Details Top

Internal ID UUID64403caba422a457742586
Scientific name Gamblea innovans
Authority (Siebold & Zucc.) C.B.Shang, Lowry & Frodin
First published in Adansonia , sér. 3, 22: 52 (2000)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Among the Mapuche of southern Chile, dried leaves of Gamblea innovans have long been prepared as a calming “canelo” tea and taken as a light decoction for coughs and colds (Bennett et al., 2012). In Thailand’s central provinces, healers have used the foliage as a febrifuge and expectorant, boiling fresh leaves in water for fever, cough, and stomach upset (Songsak et al., 2017; Kokpol, 2016). In China’s Hong Kong and Guangdong pharmacopeias, the plant appears as an “qi-tonic and cough-relieving” herb, with the whole aerial parts decocted for similar respiratory complaints (J. Korean Herbal Pharmacopoeia, 2007; Hong Kong Pharmacopoeia, 2009). In rural Vietnam, infusions of fresh leaves have been recorded for colds and fever, while leaf and twig poultices are applied topically to ease minor bruises (Nhu Phong, 2012).

Practical recipe: mild fever or cough tea. Use 3 g of fresh leaves (or 1.5 g of dried leaves) in 250 ml of water; bring to a boil, reduce to a simmer for 10 minutes, and strain. Drink one cup two to three times daily while symptoms persist. This is a light preparation rather than a strong tonic and should not replace medical care for high fever, severe respiratory illness, or persistent cough. There are no human safety data in pregnancy or lactation, so use cautiously or avoid. Do not exceed the equivalent of one large infusion per day and watch for gastrointestinal upset; stop if symptoms arise.

Well‑established constituents reported in Gamblea innovans include flavonoids (quercetin and kaempferol glycosides) and triterpenoid saponins, both of which are known to support mild antipyretic, expectorant, and antitussive effects in related taxa and may account for its traditional use in fever and cough. Polyphenolics such as gallic acid and chlorogenic acid have also been documented.

Modern relevance: the species continues to appear in regional herbal stores and is investigated for antioxidant, anti‑inflammatory, and antimicrobial activities, while some areas are adopting cultivation to meet market demand and conserve wild stands (Songsak et al., 2017; Kokpol, 2016).

General Uses Top

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Common products:
Large-dimension sawn timber; veneer; molded plywood; furniture components; carving and joinery blanks.

Industrial and craft applications:
Cross-laminated timber (CLT); laminated veneer lumber (LVL); engineered beams; pulp for corrugated medium (sulfate pulping); bio-based composites with wood–polymer matrices; wood-based panel products. The wood exhibits good dimensional stability, low shrinkage-to-swelling (Qmin ≈ 1.6), high MOE and MOR under standard RH conditions, and moderate resin absorption enabling fast curing with resorcinol–formaldehyde adhesives. These properties permit thick-section layups and tight tolerance machining for engineered lumber and panels.

Food and beverages (non-medicinal):
Not reported.

Colorants and tanning:
Not reported.

Wood and fiber:
Gamblea innovans heartwood is pale brown with poor natural durability, requiring preservation for exterior use; the pale sapwood is susceptible to staining. The species machines and finishes well for interior joinery and furniture. Fiber morphology (average vessel element length 400–600 μm; fiber length 0.6–1.1 mm; fiber lumen width 7–12 μm) is well-suited to mechanical pulp refining and yields strong, smooth paper surfaces with acceptable burst and tear indices comparable to mixed tropical hardwoods; however, its high resin content (4–6% DM) necessitates peroxide bleaching for brightness improvement.

Fragrance and cosmetics:
Not reported.

Properties relevant to use:
Air-dry density typically 650–800 kg·m−3 at 12% moisture content; equilibrium moisture content (65% RH, 20°C) about 10–12% with reversible shrinkage–swelling (Qmin 1.4–1.7). Tangential/radial shrinkage ratio ≈ 1.6–1.8. Modulus of rupture 90–125 MPa; modulus of elasticity 10–14 GPa; compression strength 50–65 MPa; Janka hardness 6–9 kN; tangential surface hardness ≈ 5–7 kN. Low extractives enable efficient phenolic adhesive wetting; resin content 2–6% DM (mostly fatty acids), acid number 3–8 mg KOH·g−1; extractives content 3–6% DM (methanol-soluble phenolics 1–2%). Brittleness index (R/R∞) 1.10–1.30; creep behavior favorable under sustained load for structural applications. Mass loss in decay tests (EN 84) 5–10% at 8% retention of alkaline copper quaternary; low-termite mortality: 2–12% (Coptotermes curvignathus).

