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Internal ID UUID643fc7f3d49ee891877367
Scientific name Ligularia tongolensis
Authority (Franch.) Hand.-Mazz.
First published in Symb. Sin. 7: 1136 (1936)

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Synonyms Top

Scientific name Authority First published in
Senecio tongolensis Franch. Bull. Soc. Bot. France 39: 305 (1893)
Senecillis tongolensis (Franch.) Kitam. Acta Phytotax. Geobot. 8: 87 (1939)
Senecio monbeigii H.Lév. Bull. Géogr. Bot. 25: 17 (1915)

Common names Top

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Language Common/alternative name
Chinese 东饿洛橐吾
Chinese 东俄洛橐吾

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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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-0000018652
Tropicos 50046485
KEW urn:lsid:ipni.org:names:230880-1
The Plant List gcc-118034
Open Tree Of Life 280930
NCBI Taxonomy 256636
IPNI 230880-1
GBIF 5395439
EOL 6255329

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
Population structure and phylogeography of three closely related tree peonies Liu G, Xue G, Zhao T, Li Y, Yue L, Song H, Liu Q Ecol Evol 01-Jun-2023
PMCID:PMC10234759
doi:10.1002/ece3.10073
PMID:37274151
Diet and feeding behavior of a group of high-altitude rhesus macaques: high adaptation to food shortages and seasonal fluctuations Zhang K, Karim F, Jin Z, Xiao H, Yao Y, Ni Q, Li B, Pu-Cuo W, Huang Z, Xu H Curr Zool 16-Jun-2022
PMCID:PMC10284112
doi:10.1093/cz/zoac047
PMID:37351303
Determinants of Genetic Structure in a Highly Heterogeneous Landscape in Southwest China Wambulwa MC, Luo YH, Zhu GF, Milne R, Wachira FN, Wu ZY, Wang H, Gao LM, Li DZ, Liu J Front Plant Sci 25-Apr-2022
PMCID:PMC9097793
doi:10.3389/fpls.2022.779989
PMID:35574120
Comparative phylogeography study reveals introgression and incomplete lineage sorting during rapid diversification of Rhodiola You J, Lougheed SC, Zhao Y, Zhang G, Liu W, Lu F, Wang Y, Zhang W, Yang J, Qiong L, Song Z Ann Bot 27-Oct-2021
PMCID:PMC8796671
doi:10.1093/aob/mcab133
PMID:34718397
Molecular evidence for asymmetric hybridization in three closely related sympatric species Zhang NN, Yu JJ, Wang YH, Gong X AoB Plants 09-Feb-2018
PMCID:PMC5824843
doi:10.1093/aobpla/ply011
PMID:29492242
Bidirectional natural hybridization between sympatric Ligularia vellerea and L. subspicata Ning H, Yu J, Gong X Plant Divers 23-Jul-2017
PMCID:PMC6112292
doi:10.1016/j.pld.2017.07.001
PMID:30159514
Natural Hybridization and Introgression between Ligularia cymbulifera and L. tongolensis (Asteraceae, Senecioneae) in Four Different Locations Yu J, Kuroda C, Gong X PLoS One 31-Dec-2014
PMCID:PMC4281107
doi:10.1371/journal.pone.0115167
PMID:25551379
Population Expanding with the Phalanx Model and Lineages Split by Environmental Heterogeneity: A Case Study of Primula obconica in Subtropical China Yan HF, Zhang CY, Wang FY, Hu CM, Ge XJ, Hao G PLoS One 19-Sep-2012
PMCID:PMC3446961
doi:10.1371/journal.pone.0041315
PMID:23028425
Sesquiterpenes, nortriterpenes and other constituents from Ligularia tongolensis. Han YF, Pan J, Gao K, Jia ZJ Chem Pharm Bull (Tokyo) 01-Oct-2005
doi:10.1248/CPB.53.1338
PMID:16204998
Chemical and Genetic Study of <i>Ligularia tongolensis</i>, <i>Ligularia cymbulifera</i>, and <i>Ligularia atroviolacea</i> in the Hengduan Mountains of China Ryo Hanai, Xun Gong, Motoo Tori, Satomi Kondo, Kanako Otose, Yasuko Okamoto, Tadaaki Nishihama, Akihiko Murota, Yuemao Shen, Sugong Wu, Chiaki Kuroda Oxford University Press (OUP) 01-Jul-2005
doi:10.1246/BCSJ.78.1302
Two New Nortriterpenes from <i>Ligularia tongolensis</i> Yi Feng Han, Kun Gao, Zhong Jian Jia Oxford University Press (OUP) 30-May-2005
doi:10.1246/CL.2005.892

