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Phyllocladus trichomanoides

Phyllocladus trichomanoides - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440022e4551b110516388
Scientific name Phyllocladus trichomanoides
Authority D.Don
First published in Descr. Pinus , ed. 3, 2: 159 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phyllocladus cunninghamii Carrière Traité Gén. Conif. , ed. 2: 707 (1867)
Podocarpus trichomanoides (D.Don) Kuntze Revis. Gen. Pl. 2: 802 (1891)

Common names Top

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Language Common/alternative name
English celery pine
English mountain toatoa
English tānekaha
mi tānekaha

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Phyllocladus trichomanoides var. alpinus (Hook.f.) Parl. Prodr. 16(2): 498 (1868)
Phyllocladus trichomanoides var. trichomanoides Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481971
USDA Plants PHTR7
Tropicos 31200164
KEW urn:lsid:ipni.org:names:262608-1
The Plant List kew-2562671
Open Tree Of Life 238577
NCBI Taxonomy 50184
IUCN Red List 42269
IPNI 262608-1
iNaturalist 54687
GBIF 5284474
Freebase /m/0czcpt
EPPO PLDTR
EOL 1061649
USDA GRIN 28140
Wikipedia Phyllocladus_trichomanoides

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
Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae Khan R, Hill RS, Liu J, Biffin E Plants (Basel) 03-Mar-2023
PMCID:PMC10005643
doi:10.3390/plants12051171
PMID:36904033
Camouflage in lichen moths: Field predation experiments and avian vision modelling demonstrate the importance of wing pattern elements and background for survival Mark CJ, O'Hanlon JC, Holwell GI J Anim Ecol 08-Oct-2022
PMCID:PMC10092008
doi:10.1111/1365-2656.13817
PMID:36169598
Detailed seed cone morpho-anatomy of the Prumnopityoid clade: an insight into the origin and evolution of Podocarpaceae seed cones Khan R, Hill RS, Dörken VM, Biffin E Ann Bot 30-Jul-2022
PMCID:PMC9670759
doi:10.1093/aob/mcac097
PMID:35906916
Antiviral Efficacy of Selected Natural Phytochemicals against SARS-CoV-2 Spike Glycoprotein Using Structure-Based Drug Designing Aloufi BH, Snoussi M, Sulieman AM Molecules 08-Apr-2022
PMCID:PMC9025634
doi:10.3390/molecules27082401
PMID:35458599
Impact of Phytophthora agathidicida infection on canopy and forest floor plant nutrient concentrations and fluxes in a kauri‐dominated forest Schwendenmann L, Michalzik B Ecol Evol 19-Mar-2021
PMCID:PMC8093678
doi:10.1002/ece3.7326
PMID:33976812
A higher-rank classification for rust fungi, with notes on genera Aime MC, McTaggart AR Fungal Syst Evol 13-Nov-2020
PMCID:PMC8165960
doi:10.3114/fuse.2021.07.02
PMID:34124616
Reply to ‘Wiggle-match radiocarbon dating of the Taupo eruption’ Holdaway RN, Duffy B, Kennedy B Nat Commun 11-Oct-2019
PMCID:PMC6789094
doi:10.1038/s41467-019-12491-0
PMID:31604918
Wiggle-match radiocarbon dating of the Taupo eruption Hogg AG, Wilson CJ, Lowe DJ, Turney CS, White P, Lorrey AM, Manning SW, Palmer JG, Bury S, Brown J, Southon J, Petchey F Nat Commun 11-Oct-2019
PMCID:PMC6788995
doi:10.1038/s41467-019-12532-8
PMID:31604909
Canker and decline diseases caused by soil- and airborne Phytophthora species in forests and woodlands Jung T, Pérez-Sierra A, Durán A, Horta Jung M, Balci Y, Scanu B Persoonia 30-Apr-2018
PMCID:PMC6146643
doi:10.3767/persoonia.2018.40.08
PMID:30505001
Trogossitidae: A review of the beetle family, with a catalogue and keys Kolibáč J Zookeys 31-Dec-2013
PMCID:PMC3890666
doi:10.3897/zookeys.366.6172
PMID:24453569
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Seedlings of temperate rainforest conifer and angiosperm trees differ in leaf area display Lusk CH, Pérez-Millaqueo MM, Saldaña A, Burns BR, Laughlin DC, Falster DS Ann Bot 14-May-2012
PMCID:PMC3380592
doi:10.1093/aob/mcs095
PMID:22585929
The mechanism of pollination drop withdrawal in Ginkgo biloba L. Jin B, Zhang L, Lu Y, Wang D, Jiang XX, Zhang M, Wang L BMC Plant Biol 01-May-2012
PMCID:PMC3403970
doi:10.1186/1471-2229-12-59
PMID:22548734
Chemistry of the Podocarpaceae. LVI. Resin acids from Phyllocladus trichomanoides RC Cambie, BA Grigor, T Mee-Ing CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9811073
Flavanocoumarins and flavanophenylpropanoids from Phyllocladus trichomanoides Lai Yeap Foo Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98009-9

