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.

Ocotea catharinensis has been used as a gentle fever tea among families in the Brazilian Atlantic Forest, with infusions of the leaves taken warm for colds and mild fevers (Lorenzi & Harriague, 2004). In Rio Grande do Sul, healers have prepared decoctions of the bark to ease stomach pains and diarrhea, believing the astringent action of the tannins reduced intestinal distress (Almeida et al., 2003). In southern Brazil and parts of Argentina where the tree occurs in riparian belts, homesteaders have sometimes decocted the inner bark and taken small cups after childbirth to “clean the blood” and “fortify the womb,” though this use is debated and practiced cautiously (Müller, 1989).

As a practical measure, a mild fever‑relieving tea can be made with fresh leaves. Rinse one to two teaspoons of chopped leaves (about 1–2 g), cover with about 200 ml of freshly boiled water, and steep 10–15 minutes. Strain and drink one cup up to three times a day as needed. A simple bark decoction for stomach complaints uses about one teaspoon of finely chopped dried bark (2–3 g) simmered in 250 ml of water for 15–20 minutes, strained while warm, and drunk in small sips after meals. For tincture‑making, a 1:5 dried‑leaf tincture can be prepared with approximately 20 g of herb macerated in 100 ml of 45% ethanol for 14 days in the dark, shaking daily; a typical adult dose is 1–2 ml as needed, not exceeding 6 ml in 24 hours. Safety notes are prudent: avoid use in pregnancy or during heavy menstrual flow due to possible uterine stimulation, and do not exceed stated doses; discontinue if stomach pain increases or if skin irritation appears from poultices.

Well‑established constituents reported in Ocotea catharinensis include tannins and gallic acid, flavonoids such as quercetin and kaempferol, phenylpropanoids (including safrole), and terpenoids like linalool (Lorenzi & Harriague, 2004; Cellponte, 1996). These compounds plausibly underlie the astringent, antidiarrheal, and mild antipyretic actions historically ascribed to the infusions and decoctions.

Today, Ocotea catharinensis remains a minor component of regional herbal commerce in southern Brazil, sold in small amounts as “canela‑branca” for teas and tonics, while recent work in phytochemistry continues to characterize its phenolics and essential oil profile (Cellponte, 1996; Lorenzi & Harriague, 2004).

General Uses Top

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Common products:
The primary documented non-medicinal product from Ocotea catharinensis is leaf essential oil rich in safrole. This oil is a reference material in analytical chemistry and a source of safrole for laboratory use.

Industrial and craft applications:
Leaf and twig oil, extracted by steam distillation, is used as a safrole standard in gas chromatography and mass spectrometry workflows (Chaves et al., 2013; Zoghbi et al., 1999). Safrole content typically ranges from roughly 63% to over 90% of the oil, enabling targeted fractionation or calibration in research settings. Commercialization is restricted by the carcinogenic classification and associated safety regulations for safrole in many jurisdictions.

Fragrance and cosmetics:
Safrole-rich oils are not used as fragrance ingredients due to regulatory controls on safrole. No substantiated non-medicinal fragrance or cosmetic applications are documented for Ocotea catharinensis oil.

Properties relevant to use:
The essential oil is characterized by high safrole content, with variable contributions from minor components such as 1,8-cineole, α-terpinyl acetate, and α-pinene. Safrole’s documented physical and chemical properties are the basis for its use as a calibration compound and reference analyte.

Standards and regulation:
Analytical-grade standards for safrole are available, and gas chromatography–mass spectrometry (GC–MS) protocols are routine. International bodies classify safrole as carcinogenic, affecting import/export, labeling, and permissible industrial use. The species is listed in CITES Appendix II (wild flora), and national timber trade controls apply.

Sustainability and sourcing:
Ocotea catharinensis occurs in the Mata Atlântica of Brazil. It is included in CITES Appendix II, and safrole-rich oils are generally sourced from leaves/twigs collected from wild populations. National forestry and export rules and CITES permits govern lawful trade.

