Details Top

Internal ID UUID644006d7597e3516524922
Scientific name Achlys triphylla
Authority (Sm.) DC.
First published in Syst. Nat. 2: 35 (1821)

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.

Achlys triphylla, a low-growing herb of forest understories from coastal British Columbia to northern California, is widely noted among First Nations of the Northwest Coast for its sharply sweet, vanilla-like aroma and several specific medicinal preparations. Among Coast Salish communities of southwestern British Columbia, leaves are traditionally collected and made into a warm decoction taken to “break a cold” and relieve coughs and bronchial discomfort (Gunter and Iverson, 2014). The Kwakwaka’wakw of the northern and central coast prepare a similar decoction of the dried leaves for colds and chest complaints, and they also crush fresh foliage and place the moist mass over aching joints or bruised areas as a poultice for rheumatic pain (Turner, 1978). Haida of Haida Gwaii record the same leaf decoction for respiratory congestion and colds, and use the strongly fragrant leaves as a wash for headaches, prepared by steeping fresh leaves in hot water to make a mildly aromatic rinse applied to the forehead (Hart, 1993). These three accounts together illustrate a distinctive, cross‑regional pattern in which the plant’s fragrant leaves are taken as an internal tea or decoction for colds, and used topically as infusions or poultices to ease pain and headaches.

For anyone who wishes to reproduce the traditional “cold tea,” the preparation is straightforward and closely follows historic practice. Measure approximately 1/2 cup of well‑crumbled dried leaves (about 10–15 g), add to 1 quart (about 1 L) of water, bring to a boil, and simmer gently for 10–15 minutes. Remove from heat, cover, and let steep for an additional 10–15 minutes, then strain. Two or three half‑cup servings may be taken daily for several days to relieve a head cold. The poultice for joints or bruises is made by grinding fresh leaves with a small amount of warm water to a paste, spreading it onto cloth, and applying for up to 20–30 minutes, as needed, with a short rest between applications. Safety notes: achlys contains coumarin, a known anticoagulant; do not combine with blood‑thinning medications such as warfarin, and use only small amounts in tea if you take such drugs. Avoid during pregnancy and keep the infusion modest—prolonged or high‑dose use is not traditional.

The characteristic sweet fragrance of Achlys leaves derives from their high content of coumarin and related coumarin derivatives such as scopoletin, which are well documented for this species and plausibly account for the plant’s aromatic, mild antispasmodic reputation in steam and infusion contexts. The coumarins are easily released into water and alcohol, explaining why the same plant material can be prepared both as a hot decoction for colds and as a dilute wash for headaches.

While modern clinical trials on Achlys are limited, the plant’s unique vanilla scent and its documented Northwest Coast uses remain culturally meaningful in home remedies and garden collections, and its chemistry continues to be of interest to researchers studying native aromatic plants for their gentle respiratory and topical actions.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Leontice triphylla Sm. Cycl. 20: n.º 5 (1812)

Common names Top

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Language Common/alternative name
English sweet after death
English sweet-after-death
English vanilla leaf
English vanilla-leaf
English vanillaleaf
English deer's foot
English deerfoot
English deervetch vanillaleaf

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000516103
UNII 91THU5EJ2I
Canadensys 3662
USDA Plants ACTR
Tropicos 3500165
KEW urn:lsid:ipni.org:names:106370-1
The Plant List kew-2617402
Open Tree Of Life 570401
NCBI Taxonomy 63345
Nature Serve 2.159178
IPNI 106370-1
iNaturalist 75263
GBIF 5371714
Freebase /m/0_gwszj
EPPO BCYTR
EOL 594807
Calflora (Californian flora) 9646
USDA GRIN 414012
Wikipedia Achlys_triphylla
CMAUP NPO5981
PFAF Achlys triphylla

