Chemical Formula: C30H44O8
Chemical Formula C30H44O8
Found 64 metabolite its formula value is C30H44O8
Ganoderic acid G
Ganoderic acid G is found in mushrooms. Ganoderic acid G is a constituent of Ganoderma lucidum (reishi) Constituent of Ganoderma lucidum (reishi). Ganoderic acid G is found in mushrooms. Ganoderic acid G is a triterpenoid. Ganoderic acid G is a triterpene isolated from the surface part of gills of Ganoderma lucidum[1]. Ganoderic acid G is a triterpene isolated from the surface part of gills of Ganoderma lucidum[1].
Ganoderic acid I
Ganoderic acid I is found in mushrooms. Ganoderic acid I is a constituent of Ganoderma lucidum (reishi). Constituent of Ganoderma lucidum (reishi). Ganoderic acid I is found in mushrooms. Ganoderic acid I is a triterpenoid found in ganoderma lucidum[1]. Ganoderic acid I is a triterpenoid found in ganoderma lucidum[1].
Ganoderic acid eta
Ganoderic acid eta is found in mushrooms. Ganoderic acid eta is a constituent of Ganoderma lucidum (reishi)
Cochlioquinone A
[Raw Data] CB284_Cochlioquinone-A_neg_50eV_000047.txt [Raw Data] CB284_Cochlioquinone-A_neg_40eV_000047.txt [Raw Data] CB284_Cochlioquinone-A_neg_30eV_000047.txt [Raw Data] CB284_Cochlioquinone-A_neg_20eV_000047.txt [Raw Data] CB284_Cochlioquinone-A_pos_50eV_rep000005.txt [Raw Data] CB284_Cochlioquinone-A_pos_40eV_rep000005.txt [Raw Data] CB284_Cochlioquinone-A_pos_30eV_rep000005.txt [Raw Data] CB284_Cochlioquinone-A_pos_20eV_rep000005.txt [Raw Data] CB284_Cochlioquinone-A_pos_10eV_rep000005.txt
Isocochlioquinone A
[Raw Data] CB285_Isocochlioquinone-A_pos_50eV_rep000006.txt [Raw Data] CB285_Isocochlioquinone-A_pos_40eV_rep000006.txt [Raw Data] CB285_Isocochlioquinone-A_pos_30eV_rep000006.txt [Raw Data] CB285_Isocochlioquinone-A_pos_20eV_rep000006.txt [Raw Data] CB285_Isocochlioquinone-A_pos_10eV_rep000006.txt
Wikstroelide E
A natural product found particularly in Wikstroemia retusa and Pimelea simplex.
Caseargrewiin A
A diterpenoid of the clerodane group isolated from the bark of Casearia grewiifolia and has been shown to exhibit antimalarial and antimycobacterial activity.
(5R,6S,8S,9S,10R,12S,13S,14S,17S,20R,22R)-3,4-secocycloarta-1,24-diene-6,12,20,27-tetrahydroxy-3,4-lactone-22,26-lactone|angustifodilactone A
(6R)-6-hydroxyoleaside A|(9S)-9-(2,5-dihydro-5-oxo-furan-3-yl)tetradecahydro-5-hydroxy-10,12b-dimethyl-13-oxo-1H-6a,10-methanocycloocta[a]naphthalen-3-yl 2,6-dideoxy-3-O-methylhexopyranoside|4-[(3S,4aR,5R,6aS,9R,10R,12aR,12bR)-tetradecahydro-5-hydroxy-10,12b-dimethyl-13-oxo-3-{[(2R,4R,5S,6R)-tetrahydro-5-hydroxy-4-methoxy-6-methyl-2H-pyran-2-yl]oxy}-1H-6a,10-methanocycloocta[a]naphthalen-9-yl]furan-2(5H)-one
(17R,20S,22R,24S,25S,26R)-16alpha-acetoxy-22,26:24,25-diepoxy-5alpha,6beta,26-trihydroxyergost-2-en-1-one|salpichrolide Q
(7S)-7-hydroxyoleaside A|(9S)-9-(2,5-dihydro-5-oxofuran-3-yl)tetradecahydro-6-hydroxy-10,12b-dimethyl-13-oxo-1H-6a,10-methanocycloocta[a]naphthalen-3-yl 2,6-dideoxy-3-O-methylhexopyranoside|4-[(3S,4aR,6S,6aR,9R,10R,12aR,12bS)-tetradecahydro-6-hydroxy-10,12b-dimethyl-13-oxo-3-{[(2R,4R,5S,6R)-tetrahydro-5-hydroxy-4-methoxy-6-methyl-2H-pyran-2-yl]oxy}-1H-6a,10-methanocycloocta[a]naphthalen-9-yl]furan-2(5H)-one
(5alpha,7alpha,13alpha,17alpha)-17-(3,4-dihydroxy-2,5-dimethoxytetrahydrofuran-3-yl)-4,4,8-trimethyl-3-oxoandrosta-1,14-dien-7-yl acetate|7-O-acetyl-7-O-debenzoyl-22-hydroxy-21-methoxylimocinin|7alpha-acetoxy-21,23-epoxy-20xi,22xi-dihydroxy-21xi,23xi-dimethoxy-24,25,26,27-tetranorapoeupha-1,14-dien-3-one
3beta-(3?-O-acetyl-alpha-l-fucopyranosyloxy)pregn-20-en-19-acetate|sclerosteroid G