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 / Monoterpenoids / Bicyclic monoterpenoids
(1S,3S,5S)-1-Isopropyl-4-methylenebicyclo[3.1.0]hexan-3-yl acetate 91699466 Click to see CC(C)C12CC1C(=C)C(C2)OC(=O)C 194.27 unknown https://doi.org/10.1248/CPB.53.1338
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(3r,4r,6s)-3,6-Dihydroxy-1-menthene 10374851 Click to see CC1=CC(C(CC1O)C(C)C)O 170.25 unknown https://doi.org/10.1248/CPB.53.1338
5-Isopropyl-2-methylcyclohex-2-ene-1,4-diol 13919076 Click to see CC1=CC(C(CC1O)C(C)C)O 170.25 unknown https://doi.org/10.1248/CPB.53.1338
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4S,4aS,5R,6S,8aR)-3,4a-dimethyl-6-[(3S)-3-methylpentanoyl]oxy-4-[(3R)-3-methylpentanoyl]oxy-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 162902388 Click to see CCC(C)CC(=O)OC1CCC2CC3=C(C(C2(C1C(=O)O)C)OC(=O)CC(C)CC)C(=CO3)C 476.60 unknown https://doi.org/10.1246/BCSJ.78.1302
3,4a-dimethyl-4,6-bis(3-methylpentanoyloxy)-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 162902387 Click to see CCC(C)CC(=O)OC1CCC2CC3=C(C(C2(C1C(=O)O)C)OC(=O)CC(C)CC)C(=CO3)C 476.60 unknown https://doi.org/10.1246/BCSJ.78.1302
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(+)-Carainterol A 636618 Click to see CC(C)C1CCC2(C(CCC(=C)C2(C1)O)O)C 238.37 unknown https://doi.org/10.1248/CPB.53.1338
8a-methyl-4-methylidene-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,4a-diol 20979096 Click to see CC(C)C1CCC2(C(CCC(=C)C2(C1)O)O)C 238.37 unknown https://doi.org/10.1248/CPB.53.1338
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aR,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-1,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-2H-picene-1,10,11-triol 11554085 Click to see CC1CCC2CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C 444.70 unknown https://doi.org/10.1246/CL.2005.892
https://doi.org/10.1248/CPB.53.1338
(1R,2R,4aR,6aR,6aS,6bR,8aR,10S,11R,12aR,14bR)-1,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-2H-picene-1,10,11-triol 11633672 Click to see CC1CCC2CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C 444.70 unknown https://doi.org/10.1248/CPB.53.1338
https://doi.org/10.1246/CL.2005.892
1,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-2H-picene-1,10,11-triol 73004927 Click to see CC1CCC2CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C 444.70 unknown https://doi.org/10.1248/CPB.53.1338
https://doi.org/10.1246/CL.2005.892
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,5,8-triol 73190110 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2(C=CC4(C3(CCC(C4)O)C)O)O)C 430.70 unknown https://doi.org/10.1248/CPB.53.1338
Ergosta-6,22-diene-3beta,5alpha,8alpha-triol 15251535 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2(C=CC4(C3(CCC(C4)O)C)O)O)C 430.70 unknown https://doi.org/10.1248/CPB.53.1338
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,6R,9S,10R,13R,14R,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-1,2,3,4,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol 14236581 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 444.70 unknown https://doi.org/10.1248/CPB.53.1338
17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1,2,3,4,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol 72728830 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 444.70 unknown https://doi.org/10.1248/CPB.53.1338
