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Parasenecio auriculatus

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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 UUID643fc8fbbee8d109769660
Scientific name Parasenecio auriculatus
Authority (DC.) J.R.Grant
First published in Novon 3(2): 154 (1993)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cacalia auriculata DC. Prodr. 6: 329 (1838)
Koyamacalia auriculata (DC.) H.Rob. & Brettell Phytologia 27(4): 271 (1973)
Cacalia bulbifera Koidz.
Senecio dahuricus Sch.Bip. Flora 28: 499 (1845)
Cacalia kamtschatica var. bulbifera (Koidz.) Kitam.
Cacalia auriculata subsp. kamtschatica (Maxim.) Hultén Flora of Alaska and Neighboring Territories; A Manual of the Vascular Plants 924 1968
Ligularia auriculata Turcz. ex DC. Prodr. 6: 329 (1838)
Senecio dahuricus var. ochotensis Maxim. Bull. Acad. Imp. Sci. Saint-Petersbourg 19: 485 1874
Parasenecio auriculatus var. kamtschaticus (Maxim.) H.Koyama Fl. Jap. 3b: 50 (1995)

Common names Top

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Language Common/alternative name
English eared indian plantain
Chinese 耳叶蟹甲草
Chinese 耳叶兔儿伞

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.
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.

Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000026781
USDA Plants PAAU14
Tropicos 2743803
KEW urn:lsid:ipni.org:names:972366-1
The Plant List gcc-125881
NCBI Taxonomy 2783885
IPNI 1171991-2
iNaturalist 746704
GBIF 3090384
EOL 16994735
USDA GRIN 417183

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
Anti-atopic dermatitis effects of Parasenecio auriculatus via simultaneous inhibition of multiple inflammatory pathways Kwon Y, Cho SY, Kwon J, Hwang M, Hwang H, Kang YJ, Lee HS, Kim J, Kim WK BMB Rep 30-Jun-2022
PMCID:PMC9252893
doi:10.5483/BMBRep.2022.55.6.144
PMID:35168697
Vascular Plants Flora of Mire Ecosystem of the Bolshoy Shantar Island (the Far East of Russia) Kuptsova VA, Antonova LA, Chakov VV Plants (Basel) 08-Mar-2022
PMCID:PMC8948750
doi:10.3390/plants11060723
PMID:35336605
Non-target Effects of Naphthalene on the Soil Microbial Biomass and Bacterial Communities in the Subalpine Forests of Western China Lan L, Yang F, Zhang L, Yang W, Wu F, Xu Z, Liu Y, Yue K, Ni X, Li H, Liao S, Liu Y, Chen Y, Tan B Sci Rep 08-Jul-2019
PMCID:PMC6614484
doi:10.1038/s41598-019-46394-3
PMID:31285516
Effects of naphthalene on soil fauna abundance and enzyme activity in the subalpine forest of western Sichuan, China Liu Y, Yang F, Yang W, Wu F, Xu Z, Liu Y, Zhang L, Yue K, Ni X, Lan L, Chen Y, Tan B Sci Rep 26-Feb-2019
PMCID:PMC6391496
doi:10.1038/s41598-019-39603-6
PMID:30809005
Rhamnus davurica leaf extract inhibits Fyn activation by antigen in mast cells for anti-allergic activity Kim JH, Kim AR, Kim HS, Kim HW, Park YH, You JS, Park YM, Her E, Kim HS, Kim YM, Choi WS BMC Complement Altern Med 25-Mar-2015
PMCID:PMC4379541
doi:10.1186/s12906-015-0607-6
PMID:25887889
Plant Diversity Changes during the Postglacial in East Asia: Insights from Forest Refugia on Halla Volcano, Jeju Island Dolezal J, Altman J, Kopecky M, Cerny T, Janecek S, Bartos M, Petrik P, Srutek M, Leps J, Song JS PLoS One 16-Mar-2012
PMCID:PMC3306376
doi:10.1371/journal.pone.0033065
PMID:22438890
THE SESQUITERPENES OF <i>CACALIA</i> SPECIES Keizo Naya, Yasushi Miyoshi, Hideo Mori, Kunihiro Takai, Mikihiko Nakanishi Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1976.73
[Studies on the constituents of Cacalia spp. I. The constituents of Cacalia auriculata DC. var. kamtschatica (Maxim.) Matsumura. (1)]. Takemoto T, Kusano G, Aota K, Kaneshima M, Emary NA Yakugaku Zasshi 01-Dec-1974
doi:10.1248/YAKUSHI1947.94.12_1593
PMID:4476761

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 / Naphthalenes / Naphthols and derivatives
O-methyldehydronorcacalol 11139412 Click to see CC1CC=CC2=C(C(=C(C(=C12)C)C(=O)C)O)OC 246.30 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
Qfuxwtvaalrojb-uhfffaoysa- 50937020 Click to see CC1CC=CC2=C(C(=C(C(=C12)C)C(=O)C)O)OC 246.30 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4S)-4-hydroxy-3,4,5-trimethylbenzo[f][1]benzofuran-9-one 162845975 Click to see CC1=C2C(=CC=C1)C(=O)C3=C(C2(C)O)C(=CO3)C 242.27 unknown https://doi.org/10.1246/CL.1976.73
Cacalonol 3085072 Click to see CC1=C2C(=CC=C1)C(=O)C3=C(C2(C)O)C(=CO3)C 242.27 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
https://doi.org/10.1246/CL.1976.73
Naphtho(2,3-b)furan, 9-methoxy-3,4,5-trimethyl- 3084982 Click to see CC1=C2C(=C3C(=COC3=C(C2=CC=C1)OC)C)C 240.30 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aS,6aS,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 163069311 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593
> 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/10.1248/YAKUSHI1947.94.12_1593
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/10.1248/YAKUSHI1947.94.12_1593
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1593

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