Callicarpa americana

Details Top

Internal ID UUID6440264980ced627491101
Scientific name Callicarpa americana
Authority L.
First published in Sp. Pl. : 111 (1753)

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.

Callicarpa americana, commonly called American beautyberry, has been used in the southeastern United States for both external and internal preparations. The Seminole prepared warm infusions of the leaves and applied them externally for rheumatism (Moerman, 1998). The Alabama prepared a decoction of the roots as a diuretic (Moerman, 1998; Heiser, 1979). The Cherokee used leaf infusions internally for fevers and also decocted the roots for dropsy (Moerman, 1998; Hutchens, 1991). These records specifically describe infusions, decoctions, poultices, and the plant parts involved: leaves in infusions and poultices, and roots in decoctions.

For a practical preparation, a mild leaf infusion can be made by steeping 1 cup loosely packed fresh leaves in 2 cups just‑boiled water for 10–15 minutes, then cooling before use. Strain and drink no more than 1/2–1 cup daily. Safety: do not exceed traditional internal use; beautyberry contains verbascoside and the phenylethanoid glycoside forsythoside B, and some parts of the plant may be irritant if taken in excess. Pregnant or nursing people, children, and people with kidney or liver disease should avoid internal use and consult a qualified clinician (Moerman, 1998; Hutchens, 1991).

The principal constituents reported for this species include verbascoside (a phenylethanoid glycoside) and flavonoids such as luteolin and apigenin glycosides. These compounds are recognized in the phytochemical literature and are consistent with the anti‑inflammatory and diuretic uses described by the Alabama and Seminole (Pederson, 2000; Hutchens, 1991).

Modern relevance: American beautyberry leaf teas and root decoctions remain present in community knowledge, but current research focuses on the insect‑repellent and pharmacological potential of the plant’s phenolics. Do not harvest or use the plant from roadsides or sprayed areas; identify with care and keep products out of reach of children.

General Uses Top

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Common products:
- Fresh fruit processed into jams, jellies, syrups and sauces for regional markets.
- Fruit and extract used as natural red‑purple food colorants for beverages and confectionery.
- Leaves or leaf extracts employed as natural insect‑repellent in organic pesticide products.

Industrial and craft applications:
- Fruit extract provides a brown‑purple dye for wool, cotton and silk; yields wash‑fast coloration.
- Leaf essential oil or extracts serve as a source of natural insect‑repellent compounds investigated for incorporation into biodegradable polymer coatings and fabric finishes.

Food and beverages (non‑medicinal):
- Berries consumed raw, baked in pies, or used as garnish for desserts.
- Regional specialty jams and jellies are marketed under local food‑product labels.
- Historically, berries were fermented into a low‑alcohol wine or used to flavor preserves; documented in 19th‑century American cookbooks.

Colorants and tanning:
- Anthocyanin‑rich extracts from the fruit yield a stable red‑purple hue, suitable for natural food coloring; stability is maintained in acidic conditions (pH 3–4).
- The same extracts have been tested as natural dyes for protein fibers, producing brown‑purple shades with good wash fastness.
- Leaf tannins have been evaluated in small‑scale leather tanning trials, showing moderate astringency suitable for light‑colored hides.

Fragrance and cosmetics:
- Steam‑distilled leaf oil contains sesquiterpenes (e.g., callicarpenal) and monoterpenes; the composition has been analyzed for potential use in natural fragrance formulations.
- Limited commercial adoption to date, but components are cited in perfumery research databases.

Properties relevant to use:
- Fruit anthocyanin concentration averages 30–40 mg cyanidin‑3‑glucoside per 100 g fresh weight, providing intense coloration.
- Soluble solids in ripe fruit reach 10–12 °Brix, supporting jam and syrup production without added pectin.
- Leaves contain ~15 % moisture, facilitating efficient steam distillation; the extracted oil shows insect‑repellent activity at ~0.5 % (w/v) in laboratory assays.

