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Halenia elliptica

Halenia elliptica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64401f9f7f265037643858
Scientific name Halenia elliptica
Authority D.Don
First published in Trans. Linn. Soc. London 17: 529 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tetragonanthus centrostemma Kuntze Revis. Gen. Pl. 2: 431 (1891)
Swertia peloria Griff. Itin. Pl. Khasyah Mts. : 197 (1848)
Halenia vaniotii H.Lév. Repert. Spec. Nov. Regni Veg. 12: 182 (1913)

Common names Top

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Language Common/alternative name
Azerbaijani ellipsvari haleniya
Chinese 卵萼花锚
Chinese 黑及草
Chinese 花锚
Chinese 椭圆叶花锚
Chinese 椭圆叶花锚（椭叶花锚）
Chinese 青叶胆
Chinese 椭叶花锚

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000714556
Tropicos 13801601
KEW urn:lsid:ipni.org:names:369465-1
The Plant List kew-2837984
PFAF Halenia elliptica
Open Tree Of Life 862722
Observations.org 124294
NCBI Taxonomy 50804
IPNI 369465-1
iNaturalist 511784
GBIF 5596202
EOL 2892664
Elurikkus 553297
USDA GRIN 18213

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
Comparative Analysis of Six Complete Plastomes of Tripterospermum spp. Tu XD, Lin WJ, Fu HH, Lin YZ, Shen J, Chen S, Liu ZJ, Li MH, Chen SP Int J Mol Sci 22-Feb-2024
PMCID:PMC10931592
doi:10.3390/ijms25052534
PMID:38473781
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Flowering phenology differs among wet and dry sub-alpine meadows in southwestern China Nepal S, Trunschke J, Ren ZX, Burgess KS, Wang H AoB Plants 18-Jan-2024
PMCID:PMC10829081
doi:10.1093/aobpla/plae002
PMID:38298756
Latitudinal trends in mating system traits in the highly self‐fertilizing Lobelia inflata revealed by community science Coffey ML, Simons AM Ecol Evol 27-Nov-2023
PMCID:PMC10682567
doi:10.1002/ece3.10746
PMID:38034331
Characteristics of the complete chloroplast genome of Swertia divaricata Harry Sm. (Gentianaceae) and its phylogenetic inference Hou Y, Zhang Y, Yu J, Wang X Mitochondrial DNA B Resour 23-Oct-2023
PMCID:PMC10621253
doi:10.1080/23802359.2023.2270211
PMID:37928401
Phylogeography and ecological niche modeling implicate multiple microrefugia of Swertia tetraptera during quaternary glaciations Yang L, Zhou G BMC Plant Biol 26-Sep-2023
PMCID:PMC10521563
doi:10.1186/s12870-023-04471-w
PMID:37749488
Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny Yang L, Deng S, Zhu Y, Da Q BMC Plant Biol 28-Mar-2023
PMCID:PMC10044379
doi:10.1186/s12870-023-04183-1
PMID:36977991
Transcriptome and proteome analyses reveal the potential mechanism of seed dormancy release in Amomum tsaoko during warm stratification Pan C, Yao L, Yu L, Qiao Z, Tang M, Wei F, Huang X, Zhou Y BMC Genomics 02-Mar-2023
PMCID:PMC9983222
doi:10.1186/s12864-023-09202-x
PMID:36864423
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Phenotypic Selection in Halenia elliptica D. Don (Gentianaceae), an Alpine Biennial with Mixed Mating System Huang X, Chen M, Wang L, Yang M, Yang N, Li Z, Duan Y Plants (Basel) 31-May-2022
PMCID:PMC9183009
doi:10.3390/plants11111488
PMID:35684261
Migration patterns of Gentiana crassicaulis, an alpine gentian endemic to the Himalaya–Hengduan Mountains Ni L, Li W, Zhao Z, Gaawe D, Liu T Ecol Evol 18-Mar-2022
PMCID:PMC8933255
doi:10.1002/ece3.8703
PMID:35342601
Pollinator individual‐based networks reveal the specialized plant–pollinator mutualism in two biodiverse communities Wang L, Yang Y, Duan Y Ecol Evol 25-Nov-2021
PMCID:PMC8668776
doi:10.1002/ece3.8384
PMID:34938525
A Review on the Ethnomedicinal Usage, Phytochemistry, and Pharmacological Properties of Gentianeae (Gentianaceae) in Tibetan Medicine Chi X, Zhang F, Gao Q, Xing R, Chen S Plants (Basel) 05-Nov-2021
PMCID:PMC8620629
doi:10.3390/plants10112383
PMID:34834747
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
Multiple lines of evidence supports the two varieties of Halenia elliptica (Gentianaceae) as two species Wu JF, Jia DR, Liu RJ, Zhou ZL, Wang LL, Chen MY, Meng LH, Duan YW Plant Divers 23-Sep-2021
PMCID:PMC9209875
doi:10.1016/j.pld.2021.09.004
PMID:35769593

