Common products:
The primary commercial product derived from Bursaria spinosa is honey from European honey bee (Apis mellifera) colonies that forage on its nectar. It is documented as a nectar source for honey in south-eastern and south-western Australia and is recognized in honeyflora surveys and industry assessments for pollen and honey marketing.

Food and beverages (non-medicinal):
Honey is the principal food product associated with Bursaria spinosa. When nectar flow is significant, beekeepers recognize Bursaria-derived honey in regional flow records and palynological (pollen) profiles used to substantiate honey source attribution and lot traceability. Products are marketed in accordance with national food standards and industry traceability practices for floral-source honey.

Properties relevant to use:
In honey, the attribute of interest is floral-source verification by pollen analysis under standardized microscopic protocols. Bursaria spinosa pollen occurs in the diet of foraging A. mellifera, and its presence in filtered honey samples at specified proportions is used to support claims of nectar contribution; thresholds and reporting conventions follow established melissopalynology practices.

Standards and regulation:
Honey sourced from regions where Bursaria spinosa grows is subject to national food standards for honey labeling and compositional criteria. Commercial lots marketed as monofloral or with floral-source claims must meet industry requirements for pollen identification and reporting, as defined by melissopalynology methodology and associated quality assurance protocols. Bulk honey destined for further processing follows export/import regulations and buyer specifications for floral source documentation and residue compliance.

Synonyms Top

Scientific name	Authority	First published in
Bursaria pantonii	Guilf.	Vict. Naturalist 17: 3 (1900)
Bursaria spinosa var. australis	E.M.Benn.	Nuytsia 2: 195 (1978)
Bursaria spinosa f. grandifolia	Wawra	Itin. Princ. S. Coburgi 1: 5 1883
Bursaria spinosa var. inermis	Daveau	Dict. Hort. 1: 220 1895
Bursaria spinosa var. inernis	Daveau	Dictionnaire d'Horticulture 1899
Bursaria spinosa var. lanceolata	E.M.Benn.	Nuytsia 2: 195 (1978)
Bursaria spinosa var. macrophylla	Daveau	Dict. Hort. 1: 220 (1893)
Bursaria spinosa var. microphylla	Ewart, B.Rees & B.Wood	Proc. Roy. Soc. Victoria , n.s., 23: 55 (1910)
Bursaria spinosa var. pantonii	Ewart	Fl. Victoria : 564 (1931)
Cyrilla spinosa	Spreng.	Novi Provent. : 15 (1818)
Itea spinosa	Andrews	Bot. Repos. 5: t. 314 (1803)
Bursaria spinosa var. normalis	Domin	Biblioth. Bot. 22(89): 160 (1926)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	بيهن شائك
Finnish	piikkikielopensas

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Bursaria spinosa subsp. lasiophylla	(E.M.Benn.) L.W.Cayzer, Crisp & I.Telford	Austral. Syst. Bot. 12: 129 (1999)
Bursaria spinosa subsp. spinosa		Unknown

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Bursaria spinosa var. obovata	E.M.Benn.	Nuytsia 2: 197 (1978)

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

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - South Australia
  - Tasmania
  - Victoria

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000576092
KEW	urn:lsid:ipni.org:names:684293-1
The Plant List	kew-2687443
Open Tree Of Life	726459
NCBI Taxonomy	105281
IPNI	684293-1
iNaturalist	83571
GBIF	7303844
Freebase	/m/03g_gr0
EPPO	BUSSP
EOL	2944005
USDA GRIN	8165
Wikipedia	Bursaria_spinosa
CMAUP	NPO25529

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

Rare, common, alien and native species follow different rules in an understory plant community

Reeve S, Deane DC, McGrannachan C, Horner G, Hui C, McGeoch M

Ecol Evol

21-Mar-2022

PMCID:	PMC8938312
doi:	10.1002/ece3.8734
PMID:	35356560

Changing bird communities of an agricultural landscape: declines in arboreal foragers, increases in large species

Bain GC, MacDonald MA, Hamer R, Gardiner R, Johnson CN, Jones ME

R Soc Open Sci

11-Mar-2020

PMCID:	PMC7137982
doi:	10.1098/rsos.200076
PMID:	32269823

Evolution of lifestyles in Capnodiales

Abdollahzadeh J, Groenewald JZ, Coetzee MP, Wingfield MJ, Crous PW

Stud Mycol

05-Mar-2020

PMCID:	PMC7426231
doi:	10.1016/j.simyco.2020.02.004
PMID:	32855743

Balancing fire risk and human thermal comfort in fire-prone urban landscapes

MacLeod TA, Hahs AK, Penman TD

PLoS One

27-Dec-2019

PMCID:	PMC6934286
doi:	10.1371/journal.pone.0225981
PMID:	31881034

Rise of the killer plants: investigating the antimicrobial activity of Australian plants to enhance biofilter-mediated pathogen removal

