Details Top

Internal ID UUID643fe3b4091b4670267759
Scientific name Mosla japonica
Authority (Oliv.) Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 461 (1875)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Popcorn and picnics are classic ways to enjoy this flower, especially since each kernel is a miniature burst of flavor. The small size means the taste is subtle, and the floral, green, and sweet notes are often highlighted when lightly tossed with herbs or salt. For a bright, summery side, toss popcorn kernels with fresh herbs like parsley, chives, or basil, a drizzle of olive oil, and a pinch of sea salt. The crisp freshness of herbs complements the kernels’ delicate crunch and adds a refreshing lift.

The kernels pair beautifully with warm dishes too. Consider tossing them into a warm salad with blistered tomatoes, avocado, and a squeeze of lemon, or folding them into an herb omelet for textural contrast and a pop of brightness at breakfast. Their floral sweetness also plays well against mildly bitter greens like arugula, making them great for quick salads where you want crunch without the heaviness of nuts or croutons.

A simple garnish is often enough to bring out the best in popcorn kernels. Try a light drizzle of good olive oil or melted butter, a pinch of flaky salt, and a shower of minced herbs such as dill, mint, or chives. You can also give the kernels a brief toast in a dry skillet with garlic, which adds warmth and a gentle aroma before finishing with a squeeze of lemon.

Use them wherever you’d enjoy a small, edible flower with fresh flavor—spooned over grilled fish or chicken, folded into a grain bowl with lemon and feta, or scattered over cucumber salads. Their gentle sweetness works with citrus and creamy textures too, so a spoon of ricotta or mascarpone spooned onto the kernels, with a bit of lemon zest and black pepper, makes a light, elegant bite.

Recipe idea: Make a quick popcorn-kernel “relish” by tossing cooked kernels with finely chopped shallot, red wine vinegar, olive oil, chopped parsley, and a pinch of salt. Let it sit 10 minutes, then spoon over grilled fish or chicken.

General Uses Top

Suggest a correction!

Common products:
Essential oil; culinary herb (fresh or dried leaves).

Industrial and craft applications:
No industrial or craft applications are documented.

Food and beverages (non-medicinal):
Fresh or dried aerial parts are used as a flavoring herb in Japanese home cooking and regional dishes. Commercial spice products list Mosla japonica alongside herbs such as perilla and mint, typically under Japanese names like “soba-miso” herb mixes; products are offered as dried whole leaf or ground leaf for seasoning savory foods (e.g., pickles, noodles, grilled fish and meat). Processing is limited to dehydration or chopping, with no added extracts or health claims.

Colorants and tanning:
No documented dye, ink, or tannin uses.

Wood and fiber:
No documented timber or fiber uses.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
Essential oil composition varies but commonly includes monoterpenes (e.g., p-cymene, γ-terpinene, thymol, carvacrol) that confer aromatic, pungent herbaceous notes; leaves are small and highly aromatic, making them suitable for direct culinary use as flavoring.

Standards and regulation:
No plant-specific food standards identified; products are marketed as culinary herbs under general food labeling rules.

Sustainability and sourcing:
Wild-harvested; conservation measures in Japan generally require permits, and sustainable harvesting practices are recommended to maintain wild populations.