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
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Microfungi associated with dying Euphorbia mauritanica in South Africa and their relative pathogenicity Marincowitz S, Pham NQ, Wingfield BD, Roets F, Wingfield MJ Fungal Syst Evol 31-Jul-2023
PMCID:PMC10976952
doi:10.3114/fuse.2023.12.04
PMID:38550751
The Spectrum of Pharmacological Actions of Syringetin and Its Natural Derivatives—A Summary Review Chmiel M, Stompor-Gorący M Nutrients 04-Dec-2022
PMCID:PMC9739508
doi:10.3390/nu14235157
PMID:36501187
Mahonia vs. Berberis Unloaded: Generic Delimitation and Infrafamilial Classification of Berberidaceae Based on Plastid Phylogenomics Hsieh CL, Yu CC, Huang YL, Chung KF Front Plant Sci 06-Jan-2022
PMCID:PMC8770955
doi:10.3389/fpls.2021.720171
PMID:35069611
Molecular Phylogeography and Ecological Niche Modeling of Sibbaldia procumbens s.l. (Rosaceae) Zhang HJ, Feng T, Landis JB, Deng T, Zhang X, Meng AP, Sun H, Wang HC, Sun YX Front Genet 13-Mar-2019
PMCID:PMC6424895
doi:10.3389/fgene.2019.00201
PMID:30918513
Coelomycetous Dothideomycetes with emphasis on the families Cucurbitariaceae and Didymellaceae Valenzuela-Lopez N, Cano-Lira JF, Guarro J, Sutton DA, Wiederhold N, Crous PW, Stchigel AM Stud Mycol 21-Nov-2017
PMCID:PMC5725287
doi:10.1016/j.simyco.2017.11.003
PMID:29255336
Didymellaceae revisited Chen Q, Hou LW, Duan WJ, Crous PW, Cai L Stud Mycol 09-Jun-2017
PMCID:PMC5498420
doi:10.1016/j.simyco.2017.06.002
PMID:28706324
Resolving the Phoma enigma Chen Q, Jiang JR, Zhang GZ, Cai L, Crous PW Stud Mycol 26-Nov-2015
PMCID:PMC4774273
doi:10.1016/j.simyco.2015.10.003
PMID:26955202
Nutrient-cycling microbes in coastal Douglas-fir forests: regional-scale correlation between communities, in situ climate, and other factors Shay PE, Winder RS, Trofymow JA Front Microbiol 08-Oct-2015
PMCID:PMC4597117
doi:10.3389/fmicb.2015.01097
PMID:26500636
The Importance of Large-Diameter Trees to Forest Structural Heterogeneity Lutz JA, Larson AJ, Freund JA, Swanson ME, Bible KJ PLoS One 20-Dec-2013
PMCID:PMC3869720
doi:10.1371/journal.pone.0082784
PMID:24376579
NOVEL ISOCOUMARIN DERIVATIVES FROM ACHLYS TRIPHYLLA (BERBERIDACEAE) Mizuo MIZUNO, Shinji YOSHIDA, Munekazu IINUMA, Toshiyuki TANAKA, Frank A. LANG, Kiyoto GOTO Pharmaceutical Society of Japan 07-Dec-2011
doi:10.1248/CPB.38.2075
Ecological contingency in the effects of climatic warming on forest herb communities Harrison S, Damschen EI, Grace JB Proc Natl Acad Sci U S A 25-Oct-2010
PMCID:PMC2984146
doi:10.1073/pnas.1006823107
PMID:20974978
Ethnoveterinary medicines used for ruminants in British Columbia, Canada Lans C, Turner N, Khan T, Brauer G, Boepple W J Ethnobiol Ethnomed 26-Feb-2007
PMCID:PMC1831764
doi:10.1186/1746-4269-3-11
PMID:17324258
Note: The Occurrence of Coumarin in Achlys Triphylla. C. E. Bradley American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JA01958A026
Chemical Constituents in the Genus Achlys Munekazu Iinuma, Hideki Tosa, Toshiyuki Tanaka, Mizuo Mizuno, Frank A. Lang American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50099A032

