cell lines.
Pharm Biol. 2002 40(3):196-9.

Bezivin C, Delcros JG, Fortin H, Amoros M, Boustie J.
Toxicity and antitumor activity of a crude extract from Lepista inversa (Scop.:Fr.) Pat. (Agaricomycetideae): A preliminary study.
Int J Med Mush. 2003 5(1):25-30.

Bigelow HE, Smith AH.
The status of Lepista-a new section of Clitocybe.
Brittonia. 1969 21(2):144-77.

Boustie J, Rapior S, Fortin H, Tomasi S, Bessiere JM.
Chemotaxonomic interest of volatile components in Lepista inversa and Lepista flaccida distinction
Cryptogamie Mycologie. 2005 26(1):27-35.

Coletto B, Ausilia M, Chiari P.
[Antibiotic activity in Basidiomycetes. IX. Antibiotic activity of mycelia and cultural filtrates.] Italian
Allionia (Turin). 1995 33(0):75-9.

Fortin H, Tomasi S, Delcros JG, Bansard JY, Boustie J.
In vivo antitumor activity of clitocine, an exocyclic amino nucleoside isolated from Lepista inversa.
Chem MedChem. 2006 1(2):189-96.
Pubmed

Kubo I, Kamikawa T.
Clitocine, a new insecticidal nucleoside from the mushroom Clitocybe inversa - isolation, structure and synthesis.
Abs Pap Amer Chem Soc. 1988 195:115-AGRO Part 1.

Kubo I, Kim M..
Clitocine, a new insecticidal nucleoside from the mushroom Clitocybe inversa.
Tetra Lett. 1986 27(36):4277-80.

Lee CH, Daanen JF, Jiang M, Yu H, Kohlhaas KL, Alexander K, Jarvis MF, Kowaluk EL, Bhagwat SS.
Synthesis and biological evaluation of clitocine analogues as adenosine kinase inhibitors.
Bioorg Med Chem Lett. 2001 11(18):2419-22.
Pubmed

Moss RJ, Petrie CR, Meyer RB Jr, Nord LD, Willis RC, Smith RA, Larson SB, Kini GD, Robins RK.
Synthesis, intramolecular hydrogen bonding, and biochemical studies of clitocine, a naturally occurring exocyclic amino nucleoside.
J Med Chem. 1988 31(4):786-90.
Pubmed

Saviuc PF, Danel VC, Moreau PA, Claustre AM, Ducluzeau R, Carpentier PH.
[Acute erythermalgia: look for mushrooms!]
Rev Med Interne. 2002 23(4):394-9. French.
Pubmed

Varaprasad CVNS, Habib Q, An HY, Hong Z.
Solid-phase synthesis of 5'-deoxy-5'-amino-clitocine analogues.
Nucleosides Nucleotides & Nucleic Acids. 2006 25(1):61-72.
Pubmed

Vetter J.
Data on arsenic and cadmium contents of some common mushrooms.
Toxicon. 1994 32(1):11-5.
Pubmed

 

Last modified: 20-Apr-2008

Stropharia aeruginosa

Saturday, April 19th, 2008

Stropharia_aeruginosa.jpg
One of the few green fungi, the verdigris toadstool, Stropharia aeruginosa (Curtis) Quél.
  Source: Wikipedia

Synonyms

Agaricus aeruginosus Curtis
  Fl. Londin. 2: tab. 210 (1786)
Pratella aeruginosa (Curtis) Gray
  Nat. Arr. Brit. Pl. (London) 1: 626 (1821)
Psilocybe aeruginosa (Curtis) Noordel.
  Persoonia 16(1): 128 (1995)

Common name

Verdigris toadstool/agaric
Blue-green stropharia
Grünspan-träuschling (German)
Kopergroenzwam (Dutch)

Description

Cap: 2-8 cm diameter, when young campanulate to convex, later plane; often with low, broad umbo, covered with verdigris-green, viscid thick gluten, sometimes dotted with white scales, especially on margin (remnants of the universal veil), in age fading to yellowish; peelable pellicle.
Flesh: white or tinged blue, rather soft, thick.
Gills: broadly adnate, sometimes emarginate-sinuate, rather broad, close, whitish at first, soon grey, finally purplish chocolate-brown, edge white and minutely floccose, subevanescent.
Stem: 5-7 cm long, 4-5 mm thick, equal, hollow, soft, concolorous with cap, viscid, at first scaly or fibrillose below the annulus.
Annulus: distant from apex, narrow, submembranous, irregularly floccose, subevanescent.
Spore print: purple-brown.
Spores: pale, smooth, thick-walled, ovoid to ellipsoid, 7-9 x 4-5 µm.
Habitat: solitary to gregarious on the ground or on rotten wood in hardwood and coniferous forests; spring to late summer; common.
Taste:
indistinct, or with mildly bitter aftertaste.
Odor:
weak radish smell or none.
Edibility: some sources say edible (but undesirable), others say poisonous.