Galbraith P, Henry R, McCarthy DT

J Biol Eng

06-Jun-2019

PMCID:	PMC6555726
doi:	10.1186/s13036-019-0175-2
PMID:	31182974

Limited Cross Plant Movement and Non-Crop Preferences Reduce the Efficiency of Honey Bees as Pollinators of Hybrid Carrot Seed Crops

Gaffney A, Bohman B, Quarrell SR, Brown PH, Allen GR

Insects

23-Jan-2019

PMCID:	PMC6410176
doi:	10.3390/insects10020034
PMID:	30678092

Rarity and nutrient acquisition relationships before and after prescribed burning in an Australian box-ironbark forest

Patykowski J, Dell M, Wevill T, Gibson M

AoB Plants

16-May-2018

PMCID:	PMC6007787
doi:	10.1093/aobpla/ply032
PMID:	29942459

Habitat type and dispersal mode underlie the capacity for plant migration across an intermittent seaway

Worth JR, Holland BR, Beeton NJ, Schönfeld B, Rossetto M, Vaillancourt RE, Jordan GJ

Ann Bot

27-Jul-2017

PMCID:	PMC5737502
doi:	10.1093/aob/mcx086
PMID:	28961707

Biophysical Mechanistic Modelling Quantifies the Effects of Plant Traits on Fire Severity: Species, Not Surface Fuel Loads, Determine Flame Dimensions in Eucalypt Forests

Zylstra P, Bradstock RA, Bedward M, Penman TD, Doherty MD, Weber RO, Gill AM, Cary GJ

PLoS One

16-Aug-2016

PMCID:	PMC4986950
doi:	10.1371/journal.pone.0160715
PMID:	27529789

Noah’s Ark Conservation Will Not Preserve Threatened Ecological Communities under Climate Change

Harris RM, Carter O, Gilfedder L, Porfirio LL, Lee G, Bindoff NL

PLoS One

16-Apr-2015

PMCID:	PMC4399882
doi:	10.1371/journal.pone.0124014
PMID:	25881302

Which host-dependent insects are most prone to coextinction under changed climates?

Moir ML, Hughes L, Vesk PA, Leng MC

Ecol Evol

17-Mar-2014

PMCID:	PMC4020690
doi:	10.1002/ece3.1021
PMID:	24834327

Nurse plant effects on plant species richness in drylands: the role of grazing, rainfall and species specificity

