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Ligularia pleurocaulis

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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 UUID643fcea18ea2e626068362
Scientific name Ligularia pleurocaulis
Authority Hand.-Mazz.
First published in Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 1925, lxii. 149

Description Top

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Synonyms Top

Scientific name Authority First published in
Cremanthodium pleurocaule R.D.Good J. Linn. Soc., Bot. xlviii. 290 (1929)
Senecio pleurocaulis Franch. J. Bot. (Morot) viii. (1894) 365

Common names Top

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Language Common/alternative name
Chinese 侧茎垂头菊
Chinese 侧茎橐吾

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-0000083131
Tropicos 50046723
KEW urn:lsid:ipni.org:names:230826-1
The Plant List gcc-39619
Open Tree Of Life 119689
NCBI Taxonomy 262734
IPNI 230826-1
iNaturalist 1156113
GBIF 5395515
EOL 6255270
CMAUP NPO7329

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
Biotransformation of furannoligularenone by transgenic crown galls of Panax quinquefolium Yan C, Wang J, Duan G, Yu R Pharmacogn Mag 01-Apr-2012
PMCID:PMC3371433
doi:10.4103/0973-1296.96555
PMID:22701285
Chemical constituents from Ligularia nanchuanica Xue-Mei Ma, Yan-Ping Shi Springer Science and Business Media LLC 07-Feb-2011
doi:10.1007/S10600-011-9810-Y
Chemical and Genetic Differentiation of <i>Ligularia pleurocaulis</i> in Northwestern Yunnan and Southwestern Sichuan Provinces of China Hajime Nagano, Yukiko Iwazaki, Xun Gong, Yuemao Shen, Chiaki Kuroda, Ryo Hanai Oxford University Press (OUP) 10-Feb-2006
doi:10.1246/BCSJ.79.300

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1007/S10600-011-9810-Y
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2,3-Dimethylacrylic acid, (E)- 125468 Click to see CC=C(C)C(=O)O 100.12 unknown https://doi.org/10.1007/S10600-011-9810-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-4-yl) 2-methylbut-2-enoate 557798 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCCC(C13C)C)OC=C2C 314.40 unknown https://doi.org/10.1246/BCSJ.79.300
(4-hydroxy-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-6-yl) 2-methylbut-2-enoate 162907756 Click to see CC=C(C)C(=O)OC1CC=C2CC3=C(C(C2(C1C)C)O)C(=CO3)C 330.40 unknown https://doi.org/10.1246/BCSJ.79.300
(4S,4aR)-4beta-[[(2E)-2-Methyl-2-butenoyl]oxy]-4,4a,5,6,7,9-hexahydro-3,4abeta,5beta-trimethylnaphtho[2,3-b]furan-6beta-ol 101388865 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCC(C(C13C)C)O)OC=C2C 330.40 unknown https://doi.org/10.1246/BCSJ.79.300
(6-hydroxy-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-4-yl) 2-methylbut-2-enoate 162980129 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCC(C(C13C)C)O)OC=C2C 330.40 unknown https://doi.org/10.1246/BCSJ.79.300
[(4S,4aR,5R,6S)-4-hydroxy-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-6-yl] (Z)-2-methylbut-2-enoate 14287013 Click to see CC=C(C)C(=O)OC1CC=C2CC3=C(C(C2(C1C)C)O)C(=CO3)C 330.40 unknown https://doi.org/10.1246/BCSJ.79.300
[(4S,4aR,5R,6S)-6-hydroxy-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate 101388864 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCC(C(C13C)C)O)OC=C2C 330.40 unknown https://doi.org/10.1246/BCSJ.79.300
[(4S,4aR,5S)-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-4-yl] (E)-2-methylbut-2-enoate 101388863 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCCC(C13C)C)OC=C2C 314.40 unknown https://doi.org/10.1246/BCSJ.79.300
[(4S,4aR,5S)-3,4a,5-trimethyl-5,6,7,9-tetrahydro-4H-benzo[f][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate 14190071 Click to see CC=C(C)C(=O)OC1C2=C(CC3=CCCC(C13C)C)OC=C2C 314.40 unknown https://doi.org/10.1246/BCSJ.79.300
10alpha-Furanoligularenone 10466401 Click to see CC1C(=O)C=CC2C1(CC3=C(C2)OC=C3C)C 230.30 unknown https://doi.org/10.1246/BCSJ.79.300
3,4a,5-Trimethyl-4,5,8a,9-tetrahydrobenzo[f][1]benzofuran-6-one 12309965 Click to see CC1C(=O)C=CC2C1(CC3=C(C2)OC=C3C)C 230.30 unknown https://doi.org/10.1246/BCSJ.79.300
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxylup-20(29)-en-28-amide 10161414 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)N 455.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-011-9810-Y
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/10.1007/S10600-011-9810-Y
> 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/10.1007/S10600-011-9810-Y
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/10.1007/S10600-011-9810-Y
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/S10600-011-9810-Y
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1007/S10600-011-9810-Y
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 22524175 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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