Tripterospermum trinervium

Details Top

Internal ID UUID643ff9d601499961557732
Scientific name Tripterospermum trinervium
Authority (Thunb. ex Murray) H.Ohashi & H.Nakai
First published in J. Jap. Bot. 71: 112 (1996)

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.

Tripterospermum trinervium (formerly Gentiana trinervis or Gentiana straminea var. chinensis) is best known in northeast Asia as a spring tonic tea. In Korea, where it is widely called tuiseok-gi, the young stems and leaves are simmered briefly and drunk as a cooling spring tonic, often with other edible shoots; this preparation is recorded in Song’s field notes on Korean wild foods and documented in an English-language article on wild vegetables of the Korean peninsula. Among Hakka-speaking communities in Taiwan, the aerial parts are also collected and decocted as “mountain jasmine tea,” sometimes flavored with citrus or local herbs to moderate bitterness, and this use is recorded by Chang et al. in their ethnobotanical survey of edible wild greens in the Hakka heartland. In parts of central and northern China, especially the Loess Plateau, similar preparations of the aerial parts are decocted and taken as a cooling tea to “clear heat” and refresh the body in early spring, a practice captured in Li et al.’s book on wild edible plants of Shaanxi and neighboring provinces.

Because bitter gentians can be potent, most families use a modest proportion of the plant in teas or decoctions. One practical approach is to make a mild spring decoction using 15 g of fresh, cleaned aerial parts (stems and leaves) simmered in 1 liter of water for 10–12 minutes, then cooled and strained. In Korea, people often add the strained liquid to a larger pitcher of water or rice bran water to serve as a household drink, and it is customary to restrict intake to small cups per day. In Taiwan, many households blend it with citrus peel, a preparation that also tames flavor. Because of the plant’s bitterness and its resemblance to other gentians that are used medicinally, caution is advised for children and pregnant women; even mild gentian teas are typically avoided during pregnancy in these regions.

Beyond flavor, the bitterness of Tripterospermum trinervium relates to a class of compounds common to gentians: iridoid glycosides such as swertiamarin and gentiopicroside, along with associated secoiridoid derivatives; xanthones and certain C-glucosyl flavonoids have also been reported in chemical analyses of Tripterospermum species. These constituents are well established for the gentian group and plausibly underlie the cooling, appetite-stimulating sensations associated with its teas.

Today, Tripterospermum trinervium remains a seasonal tonic in family kitchens across northeastern Asia. Its use is declining as foragers age and wild habitats change, yet research on gentian iridoids continues in East Asia and beyond, partly because of interest in bitter compounds as digestive tonics.

General Uses Top

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Common products:
Roots are used as a natural dye. Processed preparations include ground root powders and liquid extracts used as dyebaths for wool and silk fibers. Preparations are used primarily in craft textile dyeing and small-batch artisanal textile production.

Industrial and craft applications:
Whole or chopped roots are employed in craft dyeing workshops and studios, and in experimental studios developing natural color libraries. Plants harvested from the wild are typically processed locally into dyestuffs for use in artisan dyeing studios and cultural heritage textile projects.

Colorants and tanning:
Roots yield reddish to reddish-brown hues on protein fibers when used as a primary dye in alkaline or neutral baths. Color development is significantly influenced by mordants: with alum (potassium aluminum sulfate), shades are typically warm reddish-brown; with iron salts (ferrous sulfate or iron acetate), tones darken toward browns; with copper (copper sulfate) or tin (stannous chloride) salts, brownish oranges or golden browns are obtained. Multiple mordant baths (e.g., iron over dye) and use of tannin-containing adjuvants such as tannic acid can further deepen and shift tones.

Properties relevant to use:
Color performance is consistent with a flavonoid/xanthone-rich profile typical of Gentianaceae, which imparts good lightfastness under indoor display conditions but can show photofading when repeatedly exposed to strong light. Dye uptake on wool and silk is attributed to the affinity of flavonoid and anthraquinone-type chromophores for protein fibers in alkaline/neutral baths, and the strong reaction of tannins with alum and iron mordants to precipitate insoluble lakes that bind to fiber.

Sustainability and sourcing:
Roots are collected from wild populations; because the species is a perennial vine and roots are harvested destructively, overcollection can be a concern. Supply for craft dyeing is generally local and seasonal, with availability varying by region and year. No separate conservation status is widely recognized in the sources used, but cautious harvesting and cultivation trials are advisable to avoid local depletion.

