Details Top

Internal ID UUID64401bcf0e36b002710068
Scientific name Euonymus tingens
Authority Wall.
First published in Fl. Ind. (Carey & Wallich ed.) 2: 406. 1824

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.

Among Himalayan and Bhutanese communities, Euonymus tingens is primarily used as a dye. Craftspersons in Uttarakhand macerate freshly cut branches and twigs in cold water to release a deep indigo‑to‑black dye, which they fix to wool and cotton with mordants (Singh et al., 2012). Folk practitioners in the Central Himalaya (Gurung community) and across Bhutan employ hot decoctions or infusions of leaves, bark, or wood—prepared alone or in multi‑herbal mixes—for fevers, dysentery, and minor skin complaints (Bhattarai & Silori, 2009; Wangchuk et al., 2013). In ayurvedic practice observed in Uttarakhand, bitter bark preparations are taken in small doses as digestive tonics, sometimes alongside honey or jaggery (Ahmad et al., 2012). The same dye practice is documented among Adi communities in the Eastern Himalayas (Mishra et al., 2010). Traditional uses are therefore specific to parts used and may include cold infusions of fresh branches for dye or warm decoctions of leaves/bark for fever and digestive complaints.

A practical, small‑scale, cold‑infusion dye for wool proceeds as follows. Weigh 30–40 grams of freshly cut Euonymus tingens twigs or bark (trimmed to 2–4 cm pieces) and place them in 500 ml of clean, preferably soft, cold water. Keep the vessel cool and shaded for 36–48 hours, agitating gently each day; strain and reserve the deep indigo‑black infusion. Mordant 50 grams of wool yarn in an alum solution (about 5 g alum per liter) for 15 minutes before dyeing, then simmer the mordanted yarn in the strained dye bath at 60–70 °C for 45–60 minutes with occasional gentle stirring. Rinse and dry in shade. Because all plant parts contain cardenolides, the preparation is for external use only; do not ingest, and keep away from children, pets, and pregnant individuals. High temperatures during dyeing are not recommended.

Well‑established constituents reported for Euonymus species include cardenolide glycosides such as evonimine and related cardenolides, with dihydroxy‑lupane‑type triterpenes, naphthoquinones, and steroids detected across the genus (Nakano et al., 1998; Wangchuk et al., 2013). These cardenolides plausibly underpin reported bitter and tonic actions and, together with triterpenes and naphthoquinones, may contribute to dye complexation with protein fibers in textile applications.

Commercial relevance today centers on dye plant supply and sustainable harvesting for artisans across Uttarakhand and Bhutan, while small ethnobotanical surveys continue to monitor community knowledge of fevers and digestive uses (Singh et al., 2012; Wangchuk et al., 2013).

General Uses Top

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Common products:
Euonymus tingens is cultivated primarily as an ornamental shrub. It is used in landscaping for its dense habit, glossy foliage, and small, bright fruits that attract birds. Horticulturists employ it for hedges, mixed borders, rock gardens, and container plantings. The plant is sold by specialty nurseries under the name “Himalayan Euonymus” and is valued for its evergreen leaves and autumn coloration. Mature specimens reach 2–3 m in height and have upright, slender stems with opposite, ovate to lanceolate leaves that turn from deep green to reddish‑bronze in autumn. Small greenish‑white flowers appear in late spring, followed by bright orange‑red capsules that split open to reveal fleshy seeds, providing visual interest and wildlife food. Euonymus tingens thrives in well‑drained, loamy soils in full sun to partial shade and is hardy in USDA zones 5–7. Propagation is by seed, which requires cold stratification for germination, or by semi‑hardwood cuttings taken in late summer. The species is listed in horticultural catalogues of Himalayan flora and is occasionally offered in plant exchanges focused on cold‑hardy evergreen shrubs. Its tolerance of pruning makes it suitable for formal hedges, while its natural arching habit allows informal use as a screening shrub in mixed plantings.

Sustainability and sourcing:
Euonymus tingens is native to the Himalayan region, occurring in India, Nepal, Bhutan, and parts of Pakistan at elevations of 1500–3000 m in forest margins, shrublands, and rocky slopes. Within its natural range the species is locally common and not considered threatened. Commercial cultivation supplies the ornamental market, and wild collection is minimal; most nursery stock is propagated in horticultural facilities. The plant is not listed in CITES appendices, and regional conservation assessments classify it as Least Concern. Sustainable horticultural practices—such as seed collection from cultivated specimens, propagation by cuttings, and the use of locally sourced substrate—are encouraged to reduce pressure on wild populations. In horticultural trade, Euonymus tingens is generally marketed through specialty nurseries that emphasize its native origin and suitability for temperate gardens. International seed exchange networks also include the species, facilitating its conservation ex situ.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 白皮
Chinese 染用卫矛
Chinese 有色卫矛
Chinese 脉瓣卫矛
Chinese 阿于好

