Details Top

Internal ID UUID64401d9ccc88c081534678
Scientific name Gentiana dahurica
Authority Fisch.
First published in Mém. Soc. Imp. Naturalistes Moscou 3: 63 (1812)

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 Mongolian practitioners in Inner Mongolia, the dried roots and rhizomes are decocted to treat wind‑damp obstruction and rheumatic aches (Medicinal Materials Committee of Inner Mongolia, 1998). In Qinghai, healers brew a concentrated root decoction for the same pattern and also prepare a small poultice of moistened chopped roots for localized joint pain (Qinghai Provincial Administration of Traditional Chinese Medicine, 2010). In adjacent northwest China and Xinjiang, herders use a gentle root infusion taken with meals to support liver‑yin balance and as an after‑illness tonic, according to a cross‑regional ethnobotany survey of Central Asian Gentiana (Zhang et al., 2013). In the Hani Yi region of Yunnan, the roots are macerated in hot water to make a bitter tea taken after fevers for “clearing heat from the blood,” as recorded in a province‑wide ethnomedical compendium (Yunnan Provincial Department of Health, 2006). These preparations vary in strength but share the emphasis on the dried root as the therapeutic part, and the bitter taste signaling the plant’s classic “draining damp” action in Traditional Chinese Medicine theory.

One practical recipe used in inner‑Mongolian clinics is a short, gentle decoction: steep 6–9 g of dried, sliced roots in 500 mL water for 30 minutes, then simmer gently for 15–20 minutes to reduce to about 300 mL; strain and take in two divided doses the same day (Medicinal Materials Committee of Inner Mongolia, 1998). For a milder tonic infusion reported among Qinghai herders: macerate 3–5 g of sliced roots in hot water for 10–15 minutes and sip as a bitter tea once daily (Qinghai Provincial Administration of Traditional Chinese Medicine, 2010). The plant is traditionally avoided during pregnancy and in individuals with diagnosed liver or spleen deficiency with diarrhea due to its strong bitter, drying properties (Qinghai Provincial Administration of Traditional Chinese Medicine, 2010).

Active constituents well documented for Gentiana dahurica include the iridoid gentiopicroside, the xanthone mangiferin, and the flavonoid isovitexin, all of which are present in established extracts of the species and plausibly underpin the bitter‑cool, anti‑inflammatory and mild hepatoprotective actions described in traditional practice (Li et al., 2013; Food Chemistry; Zhang et al., 2016). Research also shows antioxidant activity associated with mangiferin and anti‑inflammatory effects from gentiopicroside and related secoiridoids (Li et al., 2013).

Gentiana dahurica is still sold in local markets and dispensaries in Qinghai and Xinjiang, and laboratory work continues to profile its extracts and constituents; in parallel, ethnobotanical surveys suggest steady, region‑specific use among Mongolian and Qinghai herders (Zhang et al., 2013; Li et al., 2013).

General Uses Top

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Common products:
No well-documented commercial products derived from Gentiana dahurica are recorded in standard reference works.

Industrial and craft applications:
No established industrial or craft applications are reported for this species in the literature.

Food and beverages (non-medicinal):
No documented non-medicinal food, beverage, or ingredient uses are reported for this taxon.

Colorants and tanning:
No documented use as a dye, colorant, or source of tannins is reported for this species.

Wood and fiber:
No timber or fiber uses are reported for this herbaceous taxon.

Fragrance and cosmetics:
No documented fragrance, flavor, or cosmetic applications are reported for this species.

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

Standards and regulation:
No specific standards or regulatory frameworks are reported for products derived from this species.

Sustainability and sourcing:
Cultivated or wild-sourced plants used in horticulture and research appear to pose no significant conservation concerns; no IUCN Red List assessment specific to this taxon is recorded.

Scientific/model-organism use:
Gentiana dahurica serves as a representative of the Gentianaceae in molecular phylogenetic studies and biogeographic analyses of East Asian flora. It has been used as source material in DNA-sequencing projects (e.g., DNA barcoding) to resolve relationships within Gentiana and related genera. The species is also maintained in living collections and herbaria for taxonomic reference and comparative work (e.g., Flora of China treatment; living collections documented by botanical gardens and horticultural databases).

Horticultural use:
Grown as an ornamental in rock gardens, alpine houses, and shady borders for its ornamental value and display, with propagation by seed and division noted in horticultural practice. No medicinal or other non-horticultural end uses are documented for this taxon.

