Details Top

Internal ID UUID643ffea543a39796601837
Scientific name Trollius chinensis
Authority Bunge
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 2: 77 (1835)

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.

Based on ethnobotanical and pharmacopoeial literature, dried buds (flower buds) of Trollius chinensis are used as infusions and decoctions for respiratory and related inflammatory conditions in northern China. The China Pharmacopoeia describes the herb as a “clear heat and eliminate toxin” remedy taken as a decoction to treat wind–heat heat, sore throat, and tonsillitis (China Pharmacopoeia, 2015). In a review of Chinese materia medica, Bensky and Gamble note the same preparations—primarily hot infusions or short decoctions of the dried buds—for treating throat pain and swollen tonsils (Bensky & Gamble, 1993). A traditional drug monograph by the State Administration of Traditional Chinese Medicine (STCM) reiterates the warm infusion or decoction of the dried buds for throat ailments (State Administration of TCM, 1999). Modern herbal monographs also mention a “Jin Ling Hua Tea” marketed in China for sore throat and cold-related symptoms, prepared from the dried buds by infusion (Shanxi Yichuang Bioengineering, 2022). Collections of traditional formulas record the combination of these preparations with other herbs for tonsillitis, but the single-herb preparation is the well-documented form (Dai et al., 2015).

A simple mild tea can be prepared using about 3–4 g of dried buds in 200–250 ml of just-boiled water; steep 10–15 minutes, then drink 1–2 cups per day for 3–5 days. A stronger preparation uses the same herb quantity simmered in 200–250 ml of water for 10–12 minutes; cool and take up to one cup twice daily as needed for sore throat or tonsillitis. Safety notes: standard pharmacopoeial doses do not exceed 6–10 g per day; do not use during pregnancy or in young children without practitioner guidance; avoid concurrent use with highly anticoagulant medications. The plant contains flavonoids such as quercetin, kaempferol, and their glycosides, saponins (e.g., trollius saponins), and phenolic acids; these constituents are well reported for Trollius species and provide a plausible basis for the observed anti-inflammatory and antimicrobial activity of the bud preparations.

Commercial preparations remain available in China as bulk dried buds and as a proprietary “Jin Ling Hua tea,” and modern research has explored their anti-inflammatory effects in the context of upper respiratory inflammation (Chen et al., 2020), while traditional use in infusions and decoctions continues in both household and clinical settings.

General Uses Top

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Common products:
Ornamental plants and cut flowers. Trollius chinensis is cultivated in horticulture for its showy golden-yellow flowers, used in perennial borders, rock gardens, and as cut blooms for floral displays (Flora of China; Flora of USSR; horticultural catalogs).

Industrial and craft applications:
No non-medicinal industrial or craft uses are documented for this species.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses are reported.

Colorants and tanning:
No documented uses as a dye or tanning agent are recorded.

Wood and fiber:
No documented timber or fiber uses are reported.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses are recorded.

Properties relevant to use:
No properties relevant to non-medicinal use are documented.

Standards and regulation:
No standards or regulatory frameworks for this taxon in non-medicinal applications are reported.

Sustainability and sourcing:
No sustainability or sourcing information specific to this taxon is documented.

Synonyms Top

Scientific name Authority First published in
Trollius asiaticus var. chinensis (Bunge) Maxim. Enum. Fl. Mong. 25 1889
Trollius ledebourii var. macropetalus Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 4: 4 1861

Common names Top

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Language Common/alternative name
Finnish kesäkullero
Chinese 金莲花
Chinese 金疙瘩
Chinese 金蓮花
Chinese 中华金莲花
Chinese 中国金莲花
Chinese 中國金蓮花

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Buryatiya
      • Chita
      • Krasnoyarsk

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000455221
Tropicos 27101479
INPN 611700
KEW urn:lsid:ipni.org:names:715085-1
The Plant List kew-2514590
Plantarium 97945
Open Tree Of Life 877307
NCBI Taxonomy 78479
IPNI 715085-1
iNaturalist 84407
GBIF 7276979
EPPO TLUCH
EOL 2874032
USDA GRIN 40675
Wikipedia Trollius_chinensis
CMAUP NPO14715

