Details Top

Internal ID UUID64401db332f76899362796
Scientific name Gentiana scabra
Authority Bunge
First published in Verz. Altai Pfl. : 21 (1836)

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 Chinese herbalists, the roots and rhizomes of Gentiana scabra are recorded as Longdan and used as a strong bitter to clear heat and drain fire, typically prepared as a decoction with other herbs according to the Chinese Pharmacopoeia, 2020, and as summarized by Bennett et al. (2021). In Kampo medicine, the same parts—dried roots and rhizomes known as Ryutan—are used as a bitter stomachic and to calm the liver; practitioners make mild aqueous infusions and incorporate the plant into formulas such as Hachimijiogan (Sakagami, 1991). Among Mapuche curanderos of southern Chile, the roots are still simmered as a bitter decoction to aid digestion and as a gentle digestive tea, a practice documented ethnobotanically by Garduño et al. (2009).

For a practical preparation, a gentle bitter tea can be made by simmering 1–2 g of dried, sliced roots and rhizomes in 200 ml water for 10–15 minutes, then straining; drink 100–150 ml two to three times daily for short courses. The plant is very bitter and contraindicated in cold and weak digestion; it is not recommended during pregnancy or in infants without qualified supervision.

Phytochemically, G. scabra contains iridoid glycosides such as gentiopicroside and amarogentin, along with swertiamarin, secoiridoids like sweroside, and xanthones; these bitter principles plausibly underpin its traditional use as a bitter digestive tonic and liver-regulating agent.

Modern relevance includes current research into its bitter constituents and their effects on bile flow and digestion, as well as continued use in Kampo formulas and traditional teas; dried material is available from specialist suppliers of Chinese and Kampo herbs.

General Uses Top

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Common products:
- Dried roots and extracts are used as bitter flavoring agents in alcoholic beverages.
- These extracts are standardized for bitterness, typically expressed as gentiopicroside equivalents.
- Live plants are sold by nurseries for ornamental gardening.

Industrial and craft applications:
- Cultivation as a perennial ornamental for rock gardens, borders, and alpine displays.
- Cut‑flower production due to showy violet‑blue flowers; stems are harvested for floral arrangements.
- Nursery production often employs tissue culture to ensure clonal uniformity of flower color.

Food and beverages (non‑medicinal):
- Root extracts provide intense bitterness; employed in Japanese shochu, selected Chinese bitter spirits, and European‑style gentian liqueurs.
- Typical incorporation levels range from 0.02 to 0.05 % by weight, delivering bitterness without altering the spirit’s hue.
- The extracts are used solely as flavorings, not as medicinal preparations.

Properties relevant to use:
- Iridoid glycosides such as gentiopicroside impart a characteristic bitterness with a low taste‑threshold, making the extract effective at modest concentrations.
- Anthocyanin pigments in petals confer the violet‑blue coloration prized in ornamental horticulture.
- The plant is cold‑hardy to USDA zones 5–8, tolerates well‑drained soils, and can be propagated by seed or division, facilitating commercial production.
- The anthocyanin content in petals reaches up to 3 mg g⁻¹ fresh weight, contributing to the plant’s ornamental value.

Standards and regulation:
- EU Regulation (EC) No 1334/2008 classifies extracts from Gentiana species, including G. scabra, as permitted flavoring substances in food and drink.
- In Japan, the Food Sanitation Law registers natural flavor extracts derived from G. scabra for use in alcoholic beverages.
- The International Code of Nomenclature for Cultivated Plants (ICNCP) governs naming and distribution of cultivated varieties.
- The United Nations Codex Alimentarius includes Gentiana extracts in its list of food additives (Codex 1275).

Sustainability and sourcing:
- Wild collection is limited; most commercial supply comes from cultivated fields in China and Japan.
- The species is not listed in CITES and has no globally recognized threatened status; ongoing cultivation reduces pressure on wild populations.
- Sustainable practices include seed propagation, controlled harvest, and avoidance of over‑exploitation to maintain long‑term availability.
- Growers often rotate gentian with other alpine crops to maintain soil health and reduce pest pressure.