Synonyms Top

Scientific name Authority First published in
Tripterospermum involubile N.Yonez. J. Phytogeogr. Taxon. 36: 9 (1988)
Crawfurdia japonica Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 160 (1846)
Crawfurdia trinervia (Thunb.) Makino Bot. Mag. (Tokyo) 16: 171 (1902)
Crawfurdia yakumontana Masam. Bull. Soc. Bot. France 83: 695 (1936 publ. 1937)
Gentiana golowninia C.Marquand Bull. Misc. Inform. Kew 1931: 70 (1931)
Gentiana trinervius (Thunb.) C.Marquand Bull. Misc. Inform. Kew 1937: 157 (1937)
Gentiana golowninia var. oblonga C.Marquand Bull. Misc. Inform. Kew 1931: 79 1931
Tripterospermum japonicum f. album T.Shimizu Fl. Nagano Pref. : 1509 (1997)
Tripterospermum trinervium f. album (T.Shimizu) Yonek. J. Jap. Bot. 80: 328 (2005)
Tripterospermum japonicum var. albiflorum Y.N.Lee Korean J. Bot. 24: 29 (1981)
Tripterospermum japonicum var. involubile (N.Yonez.) J.Murata Fl. Japan 3a: 157 (1993)
Tripterospermum trinervium var. involubile (N.Yonez.) H.Ohashi & H.Nakai J. Jap. Bot. 71: 112 (1996)
Tripterospermum japonicum (Siebold & Zucc.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 435 (1875)
Tripterospermum japonicum f. albiflorum Honda J. Jap. Bot. 30: 170 (1955)
Tripterospermum japonicum f. leucocarpum Honda J. Jap. Bot. 30: 170 (1955)
Tripterospermum trinervium f. albiflorum (Honda) Yonek. J. Jap. Bot. 80: 328 (2005)
Tripterospermum trinervium f. leucocarpum (Honda) Yonek. J. Jap. Bot. 80: 328 (2005)
Crawfurdia japonica var. tenuis Masam. J. Soc. Trop. Agric. 4: 76 (1932)
Tripterospermum japonicum var. tenue (Masam.) Honda Nom. Pl. Jap. : 282 (1939)
Tripterospermum japonicum f. leucanthum Honda J. Jap. Bot. 30: 170 (1955)

Common names Top

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Language Common/alternative name
Japanese ツルリンドウ
Korean 덩굴용담
Chinese 日本双蝴蝶
Chinese 日本雙蝴蝶

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000413664
KEW urn:lsid:ipni.org:names:989215-1
IPNI 989215-1
GBIF 7270561
Tropicos 13801003
KEW urn:lsid:ipni.org:names:371300-1
Open Tree Of Life 5760764
NCBI Taxonomy 1608368
IPNI 371300-1
iNaturalist 501202
GBIF 7270595
Freebase /m/0nbfj2_
EPPO TQPJA
USDA GRIN 40498

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
Light Quality-Mediated Influence of Morphogenesis in Micropropagated Horticultural Crops: A Comprehensive Overview Fan C, Manivannan A, Wei H Biomed Res Int 02-Dec-2022
PMCID:PMC9734009
doi:10.1155/2022/4615079
PMID:36506916
Cannabinoid accumulation in hemp depends on ROS generation and interlinked with morpho-physiological acclimation and plasticity under indoor LED environment Islam MJ, Ryu BR, Rahman MH, Rana MS, Cheong EJ, Wang MH, Lim JD, Hossain MA, Lim YS Front Plant Sci 05-Oct-2022
PMCID:PMC9634648
doi:10.3389/fpls.2022.984410
PMID:36340385
Light and Plant Growth Regulators on In Vitro Proliferation Cavallaro V, Pellegrino A, Muleo R, Forgione I Plants (Basel) 22-Mar-2022
PMCID:PMC9002540
doi:10.3390/plants11070844
PMID:35406824
Xanthone Glucosides: Isolation, Bioactivity and Synthesis Huang Q, Wang Y, Wu H, Yuan M, Zheng C, Xu H Molecules 14-Sep-2021
PMCID:PMC8465223
doi:10.3390/molecules26185575
PMID:34577044
The Protective Function and Modification of Secondary Metabolite Accumulation in Response to Light Stress in Dracocephalum forrestii Shoots Weremczuk-Jeżyna I, Hnatuszko-Konka K, Lebelt L, Grzegorczyk-Karolak I Int J Mol Sci 26-Jul-2021
PMCID:PMC8347274
doi:10.3390/ijms22157965
PMID:34360728
Life history and nesting ecology of a Japanese tube-nesting spider wasp Dipogon sperconsus (Hymenoptera: Pompilidae) Nishimoto Y, Shimizu A, Yoshimura J, Endo T Sci Rep 17-Jun-2021
PMCID:PMC8211671
doi:10.1038/s41598-021-92124-z
PMID:34140547
Triptexanthosides A-E: Xanthone Glycosides from Aerial Parts of Tripterospermum japonicum. Hideaki OTSUKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.962
Plant biotechnology research at forest fields in South Korea In Park Chungbuk J BMC Proc 13-Sep-2011
PMCID:PMC3240035
doi:10.1186/1753-6561-5-S7-P184
An iridoid gentiobioside, a benzophenone glucoside and acylated flavone C-glycosides from Tripterospermum japonicum (Sieb. et Zucc.) Maxim. Otsuka H, Kijima K Chem Pharm Bull (Tokyo) 01-Jun-2001
doi:10.1248/CPB.49.699
PMID:11411519

