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Internal ID UUID64400af614249643027943
Scientific name Asarum caulescens
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 162 (1872)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Live plants of Asarum caulescens are offered by specialist nurseries as ornamental groundcovers. The product is sold in pots or as bare‑root divisions intended for garden planting in shaded, woodland or naturalistic settings. Plants typically cover 0.5–1 m² when mature and are used for low‑maintenance, evergreen groundcover, erosion control on slopes and as container specimens for patios or shade gardens.

Industrial and craft applications:
Cultivation of A. caulescens is a component of the ornamental horticulture industry, employed in landscape design for shade gardens, mixed‑border plantings, native‑species restoration projects and green‑roof or woodland‑restoration schemes. The species is also propagated by division for horticultural research on rhizomatous growth, shade tolerance and low‑maintenance landscaping techniques. In scientific contexts, sequences from A. caulescens are incorporated into molecular systematic studies of Aristolochiaceae, serving as a voucher taxon in phylogenies based on nuclear ITS and plastid markers (e.g., Nakai et al., 2016). Its inclusion provides comparative data for understanding evolutionary relationships within the family and contributes to broader comparative genomics efforts targeting the evolution of aromatic phenylpropanoids.

Properties relevant to use:
The plant exhibits a low, spreading habit with evergreen, cordate leaves that persist year‑round in shaded habitats. Its rhizomatous growth system allows rapid ground coverage and facilitates easy propagation by division. Chemically, foliage and rhizomes contain aromatic phenylpropanoids such as asarone, methyl eugenol and related compounds, which produce a characteristic scent when leaves are crushed and are of interest to fragrance research. After establishment the species shows moderate drought tolerance and requires minimal fertilization, supporting low‑maintenance plantings.

Sustainability and sourcing:
Asarum caulescens is assessed as Least Concern on the IUCN Red List, indicating that wild populations are stable throughout its native range in Japan, Korea and parts of China. Commercial supply is met primarily through cultivated propagation, reducing pressure on natural habitats. The species is not listed under CITES and its horticultural trade complies with regional plant‑health and quarantine regulations (e.g., Japan’s Plant Quarantine Law and Korea’s Agricultural Plant Export Certification), ensuring that cultivated material meets biosecurity standards while providing a sustainable source for the ornamental market.

Synonyms Top

Scientific name Authority First published in
Asarum brevistylum Franch. J. Bot. (Morot) 12: 301 (1898)
Asarum caulescens f. geroensis J.Ohara J. Phytogeogr. Taxon. 33: 72 (1985)
Asarum franchetianum Diels Bot. Jahrb. Syst. 29: 308 (1900)
Japonasarum caulescens (Maxim.) Nakai Fl. Sylv. Kor. 21: 17 (1936)

Common names Top

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Language Common/alternative name
English aoi
Japanese フタバアオイ
Chinese 尾花细辛
Chinese 土细辛
Chinese 乌金草
Chinese 双叶细辛
Chinese 对叶细辛
Chinese 雙葉細辛

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
    • Eastern Asia
      • Japan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000550799
Tropicos 2500010
KEW urn:lsid:ipni.org:names:93473-1
The Plant List kew-2654287
Open Tree Of Life 513161
NCBI Taxonomy 76081
IPNI 93473-1
iNaturalist 508488
GBIF 7313618
EPPO ASUCL

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
Germacrene B – a central intermediate in sesquiterpene biosynthesis Xu H, Dickschat JS Beilstein J Org Chem 20-Feb-2023
PMCID:PMC9972886
doi:10.3762/bjoc.19.18
PMID:36865023
Two new sesquiterpenoids from Asarum caulescens. JIRO ENDO, MOTOO NAGASAWA, HIDEJI ITOKAWA, YOICHI IITAKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.27.275
[Studies on the essential oil of Asarum caulescens. IV (author's transl)[]. Endo J Yakugaku Zasshi 01-Apr-1977
doi:10.1248/YAKUSHI1947.97.4_393
PMID:559743
[Studies on the essential oil of Asarum caulescens. III.(author's transl)]. Endo J Yakugaku Zasshi 01-Nov-1975
doi:10.1248/YAKUSHI1947.95.11_1321
PMID:1240932
[Studies on the essential oil of Asarum caulescens. II]. Endo J, Nagasawa M Yakugaku Zasshi 01-Dec-1974
doi:10.1248/YAKUSHI1947.94.12_1574
PMID:4477187
[Studies on the volatile oil of Asarum caulescens]. Endo J, Ogino T, Nagasawa M Yakugaku Zasshi 01-Jul-1972
doi:10.1248/YAKUSHI1947.92.7_874
PMID:4676228

