Scientific name	Authority	First published in
Octoclinis backhousei	W.Hill	Cat. Nat. Industr. Prod. Queensland : 16 (1862)
Callitris columellaris subsp. campestris	(Silba) Silba	J. Int. Conifer Preserv. Soc. 13(1): 2 (2006)
Callitris columellaris subsp. intratropica	(R.T.Baker & H.G.Sm.) Silba	J. Int. Conifer Preserv. Soc. 13(1): 2 (2006)
Callitris arenosa	A.Cunn. ex R.T.Baker & H.G.Sm.	Res. Pines Australia : 157 (1910)
Callitris columellaris var. campestris	Silba	Phytologia Mem. 7: 16 (1984)
Callitris columellaris f. flauca	F.M.Bailey	Compr. Cat. Queensland Pl. 510 1913
Callitris columellaris f. glauca	F.M.Bailey	Compr. Cat. Queensland Pl. , ed. 2: 510 (1913)
Callitris columellaris var. intratropica	(R.T.Baker & H.G.Sm.) Silba	Phytologia Mem. 7: 16 (1984)
Callitris columellaris var. microcarpa	(Benth.) Govaerts	World Checkl. Seed Pl. 3(1): 12 (1999)
Callitris glauca	R.Br. ex R.T.Baker & H.G.Sm.	J. Proc. Roy. Soc. New S. Wales 42: 146 (1908)
Callitris glaucophylla	Joy Thomps. & L.A.S.Johnson	Telopea 2: 731 (1986)
Callitris hugelii	(hort. ex Garr.) Franco	Anais Inst. Super. Agron. 19: 11 (1952)
Callitris intermedia	R.T.Baker & H.G.Sm.	Res. Pines Australia : 288 (1910)
Callitris intratropica	R.T.Baker & H.G.Sm.	Res. Pines Australia : 172 (1910)
Callitris robusta var. intratropica	Ewart & O.B.Davies	Fl. N. Territory : 19 (1917)
Callitris robusta var. microcarpa	F.M.Bailey	Syn. Queensl. Fl. : 497 (1883)
Frenela columellaris	(F.Muell.) Parl.	Prodr. 16(2): 451 (1868)
Frenela hugelii	hort. ex Carrière	Traité Gén. Conif. : 73 (1855)
Frenela moorei	Parl.	Prodr. 16(2): 449 (1868)
Frenela robusta var. microcarpa	Benth.	Fl. Austral. 6: 237 (1873)
Frenela verrucosa var. laevis	C.Moore	Cat. Nat. Industr. Prod. New South Wales : 28 (1862)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	white pine
English	cypress pine
English	murray river pine
English	northern cypress-pine
English	western cypress
English	western sand cypress
English	white cypress pine
English	white cypress-pine
English	murray river cypress-pine
Bulgarian	кипарисов бор
Persian	سروکاج سفید
Japanese	オーストラリアヒノキ
Russian	Кипарисовая сосна
Chinese	北澳柏

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

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - South Australia
  - Victoria
  - Western Australia

Pacific click to expand
- North-central Pacific
  - Hawaii

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000580726
USDA Plants	CACO2
Tropicos	9400368
KEW	urn:lsid:ipni.org:names:261760-1
The Plant List	kew-2692863
PFAF	Callitris columellaris
Open Tree Of Life	615102
NCBI Taxonomy	214225
IUCN Red List	42206
IPNI	261760-1
iNaturalist	52388
GBIF	2684338
Freebase	/m/0fz19k
EPPO	CLWCO
EOL	1034900
USDA GRIN	312616
Wikipedia	Callitris_columellaris

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

Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants

Kirker GT, Hassan B, Mankowski ME, Eller FJ

Insects

18-Jan-2024

PMCID:	PMC10816604
doi:	10.3390/insects15010069
PMID:	38249075

Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins

Jin L, Song Z, Cai F, Ruan L, Jiang R

Molecules

30-Dec-2022

PMCID:	PMC9822336
doi:	10.3390/molecules28010302
PMID:	36615496

Life history mediates the trade‐offs among different components of demographic resilience