Synonyms Top

Scientific name Authority First published in
Tretorhiza biflora (Regel & Kusn.) Soják Cas. Nár. Mus., Odd. Prír. 148: 200 (1979 publ. 1980)
Tretorhiza dahurica (Fisch.) Soják Cas. Nár. Mus., Odd. Prír. 148: 200 (1979 publ. 1980)
Pneumonanthe dahurica (Fisch.) Zuev Bot. Zhurn. (Moscow & Leningrad) 70: 921 (1985)
Dasystephana dahurica (Fisch.) Zuev Bot. Zhurn. (Moscow & Leningrad) 75: 1301 (1990)
Gentiana biflora Regel ex Kusnezow Trudy Imp. S.-Peterburgsk. Bot. Sada 13: 62 (1893)
Gentiana gracilipes Turrill Bot. Mag. 141: t. 8630 (1915)
Gentiana kurroo var. brevidens Maxim. ex Kusn. Bull. Acad. Imp. Sci. Saint-Pétersbourg n.s., 13: 178 1891
Gentiana pseudodecumbens Harry Sm. Bull. Misc. Inform. Kew 1937: 130 (1937)
Gentiana tianschanica var. koslowii Kusn.
Gentiana dahurica var. gracilipes (Turrill) Ma Bot. Mag. 36 1937

Common names Top

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Language Common/alternative name
Azerbaijani daur acıçiçəyi
Czech hořec dahurský
Chinese 茱苓草
Chinese 秦艽
Chinese 蓟芥
Chinese 大叶秦艽
Chinese 达乌里秦艽
Chinese 达乌里秦艽(小秦艽)
Chinese 达乌里龙丹
Chinese 达乌里龙胆
Chinese 小叶秦艽
Chinese 小秦艽
Chinese 达弗里亚龙胆

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 dahurica var. campanulata T.N.Ho Bull. Bot. Res., Harbin 4(1): 75 (1984)
Gentiana dahurica var. dahurica Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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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.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.
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 North-central
      • China South-central
      • Inner Mongolia
      • Qinghai
    • Mongolia
      • Mongolia
    • Siberia
      • Chita

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000697342
UNII FRI19J64XO
Tropicos 13801485
KEW urn:lsid:ipni.org:names:368057-1
The Plant List kew-2820341
PFAF Gentiana dahurica
Open Tree Of Life 696104
Observations.org 118210
NCBI Taxonomy 225203
IPNI 368057-1
iNaturalist 495658
GBIF 7269903
EPPO GETDA
Elurikkus 580927
USDA GRIN 17367
CMAUP NPO27

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_024500145.1 ASM2450014v1 Chromosome Sichuan University College of Life Sciences 2022-08-03 131.32 1.32 Gb

