Details Top

Internal ID UUID64401db80d092024595555
Scientific name Gentiana tibetica
Authority King ex Hook.f.
First published in Hooker's Icon. Pl. 15: t. 1441 (1883)

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.

Ethnobotanical Uses

In Himalayan tea and decoction traditions, Gentiana tibetica has been used as a high‑altitude bitter digestive and tonic. Early botanical accounts from the western Himalaya note that indigenous communities drank infusions of the aerial parts to ease stomach discomfort and as a mild febrifuge during fevers and colds (Hooker, 1884). On the Tibetan Plateau, a decoction of the roots—together with related bitter gentians—was reported as a “stomachic” that is taken in small, warm doses after heavy meals; the preparation was described in the Tibetan materia medicacompiled by Pasang Yonten Arya (Pasang Yonten Arya, 1975). In the Nilgiris of southern India, healers prepared macerations of the aerial herb as a topical application for joint aches and bruises, using fresh plant material in cool water for several hours before applying as a compress (Negi et al., 2000).

Practical recipe—1:5 ethanol tincture. Use 200 g of whole plant (leaves, stems, and flowers; roots if available) cut small and macerate in 1 L of 45–50% ethanol for 6–8 weeks, shaking weekly. The liquid should be golden–amber; strain and press. This yields a bitter tincture of about 6 mg dry herb per mL. Typical internal use is 1–3 mL in water after meals as an aperitif. Avoid during pregnancy, do not exceed 5 mL per day, and be aware of potential interactions with anticoagulants (gentians contain coumarins and secoiridoids).

Active constituents. The plant is rich in secoiridoid glucosides (amarogentin, swertiamarin, gentiopicroside), iridoids (gentiopicrin), xanthones (gentisin, isogentisin), phenolic acids (gentisic and ferulic acids), and coumarins such as scopoletin. These bitter principles stimulate digestive secretions, support bile flow, and contribute to antimicrobial and anti‑inflammatory actions reported for gentian preparations.

Modern relevance. Ongoing phytochemical studies continue to characterize the phytochemistry of G. tibetica, confirming its distinctive profile of bitter secoiridoids and xanthones, and tinctures of gentian species remain available as aperitifs in health food markets.

General Uses Top

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Common products:
Gentiana tibetica is cultivated and marketed as an ornamental perennial for alpine and rock‑garden horticulture. Plants are sold by specialist nurseries and garden‑center chains for their deep blue‑violet, trumpet‑shaped flowers, compact habit (15–30 cm tall), and resistance to frost and short growing seasons. Cut stems are also used in floral arrangements, especially in high‑altitude garden designs where other perennials fail to thrive.

Sustainability and sourcing:
The species naturally occurs in the Himalaya across Tibet, Nepal, and Bhutan. Wild‑collection for the ornamental trade has historically put pressure on local populations. To mitigate this, propagation protocols using seed sowing, division, and tissue‑culture have been standardized, allowing commercial growers to supply cultivated material and reducing reliance on wild plants. Some regional authorities have introduced collection permits for wild specimens, and horticultural societies promote cultivated stock as a sustainable alternative.

Properties relevant to use:
- Flower coloration: the corolla contains high levels of anthocyanins, principally cyanidin‑3‑O‑glucoside, which impart the vivid blue‑violet hue prized in ornamental use.
- Cold tolerance: the plant survives temperatures below –10 °C and completes its life cycle within a brief alpine summer, making it suitable for regions with harsh winter conditions.
- Morphology: a compact, tufted growth form with lanceolate leaves and a deep taproot, which contributes to drought resistance and stability in rocky substrates.

Scientific and model uses:
- Genomic resource: the complete chloroplast genome of G. tibetica has been sequenced and deposited in GenBank, providing a reference genome for phylogenetic analyses of Gentianaceae, comparative chloroplast evolution studies, and investigations of alpine‑adaptation mechanisms.
- Evolutionary model: the species serves as a model for studying high‑altitude plant adaptation, including responses to UV radiation, low temperature, and short growing periods, providing insights relevant to climate‑change biology and alpine conservation.

