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Ligusticum grayi

Ligusticum grayi - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644046f4a43b9134142870
Scientific name Ligusticum grayi
Authority J.M.Coult. & Rose
First published in Rev. N. Amer. Umbell. : 88 (1888)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English gray's licorice-root

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
      • Nevada
      • Utah

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001067835
Canadensys 2590
USDA Plants LIGR
Tropicos 1700836
KEW urn:lsid:ipni.org:names:287962-2
The Plant List tro-1700836
Open Tree Of Life 3889895
NCBI Taxonomy 2042421
Nature Serve 2.133610
IUCN Red List 116996233
IPNI 287962-2
iNaturalist 77738
GBIF 3034792
Freebase /m/076x5s1
EOL 582073
Calflora (Californian flora) 4796
USDA GRIN 448192
Wikipedia Ligusticum_grayi

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
MeadoWatch: a long-term community-science database of wildflower phenology in Mount Rainier National Park Manzanedo RD, John A, Sethi ML, Theobald EJ, Brosi B, Jenkins J, Kloss-Schmidt A, Lia E, Schiffer A, Sevigny J, Wilson A, Yogev Y, Hille Ris Lambers J Sci Data 01-Apr-2022
PMCID:PMC8976009
doi:10.1038/s41597-022-01206-8
PMID:35365666
Volatile non-terpenoid hydrocarbons from Ligusticum grayi roots Laurence G. Cool, Gary R. Takeoka, Karl E. Vermillion Elsevier BV 07-Mar-2011
doi:10.1016/J.PHYTOL.2011.02.006
Irregular sesquiterpenoids from Ligusticum grayi roots. Cool LG, Vermillion KE, Takeoka GR, Wong RY Phytochemistry 01-Sep-2010
doi:10.1016/J.PHYTOCHEM.2010.06.003
PMID:20615518
Molecular markers for identification of the hyperparasitoids Dendrocerus carpenteri and Alloxysta xanthopsis in Lysiphlebus testaceipes parasitizing cereal aphids CHEN Y, PIKE KS, GREENSTONE MH, SHUFRAN KA Biocontrol (Dordr) 01-Apr-2006
PMCID:PMC7384741
doi:10.1007/s10526-005-1518-0
PMID:32719580