Soliveres S, Eldridge DJ, Hemmings F, Maestre FT

20-Dec-2012

PMCID:	PMC4407966
doi:	10.1016/j.ppees.2012.09.003
PMID:	25914602

Mycosphaerella is polyphyletic

Crous PW, Braun U, Groenewald JZ

Stud Mycol

01-Jan-2007

PMCID:	PMC2104738
doi:	10.3114/sim.2007.58.01
PMID:	18490994

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 / Benzoic acids and derivatives / Benzoic acid esters
Dimethyl anthranilate	6826	Click to see CNC1=CC=CC=C1C(=O)OC	165.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol	14529	Click to see	150.22	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
2-M-Tolylpropene	70759	Click to see	132.20	unknown	via CMAUP database
O,alpha-dimethylstyrene	81886	Click to see	132.20	unknown	via CMAUP database
p-alpha-Dimethyl styrene	62385	Click to see	132.20	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine	854067	Click to see CNCC(C1=CC=C(C=C1)O)O	167.20	unknown	via CMAUP database
> Benzenoids / Phenols / 4-alkoxyphenols
4-(3-Methyl-2-butenoxy)phenol	11435274	Click to see CC(=CCOC1=CC=C(C=C1)O)C	178.23	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
6-Hexadecen-4-yne, (E)-	5367338	Click to see CCCCCCCCCC=CC#CCCC	220.39	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
12-Methyl-1,5,9,11-tridecatetraene	564371	Click to see	190.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Oleic Acid	445639	Click to see	282.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid	10469	Click to see	396.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate	8167	Click to see	200.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3R,3aS,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-4,9-diol	101281371	Click to see	460.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal	75427	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	via CMAUP database
beta-CITRONELLOL, (R)-	101977	Click to see	156.26	unknown	via CMAUP database
cis-alpha-Ocimene	5463455	Click to see	136.23	unknown	via CMAUP database
Citral	638011	Click to see	152.23	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Neral	643779	Click to see	152.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
Thymol	6989	Click to see	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-trans-Sabinene hydrate	11228920	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	via CMAUP database
(1S,2S,3R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-diol	21626089	Click to see CC1(C2CCC1(C(C2O)O)C)C	170.25	unknown	via CMAUP database
2-Carene, (+)-	78249	Click to see	136.23	unknown	via CMAUP database
alpha-THUJENE, (+/-)-	12444324	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
Sabinene hydrate	11744854	Click to see	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-alpha-Phellandrene	443160	Click to see	136.23	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
(5R)-5-isopropyl-2-methyl-2-cyclohexen-1-one	10888107	Click to see CC1=CCC(CC1=O)C(C)C	152.23	unknown	via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enyl acetate	11333027	Click to see CC1=CCC(CC1)C(=C)COC(=O)C	194.27	unknown	via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, trans-	12618691	Click to see	152.23	unknown	via CMAUP database
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R-trans)-	6951358	Click to see CC1=CCC(CC1OC(=O)C)C(=C)C	194.27	unknown	via CMAUP database
Alpha-Terpinene	7462	Click to see	136.23	unknown	via CMAUP database
Carvone, (-)-	439570	Click to see	150.22	unknown	via CMAUP database
Perillaldehyde, (+)-	1548901	Click to see	150.22	unknown	via CMAUP database
Phellandral, (R)-	12305140	Click to see	152.23	unknown	via CMAUP database
Terpinolene	11463	Click to see	136.23	unknown	via CMAUP database
trans-1(7),8-p-Menthadien-2-ol	6428442	Click to see	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Farnesene, (3Z,6Z)-	5317320	Click to see	204.35	unknown	via CMAUP database
alpha-Sinensal	5281534	Click to see CC(=CCC=C(C)C=C)CCC=C(C)C=O	218.33	unknown	via CMAUP database
Farnesol	445070	Click to see	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Selinene	10856614	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene	6419725	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene	16061252	Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C	540.90	unknown	via CMAUP database
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
epsilon,psi-Carotene, (6R)-	5281230	Click to see	536.90	unknown	via CMAUP database
Lycopene	446925	Click to see	536.90	unknown	via CMAUP database
Phytofluene	6436722	Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C	542.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S,3S,6R)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol	101341894	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C	600.90	unknown	via CMAUP database
(3S,3'R,5R,6S)-beta,beta-Carotene-3,3',5,6(5H,6H)-tetrol	23258402	Click to see	602.90	unknown	via CMAUP database
(3S,5R,6S)-beta-cryptoxanthin 5,6-epoxide	23256985	Click to see	568.90	unknown	via CMAUP database
(3S,5R,8R,3'R)-mutatoxanthin	21765300	Click to see	584.90	unknown	via CMAUP database
(8a(2)R)-Neochrome	14034169	Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)O)(C)C	600.90	unknown	via CMAUP database
all-trans-Neoxanthin	5281247	Click to see	600.90	unknown	via CMAUP database
beta-Cryptoxathin-5',6'-epoxide	21587177	Click to see	568.90	unknown	via CMAUP database
Cryptoxanthin	5281235	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	552.90	unknown	via CMAUP database
Rubixanthin	5281252	Click to see	552.90	unknown	via CMAUP database
Violaxanthin	448438	Click to see	600.90	unknown	via CMAUP database
Zeaxanthin	5280899	Click to see	568.90	unknown	via CMAUP database
Zeinoxanthin	5281234	Click to see	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2E,4E,6E,8E,10E,12E,14E,16E)-17-((4R)-4-Hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14,16-heptadecaoctaenal	9845703	Click to see	432.60	unknown	via CMAUP database
