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Ligularia altaica

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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 UUID643fca15ef8b2336115304
Scientific name Ligularia altaica
Authority DC.
First published in Prodr. 6: 315 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecillis altaica (DC.) Kitam. Acta Phytotax. Geobot. 8: 85 (1939)
Cineraria altaica C.A.Mey. ex DC. Prodr. 6: 315 (1838)
Senecio altaicus Sch.Bip. Flora 28: 50 (1845)
Ligularia glauca var. altaica (DC.) Krylov

Common names Top

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Language Common/alternative name
Chinese 阿勒泰橐吾

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Tuva

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000035538
Tropicos 2731828
KEW urn:lsid:ipni.org:names:230690-1
The Plant List gcc-134374
Open Tree Of Life 7051929
Observations.org 119367
NCBI Taxonomy 2126590
IPNI 230690-1
iNaturalist 859042
GBIF 5395490
CMAUP NPO12711

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
Morphometric Characteristics and Genetic Issr Marker Variability in Rhodiola rosea L. (Crassulaceae) in Different Ecological and Geographic Conditions in the Altai Republic Dorogina OV, Kuban IN, Achimova AA, Williams N, Lashchinskiy NN, Zhmud EV Int J Mol Sci 16-Oct-2023
PMCID:PMC10607822
doi:10.3390/ijms242015224
PMID:37894905
A review of the ethnobotanical value, phytochemistry, pharmacology, toxicity and quality control of Tussilago farfara L. (coltsfoot) Chen S, Dong L, Quan H, Zhou X, Ma J, Xia W, Zhou H, Fu X J Ethnopharmacol 16-Oct-2020
PMCID:PMC7561605
doi:10.1016/j.jep.2020.113478
PMID:33069788
Altaicalarins A-D, cytotoxic bisabolane sesquiterpenes from Ligularia altaica. Wang Q, Chen TH, Bastow KF, Lee KH, Chen DF J Nat Prod 26-Feb-2010
PMCID:PMC2829383
doi:10.1021/NP900489H
PMID:20073490
Altaicalarins A–D, Cytotoxic Bisabolane Sesquiterpenes from Ligularia altaica Wang Q, Chen TH, Bastow KF, Lee KH, Chen DF J Nat Prod 26-Feb-2010
PMCID:PMC2829383
doi:10.1021/np900489h
PMID:20073490

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Pretazettine 73360 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown via CMAUP database
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown via CMAUP database
Phenethylamine 1001 Click to see C1=CC=C(C=C1)CCN 121.18 unknown via CMAUP database
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1R,3S,4R,6R)-3-acetyloxy-4-[5,6-dihydroxy-6-methyl-3-[(Z)-2-methylbut-2-enoyl]oxyhept-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-2-yl] (Z)-2-methylbut-2-enoate 46881271 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(O2)C)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(=CC)C)OC(=O)C 508.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(1R,3S,4R,6R)-3-acetyloxy-4-[5,6-dihydroxy-6-methyl-3-[(Z)-2-methylbut-2-enoyl]oxyhept-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-2-yl] 2-methylbut-2-enoate 163188446 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(O2)C)C(=C)C(CC(C(C)(C)O)O)OC(=O)C(=CC)C)OC(=O)C 508.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(1S,3R,4R,6R)-4-[(3S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 162985326 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC1C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)C 432.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(1S,3R,4R,6R)-4-[4-(3,3-dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 162985327 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC1C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)C 432.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(1S,3R,4R,6R)-4-[4-(3,3-dimethyloxiran-2-yl)-3-[(Z)-2-methylbut-2-enoyl]oxybut-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 11575639 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC1C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)C 432.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(3S)-2-(2-acetyloxy-3,5-dihydroxy-4-methylphenyl)-6-methylhepta-1,5-dien-3-yl] (Z)-2-methylbut-2-enoate 139037640 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=CC(=C(C(=C1OC(=O)C)O)C)O 388.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(3S)-2-(2,3-dihydroxy-4-methylphenyl)-6-methylhepta-1,5-dien-3-yl] (Z)-2-methylbut-2-enoate 163017845 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=C(C(=C(C=C1)C)O)O 330.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[(3S)-2-[(1S,3S,4S,6S)-4-acetyloxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl]-6-methylhepta-1,5-dien-3-yl] (Z)-2-methylbut-2-enoate 162884389 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1CC2C(O2)(C(=O)C1OC(=O)C)C 390.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[2-(2-Acetyloxy-3,5-dihydroxy-4-methylphenyl)-6-methylhepta-1,5-dien-3-yl] 2-methylbut-2-enoate 75166455 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=CC(=C(C(=C1OC(=O)C)O)C)O 388.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[2-(2,3-Dihydroxy-4-methylphenyl)-6-methylhepta-1,5-dien-3-yl] 2-methylbut-2-enoate 75166456 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=C(C(=C(C=C1)C)O)O 330.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[2-(4-Acetyloxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl)-6-methylhepta-1,5-dien-3-yl] 2-methylbut-2-enoate 75166535 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1CC2C(O2)(C(=O)C1OC(=O)C)C 390.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
[4-[4-(3,3-Dimethyloxiran-2-yl)-3-(2-methylbut-2-enoyloxy)but-1-en-2-yl]-1-methyl-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylbut-2-enoate 73016667 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC1C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C)C 432.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
Altaicalarin A 46186370 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=CC(=C(C(=C1OC(=O)C)O)C)O 388.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
Altaicalarin B 46186371 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1=C(C(=C(C=C1)C)O)O 330.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
Altaicalarin C 46186620 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1CC2C(O2)(C(=O)C1OC(=O)C)C 390.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
Altaicalarin D 46186621 Click to see CC=C(C)C(=O)OC1C(C(C(=O)C2(C1O2)C)OC(=O)C)C(=C)C(CC3C(O3)(C)C)OC(=O)C(=CC)C 504.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
(3S,4R,5R,9R,10R,13R,14R,17R)-17-[(2S,3R)-3-hydroxy-6-methylhept-5-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,4-diol 11327511 Click to see CC(C1CCC2C1(CCC3C2=CCC4C3(CCC(C4O)O)C)C)C(CC=C(C)C)O 416.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829383/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Biflorin 441959 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown via CMAUP database
Undulatoside A 5321494 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2',4',6'-Trimethoxyacetophenone 123089 Click to see CC(=O)C1=C(C=C(C=C1OC)OC)OC 210.23 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,6-Dihydroxy-7-methoxy-2-methyl-4H-1-benzopyran-4-one 52918156 Click to see CC1=CC(=O)C2=C(C(=C(C=C2O1)OC)O)O 222.19 unknown via CMAUP database
Noreugenin 5375252 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)O 192.17 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(16beta)-4,12-Didehydro-9,10-(methylenedioxy)galanthan-1alpha,2beta,3alpha-triol 101649371 Click to see C1C=C2C3N1CC4=CC5=C(C=C4C3C(C(C2O)O)O)OCO5 303.31 unknown via CMAUP database
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown via CMAUP database
Dehydroanhydrolycorine 10999422 Click to see C1C2=CC3=C(C=C2C4=CC=CC5=C4N1C=C5)OCO3 249.26 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Broussin 442277 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O 256.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5,4'-dimethoxyflavan 44257196 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3OC)O 286.32 unknown via CMAUP database

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