Description adapted from Kaufmann, 1918; more microscopic characteristic may be gleaned from Van Crevel et al., 1988, p. 53 (as Psilocybe aeruginosa).

Bioactive compounds

Triterpenoids

Three lanostane triterpenoids, aeruginosols A, B and C, have been isolated and structurally characterized from the methanol extract of S. aeruginosa (Shiono et al., 2005; Shiono et al. 2007).

Lipids

In a lipid analysis of this species (Dembitsky et al., 1992), it was found that the lipid content consisted of 47.8% total lipids (mg/g dry weight), 44.8% neutral lipids, 44.0% phospholipids, and 11.2% glycolipids. It was also reported that of the phospholipids, 32.2% was phosphatidylethanolamine, 4.4% phosphatidylserine, 50.1% phosphatidylcholine, 2.1% lysophosphatidylcholine, and 11.1% phosphatidylinositol. Further information on phospholipid and fatty acid composition may be found in this reference. In addition to these 'garden variety' lipids, Dembitsky et al., (1993b) reported on the occurrence of some rare hydroxy-fatty acids in this species: 0.04% (% of total lipids) 7-hydroxy-8,14-dimethyl-9-hexadecenoic acid, 0.03% 7-hydroxy-8,16-dimethyl-9-octadecenoic acid, and 0.01% 7-hydroxy-8,18-dimethyl-9-icosenoic acid.

Medicinal properties
Antitumor effects

An extract of S. aeruginosa fruitbodies inhibited the growth of Sarcoma 180 and Ehrlich solid cancers in mice by 70% and 60%, respectively (Ohtsuka et al., 1973).

Neuromodulatory effects

Water and ethanol extracts of S. aeruginosa caused both inhibition and excitation of impulse activity of neurons from the hippocampal stratum pyramidale (CA1 region) (Moldavan et al., 2001).

Links

Mushroom Expert

References

Dembitsky VM, Rezanka T, Shubina, EE.
Chemical composition of fatty acids from some fungi.
Crypt Bot. 1993a 3(4) 383-6.

Dembitsky VM, Rezanka T, Shubina EE.
Unusual hydroxy fatty acids from some higher fungi.
Phytochem. 1993b 34(4):1057-9.

Dembitsky VM, Shubina EE, Kashin AG.
Phospholipid and fatty acid composition of some basidiomycetes.
Phytochem. 1992 31(3):845-9.

Gartz J.
Thin-layer chromatographic analysis of the constituents of fungi of the genus Stropharia.
Die Pharmazie. 1985 40(2):134-5.

Jansen PB.
The copper green fungus Stropharia aeruginosa and its relations.
Coolia. 1981 24(1):22-6.

Kauffman CH. (1918).
The Agaricaceae of Michigan. Vol 1.
Publication 26, Biological Series 5.
PDF available online

Kreisel H.
[Zur Taxonomie von Stropharia aeruginosa sensu lato.]
Taxonomy on Stropharia aeruginosa sensu lato.
Beihefte zur Sydowia Annales Mycologici Ser II. 1979 8:228-32.

Moldavan MG, Grodzynska GA, Wasser, SP, Storozhuk VM.
Effects of some higher Basidiomycetes extracts on the neurons activity.
Ukrayins'kyi Botanichnyi Zhurnal. 2001 58(2):220-8.

Ohtsuka S, Ueno S, Yoshikumi C, Hirose F, Ohmura Y, Wada T, Fujii T, Takahashi E.
Polysaccharides having an anticarcinogenic effect and a method of producing them from species of Basidiomycetes.
UK Patent 1331513, 26 September 1973.

Orton PD.
Notes on British agarics part 6.
Notes from the Royal Botanic Garden Edinburgh. 1976 35(1):147-54.

Shiono Y, Sugawara H, Nazarova M, Murayama T, Takahashi K, Ikeda M.
Three lanostane triterpenoids, aeruginosols A, B and C, from the fruiting bodies of Stropharia aeruginosa.
J Asian Nat Prod Res. 2007 9(6):531-5.
Pubmed

Shiono Y, Sugasawa H, Kurihara N, Nazarova M, Murayama T, Takahashi K, Ikeda M.
Three lanostane triterpenoids from the fruiting bodies of Stropharia aeruginosa.
J Asian Nat Prod Res. 2005 7(5):735-40.
Pubmed

Van Crevel R, Bas C, van Os J. (1988).
Flora Agaricina Neerlandica: Critical monographs on families of agarics and boleti occurring in the Netherlands. Vol 4. (Bas C, TH Kuyper, ME Noordeloos, EC Vellinga, Eds.).
Taylor and Francis: Rotterdam.

 

Last modified: 19-Apr-2008