Capdevila P, Stott I, Cant J, Beger M, Rowlands G, Grace M, Salguero‐Gómez R

Ecol Lett

25-Mar-2022

PMCID:	PMC9314072
doi:	10.1111/ele.14004
PMID:	35334148

Exploring the Roles of Dietary Herbal Essential Oils in Aquaculture: A Review

Dawood MA, El Basuini MF, Yilmaz S, Abdel-Latif HM, Alagawany M, Kari ZA, Abdul Razab MK, Hamid NK, Moonmanee T, Van Doan H

Animals (Basel)

24-Mar-2022

PMCID:	PMC8996993
doi:	10.3390/ani12070823
PMID:	35405814

Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II

Xu H, Dickschat JS

Chemistry

21-Mar-2022

PMCID:	PMC9310801
doi:	10.1002/chem.202200405
PMID:	35239190

Tree growth responses to temporal variation in rainfall differ across a continental-scale climatic gradient

O’Donnell AJ, Renton M, Allen KJ, Grierson PF

PLoS One

04-May-2021

PMCID:	PMC8096069
doi:	10.1371/journal.pone.0249959
PMID:	33945548

Calcicole–calcifuge plant strategies limit restoration potential in a regional semi‐arid flora

Cross AT, Lambers H

Ecol Evol

01-May-2021

PMCID:	PMC8207153
doi:	10.1002/ece3.7544
PMID:	34141267

Maternal Reproductive Toxicity of Some Essential Oils and Their Constituents

Dosoky NS, Setzer WN

Int J Mol Sci

27-Feb-2021

PMCID:	PMC7956842
doi:	10.3390/ijms22052380
PMID:	33673548

Quantifying carbon in tree bark: The importance of bark morphology and tree size

Neumann M, Lawes MJ

Methods Ecol Evol

14-Jan-2021

PMCID:	PMC8048897
doi:	10.1111/2041-210X.13546
PMID:	33889377

New Labdanes with Antimicrobial and Acaricidal Activity: Terpenes of Callitris and Widdringtonia (Cupressaceae)

Sadgrove NJ, Senbill H, Van Wyk BE, Greatrex BW

Antibiotics (Basel)

11-Apr-2020

PMCID:	PMC7235842
doi:	10.3390/antibiotics9040173
PMID:	32290471

Pits with aspiration explain life expectancy of a conifer species

Jansen S, McAdam S

Proc Natl Acad Sci U S A

09-Jul-2019

PMCID:	PMC6660727
doi:	10.1073/pnas.1909866116
PMID:	31289227

Beyond the extreme: recovery of carbon and water relations in woody plants following heat and drought stress

Ruehr NK, Grote R, Mayr S, Arneth A

Tree Physiol

17-May-2019

PMCID:	PMC6703153
doi:	10.1093/treephys/tpz032
PMID:	30924906

Terpenoid Compositions of Resins from Callitris Species (Cupressaceae)

Simoneit BR, Cox RE, Oros DR, Otto A

Molecules

19-Dec-2018

PMCID:	PMC6321214
doi:	10.3390/molecules23123384
PMID:	30572688

Karnatukul (Serpent’s Glen): A new chronology for the oldest site in Australia’s Western Desert

McDonald J, Reynen W, Petchey F, Ditchfield K, Byrne C, Vannieuwenhuyse D, Leopold M, Veth P

PLoS One

19-Sep-2018

PMCID:	PMC6145509
doi:	10.1371/journal.pone.0202511
PMID:	30231025

Tree Rings Show Recent High Summer-Autumn Precipitation in Northwest Australia Is Unprecedented within the Last Two Centuries