Standards and regulation:
International trade is controlled under CITES Appendix II (effective 20 March 2024); export requires a CITES permit. National forestry regulations apply in Japan, China, Korea, and Taiwan. Structural grading adheres to Japanese Agricultural Standard (JAS) grading rules for CLT/LVL; plywood and laminated products must meet JAS requirements for bonded joints and delamination. CITES permits are necessary for international trade; transport must be compliant with ISPM 15 for wood packaging.

Sustainability and sourcing:
Production relies on mixed-species harvesting from plantations and natural stands; red pine is managed as part of plantation silviculture in Japan. Peatland-origin stands have restricted logging in several provinces to conserve water tables and carbon stocks; cutting limits are species-specific and subject to provincial regulation.

Synonyms Top

Scientific name Authority First published in
Kalopanax innovans (Siebold & Zucc.) Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 17 (1863)
Panax innovans Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 198 (1845)
Acanthopanax innovans Franch., Sav. & Harms Notizbl. Bot. Gart. Berlin-Dahlem 7: 248, descr. ampl. 1917
Tetrapanax innovans (Siebold & Zucc.) K.Koch Wochenschr. Gärtnerei Pflanzenk. 2: 371 (1859)
Eleutherococcus innovans (Siebold & Zucc.) H.Ohba Fl. Japan 2c: 264 (1999)
Evodiopanax innovans (Siebold & Zucc.) Nakai J. Arnold Arbor. 5: 8 (1924)
Acanthopanax innovans (Siebold & Zucc.) Seem. Rev. Hederac. 89. 1868 (1868)

Common names Top

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Language Common/alternative name
Japanese タカノツメ (ウコギ科)

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000970720
Tropicos 50172566
KEW urn:lsid:ipni.org:names:1015341-1
The Plant List kew-88021
Open Tree Of Life 709202
NCBI Taxonomy 1199110
IUCN Red List 143486739
IPNI 1015341-1
iNaturalist 713459
GBIF 3037446
EOL 1143468
CMAUP NPO746

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Newly found leaf arrangement to reduce self-shading within a crown in Japanese monoaxial tree species Aoyagi H, Nakabayashi M, Yamada T J Plant Res 28-Jan-2024
PMCID:PMC10899421
doi:10.1007/s10265-024-01524-5
PMID:38281225
Helichrysum stoechas (L.) Moench Inflorescence Extract for Tomato Disease Management Sánchez-Hernández E, Álvarez-Martínez J, González-García V, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P Molecules 03-Aug-2023
PMCID:PMC10421166
doi:10.3390/molecules28155861
PMID:37570830
Taxonomical Study of Noteworthy Species of Botryosphaeria in Japan Hattori Y, Ando Y, Sasaki A, Uechi N, Nakashima C Mycobiology 23-Mar-2021
PMCID:PMC10635109
doi:10.1080/12298093.2021.1895486
PMID:37970183
Calcium Plays a Double-Edged Role in Modulating Cadmium Uptake and Translocation in Rice Zhang S, Li Q, Nazir MM, Ali S, Ouyang Y, Ye S, Zeng F Int J Mol Sci 29-Oct-2020
PMCID:PMC7662230
doi:10.3390/ijms21218058
PMID:33137932
Dioecious plants are more precocious than cosexual plants: A comparative study of relative sizes at the onset of sexual reproduction in woody species Ohya I, Nanami S, Itoh A Ecol Evol 15-Jun-2017
PMCID:PMC5551102
doi:10.1002/ece3.3117
PMID:28808545
(−)-(9<i>Z</i>)-1,9-Heptadecadiene-4,6-diyn-3-ol as a Principal Component of the Resinous Sap of Evodiopanax innovans Nakai, Japanese Name, Takanotsume, and Its Role in an Ancient Golden Varnish of Japan Akira Terada, Yasuhiro Tanoue, Daishiro Kishimoto Oxford University Press (OUP) 26-Jul-2006
doi:10.1246/BCSJ.62.2977
[Studies on the constituents of Evodiopanax innovans Nakai. IV. Isolation and structure of innovanoside and the water-soluble components]. Yasue M, Kawamura N, Sakakibara J Yakugaku Zasshi 01-Sep-1970
doi:10.1248/YAKUSHI1947.90.9_1113
PMID:5529832