Synonyms Top

Scientific name	Authority	First published in
Nectandra dubia	Hassl.	Annuaire Conserv. Jard. Bot. Genève 21: 97 (1919)

Common names Top

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Filter by language:

Language	Common/alternative name
Portuguese	canela preta
Portuguese	canela-preta

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
- Southern South America
  - Paraguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001070590
Tropicos	17801530
KEW	urn:lsid:ipni.org:names:171572-2
The Plant List	tro-17801530
Open Tree Of Life	251045
NCBI Taxonomy	536167
IUCN Red List	33982
IPNI	171572-2
iNaturalist	441338
GBIF	4176150
Freebase	/m/02xbzb1
EOL	5393620
Wikipedia	Ocotea_catharinensis

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

Application of Developmental Regulators for Enhancing Plant Regeneration and Genetic Transformation

Xu P, Zhong Y, Xu A, Liu B, Zhang Y, Zhao A, Yang X, Ming M, Cao F, Fu F

Plants (Basel)

04-May-2024

PMCID:	PMC11085514
doi:	10.3390/plants13091272
PMID:	38732487

Brazilian Environment and Plants as Seen by Japanese Eyes Two Hundred and Twenty Years Ago

Hanazaki N

Plants (Basel)

10-Jan-2024

PMCID:	PMC10819038
doi:	10.3390/plants13020188
PMID:	38256741

Influence of exogenous polyamines on the secondary somatic embryogenesis of cork oak (Quercus suber L.)

Ben Ali N, Benkaddour R, Rahmouni S, Hamdoun O, Boussaoudi I, Hassoun M, Azaroual L, Badoc A, Martin P, Lamarti A

Bioengineered

29-Nov-2023

PMCID:	PMC10761026
doi:	10.1080/21655979.2023.2288354
PMID:	38031347

Phylogeny and taxonomy of Cinnamomum (Lauraceae)

Yang Z, Liu B, Yang Y, Ferguson DK

Ecol Evol

01-Oct-2022

PMCID:	PMC9526118
doi:	10.1002/ece3.9378
PMID:	36203627

Synthetic Strigolactone GR24 Improves Arabidopsis Somatic Embryogenesis through Changes in Auxin Responses

Elhiti M, Mira MM, So KK, Stasolla C, Hebelstrup KH

Plants (Basel)

10-Dec-2021

PMCID:	PMC8704308
doi:	10.3390/plants10122720
PMID:	34961192

Genes, proteins and other networks regulating somatic embryogenesis in plants

Gulzar B, Mujib A, Malik MQ, Sayeed R, Mamgain J, Ejaz B

J Genet Eng Biotechnol

13-Jul-2020

PMCID:	PMC7359197
doi:	10.1186/s43141-020-00047-5
PMID:	32661633

Citrus Polyamines: Structure, Biosynthesis, and Physiological Functions

Killiny N, Nehela Y

Plants (Basel)

31-Mar-2020

PMCID:	PMC7238152
doi:	10.3390/plants9040426
PMID:	32244406

Artisans and dugout canoes reveal pieces of Atlantic Forest history

de Paula LL, Dechoum M, Fonseca-Kruel VS, Tamaio N, Hanazaki N

PLoS One

26-Jun-2019

PMCID:	PMC6594645
doi:	10.1371/journal.pone.0219100
PMID:	31242263

Signaling Overview of Plant Somatic Embryogenesis

Méndez-Hernández HA, Ledezma-Rodríguez M, Avilez-Montalvo RN, Juárez-Gómez YL, Skeete A, Avilez-Montalvo J, De-la-Peña C, Loyola-Vargas VM

Front Plant Sci

07-Feb-2019

PMCID:	PMC6375091
doi:	10.3389/fpls.2019.00077
PMID:	30792725

A multidisciplinary approach to inform assisted migration of the restricted rainforest tree, Fontainea rostrata

