Liquidambar styraciflua

Details Top

Internal ID UUID643ff48d6b1ed287458895
Scientific name Liquidambar styraciflua
Authority L.
First published in Sp. Pl. : 999 (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.

Non-pharmacopoeial liquidambar resin is still collected from wild Liquidambar styraciflua and used locally. In the Caribbean and parts of the American South, coarse resin or a syrup made by simmering the resin in water is taken by the spoonful to quiet coughs and soothe sore throats; small lozenges made from the same resin or syrup are also sucked for throat comfort (Foster and Hobbs, 2002; British Herbal Pharmacopoeia, 1990). In Appalachian folk practice, a weak decoction of the inner bark has been used for coughs and bronchial complaints; the bark is boiled briefly and the liquid drunk warm (Moerman, 1998; Grieve, 1931). In parts of Mexico and Central America, the powdered gum has been infused in hot water to make a warm tea-like drink taken for colds and congestion (Mors and Rizzini, 1966). Some herbalists also blend a small pinch of liquidambar resin with other expectorant tinctures in a traditional 1:5 ethanolic preparation for short-term cough support (British Herbal Pharmacopoeia, 1990).

To prepare a 1:5 (w:v) liquidambar resin tincture, gently warm the resin with the alcohol to dissolve, shaking to re-suspend any crystals; if you must prepare a maceration without pre-dissolving, finely grate the resin and shake the jar thoroughly every day. The final tincture is light brown, balsamic, and slightly sweet; dose 10–15 drops in a little warm water up to three times a day for a few days during acute cough. Avoid during pregnancy and breastfeeding; stop if heartburn or mouth irritation develops; the tincture is flammable and not for children (British Herbal Pharmacopoeia, 1990; Foster and Hobbs, 2002).

The aromatic activity is generally linked to phenylpropanoids and phenylpropanoid esters (for example cinnamic acid derivatives) typical of liquidambar resins, together with essential oil constituents that contribute to the expectorant, balsamic odor and taste (British Herbal Pharmacopoeia, 1990; Williamson, 2003).

Liquidambar resin remains available from specialty herb suppliers for perfumery and traditional cough preparations, and several analyses continue to profile its phenylpropanoid profile; small-scale artisanal use for lozenges and teas continues in traditional contexts (Foster and Hobbs, 2002; Mors and Rizzini, 1966).

General Uses Top

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Common products:
American sweetgum (Liquidambar styraciflua) provides lumber and veneer from its wood; industrial uses rely on kraft hardwood pulp and fiberboard derived from the wood’s fibers. The species is listed in genetic databases and used in botanical research.

Wood and fiber:
Lumber is employed for furniture, interior finish, flooring, and moldings; the wood yields veneer and is suitable for cross-laminated timber and glue-laminated products. Paper-grade pulp utilizes kraft cooking; fiberboard is produced as medium-density fiberboard (MDF) and hardboard. The species’ medium density (specific gravity ~0.52) and a mix of fibers suitable for papermaking enable these products.

Industrial and craft applications:
The wood is a recognized component in hardwood chips for kraft pulp used to manufacture printing papers, linerboard, and corrugated medium. Wood-based fiberboard and oriented strand board (OSB) utilize adhesive systems suited to hardwood species.

Scientific/model use:
The species is represented in the ForestGEO and i-Tree species databases for urban forestry planning and tree selection tools; it is a reference organism in floristic and forest ecology research programs.

Properties relevant to use:
Paper-grade pulp: lignin/cellulose ratio and hardwood fiber dimensions suitable for kraft pulping. Fiberboard: density in the medium range and fiber bonding characteristics compatible with MDF/hardboard production. Wood: typical hardwood density and grain pattern suitable for furniture and millwork applications.

Standards and regulation:
Timber grading for furniture and millwork follows North American hardwood rules; pulp and paper properties are governed by ISO/ASTM test methods for fiber analysis and pulp strength; engineered wood products (MDF, OSB) are covered by product standards including ASTM D 7907 (MDF) and product‑specific performance standards.

Sustainability and sourcing:
The species regenerates vigorously and is widespread in the eastern United States; it is commonly included in plantation and restoration programs, supporting a renewable supply for lumber and fiber products.

