Stauntonia obovatifoliola

Details Top

Internal ID UUID64404732d0e2e752213484
Scientific name Stauntonia obovatifoliola
Authority Hayata
First published in Icon. Pl. Formosan. 8: 4 (1919)

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.

Dandelion (Taraxacum officinale) has been a familiar medicine and food in many parts of the world, and the preparations most consistently described in the literature are infusions and decoctions, with occasional use as tinctures and macerations. Among the Appalachian folk tradition of eastern North America, leaves, roots, and whole plants were infused as teas for “blood purifying,” coughs, and as diuretics, while roots were decocted for liver complaints (Vargo-Gogt, 1995). In traditional Eastern European practice, as reflected in European herbal materia medica, roots and aerial parts were taken as teas to support digestion and liver function, with the roots also given as decoctions for gall-bladder complaints (Bown, 1995). Farther east, in traditional Chinese medicine recorded by the Pharmacopoeia of the People’s Republic of China, the flower heads have been used as teas (infusions) to brighten the eyes and relieve headaches (Chinese Pharmacopoeia, 2020). While leaves and flowers are also eaten as vegetables, the uses most often linked to herbal practice rely on teas or decoctions rather than whole-food preparations.

A straightforward way to prepare the familiar dandelion leaf tea is a mild infusion. For one cup, place 2–4 g of dried dandelion leaves in a teapot or infuser, pour 200–250 mL of just-boiled water, cover, and steep for 5–10 minutes. Strain and drink 1–2 cups daily. As a general note for safety, dandelion is not recommended for people with bile duct obstruction, active gallbladder disease, or known allergy to Asteraceae; the sesquiterpene lactones can irritate the stomach in sensitive individuals and, as always with diuretics, individuals on lithium or potassium-depleting medications should use with medical guidance.

The plant’s traditional profile is reflected in its established constituents. The latex-rich roots contain taraxasterol, taraxerol, and other triterpenes; leaves provide sesquiterpene lactones such as taraxinic acid β-glucoside and guaianolide lactones, plus flavonoids, phenolic acids, and vitamins including vitamin C (Phytotherapy Research, 2020; Natural Product Communications, 2022). These compounds align with the long-noted diuretic, cholagogue, and bitter tonic actions that have led to infusions and decoctions for urinary and hepatic support.

Modern relevance remains strong. Dandelion leaf teas and root decoctions are still sold as herbal teas and appear in clinical research investigating diuretic and liver-supportive effects, while the flowers persist in proprietary products for eye comfort and traditional use in China continues alongside their use in foods and wines (Food & Chemical Toxicology, 2017; Journal of Ethnopharmacology, 2016).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Stauntonia obovatifolia var. pinninervis Hayata Icon. Pl. Formosan. 8: 5–6, pl. 3, f. 7–13 1919
Stauntonia hexaphylla f. cordata H.L.Li
Stauntonia obovatifoliola var. pinninervis Hayata Icon. Pl. Formosan. 8: 6 (1919)

Common names Top

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Language Common/alternative name
Chinese 橢圓葉石月
Chinese 石月

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070177
Tropicos 17700014
KEW urn:lsid:ipni.org:names:462130-1
The Plant List tro-17700014
Open Tree Of Life 1039086
NCBI Taxonomy 161271
IPNI 462130-1
GBIF 7306119
EOL 2903972
CMAUP NPO10155

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)!
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Title Authors Publication Released IDs
A comparative study of nutrient composition, bioactive properties and phytochemical characteristics of Stauntonia obovatifoliola flesh and pericarp Li R, Ru Y, Feng L, Wang Z, He X, Zhang X Front Nutr 09-Sep-2022
PMCID:PMC9501892
doi:10.3389/fnut.2022.1013971
PMID:36159481
Chemical Structure and Biological Activities of Secondary Metabolites from Salicornia europaea L. Kim S, Lee EY, Hillman PF, Ko J, Yang I, Nam SJ Molecules 13-Apr-2021
PMCID:PMC8069253
doi:10.3390/molecules26082252
PMID:33924656
Complete chloroplast genome sequence of Stauntonia hexaphylla (Ranunculales: Lardizabalaceae), a species endemic to Korea Kim Y, Shin J, Kim DW, Lee HS, Choi C Mitochondrial DNA B Resour 15-Mar-2021
PMCID:PMC7971286
doi:10.1080/23802359.2021.1885320
PMID:33796658
The complete chloroplast genome of Akebia trifoliata subsp. australis (Lardizabalaceae), a medicinal plant in China Yu A, Tan Q, Chen J, Huang H Mitochondrial DNA B Resour 16-Sep-2020
PMCID:PMC7782757
doi:10.1080/23802359.2020.1820398
PMID:33458157
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents Kuo RY, Qian K, Morris-Natschke SL, Lee KH Nat Prod Rep 13-Aug-2009
PMCID:PMC3773821
doi:10.1039/b810774m
PMID:19779642
Anti-HIV-1 protease triterpenoids from Stauntonia obovatifoliola Hayata subsp. intermedia. Wei Y, Ma CM, Chen DY, Hattori M Phytochemistry 01-Jun-2008
doi:10.1016/J.PHYTOCHEM.2008.03.004
PMID:18433808

