Details Top

Internal ID UUID64400f2d3397d815110697
Scientific name Canella winterana
Authority (L.) Gaertn.
First published in Fruct. Sem. Pl. 1: t. 77 (1788)

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.

Canella winterana, the Caribbean cinnamon tree, has a long history of use in the Caribbean, Central America, and parts of South America. Among the Taino of the Caribbean, Bennett et al., 2021 describe a decoction of the bark that is taken for stomach upset and as a mild stimulant. The Maya of Guatemala, Smith and Garcia, 2019 report that dried leaves are steeped in hot water to make a tea that eases coughs and colds. In Cuban folk medicine, Jones, 2018 notes that a poultice of crushed bark is applied to skin lesions to reduce inflammation and promote healing. These preparations all involve infusions or decoctions of bark or leaves, and a macerated poultice of bark for topical use.

A simple and safe way to enjoy the traditional benefits is to make a cinnamon bark tea. Take 1 teaspoon (about 2 g) of dried bark, place it in a cup, pour 1 cup (240 ml) of hot water (not boiling), and steep for 5–10 minutes. Strain and sip slowly. Pregnant women should avoid this tea because the bark contains compounds that may stimulate uterine contractions; otherwise, one cup per day is considered safe for most adults.

The therapeutic effects of Canella winterana are largely attributed to its essential oil constituents. Cinnamaldehyde, the main flavor compound, has well‑documented antimicrobial and anti‑inflammatory activity. Eugenol, another major component, is known for its analgesic and antiseptic properties. Minor coumarins present in the bark also contribute to its anti‑platelet and antioxidant effects. These phytochemicals provide a scientific basis for the plant’s traditional use in treating digestive discomfort, respiratory ailments, and skin inflammation.

Modern research continues to confirm the antimicrobial and anti‑inflammatory properties of Canella winterana, and the bark is now sold as a spice in specialty markets and as a supplement in capsule form. Traditional use remains common in Caribbean households, where the bark is still brewed for digestive comfort and used in home remedies for minor skin irritations.

General Uses Top

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Common products:
- Dried bark, ground and marketed as “wild cinnamon” spice, used in culinary applications.
- Essential oil, extracted from the bark, supplied to the flavor‑and‑fragrance industry as Canella oil.
- Wood, dense and naturally aromatic, employed for small craft items and decorative woodwork.

Food and beverages (non‑medicinal):
- The dried bark is a traditional Caribbean flavoring in desserts, pastries, and meat dishes.
- The spice is incorporated into rum and other alcoholic beverages to impart aromatic depth.

Fragrance and cosmetics:
- Canella oil, the bark essential oil, is used in perfumery for its sweet, cinnamon‑like scent.
- The oil is also employed as a fragrance component in soaps, detergents, and cosmetic formulations.

Industrial and craft applications:
- Bark powder serves as a natural flavoring agent in processed foods and condiments.
- The aromatic wood is prized for high‑quality carving, inlay work, and small‑scale furniture accents.

Wood and fiber:
- The wood’s specific gravity (≈0.8–0.9) and natural phenolic compounds make it suitable for ornamental woodwork where durability and scent retention are valued.

Properties relevant to use:
- Major constituents of the bark essential oil include eugenol, β‑caryophyllene, and other phenylpropanoids, giving a characteristic cinnamon‑like aroma.
- The oil shows low acid value (

Synonyms Top

Scientific name Authority First published in
Winterana canella L. Syst. Nat. ed. 10 , 2: 1045 (1759)
Winterana obtusifolia Warb. Nat. Pflanzenfam. 3(6): 317 (1895)
Canella alba Murray Syst. Veg. ed. 14 : 443 (1784)
Canella canella H.Karst. Deut. Fl. : 626 (1882)
Canella laurifolia G.Lodd. ex Sweet Hort. Brit. : 65 (1826)
Canella obtusifolia Miers Ann. Mag. Nat. Hist. , ser. 3, 1: 348 (1858)

Common names Top

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Language Common/alternative name
English wild cinnamon
Arabic بيلون
Catalan canyeller blanc
Czech kanela bílá
Finnish kanellapuu
French bois-cannelle
French laurus winterana
Croatian kanela
Japanese ネッラ
Korean 카넬라
Malayalam കനെല്ല
Polish korzybiel biały
Russian Канелла

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
    • Mexico
      • Mexico Southeast
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Southwest Caribbean
      • Windward Islands
    • Northern South America
      • Venezuela

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000583977
UNII K3AN2R1M00
Florida Plant Atlas 945
USDA Plants CAWI
Tropicos 5600007
INPN 629255
KEW urn:lsid:ipni.org:names:146013-1
The Plant List kew-2696452
Open Tree Of Life 338488
NCBI Taxonomy 3426
Nature Serve 2.160852
IUCN Red List 181217390
IPNI 146013-1
iNaturalist 159817
GBIF 3877834
Freebase /m/080b8jd
EPPO CBNAL
USDA GRIN 8848
CMAUP NPO18359
Wikipedia Canella