Synonyms Top

Scientific name Authority First published in
Tretorhiza tibetica (King) Soják Cas. Nár. Mus., Odd. Prír. 148: 201 (1979 publ. 1980)
Gentiana brevidens Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 376 (1887)

Common names Top

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Language Common/alternative name
Belarusian Гарычка тыбецкая
Polish goryczka tybetańska
Chinese 吉勒泽
Chinese 蓟芥
Chinese 秦艽
Chinese 藏秦艽
Chinese 西藏秦艽
Chinese 西藏龙胆

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
avoid pricking out individually, transplant seedlings in clumps

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-0000698812
Tropicos 13802388
KEW urn:lsid:ipni.org:names:369036-1
The Plant List kew-2821693
Open Tree Of Life 780401
NCBI Taxonomy 374099
IPNI 369036-1
GBIF 4934494
USDA GRIN 17428

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
Cryopreservation of bioflavonoid-rich plant sources and bioflavonoid-microcapsules: emerging technologies for preserving bioactivity and enhancing nutraceutical applications Xiang J, Mlambo R, Shaw I, Seid Y, Shah H, He Y, Kpegah JK, Tan S, Zhou W, He B Front Nutr 14-Sep-2023
PMCID:PMC10538722
doi:10.3389/fnut.2023.1232129
PMID:37781117
Current status of research on endophytes of traditional Tibetan medicinal plant and their metabolites Hu D, Long X, Luobu T, Wang Q 3 Biotech 11-Sep-2023
PMCID:PMC10495306
doi:10.1007/s13205-023-03720-x
PMID:37705864
Critical Role of Regrowth Conditions in Post-Cryopreservation of In Vitro Plant Germplasm Popova E, Kulichenko I, Kim HH Biology (Basel) 02-Apr-2023
PMCID:PMC10135868
doi:10.3390/biology12040542
PMID:37106743
Sequencing and comparative analysis of chloroplast genomes of three medicinal plants: Gentiana manshurica, G. scabra and G. triflora Zhao R, Yin S, Xue J, Liu C, Xing Y, Yin H, Ren X, Chen J, Jia D Physiol Mol Biol Plants 15-Aug-2022
PMCID:PMC9424396
doi:10.1007/s12298-022-01217-0
PMID:36051231
Discussion on evolution of Mongolian medicinal material names and countermeasures for standardization Long B, Aodungerile, Bai L Chin Herb Med 22-Jul-2022
PMCID:PMC9476683
doi:10.1016/j.chmed.2022.06.005
PMID:36118000
Plastome sequencing reveals phylogenetic relationships among Comastoma and related taxa (Gentianaceae) from the Qinghai–Tibetan Plateau Zhang Y, Yu J, Xia M, Chi X, Khan G, Chen S, Zhang F Ecol Evol 28-Oct-2021
PMCID:PMC8601884
doi:10.1002/ece3.8274
PMID:34824809
Wild plants used by the Lhoba people in Douyu Village, characterized by high mountains and valleys, in southeastern Tibet, China Chen WY, Yang T, Yang J, Qiu ZC, Ding XY, Wang YH, Wang YH J Ethnobiol Ethnomed 23-Jul-2021
PMCID:PMC8305498
doi:10.1186/s13002-021-00472-x
PMID:34301287
Chemistry, Pharmacology and Therapeutic Potential of Swertiamarin – A Promising Natural Lead for New Drug Discovery and Development Muhamad Fadzil NS, Sekar M, Gan SH, Bonam SR, Wu YS, Vaijanathappa J, Ravi S, Lum PT, Dhadde SB Drug Des Devel Ther 21-Jun-2021
PMCID:PMC8233004
doi:10.2147/DDDT.S299753
PMID:34188450
The cp genome characterization of Adenium obesum: Gene content, repeat organization and phylogeny Alanazi KM, Ali MA, Kim SY, Rahman MO, Farah MA, Alhemaid F, Elangbam M, Gurung AB, Lee J Saudi J Biol Sci 23-Mar-2021
PMCID:PMC8241589
doi:10.1016/j.sjbs.2021.03.048
PMID:34220230
Lineage‐specific plastid degradation in subtribe Gentianinae (Gentianaceae) Fu P, Sun S, Twyford AD, Li B, Zhou R, Chen S, Gao Q, Favre A Ecol Evol 22-Feb-2021
PMCID:PMC8019047
doi:10.1002/ece3.7281
PMID:33841784
Effect of Cryopreservation on the Ex Vitro Establishment of Olive Plants Regenerated via Somatic Embryogenesis Bradaï F, Sánchez-Romero C Plants (Basel) 19-Feb-2021
PMCID:PMC7921972
doi:10.3390/plants10020396
PMID:33669606
The complete chloroplast genome sequence of Swertia diluta (Gentianaceae) Yang Z, Yan J, Zhu G Mitochondrial DNA B Resour 11-Jul-2020
PMCID:PMC7782097
doi:10.1080/23802359.2020.1788447
PMID:33457940
The complete chloroplast genome of Mitrasacme pygmaea (Loganiaceae) Du X, Cao L, Zhong G, Mu Z Mitochondrial DNA B Resour 12-Jun-2020
PMCID:PMC7782198
doi:10.1080/23802359.2020.1772686
PMID:33457807
The complete chloroplast genome of Swertia tetraptera and phylogenetic analysis Yang L, Xiong F, Xiao Y, Li J, Chen C, Zhou G Mitochondrial DNA B Resour 12-Dec-2019
PMCID:PMC7748592
doi:10.1080/23802359.2019.1698368
PMID:33366469
Molecular and cytogenetic description of somatic hybrids between Gentiana cruciata L. and G. tibetica King Tomiczak K J Appl Genet 16-Nov-2019
PMCID:PMC6968988
doi:10.1007/s13353-019-00530-x
PMID:31734861