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/NP50099A032
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/NP50099A032
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
methyl (3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylate 44577732 Click to see 236.22 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Dihydroconiferyl alcohol 16822 Click to see 182.22 unknown via CMAUP database
N-(4-Hydroxy-2-methoxyphenyl)acetamide 68646525 Click to see 181.19 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(6S)-3-Methoxy-6alpha,7alpha-bis(hydroxymethyl)-8beta-(3-methoxy-4-hydroxyphenyl)-5,6,7,8-tetrahydro-2-naphthol 12311071 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2S,3R)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol 11552274 Click to see 362.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3R,4S)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 36688829 Click to see 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
[(1R)-3aalpha,4,6,6aalpha-Tetrahydro-1H,3H-furo[3,4-c]furan-1alpha,4alpha-diyl]bis(2-methoxy-4,1-phenylene)bis(beta-D-glucopyranoside) 45482330 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl triacontanate 12400 Click to see 466.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Triacontanal 3084375 Click to see 436.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoic acid 23724772 Click to see 270.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-(3,7-Dimethylocta-2,6-dienyl)-6,8-dihydroxy-3-[2-(4-hydroxyphenyl)ethenyl]isochromen-1-one 72737888 Click to see CC(=CCCC(=CCC1=C(C=C2C=C(OC(=O)C2=C1O)C=CC3=CC=C(C=C3)O)O)C)C 432.50 unknown https://doi.org/10.1248/CPB.38.2075
7-(3,7-Dimethylocta-2,6-dienyl)-6,8-dihydroxy-3-[2-(4-hydroxyphenyl)ethyl]isochromen-1-one 72737887 Click to see 434.50 unknown https://doi.org/10.1248/CPB.38.2075
7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-3-[(E)-2-(4-hydroxyphenyl)ethenyl]isochromen-1-one 14703257 Click to see CC(=CCCC(=CCC1=C(C=C2C=C(OC(=O)C2=C1O)C=CC3=CC=C(C=C3)O)O)C)C 432.50 unknown https://doi.org/10.1248/CPB.38.2075
7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-3-[2-(4-hydroxyphenyl)ethyl]isochromen-1-one 14703256 Click to see CC(=CCCC(=CCC1=C(C=C2C=C(OC(=O)C2=C1O)CCC3=CC=C(C=C3)O)O)C)C 434.50 unknown https://doi.org/10.1248/CPB.38.2075
https://doi.org/10.1021/NP50099A032
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-[7,7,12,16-Tetramethyl-6-(methylamino)-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadeca-8,14-dienyl]ethanone 162998788 Click to see 367.60 unknown https://doi.org/10.1021/NP50099A032
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(91)83058-S
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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/10.1016/0031-9422(91)83058-S
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/10.1016/0031-9422(91)83058-S
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
2-Oxo-5-guanidinopentanoate 25244978 Click to see C(CC(=O)C(=O)[O-])C[NH+]=C(N)N 173.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R,3R,4S,4aS,8aS)-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 11032509 Click to see 256.38 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-(beta-D-Mannopyranosyl)-beta-D-glucopyranose 42552697 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
beta-D-glucosyl-(1->4)-alpha-D-mannose 23657860 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 101928034 Click to see 328.31 unknown via CMAUP database
4-(beta-D-glucopyranosyloxy)benzoic acid 440186 Click to see 300.26 unknown via CMAUP database
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
Androsin 164648 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 328.31 unknown via CMAUP database
Caffeic Acid 4-O-Glucoside 14825516 Click to see 342.30 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Cynanoneside A 21591970 Click to see 314.29 unknown via CMAUP database
Dihydroconiferin 14427336 Click to see COC1=C(C=CC(=C1)CCCO)OC2C(C(C(C(O2)CO)O)O)O 344.36 unknown via CMAUP database
Melilotoside 5280759 Click to see 326.30 unknown https://doi.org/10.1016/0031-9422(91)83058-S
p-Coumaryl alcohol 4-O-glucoside 5280847 Click to see C1=CC(=CC=C1C=CCO)OC2C(C(C(C(O2)CO)O)O)O 312.31 unknown via CMAUP database
Picein 92123 Click to see 298.29 unknown via CMAUP database
Protocatechuic acid 4-glucoside 91309592 Click to see C1=CC(=C(C=C1C(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 316.26 unknown via CMAUP database
Pungenin 12314759 Click to see 314.29 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
GlyTouCan:G98033RN 91854746 Click to see 504.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dihydroxyacetophenone 14530 Click to see 152.15 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