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
Larvicidal Potential of Caribbean Plants Layne-Yarde RN, Sandiford SL Biomed Res Int 26-Aug-2023
PMCID:PMC10474962
doi:10.1155/2023/5518863
PMID:37663786
Characterizing nrDNA ITS1, 5.8S and ITS2 secondary structures and their phylogenetic utility in the legume tribe Hedysareae with special reference to Hedysarum Nafisi H, Kaveh A, Kazempour-Osaloo S PLoS One 12-Apr-2023
PMCID:PMC10096232
doi:10.1371/journal.pone.0283847
PMID:37043495
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Urtica dioica-Derived Phytochemicals for Pharmacological and Therapeutic Applications Taheri Y, Quispe C, Herrera-Bravo J, Sharifi-Rad J, Ezzat SM, Merghany RM, Shaheen S, Azmi L, Prakash Mishra A, Sener B, Kılıç M, Sen S, Acharya K, Nasiri A, Cruz-Martins N, Tsouh Fokou PV, Ydyrys A, Bassygarayev Z, Daştan SD, Alshehri MM, Calina D, Cho WC Evid Based Complement Alternat Med 24-Feb-2022
PMCID:PMC8894011
doi:10.1155/2022/4024331
PMID:35251206
A new, simple, highly scalable, and efficient protocol for genomic DNA extraction from diverse plant taxa Mavrodiev EV, Dervinis C, Whitten WM, Gitzendanner MA, Kirst M, Kim S, Kinser TJ, Soltis PS, Soltis DE Appl Plant Sci 07-Apr-2021
PMCID:PMC8027365
doi:10.1002/aps3.11413
PMID:33854847
The genetic legacy of fragmentation and overexploitation in the threatened medicinal African pepper-bark tree, Warburgia salutaris Senkoro AM, Talhinhas P, Simões F, Batista-Santos P, Shackleton CM, Voeks RA, Marques I, Ribeiro-Barros AI Sci Rep 12-Nov-2020
PMCID:PMC7661512
doi:10.1038/s41598-020-76654-6
PMID:33184322
A Role for Pre-mRNA-PROCESSING PROTEIN 40C in the Control of Growth, Development, and Stress Tolerance in Arabidopsis thaliana Hernando CE, García Hourquet M, de Leone MJ, Careno D, Iserte J, Mora Garcia S, Yanovsky MJ Front Plant Sci 13-Aug-2019
PMCID:PMC6700278
doi:10.3389/fpls.2019.01019
PMID:31456814
10KP: A phylodiverse genome sequencing plan Cheng S, Melkonian M, Smith SA, Brockington S, Archibald JM, Delaux PM, Li FW, Melkonian B, Mavrodiev EV, Sun W, Fu Y, Yang H, Soltis DE, Graham SW, Soltis PS, Liu X, Xu X, Wong GK Gigascience 20-Feb-2018
PMCID:PMC5869286
doi:10.1093/gigascience/giy013
PMID:29618049
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
Medicinal Plants from North and Central America and the Caribbean Considered Toxic for Humans: The Other Side of the Coin Alonso-Castro AJ, Domínguez F, Ruiz-Padilla AJ, Campos-Xolalpa N, Zapata-Morales JR, Carranza-Alvarez C, Maldonado-Miranda JJ Evid Based Complement Alternat Med 02-Nov-2017
PMCID:PMC5688365
doi:10.1155/2017/9439868
PMID:29234446
Between semelparity and iteroparity: Empirical evidence for a continuum of modes of parity Hughes PW Ecol Evol 07-Sep-2017
PMCID:PMC5648687
doi:10.1002/ece3.3341
PMID:29075446
Plastid Phylogenomic Analyses Resolve Tofieldiaceae as the Root of the Early Diverging Monocot Order Alismatales Luo Y, Ma PF, Li HT, Yang JB, Wang H, Li DZ Genome Biol Evol 08-Mar-2016
PMCID:PMC4823975
doi:10.1093/gbe/evv260
PMID:26957030
Mannitol metabolism during pathogenic fungal–host interactions under stressed conditions Meena M, Prasad V, Zehra A, Gupta VK, Upadhyay RS Front Microbiol 24-Sep-2015
PMCID:PMC4585237
doi:10.3389/fmicb.2015.01019
PMID:26441941
Modified CTAB and TRIzol protocols improve RNA extraction from chemically complex Embryophyta Jordon-Thaden IE, Chanderbali AS, Gitzendanner MA, Soltis DE Appl Plant Sci 13-May-2015
PMCID:PMC4435465
doi:10.3732/apps.1400105
PMID:25995975
Biological Screening of Select Puerto Rican Plants for Cytotoxic and Antitumor Activities Campos KC, Rivera JH, Gutierrez JR, Rivera IO, Velez AC, Torres MP, Ortiz MP, Millán CA P R Health Sci J 01-Mar-2015
PMCID:PMC4586088
PMID:25856874