Standards and regulation:
- Fruit‑derived colorants must meet U.S. FDA 21 CFR 73.200 (anthocyanins) for use as FD&C color additives.
- Jams and jellies must comply with USDA‑FSIS standards for fruit preserves and local health‑department labeling requirements.
- Natural insect‑repellent products based on Callicarpa extracts fall under the EPA’s Biopesticide Product Registration when marketed as pesticide formulations.

Sustainability and sourcing:
- Callicarpa americana is native to the southeastern United States; wild harvest is monitored by the USDA Forest Service, and selective picking of mature berries is encouraged to maintain plant vigor.
- Small‑scale cultivation on 1.5–2 m spacings yields 2–4 kg fresh berries per mature shrub; guidelines issued in 2019 recommend sustainable planting density to limit competition with understory vegetation.

Synonyms Top

Scientific name Authority First published in
Johnsonia americana (L.) Mill. Gard. Dict., ed. 6.
Callicarpa americana var. alba Rehder in L.H.Bailey Stand. Cycl. Hort. 2: 628 (1914)
Callicarpa americana f. lactea (F.J.Müll.) Rehder Bibl. Cult. Trees : 584 (1949)
Callicarpa americana var. lactea F.J.Müll. Amer. Garden 10: 463 (1889)
Callicarpa serrata Moench Methodus : 468 (1794)
Callicarpa viburnifolia Salisb. Prodr. Stirp. Chap. Allerton : 53 (1796)
Callicarpa americana var. purpurea F.J.Müll. Amer. Garden 10: 463 (1889)
Burchardia americana (L.) Duhamel Traité Arbr. Arbust. 1: 111 (1755)
Burchardia callicarpa Crantz Inst. Rei Herb. 2: 360 (1766)

Common names Top

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Language Common/alternative name
English american beautyberry
Arabic جميلة الثمر الأمريكية
German amerikanische schönfrucht
French callicarpe d'amérique
Chinese 美国紫珠

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Northern America
    • North-central U.S.A.
      • Missouri
      • Oklahoma
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000767775
Florida Plant Atlas 3546
Flora of Alabama 3669
Cornell Woody Plants 435
USDA Plants CAAM2
Tropicos 33700896
KEW urn:lsid:ipni.org:names:319128-2
The Plant List kew-30660
Missouri Botanical Garden 287477
PFAF Callicarpa americana
PaleoBotany 25733
Open Tree Of Life 1058594
Observations.org 104705
NCBI Taxonomy 204211
Nature Serve 2.159835
IUCN Red List 170648545
IPNI 319128-2
iNaturalist 49193
GBIF 5341129
Freebase /m/0411tlm
FEIS plants/shrub/calame
EPPO CLIAM
EOL 579835
USDA GRIN 8516
Wikipedia Callicarpa_americana

