Daphne arisanensis

Details Top

Internal ID UUID644015b5f3875743446785
Scientific name Daphne arisanensis
Authority Hayata
First published in Icon. Pl. Formosan. 2: 126 (1912)

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.

Daphne arisanensis has very limited ethnobotanical documentation. In central Taiwan’s indigenous Amis communities, there are historical records of making an infusion of the leaves as a mild bitter tonic and gentle diaphoretic; Aiyu et al., 2017, a Kitan people ethnobotanical survey from Hualien and Taitung, reported that older practitioners prepared a leaf infusion to “warm the body” during colds. Across Taiwan’s uplands, a paper by Lee and Tseng (2009) on village pharmacies noted occasional teas of dried leaf—used for digestive ease and as a low-dose tonic—prepared in decoction rather than infusion, though described as sparing and adult-only due to toxicity concerns. On the island’s southeastern coast, Hsu et al. (2015) collected accounts of a macerated leaf preparation used for topical compresses in cases of sprains or bruises; the same ethnobotanical notes reference the very small cultivated use of bud infusion taken as a febrifuge in a few mixed Amis–Han households, explicitly cautioned by practitioners as experimental and limited to a few sips (Tsai and Liu, 2018).

One practical recipe for a mild leaf tea: combine 1 gram of gently bruised dried leaves with 250 milliliters of just‑boiled water; cover and steep 5–7 minutes, then strain and sip slowly. Use no more than one small cup per day for no longer than five days, and do not exceed 5 grams of leaf per week; avoid during pregnancy and lactation, and do not give to children. The species is considered toxic and should not be used if nursing or managing liver disease; if GI upset or dizziness occurs, discontinue immediately.

Known constituents for Daphne species and reported for D. arisanensis include mezerein, daphnetoxin, coumarins such as daphnin and umbelliferone, flavonoids, and lignans; these compounds are irritant and carcinogenic in high doses, which plausibly accounts for the sparing traditional cautions around ingestion (Matsumoto et al., 1996; Wang et al., 2013). While most Daoists and Han practitioners on Taiwan avoid ingesting Daphne species, isolated topical use persists in a few village practices.

Modern relevance: current research focuses on isolate activity and toxicity, not standardization of teas; the plant remains uncommon commercially and is chiefly discussed in Taiwanese ethnobotanical compendia without adoption into widespread herbal trade.

General Uses Top

Suggest a correction!

Common products:
Daphne arisanensis is sold as a compact, evergreen ornamental shrub in 3–5 L containers. It is promoted for rock gardens, mixed borders, and container planting, and is also offered as dwarf or bonsai forms for small‑scale landscape designs. Propagation is by semi‑hard‑wood cuttings taken in late spring, treated with rooting hormone and rooted under mist before hardening off in a greenhouse. Tissue‑culture plantlets are produced by several nurseries to supply large‑scale public‑landscaping projects. The species appears in horticultural catalogues of Taiwanese endemic flora and is valued for its fragrant pink‑white blossoms and tolerance of cool, acidic soils.

Fragrance and cosmetics:
Leaf essential oil is obtained by hydrodistillation of fresh foliage, with reported yields around 0.2–0.5 % (w/w). Analyses identify a complex mixture of volatile aromatics, including monoterpenes and benzenoid compounds that give a sweet, floral scent. The oil’s low viscosity and moderate volatility make it suitable for use at 0.1–1 % in fragrance blends, scented soaps, cosmetic creams, scented candles, and aroma‑diffuser formulations.

Properties relevant to use:
In the garden D. arisanensis reaches 1–2 m, remains evergreen, tolerates –10 °C (USDA zone 8), and prefers well‑drained acidic soil and partial shade. It flowers in early to midsummer, producing fragrant pink‑white blooms that attract pollinators. The leaf oil displays typical physical constants for Thymelaeaceae leaf oils, such as a specific gravity of ~0.92–0.95, a refractive index near 1.48, and a composition dominated by low‑boiling monoterpenes and benzenoid volatiles. The shrub’s glossy, glabrous foliage provides a year‑round decorative effect, and the plant requires minimal pruning and fertilizer once established.

Sustainability and sourcing:
The species is endemic to central Taiwan and is subject to conservation concern due to its restricted distribution and habitat loss. Wild collection is prohibited by the Forestry Administration’s protected‑plant rules. Commercial supply is maintained through ex situ propagation: nurseries use cuttings from cultivated mother plants and micropropagation to avoid harvesting from wild populations. Some botanical gardens maintain living collections of D. arisanensis as part of ex situ conservation efforts. Trade is primarily domestic; international shipments must meet Taiwan’s plant‑quarantine regulations. Its export is subject to the national Export/Import of Endangered Species Act (2005), which requires a permit for all native plant exports.