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000682117
Tropicos 6600006
KEW urn:lsid:ipni.org:names:161154-1
The Plant List kew-2803668
Open Tree Of Life 169628
NCBI Taxonomy 1089406
IPNI 161155-1
iNaturalist 542575
GBIF 3793460
EPPO EUOTI
EOL 2878274
CMAUP NPO849

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
Ethnomedicinal Plants Used in the Health Care System: Survey of the Mid Hills of Solan District, Himachal Pradesh, India Kumar M, Radha, Devi H, Prakash S, Rathore S, Thakur M, Puri S, Pundir A, Bangar SP, Changan S, Ilakiya T, Samota MK, Damale RD, Singh S, Berwal MK, Dhumal S, Bhoite AG, Sharma A, Senapathy M, Bhushan B, Maurya VK, Asha, Natta S, Amarowicz R, Mekhemar M Plants (Basel) 05-Sep-2021
PMCID:PMC8467016
doi:10.3390/plants10091842
PMID:34579373
Differentiation in stem and leaf traits among sympatric lianas, scandent shrubs and trees in a subalpine cold temperate forest Zhang KY, Yang D, Zhang YB, Ellsworth DS, Xu K, Zhang YP, Chen YJ, He F, Zhang JL Tree Physiol 05-Apr-2021
PMCID:PMC8597974
doi:10.1093/treephys/tpab049
PMID:33823048
Development and Validation of an HPLC-PDA Method for Biologically Active Quinonemethide Triterpenoids Isolated from Maytenus chiapensis Taddeo VA, Castillo UG, Martínez ML, Menjivar J, Jiménez IA, Núñez MJ, Bazzocchi IL Medicines (Basel) 07-Mar-2019
PMCID:PMC6473362
doi:10.3390/medicines6010036
PMID:30866563
Morphological study of floral nectaries in Euonymus and the probable origin of the echinate fruit surface Yao C, Zuo Y, Du C, Ma J Plant Divers 04-Jan-2018
PMCID:PMC6091930
doi:10.1016/j.pld.2017.12.004
PMID:30159539
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Tingenone and hydroxytingenone, triterpenoid quinone methides from Euonymus tingens P. Margaret Brown, Michael Moir, Ronald H. Thomson, Trevor J. King, Velagalety Krishnamoorthy, Tiruvenkata R. Seshadri Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19730002721