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 / Sesquiterpenoids / Agarofurans
[(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-5,7-dibenzoyloxy-4-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] benzoate 14828977 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)O 656.70 unknown https://doi.org/10.1080/10286020.2010.544254
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
[(3aS,4R,8R,8aR,9aS)-8-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-4-yl] acetate 163186175 Click to see CC(=O)OC1C2C(CC3(C1C(=C)CCC3O)C)OC(=O)C2=C 306.40 unknown https://doi.org/10.1080/10286020.2010.544254
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9R,9aS,9bS)-4,8-dihydroxy-3-methyl-6-methylidenespiro[3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-9,2'-oxirane]-2-one 11119471 Click to see CC1C2C(CC(=C)C3CC(C4(C3C2OC1=O)CO4)O)O 280.32 unknown https://doi.org/10.3184/030823402103172527
[(3aR,4S,6aR,8S,9R,9aS,9bS)-8,9-dihydroxy-4-[2-(hydroxymethyl)prop-2-enoyloxy]-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[8,7-b]furan-9-yl]methyl 2-(hydroxymethyl)prop-2-enoate 11048883 Click to see C=C1CC(C2C(C3C1CC(C3(COC(=O)C(=C)CO)O)O)OC(=O)C2=C)OC(=O)C(=C)CO 464.50 unknown https://doi.org/10.3184/030823402103172527
[8,9-Dihydroxy-4-[2-(hydroxymethyl)prop-2-enoyloxy]-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[8,7-b]furan-9-yl]methyl 2-(hydroxymethyl)prop-2-enoate 85380049 Click to see C=C1CC(C2C(C3C1CC(C3(COC(=O)C(=C)CO)O)O)OC(=O)C2=C)OC(=O)C(=C)CO 464.50 unknown https://doi.org/10.3184/030823402103172527
4,8-dihydroxy-3-methyl-6-methylidenespiro[3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-9,2'-oxirane]-2-one 85405587 Click to see CC1C2C(CC(=C)C3CC(C4(C3C2OC1=O)CO4)O)O 280.32 unknown https://doi.org/10.3184/030823402103172527
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18|A)-Oleanolic acid 7048528 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 https://doi.org/10.1016/S0031-9422(00)98097-X
3-Hydroxyolean-12-en-28-oic acid 619166 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 https://doi.org/10.1016/S0031-9422(00)98097-X
Oleanolic Acid 10494 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 https://doi.org/10.1016/S0031-9422(00)98097-X
> 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/10.1016/S0031-9422(00)98097-X
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)98097-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
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 C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1080/10286020.2010.544254
5-Ethenyl-6-(beta-D-glucopyranosyloxy)-4,4a,5,6-tetrahydro-3-methoxy-1H,3H-pyrano[3,4-c]pyran-1-one 14192589 Click to see COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C 388.40 unknown https://doi.org/10.1080/10286020.2010.544254
7-epi-Vogeloside; Epivogeloside; Isovogeloside; Nervoside 14192588 Click to see COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C 388.40 unknown https://doi.org/10.1080/10286020.2010.544254
Epivogeloside 14192590 Click to see COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C 388.40 unknown https://doi.org/10.1080/10286020.2010.544254
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1080/10286020.2010.544254
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
3,5-Dihydroxy-6-methoxy-2-methylchromen-4-one 101570902 Click to see CC1=C(C(=O)C2=C(O1)C=CC(=C2O)OC)O 222.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
4H-1-Benzopyran-4-one, 5-hydroxy-6-methoxy-2-methyl- 101570901 Click to see CC1=CC(=O)C2=C(O1)C=CC(=C2O)OC 206.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
5-Hydroxy-8-methoxy-2-methyl-4h-chromen-4-one 130032396 Click to see CC1=CC(=O)C2=C(C=CC(=C2O1)OC)O 206.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
8-Hydroxy-2-methyl-4H-1-benzopyran-4-one 57330137 Click to see CC1=CC(=O)C2=C(O1)C(=CC=C2)O 176.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
8-Hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid 15225338 Click to see C1=CC2=C(C(=C1)O)OC(=CC2=O)C(=O)O 206.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
8-methoxy-2-methyl-4H-1-benzopyran-4-one 12407421 Click to see CC1=CC(=O)C2=C(O1)C(=CC=C2)OC 190.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
8-Methoxy-4-oxochromene-2-carboxylic acid 455310 Click to see COC1=CC=CC2=C1OC(=CC2=O)C(=O)O 220.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.09.015
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-2,3,4,7-tetramethoxyxanthone 5318358 Click to see COC1=CC2=C(C=C1)OC3=C(C(=C(C(=C3C2=O)O)OC)OC)OC 332.30 unknown https://doi.org/10.1016/J.PHYMED.2009.03.015
https://doi.org/10.1016/S0031-9422(00)98097-X
1-Hydroxy-2,3,5-trimethoxyxanthen-9-one 5318372 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)O)OC)OC 302.28 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
https://doi.org/10.1016/J.LFS.2007.08.010
https://doi.org/10.1016/J.LFS.2007.10.014
1-Hydroxy-3,6,8-trimethoxyxanthen-9-one 14539318 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CC(=C3)OC)OC)O 302.28 unknown https://doi.org/10.1016/0031-9422(90)80055-L
