Ligularia duciformis - Unknown
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Internal ID UUID643fc7fe4611b907805911
Scientific name Ligularia duciformis
Authority (C.Winkl.) Hand.-Mazz.
First published in Symb. Sin. 7: 1135 (1936)

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Synonyms Top

Scientific name Authority First published in
Senecio duciformis C.Winkl. Trudy Imp. S.-Peterburgsk. Bot. Sada xiv. (1895) 155.
Senecillis duciformis (C.Winkl.) Kitam. Acta Phytotax. Geobot. 8: 87 (1939)

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Language Common/alternative name
Chinese 大黄
Chinese 大黄橐吾
Chinese 大黄橐翼吾
Chinese 网脉橐吾

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Varieties (abbr. var.) 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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000018965
Tropicos 50046441
KEW urn:lsid:ipni.org:names:230732-1
The Plant List gcc-118336
Open Tree Of Life 814910
NCBI Taxonomy 262731
IPNI 230732-1
GBIF 5395497
EOL 6255156

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
Identification of Pyrrolizidine Alkaloids in Senecio Plants by Liquid Chromatography-Mass Spectrometry Lu AJ, Lu YL, Tan DP, Qin L, Ling H, Wang CH, He YQ J Anal Methods Chem 16-Nov-2021
PMCID:PMC8610691
doi:10.1155/2021/1957863
PMID:34824876
Identification and Simultaneous Determination of the Main Toxical Pyrrolizidine Alkaloids in a Compound Prescription of Traditional Chinese Medicine: Qianbai Biyan Tablet Yang M, Tan D, Lu A, Qin L, Wang C, Ling H, Lu Y, He Y Int J Anal Chem 09-Sep-2021
PMCID:PMC8445730
doi:10.1155/2021/5209618
PMID:34539789
Molecular Mechanisms Involved in Oxidative Stress-Associated Liver Injury Induced by Chinese Herbal Medicine: An Experimental Evidence-Based Literature Review and Network Pharmacology Study Zhang C, Wang N, Xu Y, Tan HY, Li S, Feng Y Int J Mol Sci 13-Sep-2018
PMCID:PMC6165031
doi:10.3390/ijms19092745
PMID:30217028
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
Terpenoids and Phenylpropanoids in Ligularia duciformis, L. kongkalingensis, L. nelumbifolia, and L. limprichtii Kuroda C, Kobayashi R, Nagata A, Nakadozono Y, Itoh T, Okamoto Y, Tori M, Hanai R, Gong X Molecules 25-Nov-2017
PMCID:PMC6149998
doi:10.3390/molecules22122062
PMID:29186833
Evidence for continual hybridization rather than hybrid speciation between Ligularia duciformis and L. paradoxa (Asteraceae) Zhang R, Gong X, Folk R PeerJ 11-Oct-2017
PMCID:PMC5640982
doi:10.7717/peerj.3884
PMID:29038755
Sesquiterpenes from the Roots of <i>Ligularia duciformis</i> Kun Gao, Li Yang, Zhong‐Jian Jia Wiley 01-May-2015
doi:10.1002/JCCS.199900086
6β-Hy­droxy­eremophil-7(11)-en-8β,12-olide Su RN, Shi S, Wu HB, Wang WS Acta Crystallogr Sect E Struct Rep Online 07-May-2011
PMCID:PMC3120521
doi:10.1107/S1600536811016308
PMID:21754755
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
3β-Acet­oxy-8β,10β-dihy­droxy-6β-meth­oxy­eremophil-7(11)-en-8,12-olide Wu HB, Li H, Lan XC, Wang WS Acta Crystallogr Sect E Struct Rep Online 31-Jul-2010
PMCID:PMC3007320
doi:10.1107/S1600536810029831
PMID:21588445
Mechanisms of fenthion activation in rainbow trout (Oncorhynchus mykiss) acclimated to hypersaline environments Lavado R, Rimoldi JM, Schlenk D Toxicol Appl Pharmacol 09-Dec-2008
PMCID:PMC2858921
doi:10.1016/j.taap.2008.11.017
PMID:19111563
New Sesquiterpenoids from <i>Ligularia duciformis</i> Wen‐Shu Wang, Xia Dai, Li‐Ya Hong, Peng Lu, Jin‐Chao Feng, Yu‐Guo Jiao Wiley 10-Jul-2008
doi:10.1002/HLCA.200890119
Testing a hypothesis of unidirectional hybridization in plants: Observations on Sonneratia, Bruguiera and Ligularia Zhou R, Gong X, Boufford D, Wu CI, Shi S BMC Evol Biol 16-May-2008
PMCID:PMC2409324
doi:10.1186/1471-2148-8-149
PMID:18485207
Coniferyl and sinapyl alcohol derivatives from Ligularia duciformis Kun Gao, Wen-Shu Wang, Zhong-Jian Jia Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00493-7