Synonyms Top

Scientific name Authority First published in
Liquidambar gummifera Salisb. Prodr. Stirp. Chap. Allerton : 393 (1796)
Liquidambar macrophylla Oerst. Amér. Centr. : 16 (1863)
Liquidambar styraciflua var. mexicana Oerst. Amér. Centr. : 16 (1863)
Liquidambar barbata Stokes Bot. Mat. Med. 4: 332 (1812)
Liquidambar styraciflua f. pendula Rehder J. Arnold Arbor. 20: 93. 1939
Liquidambar styraciflua f. rotundiloba Rehder J. Arnold Arbor. 12: 70, fig. 1931
Liquidambar tuberculata Silba J. Int. Conifer Preserv. Soc. 22(1): 27. 2015
Liquidambar styraciflua var. macrophylla Nied. Nat. Pflanzenfam. [Engler & Prantl] 3, Abt. 2a: 124, fig. 69H. 1891

Common names Top

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Language Common/alternative name
English hazel pine
English sweet gum
English bilsted
English american storax
English redgum
English american sweetgum
English alligatorwood
English satin-walnut
English star-leaved gum
English sweetgum
Spanish Árbol del Ámbar
Arabic عنبر دماع أمريكي
Azerbaijani qatranlı likvidambar
Catalan arbre d'ambar
Catalan liquidàmbar americà
Czech ambroň styraxová
Czech ambroň západní
Danish almindelig ambratræ
Danish almindeligt ambratræ (liquidambar styraciflua)
Danish virginsk ambratræ
German seesternbaum
German amerikanischer amberbaum
Basque likidanbar
Persian شیرینژد آمریکایی
Finnish lännenambrapuu
French copalme d'amérique
French copalme d’amérique
Hebrew ליקוידמבר ליבני
Croatian američki likvidambar
Hungarian amerikai ámbrafa
Armenian լիքվիդամբար խեժատու
Italian storace americano
Japanese アメリカフウ
Japanese アメリカンレッドガム
Japanese モミジバフウ
Macedonian американски ликвидамбар
nah ocotzocuahuitl
Norwegian Bokmål ambratre
Dutch storaxboom
Dutch amberboom
Polish ambrowiec balsamiczny
Polish ambrowiec amerykański
Russian Ликвидамбар смолоносный
Russian Ликвидамбр смолоносный
Russian Амбровое дерево
Serbian Амерички ликвидамбар
Chinese 北美枫香树
Chinese 北美枫香
Chinese 北美楓香樹

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
  • Europe
    • Middle Europe
      • Belgium
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Oklahoma
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • New York
      • Pennsylvania
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
  • Southern America
    • Central America
      • Belize
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000364015
UNII L674U3X6NP
Florida Plant Atlas 3559
Flora of Alabama 2305
Cornell Woody Plants 138
USDA Plants LIST2
UConn 259
Tropicos 15100008
INPN 106361
Flora of Italy 8515
KEW urn:lsid:ipni.org:names:430718-1
The Plant List kew-2348877
Missouri Botanical Garden 281024
PaleoBotany 66765
Open Tree Of Life 62530
Observations.org 29064
NCBI Taxonomy 4400
NBN Atlas NBNSYS0500000235
Nature Serve 2.148447
IUCN Red List 33966
IPNI 430718-1
iNaturalist 49658
GBIF 3152824
Freebase /m/02f4d0
FEIS plants/tree/liqsty
EPPO LIQST
EOL 594658
Elurikkus 366173
Calflora (Californian flora) 8598
USDA GRIN 22379
Wikipedia Liquidambar_styraciflua
PFAF Liquidambar styraciflua

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_041721615.1 ASM4172161v1 Chromosome Chinese Academy Of Sciences 2024-09-03 260.4 631.79 Mb