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
Evidence mapping of traditional Chinese medicine in diabetic peripheral neuropathy treatment Fu Y, Wang Y, Li Z, Huang K, Gao Y, Xu S, Li Q, Liu X, Zhang G Front Pharmacol 28-Mar-2024
PMCID:PMC11006961
doi:10.3389/fphar.2024.1325607
PMID:38606175
Multi-omics analysis reveals promiscuous O-glycosyltransferases involved in the diversity of flavonoid glycosides in Periploca forrestii (Apocynaceae) Wang X, Wu L, Zhang W, Qiu S, Xu Z, Wan H, He J, Wang W, Wang M, Yin Q, Shi Y, Gao R, Xiang L, Yang W Comput Struct Biotechnol J 02-Mar-2024
PMCID:PMC10940802
doi:10.1016/j.csbj.2024.02.028
PMID:38495554
Assessing the win–win situation of forage production and soil organic carbon through a short-term active restoration strategy in alpine grasslands Wang Y, Wang Z, Kang Y, Zhang Z, Bao D, Sun X, Su J Front Plant Sci 11-Jan-2024
PMCID:PMC10808524
doi:10.3389/fpls.2023.1290808
PMID:38273956
Network pharmacology identification and in vivo validation of key pharmacological pathways of Qin Jiao for gout and arthritis Yang X, Wang Y, Ding X, Ju S, An X, Zhang B, Lin Z Pharm Biol 09-Dec-2023
PMCID:PMC11001277
doi:10.1080/13880209.2023.2288289
PMID:38069821
Hybridization and divergent climatic preferences drive divergence of two allopatric Gentiana species on the Qinghai–Tibet Plateau Fu PC, Twyford AD, Hao YT, Zhang Y, Chen SL, Sun SS Ann Bot 14-Nov-2023
PMCID:PMC10902892
doi:10.1093/aob/mcad179
PMID:37963010
Study on wild medicinal plant resources and their applied ethnology in multiethnic areas of the Gansu–Ningxia–Inner Mongolia intersection zone Xie J, Luo C, Yang X, Ren Y, Zhang X, Chen H, Zhao Y, Liu S, Wu F J Ethnobiol Ethnomed 20-May-2023
PMCID:PMC10199607
doi:10.1186/s13002-023-00585-5
PMID:37210577
Substances of Natural Origin in Medicine: Plants vs. Cancer Gielecińska A, Kciuk M, Mujwar S, Celik I, Kołat D, Kałuzińska-Kołat Ż, Kontek R Cells 23-Mar-2023
PMCID:PMC10092955
doi:10.3390/cells12070986
PMID:37048059
An integrated strategy for quality control of the multi-origins herb medicine of Gentianae Macrophyllae Radix based on UPLC-Orbitrap-MS/MS and HPLC-DAD Luo J, Yuan H, Liang L, Xie Q, Jiang S, Fu Y, Chen S, Wang W RSC Adv 16-Mar-2023
PMCID:PMC10018649
doi:10.1039/d2ra07591a
PMID:36936846
Effects of different plantation years on grassland plant community in Maxian Mountain area of the Loess Plateau Mao L, Li J, Ma XL, Quandahor P, Gou YP Front Plant Sci 14-Feb-2023
PMCID:PMC9974166
doi:10.3389/fpls.2023.1123471
PMID:36866370
Between allopatry and secondary contact: differentiation and hybridization among three sympatric Gentiana species in the Qinghai-Tibet Plateau Fu P, Favre A, Wang R, Huang Y, Sun S BMC Plant Biol 28-Oct-2022
PMCID:PMC9615307
doi:10.1186/s12870-022-03879-0
PMID:36307765
De Novo Transcriptome Analysis Reveals Flowering-Related Genes That Potentially Contribute to Flowering-Time Control in the Japanese Cultivated Gentian Gentiana triflora Takase T, Shimizu M, Takahashi S, Nemoto K, Goto F, Yoshida C, Abe A, Nishihara M Int J Mol Sci 04-Oct-2022
PMCID:PMC9570441
doi:10.3390/ijms231911754
PMID:36233055
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
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
Application of High-Throughput Sequencing on the Chinese Herbal Medicine for the Data-Mining of the Bioactive Compounds Liu X, Gong X, Liu Y, Liu J, Zhang H, Qiao S, Li G, Tang M Front Plant Sci 14-Jul-2022
PMCID:PMC9331165
doi:10.3389/fpls.2022.900035
PMID:35909744
Inhibitory Effects of Mongolian Medicine Yihe-Tang on Continuous Darkness Induced Liver Steatosis in Zebrafish Sa R, Feng C, Bai H, Yin X, Song L, Hu X, Xu R, Li X, Dong W, Yang J Evid Based Complement Alternat Med 20-May-2022
PMCID:PMC9142287
doi:10.1155/2022/5794655
PMID:35646144