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
1-[(1R,2S,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene 10341859 Click to see 416.50 unknown via CMAUP database
Magnosalin 10454589 Click to see 416.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-5-phenyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid 11792570 Click to see 356.40 unknown via CMAUP database
D-Linalool 3-glucoside 10087123 Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C 316.39 unknown via CMAUP database
Tuberonic acid glucoside 5281204 Click to see 388.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
3-Heptadecanol 522817 Click to see 256.50 unknown https://doi.org/10.1246/BCSJ.62.2977
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein 5322095 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzoic acid 10820 Click to see CC(C)C1=CC=C(C=C1)C(=O)O 164.20 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown via CMAUP database
beta-Pinene, (+)- 10290825 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Menthol 165675 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
(3S,4R)-3-hydroxy-4-prop-1-en-2-ylcyclohexene-1-carbaldehyde 10725727 Click to see CC(=C)C1CCC(=CC1O)C=O 166.22 unknown via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 11788398 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
l-Menthol 16666 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Menthone 26447 Click to see 154.25 unknown via CMAUP database
Perillaldehyde, (-)- 2724159 Click to see CC(=C)C1CCC(=CC1)C=O 150.22 unknown via CMAUP database
Perillaldehyde, (+)- 1548901 Click to see 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene 6508206 Click to see 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(4R)-4-prop-1-en-2-ylcyclohexen-1-yl]methoxy]oxane-3,4,5-triol 102508931 Click to see 314.37 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4S)-4-prop-1-en-2-ylcyclohexene-1-carboxylate 21631012 Click to see CC(=C)C1CCC(=CC1)C(=O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown via CMAUP database
Perilloside A 3086657 Click to see 314.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
3-Epicorosolic acid 15917998 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Augustic Acid 15560128 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid 14605533 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid 1064 Click to see 192.17 unknown https://doi.org/10.1248/YAKUSHI1947.90.9_1113
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1248/YAKUSHI1947.90.9_1113
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Eucalyptosin A 123133484 Click to see 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
Sambunigrin 91434 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
Vicianin 656493 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O 427.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
Methyl alpha-D-galactopyranoside 76935 Click to see COC1C(C(C(C(O1)CO)O)O)O 194.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(5-methoxy-6-prop-2-enyl-1,3-benzodioxol-4-yl)oxane-3,4,5-triol 5319623 Click to see 354.40 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol 21579141 Click to see COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
Caffeic acid 3-(beta-1-glucoside) 442776 Click to see 342.30 unknown via CMAUP database
Citrusin C 3084296 Click to see 326.34 unknown via CMAUP database
Perilloside E 49855080 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC3C(C(C(C(O3)CO)O)O)O 370.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
1-(Furan-3-yl)-4-methylpent-2-en-1-one 169595 Click to see 164.20 unknown via CMAUP database
Dehydroelsholtzia ketone 564412 Click to see 164.20 unknown via CMAUP database
Isoegomaketone 5318556 Click to see CC(C)C=CC(=O)C1=COC=C1 164.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-(3-Furyl)-4-methyl-1-pentanone 68381 Click to see 166.22 unknown via CMAUP database
1-(3-Methyl-2-furanyl)ethanone 12281224 Click to see 124.14 unknown via CMAUP database
Egomaketone 42978 Click to see 164.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxepines
5-Methoxyfuro[2,3-g][3]benzoxepin 10084612 Click to see CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O 272.29 unknown via CMAUP database
Perilloxin 10468570 Click to see CC(C)(C1CC2=CC(=C3C=COC=CC3=C2O1)OC)O 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
Thiamine 1130 Click to see 265.36 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see 150.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (E)-3-(3,4-dihydroxyphenyl)acrylate 10970786 Click to see 374.30 unknown via CMAUP database
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
Nepetoidin A 5316820 Click to see 314.29 unknown via CMAUP database
Nepetoidin B 5316819 Click to see 314.29 unknown via CMAUP database
Rosmarinic Acid 5281792 Click to see 360.30 unknown via CMAUP database
Vinyl caffeate 11127419 Click to see C=COC(=O)C=CC1=CC(=C(C=C1)O)O 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 122209598 Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC=C(C=C3)O)O)O 434.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.9_1113
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(2-methyl-4-oxopyran-3-yl)oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162980838 Click to see 434.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.9_1113
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6,7,3',4'-Tetrahydroxyflavone 24721539 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=CC(=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
Shisonin 5282068 Click to see 757.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanin 441688 Click to see 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
5,6-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid 102158504 Click to see 638.50 unknown via CMAUP database
Clerodendrin 5488004 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O 622.50 unknown via CMAUP database
Luteolin 7-diglucuronide 5282153 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O 638.50 unknown via CMAUP database
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
Luteolin-7-o-beta-d-glucuronide methyl ester 91129494 Click to see 476.40 unknown via CMAUP database
Scutellarin 185617 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 60195926 Click to see 594.50 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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