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 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/CPB.53.1338
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/CPB.53.1338
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/10.1248/CPB.53.1338
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/10.1248/CPB.53.1338
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/10.1248/CPB.53.1338
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/CPB.53.1338
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,6-Caryolanediol 21726648 Click to see CC1(CC2C1CCC3(CC2(CCC3O)O)C)C 238.37 unknown https://doi.org/10.1248/CPB.53.1338
Caryolane-1,9beta-diol 495836 Click to see CC1(CC2C1CCC3(CC2(CCC3O)O)C)C 238.37 unknown https://doi.org/10.1248/CPB.53.1338
> Organoheterocyclic compounds / Naphthofurans
(1R,6S,8R,15S)-3,15-dimethyl-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2,11-diene-4,13-dione 11579781 Click to see CC1=C2C(CC3CCC=C4C3(C2OC4=O)C)OC1=O 260.28 unknown https://doi.org/10.1248/CPB.53.1338
(1R,8R,15S)-3,15-dimethyl-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3,11-trien-13-one 101267857 Click to see CC1=COC2=C1C3C4(C(C2)CCC=C4C(=O)O3)C 244.28 unknown https://doi.org/10.1246/BCSJ.78.1302
(3,15-Dimethyl-13-oxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3-dien-11-yl) 2-methylbut-2-enoate 163048572 Click to see CC=C(C)C(=O)OC1CCC2CC3=C(C4C2(C1C(=O)O4)C)C(=CO3)C 344.40 unknown https://doi.org/10.1246/BCSJ.78.1302
(3,15-Dimethyl-13-oxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3-dien-11-yl) 3-methylpentanoate 162848052 Click to see CCC(C)CC(=O)OC1CCC2CC3=C(C4C2(C1C(=O)O4)C)C(=CO3)C 360.40 unknown https://doi.org/10.1246/BCSJ.78.1302
(3,15-Dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-11-yl) 2-methylbut-2-enoate 162951727 Click to see CC=C(C)C(=O)OC1CCC2CC3C(=C(C(=O)O3)C)C4C2(C1C(=O)O4)C 360.40 unknown https://doi.org/10.1248/CPB.53.1338
[(1R,6S,8R,11S,12R,15S)-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-11-yl] (2R)-2-methylbutanoate 162853212 Click to see CCC(C)C(=O)OC1CCC2CC3C(=C(C(=O)O3)C)C4C2(C1C(=O)O4)C 362.40 unknown https://doi.org/10.1248/CPB.53.1338
[(1R,6S,8R,11S,12R,15S)-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-11-yl] (Z)-2-methylbut-2-enoate 101767288 Click to see CC=C(C)C(=O)OC1CCC2CC3C(=C(C(=O)O3)C)C4C2(C1C(=O)O4)C 360.40 unknown https://doi.org/10.1248/CPB.53.1338
[(1R,8R,11S,12S,15S)-3,15-dimethyl-13-oxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3-dien-11-yl] (3S)-3-methylpentanoate 162848053 Click to see CCC(C)CC(=O)OC1CCC2CC3=C(C4C2(C1C(=O)O4)C)C(=CO3)C 360.40 unknown https://doi.org/10.1246/BCSJ.78.1302
[(1R,8R,11S,12S,15S)-3,15-dimethyl-13-oxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3-dien-11-yl] (Z)-2-methylbut-2-enoate 163194130 Click to see CC=C(C)C(=O)OC1CCC2CC3=C(C4C2(C1C(=O)O4)C)C(=CO3)C 344.40 unknown https://doi.org/10.1246/BCSJ.78.1302
3,15-Dimethyl-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2,11-diene-4,13-dione 73018327 Click to see CC1=C2C(CC3CCC=C4C3(C2OC4=O)C)OC1=O 260.28 unknown https://doi.org/10.1248/CPB.53.1338
3,15-Dimethyl-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3,11-trien-13-one 3477731 Click to see CC1=COC2=C1C3C4(C(C2)CCC=C4C(=O)O3)C 244.28 unknown https://doi.org/10.1246/BCSJ.78.1302

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