Common products:
Industrial and craft applications:
Food and beverages (non-medicinal):
Colorants and tanning:
Wood and fiber:
Fragrance and cosmetics:
Properties relevant to use:
Standards and regulation:
Sustainability and sourcing:

Synonyms Top

Scientific name	Authority	First published in
Ligusticum tenuifolium var. dissimilis	A.Nelson	Bot. Gaz. 53: 224. 1912

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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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- 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

Add a new one!

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
> 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
m-Methylallylbenzene	15263	Click to see	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	354.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.06.003

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Ligusticum grayi

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top