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Soroseris hookeriana

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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 UUID643fc96cca0a1541854152
Scientific name Soroseris hookeriana
Authority Stebbins
First published in Mem. Torrey Bot. Club 19(3): 45 (1940)

Description Top

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Synonyms Top

Scientific name Authority First published in
Crepis gillii var. hirsuta J.Anthony Notes Roy. Bot. Gard. Edinburgh 18: 193 (1934)
Soroseris hirsuta (J.Anthony) C.Shih Acta Phytotax. Sin. 31: 446 (1993): (1993)
Soroseris gillii subsp. hirsuta (J.Anthony) Stebbins Stebbins in Mem. Torrey Bot. Club 19(3). 1940 44 1940
Soroseris gillii subsp. typica Stebbins Memoirs of the Torrey Botanical Club 19(3): 41-42 1940
Soroseris gillii subsp. handelii Stebbins Mem. Torrey Bot. Club 19: 42 (1940)
Soroseris hookeriana subsp. typica Stebbins Memoirs of the Torrey Botanical Club 19(3): 45 1940

Common names Top

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Language Common/alternative name
Chinese 空桶参
Chinese 羽裂绢毛苣
Chinese 皱叶绢毛苣
Chinese 皱叶绢毛菊
Chinese 皱叶绢毛菊*(虎克絹毛菊）
Chinese 绢毛菊
Chinese 金沙绢毛菊(絹毛菊）
Chinese 高粱根

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Soroseris hookeriana subsp. handelii (Stebbins) Yu J.Wang & L.M.Heng PhytoKeys 114:22:00. 2018
Soroseris hookeriana subsp. hirsuta (J.Anthony) Yu J.Wang & L.M.Heng PhytoKeys 114:22:00. 2018
Soroseris hookeriana subsp. occidentalis (Stebbins) Yu J.Wang & L.M.Heng PhytoKeys 114:22:00. 2018

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000030331
Tropicos 50102588
KEW urn:lsid:ipni.org:names:250415-1
The Plant List gcc-129322
Open Tree Of Life 1096837
Observations.org 310512
NCBI Taxonomy 996406
IPNI 250415-1
iNaturalist 794605
GBIF 3137744

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
Medicinal plants of Dagala region in Bhutan: their diversity, distribution, uses and economic potential Wangchuk P, Namgay K, Gayleg K, Dorji Y J Ethnobiol Ethnomed 24-Jun-2016
PMCID:PMC4921017
doi:10.1186/s13002-016-0098-7
PMID:27342801
Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP J Ethnobiol Ethnomed 03-May-2016
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597
Exploring the patterns of alpine vegetation of Eastern Bhutan: a case study from the Merak Himalaya Jamtsho K, Sridith K Springerplus 01-Jul-2015
PMCID:PMC4486651
doi:10.1186/s40064-015-1066-8
PMID:26155443
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
Ethnopharmacological evaluation of radal (leaves of Lomatia hirsuta) and isolation of 2-methoxyjuglone Simonsen HT, Adsersen A, Berthelsen L, Christensen SB, Guzmán A, Mølgaard P BMC Complement Altern Med 31-Aug-2006
PMCID:PMC1564040
doi:10.1186/1472-6882-6-29
PMID:16945129
New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides. Meng JC, Zhu QX, Tan RX Planta Med 01-Aug-2000
doi:10.1055/S-2000-8607
PMID:10985081

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 / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1055/S-2000-8607
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1055/S-2000-8607
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4,7,7-Trimethyl-5-oxo-2-bicyclo[2.2.1]heptanyl) benzoate 10061788 Click to see CC1(C2CC(=O)C1(CC2OC(=O)C3=CC=CC=C3)C)C 272.34 unknown https://doi.org/10.1055/S-2000-8607
[(1R,2R,4R)-4,7,7-trimethyl-5-oxo-2-bicyclo[2.2.1]heptanyl] benzoate 53990904 Click to see CC1(C2CC(=O)C1(CC2OC(=O)C3=CC=CC=C3)C)C 272.34 unknown https://doi.org/10.1055/S-2000-8607
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1R,4R,5R)-1,7,7-trimethyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybicyclo[2.2.1]heptan-2-one 54521802 Click to see CC1(C2CC(=O)C1(CC2OC3C(C(C(C(O3)CO)O)O)O)C)C 330.37 unknown https://doi.org/10.1055/S-2000-8607
1,7,7-Trimethyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybicyclo[2.2.1]heptan-2-one 73815102 Click to see CC1(C2CC(=O)C1(CC2OC3C(C(C(C(O3)CO)O)O)O)C)C 330.37 unknown https://doi.org/10.1055/S-2000-8607
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,4R,6aR,8S,9aR,9bR)-4,8-dihydroxy-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 184984 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1055/S-2000-8607
(3aS,6R,6aR,8S,9aR,9bS)-6,8-dihydroxy-6-methyl-3,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 15127108 Click to see CC1(CCC2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1055/S-2000-8607
(3aS)-3a,4,5,6,6abeta,7,8,9,9abeta,9balpha-Decahydro-8alpha-(beta-D-glucopyranosyloxy)-3,6,9-tris(methylene)azuleno[4,5-b]furan-2(3H)-one 321680 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1055/S-2000-8607
(3R,3aR,4R,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 163023273 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1055/S-2000-8607
(3R,3aR,4R,6aR,8S,9R,9aR,9bR)-4,8-dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 14589529 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown https://doi.org/10.1055/S-2000-8607
4-Hydroxy-3,6,9-trimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 14733660 Click to see C=C1CC(C2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C)O 424.40 unknown https://doi.org/10.1055/S-2000-8607
4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 15628151 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1055/S-2000-8607
4,8-Dihydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 14589527 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown https://doi.org/10.1055/S-2000-8607
6,8-Dihydroxy-6-methyl-3,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 72745627 Click to see CC1(CCC2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1055/S-2000-8607
8-Epicrepiside E 21636138 Click to see C=C1CC(C2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C)O 424.40 unknown https://doi.org/10.1055/S-2000-8607
Deacylcynaropicrin 3084544 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1055/S-2000-8607
Vernoflexuoside 442320 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1055/S-2000-8607
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1055/S-2000-8607
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2000-8607
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2000-8607
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-2000-8607
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-2000-8607
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1055/S-2000-8607
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1055/S-2000-8607
Benzyl glucopyranoside 11076492 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1055/S-2000-8607
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2-methoxyphenoxy]oxane-3,4,5-triol 69086659 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1055/S-2000-8607
Vanilloloside 44577222 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1055/S-2000-8607
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2000-8607
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1055/S-2000-8607

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