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Ligularia lankongensis

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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 UUID643fd3c94aa01414110060
Scientific name Ligularia lankongensis
Authority (Franch.) Hand.-Mazz.
First published in Symb. Sin. 7: 1139 (1936)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ligularia lankongensis var. laxa (Franch.) Hand.-Mazz. Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 69(1): 125 1938
Senecio lankongensis Franch. Bull. Soc. Bot. France 39: 301 (1893)
Senecillis lankongensis (Franch.) Kitam. Acta Phytotax. Geobot. 8: 87 (1939)
Senecio lankongensis var. laxus Franch. Bulletin de la Societe Botanique de France 39: 301 1892
Ligularia lankongensis var. minor Lauener & D.K.Ferguson Notes Roy. Bot. Gard. Edinburgh 34(3): 369 (1976)

Common names Top

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Language Common/alternative name
Chinese 洱源橐吾

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-0000134894
Tropicos 50046619
KEW urn:lsid:ipni.org:names:230776-1
The Plant List gcc-95664
Open Tree Of Life 949838
NCBI Taxonomy 268471
IPNI 230776-1
GBIF 5395433

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
A Novel Pyrrolizidine Alkaloid from Ligularia lankongensis Aimin Tan, Mian Zhang, Zhengtao Wang, Hua Zhang The Japan Institute of Heterocyclic Chemistry 11-May-2011
doi:10.3987/COM-10-12003
Chemical constituents and diversity of Ligularia lankongensis in Yunnan Province of China. Onuki H, Yamazaki M, Nakamura A, Hanai R, Kuroda C, Gong X, Shen Y, Hirota H J Nat Prod 01-Apr-2008
doi:10.1021/NP070195P
PMID:18260639
Two New Sesquiterpenes from <i>Ligularia lankongensis</i> Ai‐Min Tan, Hong‐Ping He, Mian Zhang, Zheng‐Tao Wang, Xiao‐Jiang Hao Wiley 26-Jan-2007
doi:10.1002/HLCA.200790000
Two New Nortriterpenes from Ligularia tongolensis. Yi Feng Han, Kun Gao, Zhong Jian Jia Wiley 17-Nov-2005
doi:10.1002/CHIN.200550170