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 / Methoxybenzenes / Dimethoxybenzenes
(3E,6E)-8-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]-2,6-dimethylocta-3,6-dien-2-ol 101939209 Click to see CC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)CC=CC(C)(C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
(3R,6E)-8-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]-2,6-dimethylocta-1,6-dien-3-ol 163185640 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
3-[4-(3,7-Dimethylocta-2,5,7-trienoxy)-3,5-dimethoxyphenyl]prop-2-en-1-ol 162917476 Click to see CC(=C)C=CCC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C 344.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-[4-(3-Hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]-2,6-dimethylocta-1,6-dien-3-ol 162894225 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-[4-(3-Hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]-2,6-dimethylocta-1,6-dien-4-one 163053420 Click to see CC(=C)CC(=O)CC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C 360.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-[4-(3-Hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]-2,6-dimethylocta-3,6-dien-2-ol 162990839 Click to see CC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)CC=CC(C)(C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
3-Ethoxy-5-hydroxy-7-methoxyphenanthrene-1,4-dione 21668767 Click to see CCOC1=CC(=O)C2=C(C1=O)C3=C(C=C(C=C3C=C2)OC)O 298.29 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
3-(4-((3,7-Dimethylocta-2,6-dien-1-yl)oxy)-3-methoxyphenyl)prop-2-en-1-ol 131097 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)C 316.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
3-[4-(3,7-Dimethylocta-2,6-dienoxy)-3,5-dimethoxyphenyl]prop-2-en-1-ol 132473 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C)C 346.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
Nelumol A 6439446 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C)C 346.50 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
O-Geranylconiferyl alcohol 6439279 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)C 316.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3S,5S,8aS)-3-methyl-8-methylidene-5-propan-2-yl-1,2,5,6,7,8a-hexahydroazulene-1,3-diol 15858055 Click to see CC(C)C1CCC(=C)C2C(CC(C2=C1)(C)O)O 236.35 unknown https://doi.org/10.1002/JCCS.199900086
3-Methyl-8-methylidene-5-propan-2-yl-1,2,5,6,7,8a-hexahydroazulene-1,3-diol 162981480 Click to see CC(C)C1CCC(=C)C2C(CC(C2=C1)(C)O)O 236.35 unknown https://doi.org/10.1002/JCCS.199900086
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2R,6S,8aR)-5,8a-dimethyl-3-propan-2-yl-2,6,7,8-tetrahydro-1H-naphthalene-2,6-diol 15858056 Click to see CC1=C2C=C(C(CC2(CCC1O)C)O)C(C)C 236.35 unknown https://doi.org/10.1002/JCCS.199900086
4-Hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 14681769 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown https://doi.org/10.1002/JCCS.199900086
5,8a-dimethyl-3-propan-2-yl-2,6,7,8-tetrahydro-1H-naphthalene-2,6-diol 162874108 Click to see CC1=C2C=C(C(CC2(CCC1O)C)O)C(C)C 236.35 unknown https://doi.org/10.1002/JCCS.199900086
Ligucyperonol 14681770 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown https://doi.org/10.1002/JCCS.199900086
Platambin 613194 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1002/JCCS.199900086
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1002/JCCS.199900086
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(-)-Alismoxide 10243299 Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O 238.37 unknown https://doi.org/10.1002/JCCS.199900086
1alphaH,5alphaH-Guaia-6-ene-4beta,10beta-diol 71773128 Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O 238.37 unknown https://doi.org/10.1002/JCCS.199900086
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4-Methoxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9a-hexahydrobenzo[f][1]benzofuran-6-yl) acetate 74350085 Click to see CC1C(CCC2=CC3C(=C(C(=O)O3)C)C(C12C)OC)OC(=O)C 320.40 unknown https://doi.org/10.1002/HLCA.200890119
(4,8a,9a-Trihydroxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl) acetate 74350110 Click to see CC1C(CCC2(C1(C(C3=C(C(=O)OC3(C2)O)C)O)C)O)OC(=O)C 340.40 unknown https://doi.org/10.1002/HLCA.200890119