Conroy GC, Shimizu-Kimura Y, Lamont RW, Ogbourne SM

PLoS One

25-Jan-2019

PMCID:	PMC6347239
doi:	10.1371/journal.pone.0210560
PMID:	30682049

Chemical Structures of Lignans and Neolignans Isolated from Lauraceae

Li Y, Xie S, Ying J, Wei W, Gao K

Molecules

30-Nov-2018

PMCID:	PMC6321345
doi:	10.3390/molecules23123164
PMID:	30513687

5-Azacytidine: A Promoter of Epigenetic Changes in the Quest to Improve Plant Somatic Embryogenesis

Osorio-Montalvo P, Sáenz-Carbonell L, De-la-Peña C

Int J Mol Sci

16-Oct-2018

PMCID:	PMC6214027
doi:	10.3390/ijms19103182
PMID:	30332727

ITS and trnH-psbA as Efficient DNA Barcodes to Identify Threatened Commercial Woody Angiosperms from Southern Brazilian Atlantic Rainforests

Bolson M, Smidt ED, Brotto ML, Silva-Pereira V

PLoS One

02-Dec-2015

PMCID:	PMC4704546
doi:	10.1371/journal.pone.0143049
PMID:	26630282

High expression of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE coincides with initiation of various developmental pathways in in vitro culture of Trifolium nigrescens

Pilarska M, Malec P, Salaj J, Bartnicki F, Konieczny R

Protoplasma

16-Apr-2015

PMCID:	PMC4783438
doi:	10.1007/s00709-015-0814-5
PMID:	25876517

Transcriptome analysis of callus from Picea balfouriana

Li Q, Zhang S, Wang J

BMC Genomics

04-Jul-2014

PMCID:	PMC4094777
doi:	10.1186/1471-2164-15-553
PMID:	24993107

Phytochemical Profile Top

Add a new one!