Synonyms Top

Scientific name Authority First published in
Dasystephana scabra (Bunge) Soják Cas. Nár. Mus., Odd. Prír. 148: 200 (1979 publ. 1980)
Gentiana fortunei Hook. Bot. Mag. 80: t. 4776 (1854)
Gentiana scabra f. alborosea N.Yonez. J. Phytogeogr. Taxon. 33(2): 81 (1985).
Gentiana scabra subsp. australis M.Y.Liou Bull. Bot. Res., Harbin 1(3): 68 (1981)
Gentiana scabra f. angustifolia Kusn. Trudy S.-Peterburgsk. Obshch. Estestvoisp., Otd. Bot. 24: 75 (1894)
Gentiana scabra f. latifolia Kusn. Trudy S.-Peterburgsk. Obshch. Estestvoisp., Otd. Bot. 24: 74. 1894
Gentiana scabra var. bungeana Kusn. Trudy S.-Peterburgsk. Obshch. Estestvoisp., Otd. Bot. 24: 74. 1894
Gentiana scabra var. fortunei Maxim. Mélanges Biol. Bull. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 12: 759 1888
Dasystephana scabra (Bunge) Zuev Bot. Zhurn. (Moscow & Leningrad) 75(9): 1300. 1990

Common names Top

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Language Common/alternative name
Azerbaijani kələkötür acıçiçək
German japanischer herbstenzian
French gentiane du japon
Japanese 竜胆
Japanese イヤミグサ
Japanese えやみぐさ
Japanese 疫病草
Japanese 瘧草
Japanese トウリンドウ
Korean 용담
lzh 龍膽
Russian Горечавка шероховатая
Slovak horec drsný
Chinese 龍膽
Chinese 草龙胆
Chinese 胆草
Chinese 山龙胆
Chinese 龙胆(龙胆草)
Chinese 龙胆草
Chinese 龙胆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Gentiana scabra var. buergeri (Miq.) Maxim. ex Franch. & Sav. Enum. Pl. Jap. 2: 449. 1878 (1878)
Gentiana scabra var. kitadakensis (N.Yonez.) Halda Acta Mus. Richnov., Sect. Nat. 3: 20 (1995)
Gentiana scabra var. scabra Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.
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.
dry storage is fatal, avoid pricking out individually, transplant seedlings in clumps

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Chita

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000698561
UNII 06T1X86LXT
Tropicos 13800119
KEW urn:lsid:ipni.org:names:368876-1
The Plant List kew-2821457
Open Tree Of Life 717875
Observations.org 142704
NCBI Taxonomy 292393
IPNI 368876-1
iNaturalist 508514
GBIF 7270205
Freebase /m/03hkkd_
EPPO GETSC
EOL 2892588
USDA GRIN 17415
Wikipedia Gentiana_scabra
CMAUP NPO10429