Synonyms Top

Scientific name Authority First published in
Micromeria perforata Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 106 (1865)
Mosla hadai Nakai Bot. Mag. (Tokyo) 29: 1 (1915)
Mosla japonica var. angustifolia Makino Bot. Mag. (Tokyo) 21: 157. 1907
Mosla japonica f. thymolifera (Makino) T.Yamaz. & Murata Fl. Japan 3a: 287 (1993)
Mosla leucantha Nakai Bot. Mag. (Tokyo) 35: 179 (1921)
Mosla orthodon Nakai Bot. Mag. (Tokyo) 35: 179 (1921)
Mosla perforata Koidz. Fl. Symb. Orient.-Asiat. : 15 (1930)
Mosla thymolifera Makino J. Jap. Bot. 3: 28 (1926)
Orthodon hadae (Nakai) Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 77 (1929)
Orthodon leucanthus Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 78 (1929)
Orthodon nakaii (Kudô) Okuyama J. Jap. Bot. 15: 564 (1939)
Orthodon perforatus (Miq.) Ohwi Acta Phytotax. Geobot. 5: 56 (1936)
Orthodon thymolifer Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 77 (1929)
Mosla nakaii Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 78 (1929)
Orthodon japonicus Benth. J. Linn. Soc., Bot. 9: 167 (1865)
Mosla leucantha var. robusta Nakai Bot. Mag. (Tokyo) 35: 180 (1921)
Mosla japonica var. robusta Ohwi Fl. Jap. , rev. ed.: 1164 (1965)
Orthodon japonicus var. thymolifer (Makino) Ohwi Fl. Jap. : 1013 (1953)
Mosla japonica var. hadae (Nakai) Kitam. Acta Phytotax. Geobot. 17: 10 (1957)
Orthodon japonicus var. hadae (Nakai) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 85 (1953)
Mosla japonica var. thymolifera (Makino) Kitam. Acta Phytotax. Geobot. 17: 10 (1957)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000246358
Tropicos 100226107
KEW urn:lsid:ipni.org:names:452202-1
The Plant List kew-130190
Open Tree Of Life 5800947
NCBI Taxonomy 2006541
IPNI 452202-1
iNaturalist 919869
GBIF 7309478
USDA GRIN 407932
CMAUP NPO7653

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.

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 / Methoxybenzenes / Dimethoxybenzenes
3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one 10523042 Click to see 368.40 unknown via CMAUP database
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one 20056151 Click to see 384.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3-hydroxy-4-methoxyphenyl)methyl]-2H-furan-5-one 21592358 Click to see 370.40 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Chinensin 5315827 Click to see 364.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C 11796268 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
4-[(3S,3aS,6S,6aS)-6-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxy-phenol 12309695 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown via CMAUP database
(3R,4R)-3-(4-Hydroxy-3-methoxy-benzyl)-4-(4-hydroxy-3,5-dimethoxybenzyl)dihydrofuran-2(3H)-one 10249666 Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC 388.40 unknown via CMAUP database
(3R,4R)-3-[(3,4-dimethoxyphenyl)methyl]-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 11164637 Click to see 372.40 unknown via CMAUP database
(3R,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methyl]oxolan-2-one 101630410 Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 356.40 unknown via CMAUP database
(3R,4R)-4-[(3-hydroxy-4-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101097988 Click to see 358.40 unknown via CMAUP database
(3R,4R)-4-[(3,4-dihydroxyphenyl)methyl]-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 14682324 Click to see 358.40 unknown via CMAUP database
(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-3-hydroxyoxolan-2-one 14630578 Click to see 386.40 unknown via CMAUP database
(3S,4S)-3-hydroxy-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101681939 Click to see 404.40 unknown via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]oxolan-2-one 101630409 Click to see 354.40 unknown via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylidene]oxolan-2-one 6506046 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown via CMAUP database
(3Z,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one 643806 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O 356.40 unknown via CMAUP database
[(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-2-oxooxolan-3-yl] acetate 14630580 Click to see CC(=O)OC1(C(COC1=O)CC2=CC3=C(C=C2)OCO3)CC4=CC(=C(C=C4)OC)OC 428.40 unknown via CMAUP database
Arctigenin methyl ether 384877 Click to see 386.40 unknown via CMAUP database
Arctigenin, (+)- 28125531 Click to see 372.40 unknown via CMAUP database
Bursehernin 94504 Click to see 370.40 unknown via CMAUP database
Epinortrachelogenin 14159539 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Hydroxymatairesinol 10948757 Click to see 374.40 unknown via CMAUP database
Isosalicifolin 638390 Click to see 356.40 unknown via CMAUP database
Kaerophyllin 6440534 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see 374.40 unknown via CMAUP database
Salicifolin 101681940 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O 356.40 unknown via CMAUP database
Thujaplicatin methyl ether 192827 Click to see 388.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(3R,3aR,6aR)-3-(1,3-benzodioxol-5-yl)-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one 16038940 Click to see 248.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,6,7-Trimethoxycoumarin 148724 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC 236.22 unknown via CMAUP database
5,7-Dimethoxycoumarin 2775 Click to see 206.19 unknown via CMAUP database
6,7,8-Trimethoxycoumarin 3083928 Click to see 236.22 unknown via CMAUP database
Methylumbelliferone 10748 Click to see 176.17 unknown via CMAUP database
Scoparone 8417 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.