(3E,5E,7E,9E,11E,13E,15E,17E,19E)-20-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-5,9,14,18-tetramethylicosa-3,5,7,9,11,13,15,17,19-nonaen-2-one	101306769	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C)C)C	472.70	unknown	via CMAUP database
Apocarotenal	5478003	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C	416.60	unknown	via CMAUP database
beta-Citraurinene	90429320	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C)C)C	418.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	98050000	Click to see	502.50	unknown	via CMAUP database
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	92966492	Click to see	470.50	unknown	via CMAUP database
(2'R,5aR,7aR,8R,9S,11aR,11bR)-9-[(S)-furan-3-yl-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,5,7a,9,11b-pentamethyl-3,7-dioxospiro[6,10,11,11a-tetrahydro-5aH-benzo[g][2]benzoxepine-8,3'-oxirane]-2'-carboxylic acid	53363753	Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC(C34C(O4)C(=O)O)(C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O)C)C	634.70	unknown	via CMAUP database
Limonin	179651	Click to see	470.50	unknown	via CMAUP database
Nomilin	72320	Click to see	514.60	unknown	via CMAUP database
Obacunone	119041	Click to see	454.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5,5'-Oxybis(5-methylene-2-furaldehyde)	12366272	Click to see C1=C(OC(=C1)C=O)COCC2=CC=C(O2)C=O	234.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(R)-alpha-Citronellal	72941638	Click to see	154.25	unknown	via CMAUP database
Decanal	8175	Click to see	156.26	unknown	via CMAUP database
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
Octanal	454	Click to see	128.21	unknown	via CMAUP database
Undecanal	8186	Click to see CCCCCCCCCCC=O	170.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see	126.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,4R,6S)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane	6857487	Click to see CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
Carvone-5,6-oxide, cis-(-)-	11030188	Click to see	166.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-(4-Hydroxyphenyl)ethyl 3-(4-hydroxyphenyl)prop-2-enoate	86163337	Click to see	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin	66548	Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C	258.27	unknown	via CMAUP database
Xanthyletin	65188	Click to see	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,6,7,4'-tetramethoxyflavone	24752965	Click to see	358.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperidin	10621	Click to see	610.60	unknown	via CMAUP database
Naringin	442428	Click to see	580.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Takakin	44258588	Click to see	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6-dimethoxyflavone	5481646	Click to see	314.29	unknown	via CMAUP database
Eupatilin	5273755	Click to see	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,6,7,4'-Tetramethoxyflavone	14887080	Click to see	342.30	unknown	via CMAUP database
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone	152430	Click to see	358.30	unknown	via CMAUP database
5,7,3',4',5'-Pentamethoxyflavone	493376	Click to see	372.40	unknown	via CMAUP database
8-Hydroxy-4',5,7-trimethoxyflavone	5318368	Click to see	328.30	unknown	via CMAUP database
Apigenin trimethyl ether	79730	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC	312.30	unknown	via CMAUP database
Cirsilineol	162464	Click to see	344.30	unknown	via CMAUP database
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	via CMAUP database
Salvigenin	161271	Click to see	328.30	unknown	via CMAUP database
Sinensetin	145659	Click to see	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6,8-trimethoxy-4H-1-benzopyran-4-one	10452846	Click to see	388.40	unknown	via CMAUP database
3,5,6,7,8,3',4'-Heptamethoxyflavone	150893	Click to see	432.40	unknown	via CMAUP database
3'-Demethylnobiletin	183466	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O	388.40	unknown	via CMAUP database
3',4'-Didemethylnobiletin	5318041	Click to see	374.30	unknown	via CMAUP database
4'-Demethylnobiletin	21593928	Click to see	388.40	unknown	via CMAUP database
4'-Hydroxy-5,6,7,8-Tetramethoxyflavone	3010100	Click to see	358.30	unknown	via CMAUP database
4',5-Dihydroxy-3',6,7,8-tetramethoxyflavone	181092	Click to see	374.30	unknown	via CMAUP database
4',5-Dihydroxy-7,8-dimethoxyflavone	14585506	Click to see	314.29	unknown	via CMAUP database
5-Demethoxynobiletin	44584772	Click to see	372.40	unknown	via CMAUP database
5-Demethylnobiletin	358832	Click to see	388.40	unknown	via CMAUP database
5-Hydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one	14353376	Click to see	328.30	unknown	via CMAUP database
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one	177696	Click to see	360.30	unknown	via CMAUP database
6-Demethoxytangeretin	629964	Click to see	342.30	unknown	via CMAUP database
7-Hydroxy-4',5,6,8-tetramethoxyflavone	5318356	Click to see	358.30	unknown	via CMAUP database
Gardenin B	96539	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	358.30	unknown	via CMAUP database
Gardenin D	3080750	Click to see	374.30	unknown	via CMAUP database
Isosinensetin	632135	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC	372.40	unknown	via CMAUP database
Linderoflavone B	97151	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC	386.40	unknown	via CMAUP database
Nobiletin	72344	Click to see	402.40	unknown	via CMAUP database
Sudachitin	12443122	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O	360.30	unknown	via CMAUP database
Tangeretin	68077	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4'-Hydroxy-3,6-dimethoxy-6'',6''-dimethylpyrano[2,3:7,8]flavone	44258693	Click to see	380.40	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.

Bursaria spinosa

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top