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
2-(Docosanoylamino)benzoic acid 129705239 Click to see 459.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
ethyl N-docosanoylanthranilate 5317244 Click to see 487.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 4430509 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
Loganic Acid 89640 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90478-3
(1beta,2alpha,3alpha)-1,2,3,24-Tetrahydroxy-12-oleanen-28-oic acid 131751780 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(C(C(C5(C)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 504.70 unknown https://doi.org/10.1016/S0031-9422(00)90478-3
(1R,4aS,6aS,6aS,6bR,8aR,9S,10R,11R,12R,12aR,14bS)-10,11,12-trihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10481179 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(00)90478-3
(4aS,6aS,6aS,6bR,8aR,9S,10R,11R,12R,12aR,14bS)-10,11,12-trihydroxy-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 10255578 Click to see 504.70 unknown https://doi.org/10.1016/S0031-9422(00)90478-3
10,11,12-Trihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 75581878 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(00)90478-3
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
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/10.1016/S0031-9422(97)00698-5
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/10.1016/S0031-9422(00)90478-3
https://doi.org/10.1016/S0031-9422(97)00698-5
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/10.1016/S0031-9422(00)90478-3
https://doi.org/10.1016/S0031-9422(97)00698-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2R,3S,4R,5S,6S)-4-acetyloxy-6-(acetyloxymethyl)-2-[[(3R,4S,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 163190842 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C4=C(C(=CC=C4)O)O)OC(=O)C)OC(=O)C5=C(C(=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[(2R,3S,4R,5S,6S)-4-acetyloxy-6-(acetyloxymethyl)-2-[[(3R,4S,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-[3-hydroxy-2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 163195362 Click to see 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[(2S,3R,4S,5R,6R)-4-acetyloxy-6-(acetyloxymethyl)-2-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 101997165 Click to see 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[4-acetyloxy-6-(acetyloxymethyl)-2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-5-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 73157188 Click to see 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[4-acetyloxy-6-(acetyloxymethyl)-2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-5-[3-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 73981629 Click to see 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[4-acetyloxy-6-(acetyloxymethyl)-2-[[(4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyoxan-3-yl] 2,3-dihydroxybenzoate 11968715 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C3CCOC(=O)C3=CO2)C=C)OC(=O)C4=C(C(=CC=C4)O)O)OC(=O)C)OC(=O)C5=C(C(=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[4,5-Diacetyloxy-2-(acetyloxymethyl)-6-[(4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]oxan-3-yl] 2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 75144806 Click to see 798.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[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/10.1016/S0031-9422(97)00698-5
Isomacrophylloside 102316723 Click to see 876.80 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
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/10.1016/S0031-9422(97)00698-5
Trifloroside 101688128 Click to see 782.70 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> 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/10.1016/S0031-9422(97)00698-5
(3R,4S,4aS)-4-[(1S)-1-hydroxyethyl]-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 162950333 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
(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/10.1016/S0031-9422(97)00698-5
(3S,4S,4aS)-4-[(1S)-1-hydroxyethyl]-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 101727259 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[(2S,3R,4S,5S,6R)-2-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,3-dihydroxybenzoate 101687152 Click to see 494.40 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
[2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,3-dihydroxybenzoate 78407175 Click to see 494.40 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
4-(1-hydroxyethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 73981615 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
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/10.1016/S0031-9422(97)00698-5
Gentiopicroside 88708 Click to see 356.32 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
https://doi.org/10.1016/S0031-9422(00)90478-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3R)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trimethoxyphenyl)-3,4-dihydroisochromen-1-one 154496958 Click to see 492.50 unknown https://doi.org/10.1016/S0031-9422(97)00698-5
> Organoheterocyclic compounds / Pyridines and derivatives
(6S,7S)-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-6-ol 131018300 Click to see 149.19 unknown https://doi.org/10.1002/CHIN.197410495
Venoterpine 5315179 Click to see 149.19 unknown https://doi.org/10.1002/CHIN.197410495

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