Details Top

Internal ID UUID644015b611b20750064768
Scientific name Daphne aurantiaca
Authority Diels
First published in Notes Roy. Bot. Gard. Edinburgh 5: 285 (1912)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Daphne aurantiaca is primarily cultivated as an ornamental shrub. Commercial nurseries in China, Europe, and North America list the species for sale as a potted or container plant for garden borders, rock gardens, and small shrub plantings. Its evergreen habit, compact growth, and fragrant, yellow‑orange tubular flowers are valued in landscape design. The plant is offered under cultivar names such as “Golden Dawn” and “Aurantiaca” in specialty horticultural catalogs (RHS Plant Finder 2023; Flora of China, 1999). Retail sales focus on potted specimens ranging from 15 cm to 30 cm in height at the time of purchase. In urban landscaping projects, the species is selected for its low maintenance and ability to thrive in compact soil volumes, making it suitable for rooftop gardens and small courtyards. Plants are typically supplied in 2‑liter pots, with a root ball suitable for immediate planting or transplanting.

Properties relevant to use:
- Evergreen foliage provides winter interest and structural continuity.
- Flower scent originates from volatile phenylpropanoids and terpenes, attractive to gardeners.
- Typical mature size 0.5–1.5 m tall and wide fits limited garden spaces.
- Responds well to light pruning, allowing use as low hedges or topiary forms.
- The plant tolerates partial shade and well‑drained soils, increasing its versatility in mixed plantings.

Sustainability and sourcing:
- Propagation is primarily through semi‑hardwood cuttings and seed under controlled nursery conditions; wild harvesting is discouraged because of the species’ toxicity and limited distribution.
- The IUCN Red List categorizes Daphne aurantiaca as Data Deficient, indicating insufficient information on population trends; accordingly, conservation‑oriented nurseries avoid wild extraction.
- Sustainable supply chains depend on certified nursery production and adherence to regional plant trade regulations, ensuring that the ornamental trade does not threaten wild populations.

Synonyms Top

Scientific name Authority First published in
Daphne aurantiaca var. calcicola (W.W.Sm.) Halda Acta Mus. Richnov., Sect. Nat. 8: 31 (2001)
Daphne calcicola W.W.Sm. Notes Roy. Bot. Gard. Edinburgh 8: 185 (1914)
Wikstroemia aurantiaca (Diels) Domke Notizbl. Bot. Gart. Berlin-Dahlem 11: 358 (1932)
Wikstroemia aurantiaca var. pulvinata Domke Notizbl. Bot. Gart. Berlin-Dahlem 11(105): 358–359 1932
Wikstroemia calcicola (W.W.Sm.) Domke Notizbl. Bot. Gart. Berlin-Dahlem 13: 387 (1936)

Common names Top

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Language Common/alternative name
Arabic دفنة برتقالية
Chinese 万年青
Chinese 橙黄瑞香
Chinese 云南瑞香
Chinese 橙花瑞香
Chinese 黄花瑞香

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000637474
Tropicos 32000602
KEW urn:lsid:ipni.org:names:831152-1
The Plant List kew-2756845
Open Tree Of Life 5747007
NCBI Taxonomy 2918710
IPNI 831152-1
GBIF 7311457
EPPO DAPAU
EOL 2889991
Wikipedia Daphne_aurantiaca
CMAUP NPO2035

