ORGANISM
Japanese callicarpa
Callicarpa japonica
37 molecules reported in this organism, across 38 literature references.
Taxonomy
Classification
- Kingdom
- Archaeplastida
- Order
- Lamiales
- Family
- Lamiaceae
- Genus
- Callicarpa
Provenance
Contributing sources
- LOTUS
- Taxonomy: LOTUS (GBIF / NCBI / OTT)
Composition
Molecules reported in Callicarpa japonica
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Spathulenol 2 references Aromadendrane sesquiterpenoids
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1,6-Methanonaphthalene, decahydro-1,4,8a-trimethyl-9-methylene-, (1S,4S,4aS,6R,8aS)-(-)- 1 reference Rotundane sesquiterpenoids
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(1aR,4aR,7S,7aS,7bR)-1,1,7-Trimethyl-4-methylidenedecahydro-1H-cyclopropa[e]azulen-7-ol 1 reference Aromadendrane sesquiterpenoids
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(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 1 reference Aromadendrane sesquiterpenoids
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1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 1 reference Elemane sesquiterpenoids
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1-Naphthalenol, decahydro-1,4a-dimethyl-7-(1-methylethylidene)- 1 reference Eudesmane sesquiterpenoids
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1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)- 1 reference Pimarane and Isopimarane diterpenoids
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(1R,3E,7E,11R)-1,5,5,7-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 1 reference Humulane sesquiterpenoids
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(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 1 reference Bicyclogermacrane sesquiterpenoids $ Cyclogermacrane sesquiterpenoids
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(1S,2R,4aR,8aR)-1,2,3,4,4a,7,8,8a-Octahydro-1,2,4a,5-tetramethyl-1-naphthaleneacetaldehyde 1 reference Colensane and Clerodane diterpenoids
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2,6,6,9-Tetramethylcycloundeca-1,4,8-triene 1 reference Humulane sesquiterpenoids
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2'-O-Acetylpoliumoside 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 1 reference Flavones
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[(2R,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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[(2S,3S,4S,5R,6S)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]methoxy]-4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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[(2S,3S,4S,5S,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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5,6,7-Trimethoxy-2-phenyl-4H-1-benzopyran-4-one 1 reference Flavones
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alpha-Guaiene 1 reference Guaiane sesquiterpenoids
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Beta-Elemene 1 reference Elemane sesquiterpenoids
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Bicyclogermacrene 1 reference Bicyclogermacrane sesquiterpenoids $ Cyclogermacrane sesquiterpenoids
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Curcuphenol 1 reference Bisabolane sesquiterpenoids
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Elemene 1 reference Elemane sesquiterpenoids
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Eugenol 1 reference Cinnamic acids and derivatives
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Forsythoside B 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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Gamma-elemene, (+)- 1 reference Elemane sesquiterpenoids
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Germacrene B 1 reference Germacrane sesquiterpenoids
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Germacrene D 1 reference Germacrane sesquiterpenoids
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Globulol 1 reference Aromadendrane sesquiterpenoids
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Humulene 1 reference Humulane sesquiterpenoids
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(-)-Humulene epoxide II 1 reference Humulane sesquiterpenoids
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(+)-Intermedeol 1 reference Eudesmane sesquiterpenoids
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Ledum camphor 1 reference Aromadendrane sesquiterpenoids
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Npc186905 1 reference Humulane sesquiterpenoids
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(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 1 reference Germacrane sesquiterpenoids
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Verbascoside 1 reference Cinnamic acids and derivatives $ Phenylethanoids
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Viridiflorol 1 reference Aromadendrane sesquiterpenoids
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α-Humulene 1 reference Humulane sesquiterpenoids
Occurrence records from LOTUS. A molecule being reported in an organism means it was detected there in the cited work; it does not mean the organism is a commercial source of it.