1,3,6-trimethoxy-8-[(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 14539320 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 596.50 unknown https://doi.org/10.1016/0031-9422(90)80055-L
1,3,6-Trimethoxy-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 14539319 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 596.50 unknown https://doi.org/10.1016/0031-9422(90)80055-L
1,5-Dihydroxy-2,3,4-trimethoxyxanthen-9-one 162893843 Click to see COC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)OC)OC 318.28 unknown https://doi.org/10.1080/10286020.2010.544254
1,7-Dihydroxy-2,3,4,5-tetramethoxy-9H-xanthen-9-one 71323009 Click to see COC1=CC(=CC2=C1OC3=C(C(=C(C(=C3C2=O)O)OC)OC)OC)O 348.30 unknown https://doi.org/10.1016/J.PHYMED.2009.03.015
2,3,4,5-tetramethoxy-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 102403118 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 656.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,4,5-tetramethoxy-1-[(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 5315183 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 626.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,4,5-Tetramethoxy-1-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 162987958 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 656.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,4,7-tetramethoxy-1-[(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 5321890 Click to see COC1=CC2=C(C=C1)OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 626.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,4,7-Tetramethoxy-1-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 73981750 Click to see COC1=CC2=C(C=C1)OC3=C(C2=O)C(=C(C(=C3OC)OC)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 626.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,5-trimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 14412263 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 464.40 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
2,3,5-trimethoxy-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 102154410 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC)OC 626.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,5-trimethoxy-1-[(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 102145651 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC)OC 596.50 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,5-Trimethoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 14412262 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 464.40 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
2,3,5-Trimethoxy-1-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 162847336 Click to see COC1=CC=CC2=C1OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC)OC 626.60 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,7-trimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 14412261 Click to see COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 464.40 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
2,3,7-trimethoxy-1-[(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 102145640 Click to see COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC)OC 596.50 unknown https://doi.org/10.1080/10286020.2010.544254
2,3,7-Trimethoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 14412260 Click to see COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 464.40 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
2,3,7-Trimethoxy-1-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 74929853 Click to see COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC)OC 596.50 unknown https://doi.org/10.1080/10286020.2010.544254
9H-Xanthen-9-one, 1-hydroxy-2,3,4,5-tetramethoxy- 5318357 Click to see COC1=CC=CC2=C1OC3=C(C(=C(C(=C3C2=O)O)OC)OC)OC 332.30 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
https://doi.org/10.1016/J.PHYMED.2009.03.015
9H-Xanthen-9-one, 1,5-dihydroxy-2,3-dimethoxy- 11580116 Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O)OC 288.25 unknown https://doi.org/10.1016/J.LFS.2007.10.014
Xanthone, 1-hydroxy-2,3,7-trimethoxy- 6426908 Click to see COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)O)OC)OC 302.28 unknown https://doi.org/10.1016/S0031-9422(00)98097-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1080/10286020.2010.544254
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/10286020.2010.544254
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/10286020.2010.544254
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 14769196 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/10286020.2010.544254
apigenin-7-O-gentiobioside 10841200 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/10286020.2010.544254
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/10286020.2010.544254
luteolin-7-O-gentiobioside 14032967 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/10286020.2010.544254
luteolin-7-O-gentiobiside 14032965 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/10286020.2010.544254

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