(8a-Hydroxy-4,9a-dimethoxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl) acetate 74350109 Click to see CC1C(CCC2(C1(C(C3=C(C(=O)OC3(C2)OC)C)OC)C)O)OC(=O)C 368.40 unknown https://doi.org/10.1002/HLCA.200890119
(9a-hydroxy-4-methoxy-3,4a,5-trimethyl-2-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-6-yl) acetate 74350084 Click to see CC1C(CCC2=CC3(C(=C(C(=O)O3)C)C(C12C)OC)O)OC(=O)C 336.40 unknown https://doi.org/10.1002/HLCA.200890119
[(4S,4aR,5R,6S,9aR)-4-methoxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9a-hexahydrobenzo[f][1]benzofuran-6-yl] acetate 24905756 Click to see CC1C(CCC2=CC3C(=C(C(=O)O3)C)C(C12C)OC)OC(=O)C 320.40 unknown https://doi.org/10.1002/HLCA.200890119
[(4S,4aR,5R,6S,9aR)-9a-hydroxy-4-methoxy-3,4a,5-trimethyl-2-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-6-yl] acetate 24905755 Click to see CC1C(CCC2=CC3(C(=C(C(=O)O3)C)C(C12C)OC)O)OC(=O)C 336.40 unknown https://doi.org/10.1002/HLCA.200890119
[(4S,4aS,5R,6S,8aS,9aS)-4,8a,9a-trihydroxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl] acetate 24905803 Click to see CC1C(CCC2(C1(C(C3=C(C(=O)OC3(C2)O)C)O)C)O)OC(=O)C 340.40 unknown https://doi.org/10.1002/HLCA.200890119
[(4S,4aS,5R,6S,8aS,9aS)-8a-hydroxy-4,9a-dimethoxy-3,4a,5-trimethyl-2-oxo-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl] acetate 24905802 Click to see CC1C(CCC2(C1(C(C3=C(C(=O)OC3(C2)OC)C)OC)C)O)OC(=O)C 368.40 unknown https://doi.org/10.1002/HLCA.200890119
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1S,3aR,5aS,8R,8aR,9aR)-8-hydroxy-1,5,8-trimethyl-1,3a,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 163010953 Click to see CC1C2CC3C(CCC3(C)O)C(=CC2OC1=O)C 250.33 unknown https://doi.org/10.1002/JCCS.199900086
[(3aS,4S,5S,6R,6aS,7R,9aR,9bR)-5,7-dihydroxy-9-methyl-3-methylidene-2-oxospiro[4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-6,2'-oxirane]-4-yl] (E)-2-methylbut-2-enoate 163185936 Click to see CC=C(C)C(=O)OC1C2C(C3C(C(C=C3C)O)C4(C1O)CO4)OC(=O)C2=C 376.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-Hydroxy-1,5,8-trimethyl-1,3a,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 14282660 Click to see CC1C2CC3C(CCC3(C)O)C(=CC2OC1=O)C 250.33 unknown https://doi.org/10.1002/JCCS.199900086
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(97)00493-7
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/10.1016/S0031-9422(97)00493-7
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/10.1016/S0031-9422(97)00493-7
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/10.1007/S10600-011-9810-Y
https://doi.org/10.1016/S0031-9422(97)00493-7
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(3E,6E)-8-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]-2,6-dimethylocta-3,6-dien-2-ol 101939205 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)CC=CC(C)(C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
(3R,6E)-8-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]-2,6-dimethylocta-1,6-dien-3-ol 163193459 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
(E)-3-[4-[(2E,5E)-7-hydroperoxy-3,7-dimethylocta-2,5-dienoxy]-3-methoxyphenyl]prop-2-en-1-ol 101939207 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)CC=CC(C)(C)OO 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
(E)-3-[4-[(2E,6R)-6-hydroperoxy-3,7-dimethylocta-2,7-dienoxy]-3-methoxyphenyl]prop-2-en-1-ol 163190227 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)OO 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
3-[4-(6-Hydroperoxy-3,7-dimethylocta-2,7-dienoxy)-3-methoxyphenyl]prop-2-en-1-ol 162999734 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)OO 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
3-[4-(7-Hydroperoxy-3,7-dimethylocta-2,5-dienoxy)-3-methoxyphenyl]prop-2-en-1-ol 162868720 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)CC=CC(C)(C)OO 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-[4-(3-Hydroxyprop-1-enyl)-2-methoxyphenoxy]-2,6-dimethylocta-1,6-dien-3-ol 85382787 Click to see CC(=C)C(CCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7
8-[4-(3-Hydroxyprop-1-enyl)-2-methoxyphenoxy]-2,6-dimethylocta-3,6-dien-2-ol 162853738 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)CC=CC(C)(C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(97)00493-7

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