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
Potential JAK2 Inhibitors from Selected Natural Compounds: A Promising Approach for Complementary Therapy in Cancer Patients Vaziri-Amjad S, Rahgosha R, Taherkhani A Evid Based Complement Alternat Med 26-Apr-2024
PMCID:PMC11068457
doi:10.1155/2024/1114928
PMID:38706884
Advances in Flavonoid Research: Sources, Biological Activities, and Developmental Prospectives Hao B, Yang Z, Liu H, Liu Y, Wang S Curr Issues Mol Biol 26-Mar-2024
PMCID:PMC11049524
doi:10.3390/cimb46040181
PMID:38666911
Combination of ethyl acetate fraction from Calotropis gigantea stem bark and sorafenib induces apoptosis in HepG2 cells Chaisupasakul P, Pekthong D, Wangteeraprasert A, Kaewkong W, Somran J, Kaewpaeng N, Parhira S, Srisawang P PLoS One 25-Mar-2024
PMCID:PMC10962855
doi:10.1371/journal.pone.0300051
PMID:38527038
Nitrogen acquisition strategy shifts with tree age depending on root functional traits and soil properties in Larix principis-rupprechtii plantations Liu Q, Chen Y, Chen Y Front Plant Sci 12-Mar-2024
PMCID:PMC10964345
doi:10.3389/fpls.2024.1358367
PMID:38533407
Highly Promiscuous Flavonoid Di-O-glycosyltransferases from Carthamus tinctorius L. Xu X, Xia M, Han Y, Tan H, Chen Y, Song X, Yuan S, Zhang Y, Su P, Huang L Molecules 26-Jan-2024
PMCID:PMC10856022
doi:10.3390/molecules29030604
PMID:38338349
Trollius chinensis Bunge: A Comprehensive Review of Research on Botany, Materia Medica, Ethnopharmacological Use, Phytochemistry, Pharmacology, and Quality Control He L, Wang Z, Lu J, Qin C, He J, Ren W, Liu X Molecules 15-Jan-2024
PMCID:PMC10819464
doi:10.3390/molecules29020421
PMID:38257334
Biosynthetic pathway of prescription bergenin from Bergenia purpurascens and Ardisia japonica Liu XY, Wang YN, Du JS, Chen BH, Liu KY, Feng L, Xiang GS, Zhang SY, Lu YC, Yang SC, Zhang GH, Hao B Front Plant Sci 04-Jan-2024
PMCID:PMC10794647
doi:10.3389/fpls.2023.1259347
PMID:38239219
Karyotypes and Physical Mapping of Ribosomal DNA with Oligo-Probes in Eranthis sect. Eranthis (Ranunculaceae) Mitrenina EY, Alekseeva SS, Badaeva ED, Peruzzi L, Artemov GN, Krivenko DA, Pinzani L, Aytaç Z, Çeçen Ö, Baasanmunkh S, Choi HJ, Mesterházy A, Tashev AN, Bancheva S, Lian L, Xiang K, Wang W, Erst AS Plants (Basel) 22-Dec-2023
PMCID:PMC10780877
doi:10.3390/plants13010047
PMID:38202355
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Integrated Metabolomic and Transcriptomic Analysis of Puerarin Biosynthesis in Pueraria montana var. thomsonii at Different Growth Stages Hu X, Zhu T, Min X, He J, Hou C, Liu X Genes (Basel) 18-Dec-2023
PMCID:PMC10742406
doi:10.3390/genes14122230
PMID:38137052
Comparative plastome genomics and phylogenetic relationships of the genus Trollius Li J, Du Y, Xie L, Jin X, Zhang Z, Yang M Front Plant Sci 17-Nov-2023
PMCID:PMC10690957
doi:10.3389/fpls.2023.1293091
PMID:38046610
Structure-function and engineering of plant UDP-glycosyltransferase Wang M, Ji Q, Lai B, Liu Y, Mei K Comput Struct Biotechnol J 27-Oct-2023
PMCID:PMC10641439
doi:10.1016/j.csbj.2023.10.046
PMID:37965058
Identification and Characterization of CtUGT3 as the Key Player of Astragalin Biosynthesis in Carthamus tinctorius L. Ren C, Xi Z, Xian B, Chen C, Huang X, Jiang H, Chen J, Peng C, Pei J J Agric Food Chem 23-Oct-2023
PMCID:PMC10623559
doi:10.1021/acs.jafc.3c05117
PMID:37870279
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Complete chloroplast genome of Adonis pseudoamurensis W.T.Wang (Ranunculaceae) Zhang XY, Zhang ZL, Zhang LQ, Zhang LF, Zhu JY, Xue CS Mitochondrial DNA B Resour 15-Sep-2023
PMCID:PMC10506428
doi:10.1080/23802359.2023.2256493
PMID:37727834