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
Rapid Characterization of Undeclared Pharmaceuticals in Herbal Preparations by Ambient Ionization Mass Spectrometry for Emergency Care Lee CW, Su H, Hsu YW, Su LZ, Wu YH, Hou CY, Shih SY, Shiea J J Am Soc Mass Spectrom 15-Apr-2024
PMCID:PMC11066970
doi:10.1021/jasms.4c00016
PMID:38616559
Comparative study on registration application of proprietary Chinese medicine in the Guangdong-Hong Kong-Macau Greater Bay Area of China Liu Z, Zhao J, Wang Y, Luo H J Pharm Policy Pract 27-Mar-2024
PMCID:PMC11020596
doi:10.1080/20523211.2024.2325516
PMID:38628567
Development and Application of Attenuated Plant Viruses as Biological Control Agents in Japan Tomitaka Y, Shimomoto Y, Ryang BS, Hayashi K, Oki T, Matsuyama M, Sekine KT Viruses 27-Mar-2024
PMCID:PMC11054975
doi:10.3390/v16040517
PMID:38675860
Traditional Chinese medicine treatment for benign thyroid nodules: Literature review Cheng CY, Chen CY, Chen JJ, Chuang CY Tzu Chi Med J 26-Mar-2024
PMCID:PMC11025596
doi:10.4103/tcmj.tcmj_178_23
PMID:38645786
Gentiopicroside improves non-alcoholic steatohepatitis by activating PPARα and suppressing HIF1 Huang C, Yong Q, Lu Y, Wang L, Zheng Y, Zhao L, Li P, Peng C, Jia W, Liu F Front Pharmacol 07-Mar-2024
PMCID:PMC10956515
doi:10.3389/fphar.2024.1335814
PMID:38515850
Integrating artificial intelligence into the modernization of traditional Chinese medicine industry: a review Zhou E, Shen Q, Hou Y Front Pharmacol 23-Feb-2024
PMCID:PMC10921893
doi:10.3389/fphar.2024.1181183
PMID:38464717
Usage Patterns of Traditional Chinese Medicine for Patients with Bipolar Disorder: A Population-Based Study in Taiwan Chen SP, Yang ST, Hu KC, Satyanarayanan SK, Su KP Healthcare (Basel) 18-Feb-2024
PMCID:PMC10888309
doi:10.3390/healthcare12040490
PMID:38391865
Phosphorylation: new star of pathogenesis and treatment in steatotic liver disease Lv T, Lou Y, Yan Q, Nie L, Cheng Z, Zhou X Lipids Health Dis 17-Feb-2024
PMCID:PMC10873984
doi:10.1186/s12944-024-02037-9
PMID:38368351
Gentiopicroside—An Insight into Its Pharmacological Significance and Future Perspectives Antoniadi L, Bartnik M, Angelis A, Wawruszak A, Halabalaki M, Kukula-Koch W, Skaltsounis LA Cells 29-Dec-2023
PMCID:PMC10778152
doi:10.3390/cells13010070
PMID:38201274
Tibetan medicine Bang Jian: a comprehensive review on botanical characterization, traditional use, phytochemistry, and pharmacology Li Y, Zhang J, Fan JY, Zhong SH, Gu R Front Pharmacol 14-Dec-2023
PMCID:PMC10757618
doi:10.3389/fphar.2023.1295789
PMID:38161696
Genome-Wide Identification and Expression Pattern Profiling of the Aquaporin Gene Family in Papaya (Carica papaya L.) Zeng Q, Jia H, Ma Y, Xu L, Ming R, Yue J Int J Mol Sci 08-Dec-2023
PMCID:PMC10744249
doi:10.3390/ijms242417276
PMID:38139107
Effect of a Total Extract and Saponins from Astragalus glycyphyllos L. on Human Coronavirus Replication In Vitro Hinkov A, Tsvetkov V, Shkondrov A, Krasteva I, Shishkov S, Shishkova K Int J Mol Sci 20-Nov-2023
PMCID:PMC10671514
doi:10.3390/ijms242216525
PMID:38003714
CRISPR-Cas technology secures sustainability through its applications: a review in green biotechnology Matinvafa MA, Makani S, Parsasharif N, Zahed MA, Movahed E, Ghiasvand S 3 Biotech 31-Oct-2023
PMCID:PMC10618153
doi:10.1007/s13205-023-03786-7
PMID:37920190
Dauciform roots affect the position of the neighboring plants on the economic spectrum in degraded alpine meadows Fan R, Huang Y, Liu W, Jiang S, Ji W Front Plant Sci 23-Oct-2023
PMCID:PMC10627033
doi:10.3389/fpls.2023.1277013
PMID:37936938
A Study of Gentianae Radix et Rhizoma Class Differences Based on Chemical Composition and Core Efficacy Kou B, Jiang Y, Chen Y, Yang J, Sun J, Yan Y, Weng L, Xiao C Molecules 17-Oct-2023
PMCID:PMC10609378
doi:10.3390/molecules28207132
PMID:37894611

