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Chemical compound
Lanostane or 4,4,14α-trimethylcholestane is a tetracyclic chemical compound with formula C 30H 54. It is a polycyclic hydrocarbon, specifically a triterpene
Lanostane
Organism belonging to kingdom Fungi
Halawany AM, Ma CM, Hattori M (June 2008). "Anti-HIV-1 protease activity of lanostane triterpenes from the Vietnamese mushroom Ganoderma colossum". Journal
Fungus
Chemical compound
Euphane is a tetracyclic triterpene that is the 13α,14β-stereoisomer of lanostane. Its derivatives are widely distributed in many plants. Euphanes is also
Euphane
Enzyme
hypothetical steroid nucleus can be demonstrated by a structure of 24-ethyl-lanostane, a prototypical steroid with 32 carbon atoms. Its core ring system (ABCD)
3α-Hydroxysteroid dehydrogenase
3α-Hydroxysteroid_dehydrogenase
Species of fungus
particularly lanosterol, an intermediate in the synthesis of ergosterol and lanostane-type triterpenes. It is commonly marketed as a dietary supplement for
Inonotus_obliquus
Polycyclic organic compound having sterane as a core structure
Structure of 24-ethyl-lanostane, a prototypical steroid with 32 carbon atoms. Its core ring system (ABCD), composed of 17 carbon atoms, is shown with
Steroid
Chemical compound
polycyclic hydrocarbon, specifically triterpene. It is also an isomer of lanostane (specifically 19(10→9β)-abeolanostane), from which it differs by the formal
Cucurbitane
Chemical compound
Lanosterol is a tetracyclic triterpenoid from which all animal and fungal steroids are derived. By contrast, plant steroids are produced via cycloartenol
Lanosterol
Index of chemical compounds with the same molecular formula
Baccharane Cucurbitane Dammarane Dinosterane Euphane 24-Isopropylcholestane Lanostane 24-n-Propylcholestane Protostane Tirucallane This set index page lists
C30H54
Chemical compound
masticadienolic acid and other triterpenoid compounds. This compound has a lanostane skeleton with a carboxylic acid group and a conjugated enone system. It
Masticadienonic_acid
Chemical compound
Clavaric acid is a lanostane type steroid produced by the mushroom Hypholoma lateritium. Clavaric acid was discovered by Merck Research Laboratories in
Clavaric_acid
Chemical compound
Lanostane, one of many steroids with a hydrindane core.
Hydrindane
Chemical compound
sterane is used as a biomarker for early eukaryotes. Cholane Cholestane Lanostane Glotter, E. (1991). "Withanolides and related ergostane-type steroids"
Ergostane
Class of chemical compounds
of rings Examples 0 Squalene 1 Achilleol A 2 Polypodatetraene 3 Malabaricane 4 Lanostane, Cucurbitacin 5 Hopane, Oleanane, Ursolic acid 6 Chamaecydin
Triterpene
Species of fern
Ali, Mohammad; Niwa, Masatake (1 May 2000). "Normethyl pentacyclic and lanostane-type triterpenes from Adiantum venustum". Phytochemistry. 54 (2): 215–220
Adiantum_venustum
Chemical compound
is the starting point for the synthesis of almost all plant steroids. Lanostane Cycloastragenol Cycloartenyl ferulate Calculated using Advanced Chemistry
Cycloartane
Genus of fungi
Phosri Astraeus telleriae M.P.Martín, Phosri & Watling In 2008, five lanostane-type triterpenes were isolated and identified from the fruit bodies of
Astraeus_(fungus)
Cosmopolitan species of fungus
22-tetraene-3-one, three unique triterpenes—derivatives of 3-hydroxy-lanostane—have been isolated from fruit bodies of A. hygrometricus. The compounds
Astraeus_hygrometricus
Chemical compound
Pachymic acid is a naturally occurring steroid that can be extracted from the parasitic fungus Wolfiporia extensa (synonym Wolfiporia cocos). The dried
Pachymic_acid
Chemical compound
been used for its medicinal properties. This natural product contains a lanostane-type skeleton with a carboxylic acid group and also a hydroxyl group.
Masticadienolic_acid
Chemical compound
of cycloartane triterpene alcohols. The formation of cucurbitane- and lanostane-type isomers". The Journal of Organic Chemistry. 49 (4): 709–712. doi:10
Parkeol
Chemical compound
it is considered to be the "prototype" of steroids. Fusidane Dammarane Lanostane International Union of Pure and Applied Chemistry (2014). Nomenclature
Protostane
Protopanaxatriol, Dammarendiol, Dammarenediol‑II, & Ocotillol‑type aglycones. Lanostane-type, e.g. Lanosterol, Cycloartenol, Parkeol, Schiglauzic acid, Ganoderic
Sapogenin
Photochemical reaction
photolysis in the presence of oxygen. An improved synthesis of 32-oxygenated lanostanes". Journal of the Chemical Society, Perkin Transactions 1: 2402. doi:10
Barton_nitrite_ester_reaction
C30H52O7 cubensic acid 136156-79-1 C30H52O8 boldoglucin 1398-22-7 C30H54 lanostane 474-20-4 C30H58O4 didodecyl hexanedioate 3072-02-4 C30H58O4 ethylene dimyristate
List of compounds with carbon numbers 30–39
List_of_compounds_with_carbon_numbers_30–39
Chemical compound
Tirucallane Names IUPAC name (20S)-13α,14β,17α-Lanostane Systematic IUPAC name (1S,3aR,3bR,5aS,9aR,9bS,11aS)-3a,6,6,9a,11a-Pentamethyl-1-[(2S)-6-meth
Tirucallane
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