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 / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3-(4-Hydroxyphenyl)propanol 82452 Click to see 152.19 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)- 11063784 Click to see 214.21 unknown via CMAUP database
3-(Hydroxymethyl)-5-methoxyphenol 592986 Click to see COC1=CC(=CC(=C1)O)CO 154.16 unknown via CMAUP database
Dihydroconiferyl alcohol 16822 Click to see 182.22 unknown via CMAUP database
Erythro-Guaiacylglycerol 12310250 Click to see 214.21 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
erythro-Guaiacylglycerol beta-dihydroconiferyl ether 13893597 Click to see 378.40 unknown via CMAUP database
threo-(7R,8R)-3-methoxy-8,4'-oxyneoligna-3',4,7,9,9'-pentol 11793120 Click to see 364.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 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
(-)-Matairesinol 119205 Click to see 358.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2R,3R)-2,3-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10883321 Click to see 376.36 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R,3S)-2,3-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11824948 Click to see COC1=C(C=CC(=C1)C(C(COC2C(C(C(C(O2)CO)O)O)O)O)O)O 376.36 unknown via CMAUP database
1-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-1-one 51136357 Click to see COC1=C(C=CC(=C1)C(=O)CCOC2C(C(C(C(O2)CO)O)O)O)O 358.34 unknown via CMAUP database
6S,9R-Roseoside 9930064 Click to see 386.40 unknown via CMAUP database
Citrusin D 10914828 Click to see 342.34 unknown via CMAUP database
icariside B5 14135399 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 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 / Prenol lipids / Diterpenoids
(1R,2R,4aR,8aS)-2,5,5,8a-tetramethyl-1-(3-methylidenepent-4-enyl)-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 6565031 Click to see 290.50 unknown via CMAUP database
(1R,4aR,4bR,10aR)-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4,4b,5,10,10a-hexahydro-2H-phenanthrene-1-carboxylic acid 52325861 Click to see 316.40 unknown via CMAUP database
(1R,4aR,4bR,6S,10aS)-6-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 52325855 Click to see CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C 318.40 unknown via CMAUP database
(3S)-5-[(1S,4aR,5R,8aR)-5-(acetyloxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 101006381 Click to see 364.50 unknown via CMAUP database
(3S)-5-[(1S,4aR,5R,8aR)-5-methoxycarbonyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 51693032 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC(=O)O 350.50 unknown via CMAUP database
[(1R,4aR,4bS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl]methanol 92261496 Click to see 288.50 unknown via CMAUP database
12-Hydroxyabietic acid 52325853 Click to see 318.40 unknown via CMAUP database
12-Hydroxydehydroabietic Acid 13370050 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O 316.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see 316.40 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Isoabienol 11220007 Click to see 290.50 unknown via CMAUP database
Pinifolic Acid 12314311 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O 336.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,7-dimethylchromen-5-ol 45278176 Click to see 326.50 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
beta-Pinene, (+)- 10290825 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
gamma-Terpineol 11467 Click to see CC(=C1CCC(CC1)(C)O)C 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
2-[(1S)-3-methylcyclohex-2-en-1-yl]propan-2-ol 101198558 Click to see 154.25 unknown via CMAUP database
3,6,6-Trimethylcyclohepta-2,4-dien-1-one 14314225 Click to see CC1=CC(=O)CC(C=C1)(C)C 150.22 unknown via CMAUP database
3,7,7-Trimethyl1,3,5-cycloheptatriene 576718 Click to see 134.22 unknown via CMAUP database
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown via CMAUP database
Sylveterpinolene 524200 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown via CMAUP database
Grifolin 5372312 Click to see CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 328.50 unknown via CMAUP database
Neogrifolin 9874426 Click to see 328.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacra-1(10),5-dien-4beta-ol 11148775 Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
25-Methylpisolactone 101705403 Click to see 484.80 unknown via CMAUP database
Pisolactone 14167274 Click to see CC(C)C1CC(OC1=O)C(C)C2CCC3(C2(CCC4=C3CCC5C4(CCC(C5(C)C)O)C)C)C 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Androstenedione 6128 Click to see 286.40 unknown via CMAUP database
> 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 via CMAUP database
Sitostanol 241572 Click to see 416.70 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Enniatin B 164754 Click to see 639.80 unknown via CMAUP database
Enniatin B1 11262300 Click to see 653.80 unknown via CMAUP database
Enniatin B2 44559513 Click to see 625.80 unknown via CMAUP database
Enniatin B4 3010886 Click to see 653.80 unknown via CMAUP database
Enniatin J1 11814110 Click to see 611.80 unknown via CMAUP database
Enniatin K1 11006677 Click to see CCC1C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N(C(C(=O)OC(C(=O)N1C)C(C)C)C(C)C)C)C(C)C)C(C)C)C)C(C)C 625.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(1S,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44577289 Click to see 376.36 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
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
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
Raspberryketone glucoside 5320521 Click to see 326.34 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
Zingerone beta-D-glucopyranoside 90743708 Click to see 356.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
Acetylacetone 31261 Click to see 100.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
20alpha-Hydroxytingenone 10717799 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown https://doi.org/10.1039/P19730002721
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see 420.60 unknown https://doi.org/10.1039/P19730002721
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-(beta-D-Glucopyranosyloxy)-1-(4-hydroxy-3-methoxyphenyl)ethanone 101992980 Click to see COC1=C(C=CC(=C1)C(=O)COC2C(C(C(C(O2)CO)O)O)O)O 344.31 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxazoles
2-[[(2R,3S,6R,8S,9S)-3,9-dimethyl-2-[(2R)-1-oxo-1-(1H-pyrrol-2-yl)propan-2-yl]-1,7-dioxaspiro[5.5]undecan-8-yl]methyl]-1,3-benzoxazole-4-carboxylic acid 102499957 Click to see CC1CCC2(CCC(C(O2)C(C)C(=O)C3=CC=CN3)C)OC1CC4=NC5=C(C=CC=C5O4)C(=O)O 480.60 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
Indole-3-acetic acid 802 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)O 175.18 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
(1s,5r)-1-Methyl-9-azabicyclo[3.3.1]nonan-3-one 161131 Click to see CC12CCCC(N1)CC(=O)C2 153.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(2R)-1-[(2R)-6-methyl-2,3,4,5-tetrahydropyridin-2-yl]propan-2-ol 101651530 Click to see CC1=NC(CCC1)CC(C)O 155.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4R,5R,6S)-2-[4-[(2R,3R)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 101992984 Click to see 492.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2R,3R)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101992983 Click to see 508.50 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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
Epirobinetinidol-(4I(2),8)-catechin 13831060 Click to see 594.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
3'-O-Methylcatechin 14332899 Click to see 304.29 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Kaempferol 3-(3,6-di-p-coumaroylglucoside) 10032927 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 740.70 unknown via CMAUP database
quercetin 3-O-(3',6"-O-di-p-coumaroyl)-glucoside 23265223 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 756.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Quercetin-3'-glucoside 9934142 Click to see 464.40 unknown via CMAUP database
Taxifolin 3'-glucoside 14282774 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(+)-Catechin 3-glucoside 14104302 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 452.40 unknown via CMAUP database
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Quercetin 3-O-(6-O-acetyl-beta-D-glucopyranoside) 10006384 Click to see 506.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Taxifolin 7-glucoside 14282775 Click to see 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Sylpin 44258710 Click to see CC1=CC(=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
6-Methyl-7-O-methylaromadendrin 102004632 Click to see CC1=C(C=C2C(=C1O)C(=O)C(C(O2)C3=CC=C(C=C3)O)O)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin 5280457 Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O 212.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Pinostilbenoside 23271974 Click to see 404.40 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 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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