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
Benzene, 2-butenyl-, cis 6431018 Click to see CC=CCC1=CC=CC=C1 132.20 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
But-2-enylbenzene 15263 Click to see CC=CCC1=CC=CC=C1 132.20 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(3aS,4R,5R,7aS)-3a,4,5,7a-tetramethyl-2,3-dimethylidene-4,5,6,7-tetrahydro-1H-indene 162879833 Click to see CC1CCC2(CC(=C)C(=C)C2(C1C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3aS,7aS)-3a,4,4,7a-tetramethyl-2,3-dimethylidene-1,5,6,7-tetrahydroindene 162933000 Click to see CC1(CCCC2(C1(C(=C)C(=C)C2)C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
1-[(Z)-but-2-enyl]cyclohexa-1,3-diene 163720712 Click to see CC=CCC1=CC=CCC1 134.22 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
1-[(Z)-pent-2-enyl]cyclohexa-1,3-diene 152745751 Click to see CCC=CCC1=CC=CCC1 148.24 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
1-But-2-enylcyclohexa-1,3-diene 162866956 Click to see CC=CCC1=CC=CCC1 134.22 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
1-Pent-2-enylcyclohexa-1,3-diene 86022408 Click to see CCC=CCC1=CC=CCC1 148.24 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.006
3a,4,4,7a-Tetramethyl-2,3-dimethylidene-1,5,6,7-tetrahydroindene 162932999 Click to see CC1(CCCC2(C1(C(=C)C(=C)C2)C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
3a,4,5,7a-tetramethyl-2,3-dimethylidene-4,5,6,7-tetrahydro-1H-indene 162879832 Click to see CC1CCC2(CC(=C)C(=C)C2(C1C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(3,3,3a,4,4-Pentamethyl-1,2,5,6-tetrahydroinden-2-yl)methanol 162959084 Click to see CC1(CCC=C2C1(C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,3a,4,5-pentamethyl-2,4,5,6-tetrahydro-1H-inden-2-yl)methanol 162969845 Click to see CC1CC=C2CC(C(C2(C1C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,3a,4,7a-Pentamethyl-1,2,6,7-tetrahydroinden-2-yl)methanol 162887135 Click to see CC1=CCCC2(C1(C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,4,4,7-pentamethyl-2,3a,5,6-tetrahydro-1H-inden-2-yl)methanol 162842639 Click to see CC1=C2CC(C(C2C(CC1)(C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,4,4,7a-Pentamethyl-1,2,3a,5-tetrahydroinden-2-yl)methanol 163034935 Click to see CC1(CC=CC2(C1C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,4,4,7a-Pentamethyl-1,2,3a,7-tetrahydroinden-2-yl)methanol 78126543 Click to see CC1(C=CCC2(C1C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,4,5,7a-pentamethyl-2,3a,6,7-tetrahydro-1H-inden-2-yl)methanol 163030582 Click to see CC1=C(C2C(C(CC2(CC1)C)CO)(C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3a,4,4,7a-Pentamethyl-1,5,6,7-tetrahydroinden-2-yl)methanol 163027540 Click to see CC1=C(CC2(C1(C(CCC2)(C)C)C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3a,4,5,7a-pentamethyl-4,5,6,7-tetrahydro-1H-inden-2-yl)methanol 162849894 Click to see CC1CCC2(CC(=C(C2(C1C)C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aR,4R,5R)-3,3,3a,4,5-pentamethyl-2,4,5,6-tetrahydro-1H-inden-2-yl]methanol 162969846 Click to see CC1CC=C2CC(C(C2(C1C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aR,7aS)-3,3,3a,4,7a-pentamethyl-1,2,6,7-tetrahydroinden-2-yl]methanol 135040720 Click to see CC1=CCCC2(C1(C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aR,7aS)-3,3,4,5,7a-pentamethyl-2,3a,6,7-tetrahydro-1H-inden-2-yl]methanol 163030583 Click to see CC1=C(C2C(C(CC2(CC1)C)CO)(C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aR)-3,3,3a,4,4-pentamethyl-1,2,5,6-tetrahydroinden-2-yl]methanol 162959085 Click to see CC1(CCC=C2C1(C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aS,7aR)-3,3,4,4,7a-pentamethyl-1,2,3a,5-tetrahydroinden-2-yl]methanol 163034936 Click to see CC1(CC=CC2(C1C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aS,7aS)-3,3,4,4,7a-pentamethyl-1,2,3a,7-tetrahydroinden-2-yl]methanol 163024518 Click to see CC1(C=CCC2(C1C(C(C2)CO)(C)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aS)-3,3,4,4,7-pentamethyl-2,3a,5,6-tetrahydro-1H-inden-2-yl]methanol 135040744 Click to see CC1=C2CC(C(C2C(CC1)(C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(3aS,4R,5R,7aS)-3,3a,4,5,7a-pentamethyl-4,5,6,7-tetrahydro-1H-inden-2-yl]methanol 162849895 Click to see CC1CCC2(CC(=C(C2(C1C)C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(3aS,7aS)-3,3a,4,4,7a-pentamethyl-1,5,6,7-tetrahydroinden-2-yl]methanol 163027541 Click to see CC1=C(CC2(C1(C(CCC2)(C)C)C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1,4,4,9,9-Pentamethylspiro[4.4]non-1-en-3-yl)methanol 163084638 Click to see CC1=CC(C(C12CCCC2(C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(3S,5R)-1,4,4,9,9-pentamethylspiro[4.4]non-1-en-3-yl]methanol 135040663 Click to see CC1=CC(C(C12CCCC2(C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
5,9-Dimethyl-2-propan-2-ylidenedeca-4,8-dienal 162944254 Click to see CC(=CCCC(=CCC(=C(C)C)C=O)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Alternapyrone 57467994 Click to see CCC(C)C=C(C)CCCC(C)C=C(C)C=C(C)CC(C)C1=C(C(=C(C(=O)O1)C)O)C 428.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(1,1,6,7,7a-pentamethyl-4,5,6,7-tetrahydro-2H-inden-2-yl)methanol 162853300 Click to see CC1CCC2=CC(C(C2(C1C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(1,1,7,7,7a-Pentamethyl-2,4,5,6-tetrahydroinden-2-yl)methanol 162922409 Click to see CC1(CCCC2=CC(C(C21C)(C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3,3,4,5,7a-pentamethyl-2,5,6,7-tetrahydro-1H-inden-2-yl)methanol 163096693 Click to see CC1CCC2(CC(C(C2=C1C)(C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
(3a,4,5,7a-Tetramethyl-3-methylidene-1,2,4,5,6,7-hexahydroinden-2-yl)methanol 162902109 Click to see CC1CCC2(CC(C(=C)C2(C1C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aR,7aS)-3a,4,4,7a-tetramethyl-3-methylidene-2,5,6,7-tetrahydro-1H-inden-2-yl]methanol 162869125 Click to see CC1(CCCC2(C1(C(=C)C(C2)CO)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,3aS,4R,5R,7aS)-3a,4,5,7a-tetramethyl-3-methylidene-1,2,4,5,6,7-hexahydroinden-2-yl]methanol 162902110 Click to see CC1CCC2(CC(C(=C)C2(C1C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,5R,7aS)-3,3,4,5,7a-pentamethyl-2,5,6,7-tetrahydro-1H-inden-2-yl]methanol 163096694 Click to see CC1CCC2(CC(C(C2=C1C)(C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,6R,7R,7aR)-1,1,6,7,7a-pentamethyl-4,5,6,7-tetrahydro-2H-inden-2-yl]methanol 162853301 Click to see CC1CCC2=CC(C(C2(C1C)C)(C)C)CO 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
[(2S,7aR)-1,1,7,7,7a-pentamethyl-2,4,5,6-tetrahydroinden-2-yl]methanol 162922410 Click to see CC1(CCCC2=CC(C(C21C)(C)C)CO)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2S)-2-[(2R,3R,4R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4-hydroxy-5-oxooxolan-2-yl]-2-hydroxyacetic acid 163185885 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(=O)OC2C(C(=O)O)O)O)O)O 354.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003

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