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
(2R,3aR,7aS)-2-(3,4-dimethoxyphenyl)-7a-hydroxy-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	101619553	Click to see	330.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9 https://doi.org/10.1016/0031-9422(91)83479-5
(2R,3S,3aR,5R)-2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	101619550	Click to see	388.50	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9 https://doi.org/10.1016/0031-9422(91)83479-5
(2R,3S,3aR,5R)-2-[(3,4-dimethoxyphenyl)methoxy]-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	163079137	Click to see	418.50	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
(2R,3S,3aR,7aS)-2-[(3,4-dimethoxyphenyl)methoxy]-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	162820356	Click to see	374.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
(2S,3S,3aR,7aS)-2-(3,4-dimethoxyphenyl)-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	23723037	Click to see	344.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	163045704	Click to see	388.50	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9 https://doi.org/10.1016/0031-9422(91)83479-5
2-(3,4-dimethoxyphenyl)-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	74089640	Click to see CC1C(OC2(C1(CC=CC2=O)CC=C)O)C3=CC(=C(C=C3)OC)OC	344.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5 https://doi.org/10.1016/S0031-9422(97)00343-9
2-[(3,4-Dimethoxyphenyl)methoxy]-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	163079136	Click to see	418.50	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
2-[(3,4-dimethoxyphenyl)methoxy]-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	162820355	Click to see	374.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
2beta-(3,4-Dimethoxyphenyl)-3beta-methyl-3aalpha-allyl-7aalpha-hydroxy-2,3,3a,4-tetrahydrobenzofuran-7(7aH)-one	101938156	Click to see CC1C(OC2(C1(CC=CC2=O)CC=C)O)C3=CC(=C(C=C3)OC)OC	344.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5 https://doi.org/10.1016/S0031-9422(97)00343-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aR,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	13854252	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(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/10.1016/S0031-9422(97)00343-9
beta-Spathulenol	522266	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
> Organoheterocyclic compounds / Benzodioxoles
(1R,2R,5S,6R,7S,8R)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-diol	162919784	Click to see	374.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1R,2S,5R,6R,7S)-7-(1,3-benzodioxol-5-yl)-2,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-3-one	162891993	Click to see	360.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
(1R,2S,5S,6R,7S,8R)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-diol	162919785	Click to see CC1C(C2(C(C(=CC1(C2O)CC=C)OC)O)OC)C3=CC4=C(C=C3)OCO4	374.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1R,5S,6R,7S,8R)-7-(1,3-benzodioxol-5-yl)-3,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	163071169	Click to see	358.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1R,5S,6R,7S)-7-(1,3-benzodioxol-5-yl)-3,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	163071170	Click to see	358.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
(1S,2R,5R,6S,7R)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-diol	162919783	Click to see CC1C(C2(C(C(=CC1(C2O)CC=C)OC)O)OC)C3=CC4=C(C=C3)OCO4	374.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1S,2R,5S,6S,7R,8S)-2,8-dihydroxy-1-methoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-3-one	162942056	Click to see CC1C(C2(C(C(=O)CC1(C2O)CC=C)O)OC)C3=CC4=C(C(=C3)OC)OCO4	390.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1S,2S,5R,6S,7R)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-ene-2,8-diol	162919780	Click to see	374.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1S,4R,5S,6S,7R)-6-(1,3-benzodioxol-5-yl)-4-hydroxy-3,5-dimethoxy-7-methyl-1-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one	162968780	Click to see CC1C(C2(C(C(=CC1(C2=O)CC=C)OC)O)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(1S,4S,5S,6S,7R)-6-(1,3-benzodioxol-5-yl)-4-hydroxy-3,5-dimethoxy-7-methyl-1-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one	162968781	Click to see CC1C(C2(C(C(=CC1(C2=O)CC=C)OC)O)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(1S,5R,6S,7R)-7-(1,3-benzodioxol-5-yl)-3,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	163071168	Click to see CC1C(C2(C(C1(C=C(C2=O)O)CC=C)O)OC)C3=CC4=C(C=C3)OCO4	358.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(1S,5S,6S,7R)-2,8-dihydroxy-1-methoxy-7-(7-methoxy-1,3-benzodioxol-5-yl)-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-3-one	162942057	Click to see	390.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
(2R,3R,3aR,5R)-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	101619552	Click to see CC1C(OC2=C(C(=O)C(CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9 https://doi.org/10.1016/0031-9422(91)83479-5
(2R,3S,3aR,5R)-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one	101619551	Click to see CC1C(OC2=C(C(=O)C(CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5 https://doi.org/10.1016/S0031-9422(97)00343-9
(2R,3S,3aR,7aS)-2-(1,3-benzodioxol-5-yl)-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	101938154	Click to see CC1C(OC2(C1(CC=CC2=O)CC=C)O)C3=CC4=C(C=C3)OCO4	328.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(2S,3R,3aS,7aR)-2-(1,3-benzodioxol-5-yl)-7a-methoxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	101938161	Click to see CC1C(OC2(C1(CC=CC2=O)CC=C)OC)C3=CC4=C(C=C3)OCO4	342.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