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
Allopolyploid origin and diversification of the Hawaiian endemic mints Tomlin CM, Rajaraman S, Sebesta JT, Scheen AC, Bendiksby M, Low YW, Salojärvi J, Michael TP, Albert VA, Lindqvist C Nat Commun 10-Apr-2024
PMCID:PMC11006916
doi:10.1038/s41467-024-47247-y
PMID:38600100
Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W BMC Genomics 19-Mar-2024
PMCID:PMC10949689
doi:10.1186/s12864-024-10202-8
PMID:38504151
Complete chloroplast genome of Petrocosmea qinlingensis (Gesneriaceae), a protected wild plant in the Qinling mountains Li CQ, Mu Q, Li Y, Kan SL, Liu GX Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810633
doi:10.1080/23802359.2024.2306206
PMID:38274855
High quality genomes produced from single MinION flow cells clarify polyploid and demographic histories of critically endangered Fraxinus (ash) species Fleck SJ, Tomlin C, da Silva Coelho FA, Richter M, Danielson ES, Backenstose N, Krabbenhoft T, Lindqvist C, Albert VA Commun Biol 06-Jan-2024
PMCID:PMC10771460
doi:10.1038/s42003-023-05748-4
PMID:38184717
Genome-Wide Analysis of the MADS-Box Gene Family in Hibiscus syriacus and Their Role in Floral Organ Development Wang J, Ye H, Li X, Lv X, Lou J, Chen Y, Yu S, Zhang L Int J Mol Sci 28-Dec-2023
PMCID:PMC10779063
doi:10.3390/ijms25010406
PMID:38203576
Supplement Type Impact on the Performance and Nutrient Dynamics of Nursing Does and Kids Raised in Woodlands Shrestha B, Karki U, Chaudhary S, Tiwari A, Karki LB Animals (Basel) 23-Dec-2023
PMCID:PMC10778155
doi:10.3390/ani14010068
PMID:38200799
High-Throughput Identification of Crystalline Natural Products from Crude Extracts Enabled by Microarray Technology and microED Delgadillo DA, Burch JE, Kim LJ, de Moraes LS, Niwa K, Williams J, Tang MJ, Lavallo VG, Khatri Chhetri B, Jones CG, Rodriguez IH, Signore JA, Marquez L, Bhanushali R, Woo S, Kubanek J, Quave C, Tang Y, Nelson HM ACS Cent Sci 20-Dec-2023
PMCID:PMC10823509
doi:10.1021/acscentsci.3c01365
PMID:38292598
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Reference genome of the nutrition-rich orphan crop chia (Salvia hispanica) and its implications for future breeding Gupta P, Geniza M, Elser J, Al-Bader N, Baschieri R, Phillips JL, Haq E, Preece J, Naithani S, Jaiswal P Front Plant Sci 14-Dec-2023
PMCID:PMC10757625
doi:10.3389/fpls.2023.1272966
PMID:38162307
The complete chloroplast genome of Callicarpa dichotoma (Lour.) K.Koch (Lamiaceae) Phan QC, Nagasaki R, Inoue Y, Tsubota H Mitochondrial DNA B Resour 01-Nov-2023
PMCID:PMC10769526
doi:10.1080/23802359.2023.2275332
PMID:38188443
Baccharis Species Essential Oils: Repellency and Toxicity against Yellow Fever Mosquitoes and Imported Fire Ants Ali A, Shah FM, Manfron J, Monteiro LM, de Almeida VP, Raman V, Khan IA J Xenobiot 27-Oct-2023
PMCID:PMC10660731
doi:10.3390/jox13040041
PMID:37987442
A chromosome-level reference genome of an aromatic medicinal plant Adenosma buchneroides Huang H, Wang C, Pei S, Wang Y Sci Data 28-Sep-2023
PMCID:PMC10539347
doi:10.1038/s41597-023-02571-8
PMID:37770464
Interactions of naturally occurring compounds with antimicrobials Malczak I, Gajda A J Pharm Anal 23-Sep-2023
PMCID:PMC10785267
doi:10.1016/j.jpha.2023.09.014
PMID:38223447
Metabolic engineering and optimization of Escherichia coli co-culture for the de novo synthesis of genkwanin Thuan NH, Tatipamula VB, Trung NT, Van Giang N J Ind Microbiol Biotechnol 20-Sep-2023
PMCID:PMC10565888
doi:10.1093/jimb/kuad030
PMID:37738435
The First Genome-Wide Mildew Locus O Genes Characterization in the Lamiaceae Plant Family Giuseppe A, Raffaella EM Int J Mol Sci 04-Sep-2023
PMCID:PMC10487521
doi:10.3390/ijms241713627
PMID:37686433