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
> Alkaloids and derivatives
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 5-ethyl-2,3-dimethyl-6-oxooxane-2-carboxylate 163192679 Click to see CCC1CC(C(OC1=O)(C)C(=O)OCC2=CCN3C2C(CC3)O)C 337.40 unknown https://doi.org/10.1002/CHIN.200550170
[7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] 5-ethyl-2,3-dimethyl-6-oxooxane-2-carboxylate 163195755 Click to see CCC1CC(C(OC1=O)(C)C(=O)OC2CCN3C2C(=CC3)CO)C 337.40 unknown https://doi.org/10.1002/CHIN.200550170
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1R,2R,3R,4R,5R,6R)-6-[(3R,5R)-3,6-dihydroxy-6-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyhept-1-en-2-yl]-2,3,5-trihydroxy-3-methyl-4-[(Z)-2-methylbut-2-enoyl]oxycyclohexyl] (Z)-2-methylbut-2-enoate 162903884 Click to see CC=C(C)C(=O)OC1C(C(C(C(C1O)(C)O)OC(=O)C(=CC)C)O)C(=C)C(CC(C(C)(C)O)OC(=O)C(=CC)C)O 582.70 unknown https://doi.org/10.1002/HLCA.200790000
[(1R,2R,3R,4R,5R,6R)-6-[(3S,5S)-5,6-dihydroxy-6-methyl-3-[(Z)-2-methylbut-2-enoyl]oxyhept-1-en-2-yl]-2,3,5-trihydroxy-3-methyl-4-[(Z)-2-methylbut-2-enoyl]oxycyclohexyl] (Z)-2-methylbut-2-enoate 162979033 Click to see CC=C(C)C(=O)OC1C(C(C(C(C1O)(C)O)OC(=O)C(=CC)C)O)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(=CC)C 582.70 unknown https://doi.org/10.1002/HLCA.200790000
[(1R,2R,3R,4S,5R,6S)-4-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-2-hydroxy-1-methyl-5-[(Z)-2-methylbut-2-enoyl]oxy-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 162882022 Click to see CC=C(C)C(=O)OC1C(C(C2C(C1O)(O2)C)OC(=O)C(=CC)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 546.60 unknown https://doi.org/10.1021/NP070195P
[(1R,2R,3R,4S,6S)-4-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-2-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] (2R)-2-methylbutanoate 162912523 Click to see CCC(C)C(=O)OC1C(CC2C(C1O)(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 450.60 unknown https://doi.org/10.1021/NP070195P
[(1R,2R,3R,4S,6S)-4-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-2-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 162964085 Click to see CC=C(C)C(=O)OC1C(CC2C(C1O)(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 448.50 unknown https://doi.org/10.1021/NP070195P
[(1S,2R,3R,4S,6S)-4-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-3-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-2-yl] (Z)-2-methylbut-2-enoate 163019807 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)O 448.50 unknown https://doi.org/10.1021/NP070195P
[(1S,2S,3S,5R,6S)-3-chloro-5-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-2,6-dihydroxy-2-methylcyclohexyl] (Z)-2-methylbut-2-enoate 162891238 Click to see CC=C(C)C(=O)OC1C(C(CC(C1(C)O)Cl)C(=C)C(CC2C(O2)(C)C)OC(=O)C(=CC)C)O 485.00 unknown https://doi.org/10.1021/NP070195P
[3-Chloro-5-[4-(3,3-dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-2,6-dihydroxy-2-methylcyclohexyl] 2-methylbut-2-enoate 162891237 Click to see CC=C(C)C(=O)OC1C(C(CC(C1(C)O)Cl)C(=C)C(CC2C(O2)(C)C)OC(=O)C(=CC)C)O 485.00 unknown https://doi.org/10.1021/NP070195P
[4-[4-(3,3-Dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-2-hydroxy-1-methyl-5-(2-methylbut-2-enoyloxy)-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylbut-2-enoate 74336825 Click to see CC=C(C)C(=O)OC1C(C(C2C(C1O)(O2)C)OC(=O)C(=CC)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 546.60 unknown https://doi.org/10.1021/NP070195P
[4-[4-(3,3-Dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-2-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylbut-2-enoate 162964084 Click to see CC=C(C)C(=O)OC1C(CC2C(C1O)(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 448.50 unknown https://doi.org/10.1021/NP070195P
[4-[4-(3,3-Dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-2-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylbutanoate 162912522 Click to see CCC(C)C(=O)OC1C(CC2C(C1O)(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 450.60 unknown https://doi.org/10.1021/NP070195P
[4-[4-(3,3-Dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-3-hydroxy-1-methyl-7-oxabicyclo[4.1.0]heptan-2-yl] 2-methylbut-2-enoate 73031611 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(O2)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)O 448.50 unknown https://doi.org/10.1021/NP070195P
[6-[3,6-Dihydroxy-6-methyl-5-(2-methylbut-2-enoyloxy)hept-1-en-2-yl]-2,3,5-trihydroxy-3-methyl-4-(2-methylbut-2-enoyloxy)cyclohexyl] 2-methylbut-2-enoate 162903883 Click to see CC=C(C)C(=O)OC1C(C(C(C(C1O)(C)O)OC(=O)C(=CC)C)O)C(=C)C(CC(C(C)(C)O)OC(=O)C(=CC)C)O 582.70 unknown https://doi.org/10.1002/HLCA.200790000
[6-[5,6-Dihydroxy-6-methyl-3-(2-methylbut-2-enoyloxy)hept-1-en-2-yl]-2,3,5-trihydroxy-3-methyl-4-(2-methylbut-2-enoyloxy)cyclohexyl] 2-methylbut-2-enoate 162979032 Click to see CC=C(C)C(=O)OC1C(C(C(C(C1O)(C)O)OC(=O)C(=CC)C)O)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(=CC)C 582.70 unknown https://doi.org/10.1002/HLCA.200790000
> Organoheterocyclic compounds / Pyrrolizidines
(1R,4S,6S,7S,11S,17R,18R)-4-hydroxy-6,7,18-trimethyl-2,9-dioxa-14-azatetracyclo[9.5.1.14,7.014,17]octadecane-3,8-dione 162889146 Click to see CC1CC2(C(C1(C(=O)OCC3CCN4C3C(CC4)OC2=O)C)C)O 337.40 unknown https://doi.org/10.3987/COM-10-12003

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