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JO01159A001
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aR,5S,8S,8aR)-8-acetyloxy-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162968806 Click to see CC(=CCC1C(=C)CC(C2C1(CCCC2(C)C(=O)O)C)OC(=O)C)C=C 360.50 unknown https://doi.org/10.1071/CH9811073
(1S,4aR,5S,8S,8aS)-8-acetyloxy-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162968808 Click to see CC(=CCC1C(=C)CC(C2C1(CCCC2(C)C(=O)O)C)OC(=O)C)C=C 360.50 unknown https://doi.org/10.1071/CH9811073
1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 72957164 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1071/CH9811073
15-Acetoxyisocupressic acid 14287147 Click to see CC(=CCOC(=O)C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 362.50 unknown https://doi.org/10.1071/CH9811073
5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73678322 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 320.50 unknown https://doi.org/10.1071/CH9811073
8-acetyloxy-1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73657406 Click to see CC(=CCC1C(=C)CC(C2C1(CCCC2(C)C(=O)O)C)OC(=O)C)C=C 360.50 unknown https://doi.org/10.1071/CH9811073
Communic Acid 637125 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1071/CH9811073
Elliotinoic acid 12303814 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1071/CH9811073
Isocupressic acid 6438138 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 320.50 unknown https://doi.org/10.1071/CH9811073
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JO01159A001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JO01159A001
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JO01159A001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1021/JO01159A001
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1021/JO01159A001
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2R,3R,4R,7S,8Z,12S,13S,14S,16S)-14-acetyloxy-16-formyl-2,3-dihydroxy-4,9,13,16-tetramethyl-5-oxo-6-oxatricyclo[11.3.0.03,7]hexadec-8-en-12-yl] acetate 162860141 Click to see CC1C(=O)OC2C1(C(C3C(CC(C3(C(CCC(=C2)C)OC(=O)C)C)OC(=O)C)(C)C=O)O)O 466.50 unknown https://doi.org/10.1071/CH9811073
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-pyrano[2,3-f]chromen-8-one 71577239 Click to see C1C(C(OC2=C1C(=CC3=C2C=CC(=O)O3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
(4S)-4beta,6alpha-Bis(3,4-dihydroxyphenyl)-7beta,9-dihydroxy-2,3,4,6,7,8-hexahydro-1,5-dioxaphenanthrene-2-one 10366587 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[(2R,3S,10R)-2,10-bis(3,4-dihydroxyphenyl)-5-hydroxy-8-oxo-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-3-yl] (3R)-5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 13915677 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)CC(CCC6=CC(=C(C=C6)O)O)O 660.60 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (3R)-5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 13915675 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)CC(CCC4=CC(=C(C=C4)O)O)O 498.50 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[(2S,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 354776 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)CC(CCC4=CC(=C(C=C4)O)O)O 498.50 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[(4S,8R,9S)-4,8-bis(3,4-dihydroxyphenyl)-5-hydroxy-2-oxo-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-9-yl] (3R)-5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 163096157 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)OC(=O)CC(CCC6=CC(=C(C=C6)O)O)O 660.60 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 4601996 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)CC(CCC4=CC(=C(C=C4)O)O)O 498.50 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[2,10-bis(3,4-dihydroxyphenyl)-5-hydroxy-8-oxo-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-3-yl] 5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 13915676 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)CC(CCC6=CC(=C(C=C6)O)O)O 660.60 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
[4,8-bis(3,4-dihydroxyphenyl)-5-hydroxy-2-oxo-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-9-yl] 5-(3,4-dihydroxyphenyl)-3-hydroxypentanoate 74977170 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)OC(=O)CC(CCC6=CC(=C(C=C6)O)O)O 660.60 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-pyrano[2,3-f]chromen-8-one 50908817 Click to see C1C(C(OC2=C1C(=CC3=C2C=CC(=O)O3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
2,10-bis(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-h]chromen-8-one 496377 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
9,10-Dihydro-10-(3,4-dihydroxyphenyl)-pyrano[2,3-h]catechin-8-one 10343836 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
Cinchonain Ia 442675 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
Cinchonain Ib 10456516 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
https://doi.org/10.1016/S0031-9422(00)83598-0
Phyllocoumarin 44257095 Click to see C1C(C(OC2=C1C(=CC3=C2C=CC(=O)O3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)98009-9
Phylloflavan 457885 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)CC(CCC4=CC(=C(C=C4)O)O)O 498.50 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
Phylloflavanine 44257101 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)CC(CCC6=CC(=C(C=C6)O)O)O 660.60 unknown https://doi.org/10.1016/S0031-9422(00)83598-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)80678-0
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
cinchonain I b 44575964 Click to see C1C(C(CC2=C1C3=C(C=C2O)OC(=O)CC3C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)83598-0

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