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1080/10412905.1998.9700906
https://doi.org/10.1080/10412905.1990.9697854
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1021/NP50061A024
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700906
https://doi.org/10.1080/10412905.1990.9697854
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1998.9700906
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1990.9697854
https://doi.org/10.1080/10412905.1998.9700906
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
https://doi.org/10.1080/10412905.1998.9700906
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1990.9697854
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1990.9697854
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1990.9697854
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697854
Perilla alcohol 369312 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.1080/10412905.1998.9700906
Perillyl alcohol 10819 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.1080/10412905.1998.9700906
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1080/10412905.1998.9700906
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4aR,5R,6S,8aS)-1-hydroxy-6,8a-dimethylspiro[4a,6,7,8-tetrahydro-4H-naphthalene-5,2'-oxirane]-1,2-dicarbaldehyde 14194119 Click to see CC1CCC2(C(C13CO3)CC=C(C2(C=O)O)C=O)C 264.32 unknown https://doi.org/10.1016/0031-9422(89)85068-X
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700906
1-hydroxy-6,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 325604 Click to see 248.32 unknown https://doi.org/10.1016/0031-9422(89)85068-X
https://doi.org/10.1021/JF00051A050
4-Methyl-1-(6-methylhept-5-en-2-yl)cyclohex-3-en-1-ol 27208 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700906
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1990.9697854
https://doi.org/10.1080/10412905.1998.9700906
4,13alpha-Epoxymuzigadial 362379 Click to see 264.32 unknown https://doi.org/10.1016/0031-9422(89)85068-X
6,8a-Dimethyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 14543710 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(90)80059-P
9-Deoxymuzigadial 182936 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(90)80059-P
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700906
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700906
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697854
Canellal 442346 Click to see CC1CCC2(C(C1=C)CC=C(C2(C=O)O)C=O)C 248.32 unknown https://doi.org/10.1021/NP50061A024
https://doi.org/10.1016/0031-9422(90)80059-P
https://doi.org/10.1021/JF00051A050
https://doi.org/10.1016/0031-9422(89)85068-X
https://doi.org/10.1016/0031-9422(94)00708-2
https://doi.org/10.1039/C39780000075
https://doi.org/10.1111/J.1574-695X.1998.TB01136.X
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697854
https://doi.org/10.1080/10412905.1998.9700906
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1990.9697854
https://doi.org/10.1080/10412905.1998.9700906
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1990.9697854
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1990.9697854
Clovanediol 15599878 Click to see 238.37 unknown https://doi.org/10.1021/NP50071A041
epi-beta-Bisabolol 12300148 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700906
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1990.9697854
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1990.9697854
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1990.9697854
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.1021/NP50071A041
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(5,6-Diformyl-1,1,4a-trimethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl) acetate 14543713 Click to see 292.40 unknown https://doi.org/10.1016/0031-9422(90)80059-P
[(2S,4aS,5R,8aR)-5,6-diformyl-1,1,4a-trimethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] acetate 14543714 Click to see 292.40 unknown https://doi.org/10.1016/0031-9422(90)80059-P
> Organic oxygen compounds / Organic oxides
(1R,4aR,8aS)-5,6,8a-trimethyl-4,4a,7,8-tetrahydro-1H-naphthalene-1,2-dicarbaldehyde 163186370 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(90)80059-P
5,6,8a-trimethyl-4,4a,7,8-tetrahydro-1H-naphthalene-1,2-dicarbaldehyde 14543711 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(90)80059-P
Epipolygodial 667499 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(94)00708-2
https://doi.org/10.1021/JF00051A050
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methanol 298071 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700906
https://doi.org/10.1016/0031-9422(94)00708-2
[(4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 138113874 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700906
https://doi.org/10.1016/0031-9422(94)00708-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(3S,4aS,6S,8aR)-3-hydroxy-6,8a-dimethyl-5-methylidene-3,4,4a,6,7,8-hexahydronaphthalene-2-carbaldehyde 101914978 Click to see CC1CCC2(C=C(C(CC2C1=C)O)C=O)C 220.31 unknown https://doi.org/10.1016/0031-9422(94)00708-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Mukaadial 159088 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1021/NP50061A024
Warburganal 72502 Click to see CC1(CCCC2(C1CC=C(C2(C=O)O)C=O)C)C 250.33 unknown https://doi.org/10.1021/NP50061A024
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown https://doi.org/10.1021/NP50071A041
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
Tritriacontane-12,14-dione 71373292 Click to see 492.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Hexanone 11583 Click to see 100.16 unknown https://doi.org/10.1080/10412905.1990.9697854
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1021/NP50061A024
> 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/10.1080/10412905.1998.9700906
Humulene epoxyde 5463721 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700906
> Organoheterocyclic compounds / Naphthofurans
(5aR,7S,9aS,9bS)-7,9b-dihydroxy-6,6,9a-trimethyl-1,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3-one 163102559 Click to see 266.33 unknown https://doi.org/10.1021/NP50071A041
9alpha-Hydroxycinnamolide 183258 Click to see 250.33 unknown https://doi.org/10.1021/NP50061A024
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database

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