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
Climate change could negate U.S. forest ecosystem service benefits gained through reductions in nitrogen and sulfur deposition Phelan JN, Van Houtven G, Clark CM, Buckley J, Cajka J, Hargrave A, Horn K, Thomas RQ, Sabo RD Sci Rep 10-May-2024
PMCID:PMC11087459
doi:10.1038/s41598-024-60652-z
PMID:38730011
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
What drives wild pig (Sus scrofa) movement in bottomland and upland forests? Evans TS, Ellison N, Boudreau MR, Strickland BK, Street GM, Iglay RB Mov Ecol 25-Apr-2024
PMCID:PMC11044336
doi:10.1186/s40462-024-00472-y
PMID:38664784
Impacts of Invasive Plants on Native Vegetation Communities in Wetland and Stream Mitigation DeBerry DA, Hunter DM Biology (Basel) 18-Apr-2024
PMCID:PMC11048567
doi:10.3390/biology13040275
PMID:38666887
An inexpensive moist chamber culture technique for finding microbiota on live tree bark Bordelon AP, Keller HW, Scarborough AR Appl Plant Sci 16-Apr-2024
PMCID:PMC11022227
doi:10.1002/aps3.11578
UV reflectance in crop remote sensing: Assessing the current state of knowledge and extending research with strawberry cultivars Heath M, St-Onge D, Hausler R PLoS One 25-Mar-2024
PMCID:PMC10962828
doi:10.1371/journal.pone.0285912
PMID:38527020
Waterlogging in soil restricts the growth of Gleditsia sinensis seedlings and inhibits the accumulation of lignans and phenolic acids in thorns Luo ZQ, Shi XQ, Wang XY, Yang QL, Pan X, Pan WX, Luo CL, Yu SS, Zhou WW, Ren BR, Yi Y, Zhang XM PeerJ 22-Mar-2024
PMCID:PMC10962338
doi:10.7717/peerj.17137
PMID:38529310
First Record of Comparative Plastid Genome Analysis and Phylogenetic Relationships among Corylopsis Siebold & Zucc. (Hamamelidaceae) Kim TH, Ha YH, Setoguchi H, Choi K, Kim SC, Kim HJ Genes (Basel) 20-Mar-2024
PMCID:PMC10970243
doi:10.3390/genes15030380
PMID:38540439
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Proper doses of brassinolide enhance somatic embryogenesis in different competent Korean pine cell lines during embryogenic callus differentiation Nie S, Yan Y, Wang Y, Liu S, Guo W, Yang L, Shen H Front Plant Sci 23-Jan-2024
PMCID:PMC10845146
doi:10.3389/fpls.2024.1330103
PMID:38322821
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
The WOX Genes from the Intermediate Clade: Influence on the Somatic Embryogenesis in Medicago truncatula Yakovleva DV, Efremova EP, Smirnov KV, Simonova VY, Konstantinov ZS, Tvorogova VE, Lutova LA Plants (Basel) 13-Jan-2024
PMCID:PMC10819790
doi:10.3390/plants13020223
PMID:38256776
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Bridging the gap: A new species of arboreal Abronia (Squamata: Anguidae) from the Northern Highlands of Chiapas, Mexico Clause AG, Luna-Reyes R, Mendoza-Velázquez OM, Nieto-Montes de Oca A, Solano-Zavaleta I PLoS One 03-Jan-2024
PMCID:PMC10763973
doi:10.1371/journal.pone.0295230
PMID:38170723
MtWOX2 and MtWOX9-1 Effects on the Embryogenic Callus Transcriptome in Medicago truncatula Krasnoperova EY, Tvorogova VE, Smirnov KV, Efremova EP, Potsenkovskaia EA, Artemiuk AM, Konstantinov ZS, Simonova VY, Brynchikova AV, Yakovleva DV, Pavlova DB, Lutova LA Plants (Basel) 28-Dec-2023
PMCID:PMC10780917
doi:10.3390/plants13010102
PMID:38202410

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 / Anthracenes
Anthracene 8418 Click to see 178.23 unknown https://doi.org/10.1055/S-2008-1074841
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see 278.34 unknown https://doi.org/10.1055/S-2008-1074841
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
(+)-Fenchol 6997371 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
4,6,6-Trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]bicyclo[3.1.1]hept-4-en-2-ol 56924154 Click to see 420.70 unknown https://doi.org/10.1055/S-2008-1074841
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-2008-1074841
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1055/S-2008-1074841
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6R)-rel- 85568 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.2307/2423424
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.2307/2423424
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.2307/2423424
Beta-Terpineol 8748 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
cis-Piperitol 85567 Click to see 154.25 unknown https://doi.org/10.1055/S-2008-1074841
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.2307/2423424
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
(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/10.2307/2423424
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.2307/2423424
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.2307/2423424
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.2307/2423424
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.2307/2423424
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.2307/2423424
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1055/S-2008-1074841
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.2307/2423424
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1055/S-2008-1074841
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.2307/2423424
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.2307/2423424
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown https://doi.org/10.2307/2423424
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.2307/2423424
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
Valeranone 171455 Click to see 222.37 unknown https://doi.org/10.1055/S-2008-1074841
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.2307/2423424
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1055/S-2008-1074841
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1055/S-2008-1074841
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2008-1074841
https://doi.org/10.2307/2423424
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/(SICI)1096-9063(199902)55:2<205::AID-PS870>3.0.CO;2-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see 174.15 unknown https://doi.org/10.1016/J.TETLET.2008.02.140
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.TETLET.2008.02.140
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool oxide (5-ring) 102611 Click to see 170.25 unknown https://doi.org/10.1055/S-2008-1074841
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.2307/2423424
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see 150.22 unknown https://doi.org/10.1055/S-2008-1074841
> Organoheterocyclic compounds / Tetrahydrofurans
Vitispirane 6450832 Click to see CC1CCC2(O1)C(=C)C=CCC2(C)C 192.30 unknown https://doi.org/10.2307/2423424
https://doi.org/10.1055/S-2008-1074841
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(93)85229-K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(93)85229-K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(93)85229-K
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown https://doi.org/10.1016/0031-9422(93)85229-K
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(93)85229-K

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