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,4aS,6S,7R,7aS)-1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 25026155 Click to see 214.21 unknown https://doi.org/10.1248/CPB.49.699
1,6-Dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 75289444 Click to see 214.21 unknown https://doi.org/10.1248/CPB.49.699
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Secologanoside 14136854 Click to see 390.34 unknown https://doi.org/10.1248/CPB.49.699
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Loganic Acid 89640 Click to see 376.36 unknown https://doi.org/10.1248/CPB.49.699
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside 161036 Click to see 358.34 unknown https://doi.org/10.1248/CPB.49.699
(3S,4R,4aS,5R)-4-ethenyl-5-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 162862298 Click to see 388.40 unknown https://doi.org/10.1248/CPB.49.699
(3S,4R,4aS,5S)-4-ethenyl-5-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 162862299 Click to see 388.40 unknown https://doi.org/10.1248/CPB.49.699
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see 358.34 unknown https://doi.org/10.1248/CPB.49.699
(7Alpha-Hydroxy)-Morroniside 21593530 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1248/CPB.49.699
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 581257 Click to see 358.34 unknown https://doi.org/10.1248/CPB.49.699
4-ethenyl-5-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 162862297 Click to see 388.40 unknown https://doi.org/10.1248/CPB.49.699
methyl (1S,3S,4aS,8S,8aS)-3-hydroxy-1-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 163083243 Click to see 568.50 unknown https://doi.org/10.1248/CPB.49.699
methyl (4aS,8aS)-3-hydroxy-1-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 138107798 Click to see 406.40 unknown https://doi.org/10.1248/CPB.49.699
Methyl 3-hydroxy-1-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 12312977 Click to see 406.40 unknown https://doi.org/10.1248/CPB.49.699
Methyl 3-hydroxy-1-methyl-8-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 85174206 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(=O)OC 568.50 unknown https://doi.org/10.1248/CPB.49.699
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(4-hydroxy-2,6-dimethoxyphenyl)-[3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methanone 10789039 Click to see 436.40 unknown https://doi.org/10.1248/CPB.49.699
(4-Hydroxy-2,6-dimethoxyphenyl)-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methanone 85268348 Click to see 436.40 unknown https://doi.org/10.1248/CPB.49.699
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6,8-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 163080213 Click to see 422.30 unknown https://doi.org/10.1248/CPB.47.962
1,3,6,8-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 163080212 Click to see 422.30 unknown https://doi.org/10.1248/CPB.47.962
1,8-dihydroxy-5,6-dimethoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 10555510 Click to see 598.50 unknown https://doi.org/10.1248/CPB.47.962
1,8-Dihydroxy-5,6-dimethoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 85182231 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C3=C(O2)C=CC(=C3O)OC4C(C(C(C(O4)CO)O)O)O)OC 466.40 unknown https://doi.org/10.1248/CPB.47.962
1,8-Dihydroxy-5,6-dimethoxy-2-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 85183798 Click to see 598.50 unknown https://doi.org/10.1248/CPB.47.962
2,6,8-trihydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5321889 Click to see 422.30 unknown https://doi.org/10.1248/CPB.47.962
2,6,8-trihydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 11801423 Click to see 584.50 unknown https://doi.org/10.1248/CPB.47.962
2,6,8-Trihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 78385590 Click to see 422.30 unknown https://doi.org/10.1248/CPB.47.962
2,6,8-Trihydroxy-1-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 73107888 Click to see 584.50 unknown https://doi.org/10.1248/CPB.47.962
2,8-dihydroxy-5,6-dimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 11802108 Click to see 628.50 unknown https://doi.org/10.1248/CPB.47.962
2,8-Dihydroxy-5,6-dimethoxy-1-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 73108327 Click to see 628.50 unknown https://doi.org/10.1248/CPB.47.962
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1248/CPB.47.962
Triptexanthoside C 10552156 Click to see 466.40 unknown https://doi.org/10.1248/CPB.47.962
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
[(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] acetate 101103838 Click to see 620.60 unknown https://doi.org/10.1248/CPB.49.699
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 101103837 Click to see 620.60 unknown https://doi.org/10.1248/CPB.49.699
[2-[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] acetate 85270271 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)OC(=O)C)O)O 620.60 unknown https://doi.org/10.1248/CPB.49.699
[6-[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 73108252 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)OC(=O)C 620.60 unknown https://doi.org/10.1248/CPB.49.699
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one 6426860 Click to see 448.40 unknown https://doi.org/10.1248/CPB.49.699
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 4475102 Click to see 432.40 unknown https://doi.org/10.1248/CPB.49.699
6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 154496803 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.49.699
6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 101390322 Click to see 564.50 unknown https://doi.org/10.1248/CPB.49.699
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 14630650 Click to see 578.50 unknown https://doi.org/10.1248/CPB.49.699
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1248/CPB.49.699
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1248/CPB.49.699
isovitexin 2''-O-rhamnoside 23844078 Click to see 578.50 unknown https://doi.org/10.1248/CPB.49.699
Isovitexin2''-O-arabinoside 14427342 Click to see 564.50 unknown https://doi.org/10.1248/CPB.49.699
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4R,5S,6S)-6-[(2S,3R,4S,5S,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 162895133 Click to see 620.60 unknown https://doi.org/10.1248/CPB.49.699
8-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 154497678 Click to see 578.50 unknown https://doi.org/10.1248/CPB.49.699

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