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
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1S,5S)-1,2,3,4,5,6-hexahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one 442949 Click to see 190.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Methyl phenylacetate 7559 Click to see 150.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl Benzoate 7150 Click to see 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> 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 via CMAUP database
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
Proglobeflowery acid 132759 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)OC)O)C 236.26 unknown https://doi.org/10.1080/1028602031000147393
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1080/1028602031000147393
Methyl 3,4-Dimethoxybenzoate 16522 Click to see COC1=C(C=C(C=C1)C(=O)OC)OC 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxybenzamide 73705 Click to see COC1=C(C=C(C=C1)C(=O)N)OC 181.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetic acids / 2(hydroxyphenyl)acetic acids
2-Hydroxy-5-butoxyphenylacetic acid 15108711 Click to see 224.25 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Butyl 2-(2,5-dihydroxyphenyl)acetate 44217017 Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)O 224.25 unknown via CMAUP database
Ethyl 2,5-dihydroxyphenylacetate 297396 Click to see CCOC(=O)CC1=C(C=CC(=C1)O)O 196.20 unknown via CMAUP database
Methyl 2-(2,5-dihydroxyphenyl)acetate 13790504 Click to see 182.17 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Homovanillyl alcohol 16928 Click to see 168.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see 154.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Dimethyl Azelate 15612 Click to see COC(=O)CCCCCCCC(=O)OC 216.27 unknown via CMAUP database
Dimethyl suberate 15611 Click to see 202.25 unknown via CMAUP database
Dimethyl Succinate 7820 Click to see COC(=O)CCC(=O)OC 146.14 unknown via CMAUP database
Methyl Decanoate 8050 Click to see 186.29 unknown via CMAUP database
Methyl Octanoate 8091 Click to see 158.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Entadamide-A-beta-D-glucopyranoside 101616680 Click to see CSC=CC(=O)NCCOC1C(C(C(C(O1)CO)O)O)O 323.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72737016 Click to see 1544.60 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72737187 Click to see 1586.70 unknown via CMAUP database
phaseoloideside A 72736851 Click to see 1512.60 unknown via CMAUP database
phaseoloideside B 72736852 Click to see 1412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Salmoxanthin 10507805 Click to see CC1=CC(CC(C1(C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C)O)(C)C)O 600.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
Entagenic acid 21594206 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(C(C2O)O)C)C)(C)C)O)C)C(=O)O)C 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3R,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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 12303645 Click to see 414.70 unknown via CMAUP database
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/10.1080/1028602031000147393
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/10.1080/1028602031000147393
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/10.1080/1028602031000147393
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1080/1028602031000147393
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Entadamide A 6439215 Click to see 161.22 unknown via CMAUP database
Entadamide B 3035981 Click to see CSC(CC(=O)NCCO)SC 209.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-beta-d-Glucopyranosyloxy-5-butoxyphenylacetic acid 15108713 Click to see 386.40 unknown via CMAUP database
butyl 2-[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetate 102143698 Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 386.40 unknown via CMAUP database
Phaseoloidin 14104237 Click to see 330.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
beta-D-Fructopyranose 24310 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(a1-2a)Fruf 11005647 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown via CMAUP database
GlyTouCan:G95076SI 11972400 Click to see 990.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol 5780 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Globeflowery acid 6451636 Click to see 236.26 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Dihydrobenzofuran 10329 Click to see 120.15 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(+-)-Trolline 21574476 Click to see 219.24 unknown https://doi.org/10.3987/COM-04-10062
(S)-(-)-oleracetin E 11160309 Click to see 219.24 unknown https://doi.org/10.3987/COM-04-10062
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
3-O-galloyl gallic acid methyl ester 10131824 Click to see COC(=O)C1=CC(=C(C(=C1)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 336.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(1R,8S,9R,16R,18S,27S)-9-(3,4-dihydroxyphenyl)-5,8,16,21,23-pentahydroxy-2,10,17,26-tetraoxaheptacyclo[14.11.1.01,13.03,12.06,11.018,27.020,25]octacosa-3(12),4,6(11),13,20,22,24-heptaen-15-one 101925531 Click to see 576.50 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
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 / Flavones
4H-1-Benzopyran-4-one, 2-(3,5-dihydroxyphenyl)-5,7-dihydroxy- 5487757 Click to see 286.24 unknown via CMAUP database
7,4'-Dihydroxyflavone 5282073 Click to see 254.24 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
Rhamnocitrin 5320946 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one 73829966 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1080/1028602031000147393
8-beta-D-Glucopyranosyl-3',4',5,7-tetrahydroxyflavone 44257907 Click to see 448.40 unknown via CMAUP database
Isoswertisin 44258317 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1080/1028602031000147393
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 https://doi.org/10.1080/1028602031000147393
https://doi.org/10.1016/S0378-8741(01)00410-X
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/S0378-8741(01)00410-X
https://doi.org/10.1080/1028602031000147393
Vitexin-7-olate 49791957 Click to see 431.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see 344.30 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1080/1028602031000147393
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4,4'-Dihydroxy-2'-methoxychalcone 5319688 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Integerrimine 5281733 Click to see 335.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Tannic Acid 16129778 Click to see 1701.20 unknown via CMAUP database

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