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5S,6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-4,5-dihydro-1-benzofuran-7-one 163020125 Click to see 230.30 unknown https://doi.org/10.1248/YAKUSHI1947.95.11_1321
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R)-2-ethenyl-2-methyl-5-propan-2-ylidene-3-prop-1-en-2-ylcyclohexan-1-ol 162945888 Click to see 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.92.7_874
(1R,8aS)-1,4-dimethyl-7-propan-2-ylidene-2,3,5,6,8,8a-hexahydroazulen-1-ol 163012438 Click to see CC1=C2CCC(C2CC(=C(C)C)CC1)(C)O 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
(4aS,8aR)-5,8a-dimethyl-3-propan-2-ylidene-1,2,4,4a,7,8-hexahydronaphthalene 12442774 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
2-Ethenyl-2-methyl-5-propan-2-ylidene-3-prop-1-en-2-ylcyclohexan-1-ol 78385315 Click to see 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.92.7_874
3,7(11)-Eudesmadiene 522296 Click to see CC1=CCCC2(C1CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
8a-Methyl-5-methylidene-3-propan-2-ylidene-1,4,4a,6,7,8-hexahydronaphthalen-2-one 9859260 Click to see CC(=C1CC2C(=C)CCCC2(CC1=O)C)C 218.33 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
Selina-4(15),7(11)-dien-8-one 13986100 Click to see CC(=C1CC2C(=C)CCCC2(CC1=O)C)C 218.33 unknown https://doi.org/10.1248/CPB.27.275
https://doi.org/10.1248/YAKUSHI1947.94.12_1574
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 12309812 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,2E,6E)-2,6-dimethyl-9-propan-2-ylidenecyclodeca-2,6-dien-1-ol 21159055 Click to see 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.92.7_874
(1R)-2,6-dimethyl-9-propan-2-ylidenecyclodeca-2,6-dien-1-ol 162923508 Click to see 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.92.7_874
(1Z,4E)-germacrene B 5371080 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
(3Z,7E)-3,7-dimethyl-10-propan-2-ylidenecyclodeca-3,7-dien-1-one 5317572 Click to see 218.33 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
(5E,9E)-3,6,10-trimethyl-7,8-dihydro-4H-cyclodeca[b]furan-11-one 131881530 Click to see 230.30 unknown https://doi.org/10.1248/YAKUSHI1947.95.11_1321
(5Z,9Z)-3,6,10-trimethyl-7,8-dihydro-4H-cyclodeca[b]furan-11-one 90473733 Click to see CC1=CCC2=C(C(=O)C(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1248/YAKUSHI1947.95.11_1321
[(1R,2E,6E)-2,6-dimethyl-9-propan-2-ylidenecyclodeca-2,6-dien-1-yl] acetate 101600181 Click to see 262.40 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
[(1R)-2,6-dimethyl-9-propan-2-ylidenecyclodeca-2,6-dien-1-yl] acetate 162948397 Click to see 262.40 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
1,5-Dimethyl-8-(propan-2-ylidene)cyclodeca-1,5-diene 177602 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
3,7-Cyclodecadien-1-one, 3,7-dimethyl-10-(1-methylethylidene)-, (Z,E)- 81323 Click to see 218.33 unknown https://doi.org/10.1248/YAKUSHI1947.94.12_1574
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3Z,7E,9R)-4,8,12-trimethyl-10-oxabicyclo[7.3.1]trideca-1(12),3,7-trien-11-one 162946070 Click to see 232.32 unknown https://doi.org/10.1248/YAKUSHI1947.97.4_393
(4aR,5R,7aS)-7a-methyl-3-propan-2-ylidene-5-prop-1-en-2-yl-4a,5,6,7-tetrahydro-4H-cyclopenta[b]pyran-2-one 163003672 Click to see CC(=C1CC2C(CCC2(OC1=O)C)C(=C)C)C 234.33 unknown https://doi.org/10.1248/CPB.27.275
(4aR,5S,7aS)-7a-methyl-3-propan-2-ylidene-5-prop-1-en-2-yl-4a,5,6,7-tetrahydro-4H-cyclopenta[b]pyran-2-one 163003671 Click to see CC(=C1CC2C(CCC2(OC1=O)C)C(=C)C)C 234.33 unknown https://doi.org/10.1248/CPB.27.275
Cauleslactone 6443584 Click to see 232.32 unknown https://doi.org/10.1248/YAKUSHI1947.97.4_393
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(+)-Isofebrifugine 11208839 Click to see C1CC(C(NC1)CC(=O)CN2C=NC3=CC=CC=C3C2=O)O 301.34 unknown https://doi.org/10.1248/YAKUSHI1947.95.11_1321

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