O'Donnell AJ, Cook ER, Palmer JG, Turney CS, Page GF, Grierson PF

PLoS One

03-Jun-2015

PMCID:	PMC4454581
doi:	10.1371/journal.pone.0128533
PMID:	26039148

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
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin	2203	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1002/JPS.2600600125
Deoxypodophyllotoxin	345501	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1002/JPS.2600600125
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aR,5S,8aS)-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid	162907162	Click to see CC12CCCC(C1CCC(=C)C2CCC(=C)C=C)(C)C(=O)O	302.50	unknown	https://doi.org/10.1071/CH9710353
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2-(3,8-Dimethyl-1,2,3,4,5,6,7,8-octahydroazulen-5-yl)propan-2-ol	521245	Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-(6,10-Dimethyl-11-oxatricyclo[5.3.1.01,7]undecan-3-yl)propan-2-ol	163106900	Click to see CC1CCC(CC23C1(O2)CCC3C)C(C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-[(3S,3aS,5R)-3,8-Dimethyl-1,2,3,3a,4,5,6,7-octahydroazulen-5-yl]propan-2-ol	12302134	Click to see CC1CCC2=C(CCC(CC12)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
alpha-Bulnesene	520826	Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
alpha-Guaiene	5317844	Click to see CC1CCC(CC2=C1CCC2C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Azulene, 1,2,3,4,5,6,7,8-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, (1S,4S,7R)-	107152	Click to see CC1CCC(CC2=C1CCC2C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Bulnesol	90785	Click to see CC1CCC2=C(CCC(CC12)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
delta-Guaiene	94275	Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Guaiol	227829	Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(-)-cis-beta-Elemene	6431151	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel-	10583	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(+)-5-Epieudesmane-4alpha,11-diol	21595528	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
(3R,4aS,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6-hexahydronaphthalene	162940678	Click to see CC(=C)C1CCC2(C=CCC(=C)C2C1)C	202.33	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
(3R,4aS,8aS)-8a-Methyl-5-methylene-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene	91699613	Click to see CC(=C)C1CCC2(C=CCC(=C)C2C1)C	202.33	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
(3R,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6-hexahydronaphthalene	15381873	Click to see CC(=C)C1CCC2(C=CCC(=C)C2C1)C	202.33	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol	521215	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-ol	518516	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol	521216	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalene	605019	Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
5,11-Selinadiene	10899741	Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol	4655876	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
7-epi-alpha-Selinene	10123	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene	519361	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
alpha-Selinene	10856614	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3S,3aR,5S,6R,7aR)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one	163102713	Click to see CC1C2CC(C(CC2OC1=O)(C)C=C)C(=C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
6-Ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one	14038379	Click to see CC1C2CC(C(CC2OC1=O)(C)C=C)C(=C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aR,4aR,8aS,9aR)-3,8a-dimethyl-5-methylidene-3a,4,4a,6,9,9a-hexahydro-3H-benzo[f][1]benzofuran-2-one	163017020	Click to see CC1C2CC3C(=C)CC=CC3(CC2OC1=O)C	232.32	unknown	https://doi.org/10.1071/CH9792455
(3R,3aR,4aS,8aR,9aR)-3,8a-dimethyl-5-methylidene-3a,4,4a,6,9,9a-hexahydro-3H-benzo[f][1]benzofuran-2-one	163017021	Click to see CC1C2CC3C(=C)CC=CC3(CC2OC1=O)C	232.32	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
