Language	Common/alternative name
English	cedar
Czech	pazeravec bidwillův
Persian	سرو نیوزیلندی
Japanese	リボセドラス・ビドウィリー
mi	pāhautea
Russian	Либоцедрус Бидвилла

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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No forms added yet.

Germination/Propagation Top

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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
- New Zealand
  - New Zealand North
  - New Zealand South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000358614
Tropicos	9400756
KEW	urn:lsid:ipni.org:names:262464-1
The Plant List	kew-2338368
PaleoBotany	56721
Open Tree Of Life	791265
Observations.org	438828
NCBI Taxonomy	103974
IUCN Red List	42259
IPNI	262464-1
iNaturalist	135820
GBIF	2683840
Freebase	/m/02vtznm
EPPO	LIBBI
EOL	1034901
Elurikkus	281706
USDA GRIN	22034
Wikipedia	Libocedrus_bidwillii

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

Topoclimate effect on treeline elevation depends on the regional framework: A contrast between Southern Alps (New Zealand) and Apennines (Italy) forests

Rita A, Saracino A, Cieraad E, Saulino L, Zotti M, Idbella M, De Stefano C, Mogavero V, Allevato E, Bonanomi G

Ecol Evol

16-Jan-2023

PMCID:	PMC9843241
doi:	10.1002/ece3.9733
PMID:	36694545

Reappraisal of the Genus Exsudoporus (Boletaceae) Worldwide Based on Multi-Gene Phylogeny, Morphology and Biogeography, and Insights on Amoenoboletus

Biketova AY, Gelardi M, Smith ME, Simonini G, Healy RA, Taneyama Y, Vasquez G, Kovács Á, Nagy LG, Wasser SP, Peintner U, Nevo E, Bunyard BA, Vizzini A

J Fungi (Basel)

21-Jan-2022

PMCID:	PMC8874676
doi:	10.3390/jof8020101
PMID:	35205856

Comparative evaluation of cytotoxic, antimicrobial and antioxidant activities of the crude extracts of three Plectranthus species grown in Saudi Arabia

Mothana RA, Khaled JM, El-Gamal AA, Noman OM, Kumar A, Alajmi MF, Al-Rehaily AJ, Al-Said MS

Saudi Pharm J

25-Sep-2018

PMCID:	PMC6362157
doi:	10.1016/j.jsps.2018.09.010
PMID:	30766425

First Occurrence of Platycladus from the Upper Miocene of Southwest China and Its Phytogeographic Implications

Wu JY, Ding ST, Li QJ, Zhao ZR, Sun BN

PLoS One

17-Dec-2014

PMCID:	PMC4269418
doi:	10.1371/journal.pone.0115141
PMID:	25517767

The essential oil of <i>Libocedrus bidwillii</i>‐New Zealand Cedar

R. D. Batt, C. H. Hassell

Wiley

12-Jul-2007

doi:	10.1002/JCTB.5000681208

Flavonoid profiles of new zealand Libocedrus and related genera

Kenneth R. Markham, Adrian Franke, Brian P.J. Molloy, Rosemary F. Webby

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(90)85105-O

Quercetin-3-O-α-[2-O-p-hydroxybenzoyl-4-O-p- coumaroylrhamnopyranoside], an aglycone-like flavonol glycoside from Libocedrus bidwillii

Adrian Franke, kennetn r. Markiiam

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(89)80399-1

Lignans and sugiol from Libocedrus bidwillii

Graeme B. Russell

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(75)85256-3

SIMULATING NEW ZEALAND FOREST DYNAMICS WITH A GENERALIZED TEMPERATE FOREST GAP MODEL

Hall GM, Hollinger DY

Ecol Appl

01-Feb-2000

PMCID:	PMC7163527
doi:	10.1890/1051-0761(2000)010[0115:SNZFDW]2.0.CO;2

Antitumour lignans and cytotoxic resin acids from a New Zealand gymnosperm, Libocedrus plumosa.

Perry NB, Foster LM

Phytomedicine

01-Dec-1994

doi:	10.1016/S0944-7113(11)80070-X
PMID:	23195944

Phytochemical Profile Top

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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
(8aR)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one	5320458	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O	414.40	unknown	https://doi.org/10.1016/S0944-7113(11)80070-X
beta-Peltatin	92122	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O	414.40	unknown	https://doi.org/10.1016/S0944-7113(11)80070-X
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/10.1016/S0944-7113(11)80070-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one	275529	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/0031-9422(75)85256-3
Communic Acid	637125	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1016/S0944-7113(11)80070-X
methyl (1S,4aR,5R,8aR)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate	5316024	Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)C=C	316.50	unknown	https://doi.org/10.1016/S0944-7113(11)80070-X
Sandaracopimaric acid	221580	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1016/S0944-7113(11)80070-X
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/0031-9422(75)85256-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1002/JCTB.5000681208
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/JCTB.5000681208
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/JCTB.5000681208
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1002/JCTB.5000681208
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1002/JCTB.5000681208
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1002/JCTB.5000681208
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexa-1,3-diene	6428861	Click to see CC1=CC=C(CC1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1002/JCTB.5000681208
1-Methyl-4-[(2S)-6-methylhept-5-en-2-yl]cyclohexa-1,3-diene	71404158	Click to see CC1=CC=C(CC1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1002/JCTB.5000681208
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-	23204	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1002/JCTB.5000681208
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene	6508206	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1002/JCTB.5000681208
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl (1S,4aR,7aR)-4a-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate	10325616	Click to see COC(=O)C1=COC(C2C1(CC=C2COC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	566.50	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Echubioside	3048732	Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC)OC7C(C(C(C(O7)CO)O)O)O	680.80	unknown	https://doi.org/10.1016/0031-9422(89)80399-1
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5,7-dihydroxy-8-[2-hydroxy-5-[(2S)-5-hydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-2-yl]phenyl]-2-(4-hydroxyphenyl)chromen-4-one	162846277	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O	554.50	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
8-[5-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	44420106	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	540.50	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
Biflavonoid-flavone base + 3O and flavanone base + 2O + 1MeO	46841213	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O	554.50	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Hypolaetin	5281648	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
Isoscutellarein	5281665	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O)O	286.24	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3S,4R,5R,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-6-methyloxan-3-yl] 4-hydroxybenzoate	163002976	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	714.60	unknown	https://doi.org/10.1016/0031-9422(89)80399-1
[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4-hydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-6-methyloxan-3-yl] 4-hydroxybenzoate	74978209	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	714.60	unknown	https://doi.org/10.1016/0031-9422(89)80399-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,8-dihydroxy-7-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one	73808229	Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)O)O)O)O	434.30	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
5,8-Dihydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one	73808228	Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)O)O)O	418.30	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	21589941	Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)O)O)O	418.30	unknown	https://doi.org/10.1016/0031-9422(90)85105-O
Hypoletin-7-O-\|A-D-xylopyranoside	21589942	Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)O)O)O)O)O	434.30	unknown	https://doi.org/10.1016/0031-9422(90)85105-O

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Libocedrus bidwillii

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