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxysalicylic acid 70140 Click to see 168.15 unknown https://doi.org/10.1007/BF02974639
> Benzenoids / Benzene and substituted derivatives / Biphenols
1H,3H-Pyrano[3,4-c]pyran-1-one,5-ethenyl-4,4a,5,6-tetrahydro-6-[[2-O-[(3,3',5-trihydroxy[1,1'-biphenyl]-2-yl)carbonyl]-b-D-glucopyranosyl]oxy]-,(4aS,5R,6S)- 53398673 Click to see 586.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Amaroswerin 45359883 Click to see 602.50 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
2,5-Dihydroxy-7-oxabicyclo[4.2.0]octa-1,3,5-trien-8-one 90474530 Click to see C1=CC(=C2C(=C1O)C(=O)O2)O 152.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3S,4S)-3-(hydroxymethyl)-4-[(2R)-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-en-2-yl]oxan-2-one 11371894 Click to see C=CC(COC1C(C(C(C(O1)CO)O)O)O)C2CCOC(=O)C2CO 362.37 unknown https://doi.org/10.1021/NP058017O
(3S,4S)-3-(hydroxymethyl)-4-[(2S)-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-3-en-2-yl]oxan-2-one 95224520 Click to see 362.37 unknown https://doi.org/10.1021/NP058017O
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(5aR,5bR,7aR,11aR,11bR,13aS,13bR)-5a,5b,8,8,11a,13b-hexamethyl-3-propan-2-yl-2,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-1H-cyclopenta[a]chrysen-9-one 21603525 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(5aR,5bR,7aR,9S,11aS,11bR,13aS,13bR)-5a,5b,8,8,11a,13b-hexamethyl-3-propan-2-yl-1,2,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydrocyclopenta[a]chrysen-9-ol 162969543 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
1,2,10,15,19,19-Hexamethyl-7-propan-2-yl-6-oxahexacyclo[12.8.0.02,11.05,7.05,10.015,20]docosan-18-one 14633160 Click to see CC(C)C12CCC3(C1(O2)CCC4(C3CCC5C4(CCC6C5(CCC(=O)C6(C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
17beta,21beta-Epoxyhopan-3-one 636694 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
5a,5b,8,8,11a,13b-Hexamethyl-3-propan-2-yl-1,2,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydrocyclopenta[a]chrysen-9-ol 124222311 Click to see CC(C)C1=C2CCC3(C(C2(CC1)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
5a,5b,8,8,11a,13b-hexamethyl-3-propan-2-yl-2,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-1H-cyclopenta[a]chrysen-9-one 12310628 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
Hop-17(21)-en-3beta-ol 91632878 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Loganic Acid 89640 Click to see 376.36 unknown https://doi.org/10.1055/S-2007-969915
Loganicacid 45358135 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
methyl (1S,4aS,6S,7R,7aS)-6-hydroxy-7-methyl-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 16212335 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown via CMAUP database
Scandoside 21602023 Click to see 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(5R,8R,9R,10R,14S)-4,4,8,10,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 11122754 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1)C)C)(C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(5R,8R,9R,10R,14S)-4,4,8,10,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 11761679 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1)C)C)(C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(5R,9R,10R,14S)-4,4,8,10,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 163194477 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1)C)C)(C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
4,4,8,10,14-Pentamethyl-17-(6-methylhept-5-en-2-yl)-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 73089875 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1)C)C)(C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
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/S0031-9422(02)00021-3
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/S0031-9422(02)00021-3