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
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Editorial: Actinobacteria plant interaction: recent molecular tools and biology Wang Z, Kumar A, Singh P, Solanki MK Front Microbiol 10-May-2023
PMCID:PMC10206216
doi:10.3389/fmicb.2023.1209699
PMID:37234536
Pangenome analysis of the genus Herbiconiux and proposal of four new species associated with Chinese medicinal plants Deng Y, Jiang ZM, Han XF, Su J, Yu LY, Liu WH, Zhang YQ Front Microbiol 28-Feb-2023
PMCID:PMC10011130
doi:10.3389/fmicb.2023.1119226
PMID:36925467
Rice Phytoalexins: Half a Century of Amazing Discoveries; Part I: Distribution, Biosynthesis, Chemical Synthesis, and Biological Activities Valletta A, Iozia LM, Fattorini L, Leonelli F Plants (Basel) 05-Jan-2023
PMCID:PMC9862927
doi:10.3390/plants12020260
PMID:36678973
Phytochemistry and Pharmacological Activities of the Diterpenoids from the Genus Daphne Nie YW, Li Y, Luo L, Zhang CY, Fan W, Gu WY, Shi KR, Zhai XX, Zhu JY Molecules 31-Oct-2021
PMCID:PMC8588408
doi:10.3390/molecules26216598
PMID:34771007
A Review on Sources and Pharmacological Aspects of Sakuranetin Stompor M Nutrients 18-Feb-2020
PMCID:PMC7071307
doi:10.3390/nu12020513
PMID:32085443
Pilloin, A Flavonoid Isolated from Aquilaria sinensis, Exhibits Anti-Inflammatory Activity In Vitro and In Vivo Tsai YC, Wang SL, Wu MY, Liao CH, Lin CH, Chen JJ, Fu SL Molecules 02-Dec-2018
PMCID:PMC6320910
doi:10.3390/molecules23123177
PMID:30513815
Daphnauranins C–E, Three New Antifeedants from Daphne aurantiaca Roots Huang SZ, Ma QY, Wang Q, Dai HF, Liu YQ, Zhou J, Zhao YX Molecules 21-Sep-2018
PMCID:PMC6222359
doi:10.3390/molecules23102429
PMID:30248957
Two New Daucane Sesquiterpenoids from Daphne aurantiaca Zhao YX, Huang SZ, Ma QY, Mei WL, Dai HF Molecules 24-Aug-2012
PMCID:PMC6268740
doi:10.3390/molecules170910046
PMID:22922275
Five New Biflavonoids from <i>Daphne aurantiaca</i> Shuang Liang, Yun‐Heng Shen, Jun‐Mian Tian, Yi Feng, Zhi Xiong, Wei‐Dong Zhang Wiley 18-Jul-2011
doi:10.1002/HLCA.201000382
Terpenoids from Daphne aurantiaca and their potential anti-inflammatory activity. Liang S, Shen YH, Feng Y, Tian JM, Liu XH, Xiong Z, Zhang WD J Nat Prod 23-Apr-2010
doi:10.1021/NP9005053
PMID:20192236