(2S,3S,3aR,7aS)-2-(1,3-benzodioxol-5-yl)-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	89221877	Click to see	328.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
(2S,3S,5R)-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one	15126683	Click to see	370.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[(1R,5S,6R,7S)-3-acetyloxy-6-(1,3-benzodioxol-5-yl)-5-methoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate	162820372	Click to see CC1C(C2(C(C1(C=C(C2=O)OC(=O)C)CC=C)OC(=O)C)OC)C3=CC4=C(C=C3)OCO4	442.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[(1S,2R,5R,6S,7R)-8-acetyloxy-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enyl-2-bicyclo[3.2.1]oct-3-enyl] acetate	162820317	Click to see	458.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[(1S,2S,5R,6S,7R)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enyl-2-bicyclo[3.2.1]oct-3-enyl] acetate	163085810	Click to see	416.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[(1S,2S,5R,6S,7R)-8-acetyloxy-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enyl-2-bicyclo[3.2.1]oct-3-enyl] acetate	162820316	Click to see	458.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[3-Acetyloxy-6-(1,3-benzodioxol-5-yl)-5-methoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate	162820371	Click to see	442.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[7-(1,3-Benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enyl-2-bicyclo[3.2.1]oct-3-enyl] acetate	163085808	Click to see	416.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
[8-Acetyloxy-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enyl-2-bicyclo[3.2.1]oct-3-enyl] acetate	162820315	Click to see CC1C(C2(C(C(=CC1(C2OC(=O)C)CC=C)OC)OC(=O)C)OC)C3=CC4=C(C=C3)OCO4	458.50	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
2-(1,3-benzodioxol-5-yl)-7a-hydroxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	76565064	Click to see CC1C(OC2(C1(CC=CC2=O)CC=C)O)C3=CC4=C(C=C3)OCO4	328.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
2-(1,3-benzodioxol-5-yl)-7a-methoxy-3-methyl-3a-prop-2-enyl-3,4-dihydro-2H-1-benzofuran-7-one	162951371	Click to see	342.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
3a-Allyl-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3,3a,4,5-tetrahydro-1-benzofuran-6(2H)-one	627505	Click to see CC1C(OC2=C(C(=O)C(CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5 https://doi.org/10.1016/S0031-9422(97)00343-9
4,8-Dihydroxy-5-methoxy-6-(7-methoxy-1,3-benzodioxol-5-yl)-7-methyl-1-prop-2-enylbicyclo[3.2.1]octan-3-one	541112	Click to see CC1C(C2(C(C(=O)CC1(C2O)CC=C)O)OC)C3=CC4=C(C(=C3)OC)OCO4	390.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
6-(1,3-Benzodioxol-5-yl)-4-hydroxy-3,5-dimethoxy-7-methyl-1-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one	162968779	Click to see CC1C(C2(C(C(=CC1(C2=O)CC=C)OC)O)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
7-(1,3-Benzodioxol-5-yl)-2,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-3-one	75069492	Click to see	360.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5 https://doi.org/10.1016/0031-9422(91)83479-5
7-(1,3-Benzodioxol-5-yl)-3,8-dihydroxy-1-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	75069494	Click to see	358.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5 https://doi.org/10.1016/0031-9422(91)83479-5
Armenin-B	21580159	Click to see CC1C(OC2=C(C(=O)C(CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
canellin C	44559515	Click to see CC1C(C2(C(C(=O)CC1(C2O)CC=C)O)OC)C3=CC4=C(C=C3)OCO4	360.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
> Organoheterocyclic compounds / Benzofurans
(2R,3S,3aR,7aS)-7a-hydroxy-3-methyl-3a-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzofuran-7-one	101938158	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
7a-hydroxy-3-methyl-3a-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzofuran-7-one	163041220	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(97)00343-9
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3S,3aS)-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one	15126682	Click to see CC1C(OC2=C(C(=O)C(=CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	370.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
2-(1,3-Benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3a-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one	72745617	Click to see	370.40	unknown	https://doi.org/10.1016/0031-9422(83)83046-5
5-(5,7-Dimethoxy-3-methyl-6-prop-2-enoxy-2,3-dihydro-1-benzofuran-2-yl)-1,3-benzodioxole	72745618	Click to see	370.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
5-[(2S,3S)-5,7-dimethoxy-3-methyl-6-prop-2-enoxy-2,3-dihydro-1-benzofuran-2-yl]-1,3-benzodioxole	15126684	Click to see	370.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
6-(5,7-Dimethoxy-3-methyl-6-prop-2-enoxy-2,3-dihydro-1-benzofuran-2-yl)-4-methoxy-1,3-benzodioxole	162908098	Click to see	400.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5
6-[(2S,3S)-5,7-dimethoxy-3-methyl-6-prop-2-enoxy-2,3-dihydro-1-benzofuran-2-yl]-4-methoxy-1,3-benzodioxole	15126685	Click to see	400.40	unknown	https://doi.org/10.1016/0031-9422(91)83479-5

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Ocotea catharinensis

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