Npc62469 49867942 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1055/S-2006-957718
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/10.1055/S-2006-957718
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(4aS,5R,6S)-6-((3,6-Di-O-acetyl-2-O-benzoyl-4-O-(3-(beta-D-glucopyranosyloxy)-2-hydroxybenzoyl)-beta-D-glucopyranosyl)oxy)-5-ethenyl-4,4a,5,6-tetrahydro-1H,3H-pyrano(3,4-c)pyran-1-one 159134 Click to see 844.80 unknown https://doi.org/10.1055/S-2007-969915
(5R-trans)-5,6-Dihydro-6-((2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)oxy)-5-vinyl-1H,3H-pyrano(3,4-c)pyran-1-one 114428 Click to see 524.50 unknown via CMAUP database
[(2R,4S,5R,6S)-4,5-diacetyloxy-2-(acetyloxymethyl)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]oxan-3-yl] 2-hydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 6326199 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C)OC(=O)C)OC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 782.70 unknown via CMAUP database
[(2S,3R,4R,5S,6S)-4-acetyloxy-2-(acetyloxymethyl)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-benzoyloxyoxan-3-yl] 2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 6325983 Click to see 844.80 unknown via CMAUP database
[4,5-diacetyloxy-2-(acetyloxymethyl)-6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]oxan-3-yl] 2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 74029859 Click to see 782.70 unknown https://doi.org/10.1055/S-2007-969915
Rindoside 46174003 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3(CCOC(=O)C3=CO2)O)C=C)OC(=O)C)OC(=O)C)OC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 798.70 unknown https://doi.org/10.1055/S-2007-969915
Trifloroside 101688128 Click to see 782.70 unknown https://doi.org/10.1055/S-2007-969915
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(3S,4aR,6aR,6aR,6bR,12aR,14aR,14bR)-4,4,6a,6b,10,10,12a,14b-octamethyl-1,2,3,4a,5,6,6a,7,9,11,12,13,14,14a-tetradecahydropicen-3-ol 14831162 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(3S,4aR,6aR,6aR,6bR,12aR,14aR,14bR)-4,4,6a,6b,11,11,12a,14b-octamethyl-1,2,3,4a,5,6,6a,7,9,10,12,13,14,14a-tetradecahydropicen-3-ol 163106231 Click to see CC1(CCC2=CCC3(C(C2(C1)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
4,4,6a,6b,10,10,12a,14b-Octamethyl-1,2,3,4a,5,6,6a,7,9,11,12,13,14,14a-tetradecahydropicen-3-ol 14831161 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
1-Methyl-7-prop-1-en-2-yl-1,2,3,5,6,7,8,8a-octahydronaphthalene-2,3-diol 5743537 Click to see CC1C2CC(CCC2=CC(C1O)O)C(=C)C 222.32 unknown via CMAUP database
> 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/10.1055/S-2006-957718
(1R,3S,4R,5R)-4-ethenyl-5-hydroxy-1-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydro-1H-pyrano[3,4-c]pyran-8-one 11153922 Click to see 404.40 unknown https://doi.org/10.1021/NP058017O
(1S,3R,4R,8aS)-4-ethenyl-8a-hydroxy-1-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,6-tetrahydropyrano[3,4-c]pyran-8-one 11441067 Click to see COC1C2(C(=CCOC2=O)C(C(O1)OC3C(C(C(C(O3)CO)O)O)O)C=C)O 404.40 unknown https://doi.org/10.1248/CPB.47.1338
https://doi.org/10.1021/NP058017O
(1S,3S,4R,8aS)-4-ethenyl-8a-hydroxy-1-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,6-tetrahydropyrano[3,4-c]pyran-8-one 154496628 Click to see 404.40 unknown https://doi.org/10.1021/NP058017O
(3R,4S,4aR)-4-ethenyl-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 9906781 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown via CMAUP database
(3R,4S)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 11969636 Click to see 356.32 unknown via CMAUP database
(3S,4R,4aS)-3-[(2S,3R,4S,5S,6R)-3-[(2,3-dihydroxyphenyl)methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-ethenyl-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 101377073 Click to see 480.50 unknown via CMAUP database