(22S)-2alpha-hydroxy-3alpha-acetoxy-11beta-hydroxy-24-methyl-22,25-epoxy-5alpha-furostan-18,20beta-lactone
23-dihydrogenoderic acid N|7beta,20,23xi-trihydroxy-3,11,15-trioxolanosta-8-en-26-oic acid
(4E,8E,12E)-14-<2-hydroxy-3,4-dimethyl-5-(1-beta-L-xylopyranosyloxy)phenyl>-4,8,12-trimethyltetradeca-4,8,12-trienoic acid|(4E,8E,12E)-14-[2-hydroxy-3,4-dimethyl-5-(1-beta-L-xylopyranosyloxy)phenyl]-4,8,12-trimethyltetradeca-4,8,12-trienoic acid|Lurlene
5-Et ether-(5alpha,6beta,17betaOH,20S,22R)-5,6,14,17,20-Pentahydroxy-1-oxowitha-2,24-dienolide|5alpha-ethoxy-1-oxo-6beta,14alpha,17beta,20alphaF-tetrahydroxy-20S,22R-witha-2,24-dienolide|5alpha-ethoxy-6beta,14alpha,17beta,20-tetrahydroxy-1-oxo-20S,22R-witha-2,24-dienolide
butanoic acid rel-(1R,3S,5S,6aR,7S,8S,10R,10aR)-1-(acetyloxy)-3,5,6,6a,7,8,9,10-octahydro-5-hydroxy-7,8-dimethyl-7-(3-methyl...|caseamembrin H|rel-(2S,5R,6R,8S,9S,10R,18R,19S)-18-(acetyloxy)-18,19-epoxy-2-hydroxycleroda-3,13(16),14-trien-6,19-diyl dibutanate
(+)-(1R*,3S*,5S*,6aR*,7S*,8S*,10R*,10aR*)-1-(acetoxy)-3,5,6,6a,7,8,9,10-octahydro-10-hydroxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dien-1-yl]naphtho[1,8a-c]furan-3,5-diyl dibutanoate|casearin X
14-hydroxy-3beta-(O3-methyl-beta-D-xylo-2,6-dideoxy-hexopyranosyloxy)-11-oxo-5beta,14beta-card-20(22)-enolide|14-Hydroxy-3beta-(O3-methyl-beta-D-xylo-2,6-didesoxy-hexopyranosyloxy)-11-oxo-5beta,14beta-card-20(22)-enolid
Ganoderic Acid G
Ganoderic acid G is a triterpene isolated from the surface part of gills of Ganoderma lucidum[1]. Ganoderic acid G is a triterpene isolated from the surface part of gills of Ganoderma lucidum[1].
1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(2-methylpropanoyl)oxy]-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl 2-ethylbutanoate
1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(2-methylpropanoyl)oxy]-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl 2-ethylbutanoate_major
1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(2-methylpropanoyl)oxy]-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl 2-ethylbutanoate_69.7\\%
1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(2-methylpropanoyl)oxy]-5-oxotetracyclo[8.5.0.0²,?.0¹¹,¹³]pentadeca-3,8-dien-13-yl 2-ethylbutanoate
Ganoderic acid I
Ganoderic acid I is a triterpenoid found in ganoderma lucidum[1]. Ganoderic acid I is a triterpenoid found in ganoderma lucidum[1].
Ganoderic acid eta
cucurbitacin J
A cucurbitacin that is 9,10,14-trimethyl-4,9-cyclo-9,10-secocholesta-2,5-diene substituted by hydroxy groups at positions 2, 16, 20, 24 and 25 and oxo groups at positions 1, 11 and 22.
3β-[(6-Deoxy-3-O-methyl-β-D-galactopyranosyl)oxy]-14-oxo-8,15-cyclo-14,15-seco-5β-card-20(22)-enolide
epi-Cochlioquinone A
An organic heterotetracyclic that is 1,2,3,4a,5,6,6a,12,12a,12b-decahydropyrano[3,2-a]xanthene-8,11-dione substituted by a 2-hydroxypropan-2-yl group at position 3, hydroxy group at position 12, methyl groups at positions 6a and 12b and a 3-(acetyloxy)-4-methylhexan-2-yl moiety at position 9. Isolated from the fermentation broth of Stachybotrys bisbyi SANK 17777, it acts as an inhibitor of acyl-CoA:cholesterol acyltransferase.
[1,6-Dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-(2-methylpropanoyloxy)-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-ethylbutanoate
16-Hydroxy-4,4,9,13,14-pentamethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-1,7,8,10,12,15,16,17-octahydrocyclopenta[a]phenanthrene-2,3,11-trione
rel-12-O-Octanoylphorbol-13-acetate
A natural product found in Pimelea elongata.