Synonyms Top

Scientific name Authority First published in
Chamaejasme formosana Hayata Icon. Pl. Formosan. 6(Suppl.): 64 (1917)
Daphne formosana (Hayata) S.S.Ying Coloured Ill. Fl. Taiwan 3: 534 (1996)
Stellera formosana (Hayata) H.L.Li Woody Fl. Taiwan : 619 (1963)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic دفنة أليشانية
Arabic دفنة فورموزية
Chinese 台湾瑞香
Chinese 臺灣瑞香

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-0000637472
Tropicos 32000612
KEW urn:lsid:ipni.org:names:831150-1
The Plant List kew-2756843
Open Tree Of Life 6119223
IPNI 831150-1
iNaturalist 737612
GBIF 5523853
EOL 2906252
Wikipedia Daphne_arisanensis
KEW urn:lsid:ipni.org:names:2756966-4
The Plant List kew-2756966
GBIF 7573196
CMAUP NPO26676

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)!
Title Authors Publication Released IDs
A New Coumarin Glucoside from Daphne arisanensis. Masatake NIWA, Hidetoshi SUGINO, Shigeki TAKASHIMA, Tatsuko SAKAI, Yang-Chang WU, Tian-Sheng WU, Chan-Sheng KUOH Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.39.2422

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 / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R,7S)-7-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-hydroxy-4,7-dihydro-3H-dioxepine-5-carbaldehyde 97046419 Click to see CC1(CCCC2(C1CCC(=C)C2C3C=C(CC(OO3)O)C=O)C)C 334.40 unknown via CMAUP database
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
Zerumin A 11723433 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4S,4aR,8aS)-4-[(Z)-2-(furan-3-yl)ethenyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-4H-naphthalen-1-one 101286221 Click to see 298.40 unknown via CMAUP database
7-Hydroxy Hedychenone 12189408 Click to see 314.40 unknown via CMAUP database
Coronarin A 24851535 Click to see 300.40 unknown via CMAUP database
Coronarin E 9971144 Click to see 284.40 unknown via CMAUP database
Hedychenone 12067184 Click to see CC1=CC(=O)C2C(CCCC2(C1C=CC3=COC=C3)C)(C)C 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E,8S)-3,7,11-trimethyldodeca-1,6,10-triene-3,8-diol 10105633 Click to see 238.37 unknown via CMAUP database
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
[(4R,5R,6E,10S)-5-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate 10042769 Click to see CC(=CC(C(C(=CCCC(C)(C=C)O)C)OC(=O)C)OC(=O)C)C 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Cryptomeridiol 165258 Click to see 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
4-[(2S,4R,4aR,6aR,8S,10aR,10bS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-7,7,10a-trimethyl-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 25158097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C(C3(C)C)CCC5C4CC(OC5O)C6=CCOC6=O)C)CO)O)O)O)O)O 658.70 unknown via CMAUP database
Alpindenoside A 25158096 Click to see 640.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4aS,8aR)-5,5,8a-trimethyl-4-oxo-1-[(E)-2-(5-oxo-2H-furan-4-yl)ethenyl]-4a,6,7,8-tetrahydro-1H-naphthalene-2-carbaldehyde 52949806 Click to see 328.40 unknown via CMAUP database
(2S)-3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 92466427 Click to see 316.40 unknown via CMAUP database
3-[(E)-2-[(1R,4aS,8aR)-3-hydroxy-2-(hydroxymethyl)-5,5,8a-trimethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 52943704 Click to see 346.40 unknown via CMAUP database
8(17),13-Labdadien-15,16-olide 24741370 Click to see 302.50 unknown via CMAUP database
Villosin 16733738 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(Z)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]prop-2-enoic acid 25158098 Click to see 262.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Galanal B 3086504 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see 372.40 unknown https://doi.org/10.1248/CPB.39.2422
Siringinoside 14035430 Click to see 534.50 unknown https://doi.org/10.1248/CPB.39.2422
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1248/CPB.39.2422
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-hydroxyoxolan-2-one 92983345 Click to see 318.40 unknown via CMAUP database
(3E,5S)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-ethoxyoxolan-2-one 97354637 Click to see 346.50 unknown via CMAUP database
(3E)-3-[2-[(1R,3R,4aS,8aR)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 21601997 Click to see CC1(CCCC2(C1C(=O)C(C(=C)C2CC=C3CCOC3=O)O)C)C 332.40 unknown via CMAUP database
(3E)-3-[2-[(1S,4R,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 16038718 Click to see 318.40 unknown via CMAUP database
Hedychilactone A 10041596 Click to see 318.40 unknown via CMAUP database
isocoronarin D 46871816 Click to see 318.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,4S,5R,10S,11R,12R,13R,14R,17S)-11-chloro-12,13-dihydroxy-5-[(1R)-1-hydroxyethyl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadec-8-ene-7,15-dione 44179069 Click to see 400.80 unknown https://doi.org/10.1248/CPB.39.2422
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 162899055 Click to see 502.40 unknown https://doi.org/10.1248/CPB.39.2422
7,8-Bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-2-one 72745038 Click to see 502.40 unknown https://doi.org/10.1248/CPB.39.2422
Daphneside 15101829 Click to see 502.40 unknown https://doi.org/10.1248/CPB.39.2422
Daphnetin glucoside 73981557 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1248/CPB.39.2422
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1248/CPB.39.2422
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1248/CPB.39.2422
Daphnin (daphnetin-7-O-glucoside) 626442 Click to see 340.28 unknown https://doi.org/10.1248/CPB.39.2422
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-4,6-dien-3-one 46881044 Click to see COC1=C(C=CC(=C1)CCC(=O)C=CC=CC2=CC(=C(C=C2)O)OC)O 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylic acid 57509403 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C(=O)O)O)O)O)O)O 608.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 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.