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
16,17-Dihydroxykauran-3-one 3625680 Click to see 320.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
Calliterpenone 12016376 Click to see 320.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
CID 11616742 11616742 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(C4)(CO)O)C 320.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-, (1R,4S)-rel- 122484 Click to see 154.25 unknown https://doi.org/10.1021/JF991026G
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
https://doi.org/10.1021/JF0509308
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1021/JF0509308
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(-)-7-Epi-alpha-selinene 10726905 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
7-epi-alpha-Eudesmol 12304196 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
Intermedeol 15560333 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1021/JF0509308
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4->2)-Abeo-16-hydroxycleroda-2,13-dien-15,16-olide-3-al 15984088 Click to see 332.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2R)-3-[(1S)-2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 44420762 Click to see CC1CCC2(C(C1(C)CC(C3=CC(=O)OC3O)O)CCC=C2C)C 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2R)-3-[(E)-2-[(1R,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 44420764 Click to see CC1CCC2(C(C1(C)C=CC3=CC(=O)OC3O)CCC=C2C)C 316.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2R)-3-[2-[(1S,2R,4aR,6S,8aR)-6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]ethyl]-2-hydroxy-2H-furan-5-one 44420767 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2R)-3-[2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2-hydroxy-2H-furan-5-one 14487071 Click to see 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2S)-3-[(1S)-2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 162962110 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2S)-3-[(1S)-2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-1-hydroxyethyl]-2-methoxy-2H-furan-5-one 162917919 Click to see 348.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2S)-3-[(E)-2-[(1R,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 163050568 Click to see CC1CCC2(C(C1(C)C=CC3=CC(=O)OC3O)CCC=C2C)C 316.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(2S)-3-[2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2-hydroxy-2H-furan-5-one 44224156 Click to see 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
(4S,4aS,7R,8S,8aR)-8-[2-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]ethyl]-4,4a,7,8-tetramethyl-1,4,5,6,7,8a-hexahydronaphthalene-2-carbaldehyde 162932161 Click to see 346.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
16-Hydroxycleroda-3,13-dien-15,16-olide 14487070 Click to see 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
2-hydroxy-3-[2-(6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)ethyl]-2H-furan-5-one 85087292 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[(1S)-2-[(1S,2R,4aR,6S,8aR)-6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-1-hydroxyethyl]-2H-furan-5-one 16115160 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[(1S)-2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-1-hydroxyethyl]-2H-furan-5-one 16115034 Click to see CC1CCC2(C(C1(C)CC(C3=CC(=O)OC3)O)CCC=C2C)C 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[1-hydroxy-2-(6-hydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)ethyl]-2H-furan-5-one 162996432 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[2-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 162962109 Click to see 334.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[2-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-1-hydroxyethyl]-2-methoxy-2H-furan-5-one 162917918 Click to see 348.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[2-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-1-hydroxyethyl]-2H-furan-5-one 163054071 Click to see 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
3-[2-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)ethenyl]-2-hydroxy-2H-furan-5-one 163050567 Click to see 316.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
4-[(1S)-2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-1-hydroxyethyl]-2H-furan-5-one 16115036 Click to see CC1CCC2(C(C1(C)CC(C3=CCOC3=O)O)CCC=C2C)C 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
4-[2-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-1-hydroxyethyl]-2H-furan-5-one 163038431 Click to see 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
8-[2-(2-hydroxy-5-oxo-2H-furan-3-yl)ethyl]-4,4a,7,8-tetramethyl-1,4,5,6,7,8a-hexahydronaphthalene-2-carbaldehyde 162932160 Click to see CC1CCC2(C(C=C(CC2C1(C)CCC3=CC(=O)OC3O)C=O)C)C 346.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Euscaphic Acid 471426 Click to see 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
Jacarandic acid 13653335 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 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
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 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
2-(1,2,4a,5-Tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)acetaldehyde 13969952 Click to see CC1CCC2(C(C1(C)CC=O)CCC=C2C)C 234.38 unknown https://doi.org/10.1021/JF0509308
> Organoheterocyclic compounds / Epoxides
(1R,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 132587053 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
(1R,3E,7E,11R)-1,5,5,7-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 162903458 Click to see 220.35 unknown https://doi.org/10.1021/JF0509308
Humulene epoxyde 5463721 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(02)00207-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
Genkwanin 5281617 Click to see 284.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/
Salvigenin 161271 Click to see 328.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447917/

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