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2-Dihydroxy-6-methylanthracene-9,10-dione 5319503 Click to see 254.24 unknown via CMAUP database
Anthragallol 11768 Click to see 256.21 unknown via CMAUP database
Anthraquinone, 2-benzyl-1,3-dihydroxy- 630215 Click to see C1=CC=C(C=C1)CC2=C(C=C3C(=C2O)C(=O)C4=CC=CC=C4C3=O)O 330.30 unknown via CMAUP database
Damnacanthal 2948 Click to see COC1=C2C(=CC(=C1C=O)O)C(=O)C3=CC=CC=C3C2=O 282.25 unknown via CMAUP database
Morindone 442756 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)O)O 270.24 unknown via CMAUP database
Nordamnacanthal 160712 Click to see 268.22 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Henicos-20-en-6-ynoic acid 44203444 Click to see 320.50 unknown via CMAUP database
Nonadec-18-en-4-ynoic acid 44203446 Click to see 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2,3-Di(nonadec-18-en-4-ynoyloxy)propyl nonadec-18-en-4-ynoate 44203468 Click to see C=CCCCCCCCCCCCCC#CCCC(=O)OCC(COC(=O)CCC#CCCCCCCCCCCCCC=C)OC(=O)CCC#CCCCCCCCCCCCCC=C 915.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(1S,2S,4R,5S,6S,10R,11R,12R,13R,14R,18R)-5,6-dihydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-11-phenoxy-14-prop-1-en-2-yl-3,15,17-trioxapentacyclo[9.7.0.02,4.06,10.014,18]octadecan-13-yl] benzoate 46886775 Click to see 606.70 unknown https://doi.org/10.1021/NP9005053
Genkwadaphnin 46886776 Click to see 604.60 unknown https://doi.org/10.1021/NP9005053
Gniditrin 46905268 Click to see 646.70 unknown https://doi.org/10.1021/NP9005053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(1R,2S,6R,10S,11R,13S,14R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12-trimethyl-13-nonanoyloxy-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] benzoate 46886773 Click to see CCCCCCCCC(=O)OC12C(CC3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)CO)O)OC(=O)C5=CC=CC=C5 594.70 unknown https://doi.org/10.1021/NP9005053
[(1R,2S,6R,10S,11R,13S,14R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12-trimethyl-13-octanoyloxy-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] benzoate 46886774 Click to see CCCCCCCC(=O)OC12C(CC3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)CO)O)OC(=O)C5=CC=CC=C5 580.70 unknown https://doi.org/10.1021/NP9005053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,3aR,5S,8aS)-6-(hydroxymethyl)-3a-methyl-1-prop-1-en-2-yl-2,3,4,5,8,8a-hexahydro-1H-azulen-5-ol 46211176 Click to see 236.35 unknown https://doi.org/10.1021/NP9005053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(5R,8S,8aS)-5-[(2R)-1,2-dihydroxypropan-2-yl]-3,8-dimethyl-4,5,6,7,8,8a-hexahydro-1H-azulen-2-one 46211177 Click to see 252.35 unknown https://doi.org/10.1021/NP9005053
1alpha,7alpha,10alphaH-Guaia-4,11-dien-3-one 10082128 Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C 218.33 unknown https://doi.org/10.1021/NP9005053
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,5aS,8S,8aR)-3a,5a-dihydroxy-1,5,8-trimethyl-7,8,8a,9-tetrahydro-6H-azuleno[6,5-b]furan-2-one 46211181 Click to see 264.32 unknown https://doi.org/10.1021/NP9005053
(3aR,5aS,8S,8aS)-3a,5a-dihydroxy-1,5,8-trimethyl-7,8,8a,9-tetrahydro-6H-azuleno[6,5-b]furan-2-one 46211180 Click to see CC1CCC2(C1CC3=C(C(=O)OC3(C=C2C)O)C)O 264.32 unknown https://doi.org/10.1021/NP9005053
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-formyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 21729656 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC=O)C)C)C2C1C)C)C(=O)O 484.70 unknown via CMAUP database
(1S,2S,4S,5R,6S,11R,14R,15S,18S,21R,22S,23R)-6,10,10,14,15,21,22-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosane-9,25-dione 15240838 Click to see CC1CCC23CCC4(C5(CCC6C(C(=O)CCC6(C5C7C(C4(C2C1C)OC3=O)O7)C)(C)C)C)C 468.70 unknown via CMAUP database
(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,21R,22S,23R)-9-hydroxy-6,10,10,14,15,21,22-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 15598293 Click to see 470.70 unknown via CMAUP database
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-6a-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 102150860 Click to see 618.80 unknown via CMAUP database
3|A-Hydroxyurs-11-en-28,13|A-olide 21606663 Click to see 454.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP9005053
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Uncarinic acid E 10746421 Click to see 618.80 unknown via CMAUP database
Ursonic Acid 9890209 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 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
> Nucleosides, nucleotides, and analogues / Purine nucleotides / Purine ribonucleotides / Purine ribonucleoside triphosphates
[[(2R,3R,4S,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate 23638216 Click to see 507.18 unknown https://doi.org/10.1021/NP9005053
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,3aR,8S,8aS,9aR)-1,5,8-trimethyl-1,3a,4,7,8,8a,9,9a-octahydroazuleno[6,5-b]furan-2,6-dione 46886754 Click to see 248.32 unknown https://doi.org/10.1021/NP9005053
(1S,3aR,8S,8aS,9aS)-1,5,8-trimethyl-1,3a,4,7,8,8a,9,9a-octahydroazuleno[6,5-b]furan-2,6-dione 46886772 Click to see CC1CC(=O)C2=C(CC3C(CC12)C(C(=O)O3)C)C 248.32 unknown https://doi.org/10.1021/NP9005053
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S)-5,7-dihydroxy-3-[(2S,3S)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 101960506 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)C3C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O)O 556.50 unknown https://doi.org/10.1002/HLCA.201000382
(2S,3S)-2-(2,4-dihydroxyphenyl)-3-[(2S,3S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 101960504 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(OC5=CC(=CC(=C5C4=O)O)O)C6=C(C=C(C=C6)O)O 574.50 unknown https://doi.org/10.1002/HLCA.201000382
(2S,3S)-3-[(2S,3S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 101960505 Click to see 558.50 unknown https://doi.org/10.1002/HLCA.201000382

Gallery Top

Daphne aurantiaca
Author: Sorin
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Sorin

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