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 / Anthracenes / Anthraquinones
1,5-Dihydroxy-3-methoxy-7-methylanthraquinone 15138599 Click to see 284.26 unknown via CMAUP database
1,5-Dihydroxy-3-methylanthraquinone 5316800 Click to see 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Veratraldehyde 8419 Click to see 166.17 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
CID 14139389 14139389 Click to see 272.40 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones
Przewalskin A 16090911 Click to see 402.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
gamma-Linolenic acid 5280933 Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol 101607178 Click to see 332.50 unknown via CMAUP database
(11R)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol 14587208 Click to see 284.40 unknown via CMAUP database
(11S)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol 14587207 Click to see 284.40 unknown via CMAUP database
(11S)-12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraene-4,5-diol 10040486 Click to see 300.40 unknown via CMAUP database
(1R,8S,10S)-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),5-diene-3,4-dione 102280560 Click to see 314.40 unknown via CMAUP database
1,2-Dihydrotanshinquinone 105119 Click to see CC1=CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4C 278.30 unknown via CMAUP database
6,7-Dehydroferruginol 10978982 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O 284.40 unknown via CMAUP database
Demethylsalvicanol 11666872 Click to see 318.40 unknown via CMAUP database
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown via CMAUP database
Lanigerol 188496 Click to see 302.50 unknown via CMAUP database
Przewalskin C 11566132 Click to see 330.50 unknown via CMAUP database
Przewalskin D 101375853 Click to see CC(C)C1=C(C(=C2C=C3C=CCC(C3CCC2=C1)(C)C)O)O 298.40 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1S,6R,19R,22R,28S,30S)-19-hydroxy-13,22,31,31-tetramethyl-19-(2-oxopropyl)-25-propan-2-yl-5,7,23,35-tetraoxanonacyclo[26.6.1.01,30.03,27.04,24.06,22.08,21.09,18.012,17]pentatriaconta-3,8(21),9(18),10,12,14,16,24,26-nonaen-20-one 57404390 Click to see 648.80 unknown via CMAUP database
(6R)-6-(hydroxymethyl)-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione 56967682 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO 310.30 unknown via CMAUP database
Cryptotanshinone 160254 Click to see 296.40 unknown via CMAUP database
Danshenol A 3083514 Click to see 336.40 unknown via CMAUP database
Dehydrodanshenol A 71816415 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC=C4C)(CC(=O)C)O 334.40 unknown via CMAUP database
Dihydrotanshinone I 11425923 Click to see 278.30 unknown via CMAUP database
Isograndifoliol 71816417 Click to see 302.40 unknown via CMAUP database
Miltipolone 10086184 Click to see 300.40 unknown via CMAUP database
Miltirone 160142 Click to see 282.40 unknown via CMAUP database
Przewaquinone A 619402 Click to see 310.30 unknown via CMAUP database
Przewaquinone C 56967683 Click to see 296.30 unknown via CMAUP database
Tanshindiol B 5321620 Click to see 312.30 unknown via CMAUP database
Tanshindiol C 126072 Click to see 312.30 unknown via CMAUP database
Tanshinone I 114917 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C 276.30 unknown via CMAUP database
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Carnosol 442009 Click to see 330.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,4S,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 24970456 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2O)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13878137 Click to see 604.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
10-Hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5319375 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)O)C)C)C 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 258538 Click to see 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
16beta-Hydroxylup-20(29)-en-3-one 163095425 Click to see 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 74376474 Click to see 438.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
9-(Hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 4483448 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 604.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Calenduladiol 461835 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Hederagenin 73299 Click to see 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lup-20(29)-ene-3,16-diol 260656 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Mesembryanthemoidigenic acid 21594136 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C(=O)O)C)C)C 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Resinone 101316848 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2O)C)C)(C)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3S,4aR,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-3,10-dihydroxy-9-(hydroxymethyl)-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 102408107 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)C(C5)O)C(=O)O)C)C)(C)CO)O 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
(4aS,6aR,6aS,6bR,8aR,9S,10R,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14191225 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)(C)CO)O 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
10-Hydroxy-9-(hydroxymethyl)-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14191224 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
3,10-Dihydroxy-9-(hydroxymethyl)-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 74376473 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)C(C5)O)C(=O)O)C)C)(C)CO)O 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
2-[(3R,4R,5R,8R,9R,10R,12S,13S,14R,15R)-4-(carboxymethyl)-12-hydroxy-4,9,10,13-tetramethyl-15-prop-1-en-2-yl-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylpropanoic acid 24970454 Click to see 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
2-[4-(carboxymethyl)-12-hydroxy-4,9,10,13-tetramethyl-15-prop-1-en-2-yl-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylpropanoic acid 74376472 Click to see 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
3-Epiakebonoic acid 14036558 Click to see 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
Akebonic Acid 14036559 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.004
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 25245849 Click to see 522.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Rosmadial 15801061 Click to see 344.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Danshinspiroketallactone 56956598 Click to see 268.31 unknown via CMAUP database
Epidanshenspiroketallactone 102004791 Click to see 268.31 unknown via CMAUP database
Przewalskin B 51002763 Click to see 330.40 unknown via CMAUP database
Salprzelactone 71816414 Click to see CC1COC(=O)C1C2C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2 296.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Salvianolic Acid B 6451084 Click to see 718.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database

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