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

Add a new one! Suggest a correction!

Filter by language:

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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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

Asia-temperate click to expand
- China
  - China South-central

Links to other databases Top

Suggest others/fix!

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

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2-Dihydroxy-6-methylanthraquinone	5319503	Click to see CC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)O	254.24	unknown	via CMAUP database
Anthragallol	11768	Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)O)O	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 C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O	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
18-Nonadecene-4-yneoic acid	44203446	Click to see C=CCCCCCCCCCCCCC#CCCC(=O)O	292.50	unknown	via CMAUP database
20-Henicosene-6-yneoic acid	44203444	Click to see C=CCCCCCCCCCCCCC#CCCCCC(=O)O	320.50	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]octadec-8-en-13-yl] benzoate	46886776	Click to see CC1C(C2(C(C3C1(C4C=C(C(=O)C4(C(C5(C3O5)CO)O)O)C)OC6=CC=CC=C6)OCO2)C(=C)C)OC(=O)C7=CC=CC=C7	604.60	unknown	https://doi.org/10.1021/NP9005053
[(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 CC1CC2C3(C(C(C4(C(C3C5C(O5)(C(C2(C1=O)O)O)CO)OCO4)C(=C)C)OC(=O)C6=CC=CC=C6)C)OC7=CC=CC=C7	606.70	unknown	https://doi.org/10.1021/NP9005053
[(2R,6S,7S,8R,10S,11S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (2E,4E,6E)-deca-2,4,6-trienoate	46905268	Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C	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 CC(=C)C1CCC2(C1CC=C(C(C2)O)CO)C	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 CC1CCC(CC2=C(C(=O)CC12)C)C(C)(CO)O	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,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
2,4,4abeta,5,6,7,7a,9a-Octahydro-3,5beta,8-trimethyl-7aalpha,9aalpha-dihydroxyazuleno[6,5-b]furan-2-one	46211181	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
(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 CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1C)OC3=O)O7)C)O)(C)C)C)C	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)COC(=O)C=CC6=CC=C(C=C6)O)C(=O)O)C	618.80	unknown	via CMAUP database
3-Hydroxy-11-ursen-28,13-olide	21606663	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
Uncarinic acid E	10746421	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)COC(=O)C=CC6=CC=C(C=C6)O)C(=O)O)C	618.80	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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 C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N	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 CC1CC(=O)C2=C(CC3C(CC12)C(C(=O)O3)C)C	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 C1=CC(=CC=C1C2C(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)O	558.50	unknown	https://doi.org/10.1002/HLCA.201000382

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Daphne aurantiaca

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top