(3R,3aR,4aS,8aS,9aR)-3,8a-dimethyl-5-methylidene-3a,4,4a,6,7,8,9,9a-octahydro-3H-benzo[f][1]benzofuran-2-one	162923993	Click to see CC1C2CC3C(=C)CCCC3(CC2OC1=O)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
(3R,3aR,8aS,9aR)-Decahydro-3,8a-dimethyl-5-methylenenaphtho[2,3-b]furan-2(3H)-one	13769923	Click to see CC1C2CC3C(=C)CCCC3(CC2OC1=O)C	234.33	unknown	https://doi.org/10.1071/CH9792455
3,8a-dimethyl-5-methylidene-3a,4,4a,6,9,9a-hexahydro-3H-benzo[f][1]benzofuran-2-one	15558973	Click to see CC1C2CC3C(=C)CC=CC3(CC2OC1=O)C	232.32	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
3,8a-Dimethyl-5-methylidene-dodecahydronaphtho[2,3-b]furan-2-one	5104810	Click to see CC1C2CC3C(=C)CCCC3(CC2OC1=O)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3R,3aR,5E,9E,11aS)-3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one	162905472	Click to see CC1C2CC=C(CCC=C(CC2OC1=O)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one	131876254	Click to see CC1C2CC=C(CCC=C(CC2OC1=O)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Organoheterocyclic compounds / Indolizidines
(5S,6R,8R,8aS)-6,8-diethyl-5-pentyl-1,2,3,5,6,7,8,8a-octahydroindolizine	162964490	Click to see CCCCCC1C(CC(C2N1CCC2)CC)CC	251.50	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,3aR,8R,8aR,9aS)-1,5,8-trimethyl-3a,4,6,7,8,8a,9,9a-octahydro-1H-azuleno[6,5-b]furan-2-one	15381874	Click to see CC1CCC2=C(CC3C(CC12)C(C(=O)O3)C)C	234.33	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
(1R,3aR,8S,8aR,9aR)-1,5,8-trimethyl-3a,4,6,7,8,8a,9,9a-octahydro-1H-azuleno[6,5-b]furan-2-one	162978458	Click to see CC1CCC2=C(CC3C(CC12)C(C(=O)O3)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
(1R,3aS,8R,8aS,9aR)-1,5,8-trimethyl-3a,4,6,7,8,8a,9,9a-octahydro-1H-azuleno[6,5-b]furan-2-one	102318012	Click to see CC1CCC2=C(CC3C(CC12)C(C(=O)O3)C)C	234.33	unknown	https://doi.org/10.1071/CH9792455
(3aR,4aS,5R,9aS)-5,8-Dimethyl-3-methylene-3a,4,4a,5,6,7,9,9a-octahydroazuleno[6,5-b]furan-2(3H)-one	91704079	Click to see CC1CCC2=C(CC3C(CC12)C(=C)C(=O)O3)C	232.32	unknown	https://doi.org/10.1016/S0040-4039(01)88987-5
(3aS,8R,8aS,9aR)-5,8-dimethyl-1-methylidene-3a,4,6,7,8,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one	101316902	Click to see CC1CCC2=C(CC3C(CC12)C(=C)C(=O)O3)C	232.32	unknown	https://doi.org/10.1071/CH9792455 https://doi.org/10.1016/S0040-4039(01)88987-5
(3R,3aR,4aS,5R,9aS)-3,5,8-Trimethyl-3a,4,4a,5,6,7,9,9a-octahydroazuleno[6,5-b]furan-2(3H)-one	91711340	Click to see CC1CCC2=C(CC3C(CC12)C(C(=O)O3)C)C	234.33	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7 https://doi.org/10.1016/S0040-4039(01)88987-5
> Organoheterocyclic compounds / Tetrahydrofurans
2,6,10,10-Tetramethyl-11-oxatricyclo[7.2.1.01,5]dodecane	12302135	Click to see CC1CCC2CC3(C1CCC3C)OC2(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
Guaioxide	12302138	Click to see CC1CCC2CC3(C1CCC3C)OC2(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00158-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Einecs 250-156-0	5484218	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC(C(C(C=O)O)O)O)O)O	434.30	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3,7-Dihydroxy-2-(4-hydroxyphenyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	74978065	Click to see CC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
3,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162922618	Click to see CC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
Kaempferol 5-rhamnoside	44258917	Click to see CC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	162958067	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(O4)CO)O)O)O)O	450.30	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2
7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	162958066	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(O4)CO)O)O)O)O	450.30	unknown	https://doi.org/10.1016/S0031-9422(00)82391-2

Biological Material Top

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.

Callitris columellaris

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