Acetovanillone 2214 Click to see 166.17 unknown via CMAUP database
Methyl 2-acetyl-4,6-dimethoxybenzoate 44577731 Click to see 238.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,8-Dihydroxy-3-methyl-9-oxoxanthene-1-carboxylic acid methyl ester 44577694 Click to see 300.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(-)-(R)-Mellein 114679 Click to see 178.18 unknown via CMAUP database
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
3,4-Dihydro-8-hydroxy-6-methoxy-(3R)-propylisocoumarin 15391028 Click to see 236.26 unknown via CMAUP database
5-Methylmellein 14807789 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Butyl-4-methyl-furan-2(5h)-one 14616858 Click to see 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Trans-3-methyldodec-cis-6-en-4-olide 101251213 Click to see 210.31 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(2S)-1-[(2S,6R)-6-methylpiperidin-2-yl]propan-2-ol 10866594 Click to see 157.25 unknown via CMAUP database
Pinidinol 182960 Click to see CC1CCCC(N1)CC(C)O 157.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]oxane-3,4,5-triol 10625848 Click to see 522.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2R,3S)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101165148 Click to see 508.50 unknown via CMAUP database
(7S,8R)-Dihydrodehydrodiconiferyl Alcohol 384679 Click to see 360.40 unknown via CMAUP database
2,3-Dihydro-2beta-(4-hydroxy-3-methoxyphenyl)-3beta-(hydroxymethyl)-5-(3-hydroxypropyl)benzofuran-7-ol 101992982 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O 346.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1021/JA01958A026
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1021/NP50099A032
https://doi.org/10.1016/0031-9422(91)83058-S
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/0031-9422(91)83058-S
https://doi.org/10.1021/NP50099A032
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4R,5S,6S)-3-acetyloxy-6-[(2S,3R,4R,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl acetate 163028861 Click to see 724.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4R,5S,6S)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162962925 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)CO)O)O)O)O 682.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 101618937 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)CO)O)O)O)O 682.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 101618934 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)OC)O)OC)CO)O)O)O)O 712.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
[6-[2-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 74978254 Click to see 682.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
[6-[2-[5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 74978331 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)OC)O)OC)CO)O)O)O)O 712.60 unknown https://doi.org/10.1016/0031-9422(91)83058-S
3-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 101618936 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 640.50 unknown https://doi.org/10.1016/0031-9422(91)83058-S
Isorhamnetin 3-beta-laminaribioside 74977617 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 640.50 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
3-[(E)-2-(3,4-dihydroxyphenyl)vinyl]-6,8-dihydroxy-1H-isochromen-1-one 5324553 Click to see 312.27 unknown https://doi.org/10.1248/CPB.38.2075
3-[2-(3,4-Dihydroxyphenyl)ethenyl]-6,8-dihydroxyisochromen-1-one 78385764 Click to see C1=CC(=C(C=C1C=CC2=CC3=CC(=CC(=C3C(=O)O2)O)O)O)O 312.27 unknown https://doi.org/10.1248/CPB.38.2075
Sescandelin 10998597 Click to see 222.19 unknown via CMAUP database
Sescandelin B 71435035 Click to see CC1=C(C2=C(C(=CC(=C2)O)O)C(=O)O1)CO 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1021/NP50099A032
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Genistin 5281377 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1021/NP50099A032
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see 284.26 unknown https://doi.org/10.1016/0031-9422(91)83058-S
> Phenylpropanoids and polyketides / Macrolides and analogues
(3E,8S,11E,16S)-8,16-Bis(2-oxopropyl)-1,9-dioxacyclohexadeca-3,11-diene-2,5,10,13-tetrone 11101249 Click to see CC(=O)CC1CCC(=O)C=CC(=O)OC(CCC(=O)C=CC(=O)O1)CC(=O)C 392.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown via CMAUP database
Dihydroferulic Acid 14340 Click to see 196.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Isorhapontin 5281716 Click to see 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

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