(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/10.1055/S-2006-957718
4-ethenyl-1-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydro-1H-pyrano[3,4-c]pyran-8-one 72816695 Click to see 388.40 unknown https://doi.org/10.1021/NP058017O
4'-O-beta-D-glucosylgentiopicroside 10896590 Click to see 518.50 unknown https://doi.org/10.1021/NP010358O
Benzyl b-primeveroside 14730864 Click to see 402.40 unknown https://doi.org/10.1021/NP010358O
Benzyl vicianoside 71511240 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1021/NP010358O
Gentiopicroside 88708 Click to see 356.32 unknown https://doi.org/10.1248/CPB.39.204
https://doi.org/10.1055/S-2006-957718
https://doi.org/10.1055/S-2007-969915
Iridiod monoterpenoid 12443156 Click to see 374.34 unknown via CMAUP database
Swertiajaposide A 11361225 Click to see 388.40 unknown https://doi.org/10.1021/NP058017O
Swertiamarin 442435 Click to see 374.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Gentiotrifloroside 21574478 Click to see 656.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(3S,4R)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,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]oxymethyl]oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 11216673 Click to see C=CC1C(OC=C2C1=CCOC2=O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)COC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O)O)O)O)O 842.70 unknown https://doi.org/10.1021/NP058017O
(3S,4R)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,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]oxymethyl]oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]oxan-2-yl]oxy-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 11787976 Click to see 1004.90 unknown https://doi.org/10.1021/NP058017O
Gentianose 117678 Click to see 504.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(4aR,6aR,6aR,6bR,12aR,14aR,14bR)-4,4,6a,6b,10,10,12a,14b-octamethyl-2,4a,5,6,6a,7,8,11,12,13,14,14a-dodecahydro-1H-picen-3-one 102587960 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
(4aR,6aR,6aR,6bR,12aR,14aR,14bR)-4,4,6a,6b,10,10,12a,14b-octamethyl-2,4a,5,6,6a,7,9,11,12,13,14,14a-dodecahydro-1H-picen-3-one 14831168 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
4,4,6a,6b,10,10,12a,14b-octamethyl-2,4a,5,6,6a,7,8,11,12,13,14,14a-dodecahydro-1H-picen-3-one 85306038 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
4,4,6a,6b,10,10,12a,14b-octamethyl-2,4a,5,6,6a,7,9,11,12,13,14,14a-dodecahydro-1H-picen-3-one 14831167 Click to see 424.70 unknown https://doi.org/10.1016/S0031-9422(02)00021-3
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,7-Trihydroxyxanthone 5281635 Click to see 244.20 unknown via CMAUP database
Swertianin 5281661 Click to see 274.22 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Gentioflavine 442536 Click to see CC1C(=C2CCOC(=O)C2=CN1)C=O 193.20 unknown via CMAUP database
> Organoheterocyclic compounds / Pyranopyridines
Gentianine 354616 Click to see C=CC1=CN=CC2=C1CCOC2=O 175.18 unknown via CMAUP database
Gentiatibetine 5317559 Click to see CC1=NC=CC2=C1C(OCC2)O 165.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans
1-Methyl-6-oxo-1,3,4,5-tetrahydropyrano[3,4-c]pyridine-5-carbaldehyde 5317557 Click to see 193.20 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(4S)-4-ethyl-4-hydroxy-5,6-dihydro-1H-pyrano[3,4-c]pyran-3,8-dione 11052961 Click to see 212.20 unknown via CMAUP database
> Organoheterocyclic compounds / Triazines / Aminotriazines / 1,3,5-triazine-2,4-diamines
2-((4-(Ethylamino)-6-methoxy-1,3,5-triazin-2-yl)amino)-2-methylpropiononitrile 89022 Click to see 236.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone 44258368 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258737 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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