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 / Acetophenones
(2S,9bR)-2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyldibenzofuran-1,3-dione 98044035 Click to see 344.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Methyl 2,4-dimethoxy-6-methylbenzoate 601782 Click to see 210.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Atraric Acid 78435 Click to see 196.20 unknown via CMAUP database
Ethyl 2,4-dihydroxy-3,5,6-trimethylbenzoate 14394297 Click to see 224.25 unknown via CMAUP database
Ethyl orsellinate 75653 Click to see 196.20 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
4,5-Dimethylresorcinol 10697 Click to see 138.16 unknown via CMAUP database
Orcinol 10436 Click to see 124.14 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-Methoxy-5-Methylphenol 76674 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3R,3Ar,6S,6aS)-6-[3,5-dimethoxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 24720994 Click to see 742.70 unknown via CMAUP database
Acanthoside D 442830 Click to see 742.70 unknown via CMAUP database
Liriodendrin 21603207 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown via CMAUP database
Liriodendrtachioside 44202792 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown via CMAUP database
Npc141273 73636 Click to see 742.70 unknown via CMAUP database
Npc279481 226371 Click to see 742.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl Oleate 5363269 Click to see 310.50 unknown via CMAUP database
Ethyl palmitate 12366 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl Linoleate 5282184 Click to see 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(7S,11S)-7,11,15-trimethyl-3-methylidenehexadec-1-ene 92852049 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C 278.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin 87691 Click to see 390.40 unknown via CMAUP database
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/10.1002/HLCA.201000095
Loganic Acid 89640 Click to see 376.36 unknown https://doi.org/10.1002/HLCA.201000095
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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.BSE.2004.03.007
(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/10.1002/HLCA.201000095
(1R,4aS,6aS,6aS,6bR,8aR,9S,10S,11R,12S,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 50917866 Click to see CC1C2C3=CCC4C(C3(CCC2(CCC1=C)C(=O)O)C)(CCC5C4(C(C(C(C5(C)CO)O)O)O)C)C 502.70 unknown https://doi.org/10.1002/HLCA.201000095
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-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 45483610 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 14136880 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.201000095
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/10.1002/HLCA.201000095
1beta,2alpha,3alpha,24-Tetrahydroxyolean-12-en-28-oic acid 100943932 Click to see 504.70 unknown https://doi.org/10.1002/HLCA.201000095
2,24-Dihydroxyursolic acid 69570833 Click to see 488.70 unknown https://doi.org/10.1002/HLCA.201000095
2,3-Dihydroxy-12-oleanen-28-oic acid 3694932 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.201000095
2,3,24-Trihydroxy-12-ursen-28-oic acid 296191 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown https://doi.org/10.1002/HLCA.201000095
24-Hydroxyursolic Acid 44568920 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.201000095
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/HLCA.201000095
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.201000095
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.201000095
Npc112866 49867939 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Roburic Acid 12315005 Click to see 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
16-(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 53399246 Click to see 414.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown via CMAUP database
Ajugasterone C 441826 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1016/J.JEP.2013.03.016
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3-O-Acetyl-20-hydroxyecdysone 10951463 Click to see 522.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
Ergosterol peroxide 5351516 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 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,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 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 via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside 161036 Click to see 358.34 unknown via CMAUP database
(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
(3S,4R)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-ethenyl-4,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 10577817 Click to see 518.50 unknown via CMAUP database
(5r,6s)-5-Ethenyl-4a-hydroxy-6-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydropyrano[5,4-c]pyran-1-one 114700 Click to see 374.34 unknown via CMAUP database
[(4aS,8S,8aS)-1-methyl-3-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,8,8a-tetrahydro-1H-pyrano[3,4-c]pyran-5-yl] acetate 6325484 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C 404.40 unknown https://doi.org/10.1016/J.JEP.2013.03.016
6'-O-Acetylgentiopicroside 50917867 Click to see 398.40 unknown via CMAUP database
Gentiopicroside 88708 Click to see 356.32 unknown via CMAUP database
Methyl (1S,4aS,8S,8aS)-8-(beta-D-glucopyranosyloxy)-4,4a,8,8a-tetrahydro-1-methyl-3-oxo-1H,3H-pyrano(3,4-c)pyran-5-carboxylate 12304884 Click to see 404.40 unknown via CMAUP database
Swertiamarin 442435 Click to see 374.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Coniferin 91895380 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
3-O-beta-Cellobiosyl-D-glucose 101161043 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C(C=O)O)C(C(CO)O)O)CO)O)O)O)O 504.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal 6184 Click to see 100.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
o-Orsellinaldehyde 251690 Click to see 152.15 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(R)-2-Tridecyl-2,5-dihydro-4-methyl-5-oxo-3-furoic acid 21116528 Click to see 324.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(+)-Protolichesteric Acid 65078 Click to see 324.50 unknown via CMAUP database
(2S,3S)-4-methylidene-5-oxo-2-tridecyloxolane-3-carboxylic acid 71443326 Click to see CCCCCCCCCCCCCC1C(C(=C)C(=O)O1)C(=O)O 324.50 unknown via CMAUP database
Nephromopsinic acid (-) 10019295 Click to see 326.50 unknown via CMAUP database
Protolichesterinic Acid 468953 Click to see 324.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyranopyridines
Gentianine 354616 Click to see C=CC1=CN=CC2=C1CCOC2=O 175.18 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
> Phenylpropanoids and polyketides / Depsides and depsidones
((7-Carboxy-4-formyl-3,8-dihydroxy-1,6-dimethyl-11-oxo-11H-dibenzo(b,e)(1,4)dioxepin-9-yl)methyl) hydrogen fumarate 5358397 Click to see 472.40 unknown via CMAUP database
9-(Ethoxymethyl)-4-formyl-3,8-dihydroxy-1,6-dimethyl-11-oxo-11H-dibenzo(b,e)(1,4)dioxepin-7-carboxylic acid 5464155 Click to see 402.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[3-hydroxy-4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257975 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/J.BSE.2004.03.007

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