Agathis macrophylla - Unknown
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Internal ID UUID64403356cc6a5450675991
Scientific name Agathis macrophylla
Authority Mast.
First published in J. Roy. Hort. Soc. 14: 197 (1892)

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Synonyms Top

Scientific name Authority First published in
Agathis longifolia Warb. Monsunia 1: 186 (1900)
Dammara brownii var. macrophylla (Lindl.) Carrière Traité Gén. Conif. ed. 2: 622. 1867
Agathis brownii (Lem.) L.H.Bailey Cult. Conif. N. Amer. : 18 (1933)
Agathis macrophylla var. obtusa (Lindl.) Silba Phytologia 68: 23 (1990)
Agathis macrophylla var. vitiensis (Seem.) Silba J. Int. Conifer Preserv. Soc. 3: 19 (1996)
Agathis obtusa (Lindl.) Mast. J. Roy. Hort. Soc. 14: 270 (1892)
Agathis vitiensis Benth. & Hook.f. ex Drake Ill. Fl. Ins. Pacif. : 353 (1892)
Agathis macrophylla subsp. obtusa (Lindl.) Silba J. Int. Conifer Preserv. Soc. 16: 40 (2009)
Agathis macrophylla subsp. vitiensis (Seem.) Silba J. Int. Conifer Preserv. Soc. 16: 40 (2009)
Dammara brownii Lem. Ill. Hort. 2(Misc.): 60 (1855)
Dammara longifolia Lindl. ex Gordon Pinetum , Suppl.: 28 (1862)
Dammara macrophylla Lindl. J. Hort. Soc. London 6: 271 (1851)
Dammara obtusa Lindl. J. Hort. Soc. London 6: 270 (1851)
Dammara perousei C.Moore ex Hook. Hooker's J. Bot. Kew Gard. Misc. 4: 115 (1852)
Dammara vitiensis Seem. Fl. Vit. : 265 (1868)

Common names Top

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Language Common/alternative name
English kauri
English fijian kauri pine
hif dakua
Tonga kauli
Ukrainian agathis silbae
Ukrainian agathis vitiensis
Ukrainian agathis obtusa
Ukrainian Тихоокеанський каурі
Ukrainian Агатис тихоокеанський
Chinese 大叶贝壳杉
Chinese 斐济贝壳杉

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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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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000909190
Tropicos 2300053
KEW urn:lsid:ipni.org:names:676647-1
The Plant List kew-4526
Open Tree Of Life 1020069
NCBI Taxonomy 56990
IUCN Red List 34321
IPNI 676647-1
iNaturalist 136258
GBIF 5284401
Freebase /m/026t2rc
EPPO AGTMA
EOL 323470
USDA GRIN 410917
Wikipedia Agathis_macrophylla
CMAUP NPO7745

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Phytochemistry, Chemotaxonomy, and Biological Activities of the Araucariaceae Family—A Review Frezza C, Venditti A, De Vita D, Toniolo C, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Bianco A, Serafini M Plants (Basel) 14-Jul-2020
PMCID:PMC7412567
doi:10.3390/plants9070888
PMID:32674354
Screening of in vitro antimicrobial activity of plants used in traditional Indonesian medicine Romulo A, Zuhud EA, Rondevaldova J, Kokoska L Pharm Biol 16-Apr-2018
PMCID:PMC6130619
doi:10.1080/13880209.2018.1462834
PMID:29656672
Norditerpenoids from Agathis macrophylla Ya Li, Tong-Tong Wang, Jie Zhao, Xiang Shi, Shu-Chen Hu, Kun Gao Elsevier BV 29-Sep-2011
doi:10.1016/J.FOODCHEM.2011.09.089
Diterpenoids of the wood of Agathis vitiensis Richard C. Cambie, Jan M. Coddington, Martin J. Stone, Nobutoshi Tanaka, Yong Hua Li, Sayuti Arigayo Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97823-3

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Litmomycin 441183 Click to see CC1C2=C(C3C(O1)CC(=O)O3)C(=C4C(=C2O)C(=O)C5=C(C4=O)C6CC(C5(C(O6)C)O)O)O 444.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(1R,4aR,4bR,10aR)-1,4a-dimethyl-7-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 14705601 Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)O 276.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
(1R,4aR,4bR,7R,10aR)-7-hydroxy-1,4a-dimethyl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carboxylic acid 162866494 Click to see CC12CCCC(C1CCC3=CC(CCC23)O)(C)C(=O)O 278.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
(1R,4aR,4bR,7S,10aR)-7-hydroxy-1,4a-dimethyl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carboxylic acid 162866495 Click to see CC12CCCC(C1CCC3=CC(CCC23)O)(C)C(=O)O 278.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
methyl (1R,4aR,4bR,10aR)-1,4a-dimethyl-7-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate 14413654 Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)OC 290.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
> Lignans, neolignans and related compounds
Agatharesinol 15558522 Click to see C1=CC(=CC=C1C=CC(C2=CC=C(C=C2)O)C(CO)O)O 286.32 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aS,10aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 10591519 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
(1S)-1-[(2S,4aS,4bR,7R,8aR)-7-hydroxy-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol 163014687 Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)O)C 322.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
1,4a-dimethyl-6-methylidene-5-(3-methyl-4-oxobut-2-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 75054962 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=O 304.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
15-norlabda-8(20),12E-diene-14-carboxaldehyde-19-oic acid 44592589 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=O 304.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid 9944781 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
Agathic acid 6436877 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dorstenic acid A 636572 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC(C4CCC(=O)O)(C(=C)C)O)C)C)C)C 458.70 unknown via CMAUP database
Lambertiainc Acid 11869599 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Lambertianic acid 102582 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Methyl lambertianate 639383 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)OC 330.50 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,6R,9R,10S,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,13,14-triol 162932396 Click to see CC1(C2CCC34CC(C(C3)(CCC4C2(CCC1O)C)O)(C)O)C 322.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
(1S,4R,6R,9R,10S,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,13-diol 162923199 Click to see CC1(C2CCC34CC(=C)C(C3)(CCC4C2(CCC1O)C)O)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,13-diol 14313653 Click to see CC1(C2CCC34CC(=C)C(C3)(CCC4C2(CCC1O)C)O)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,13,14-triol 14313655 Click to see CC1(C2CCC34CC(C(C3)(CCC4C2(CCC1O)C)O)(C)O)C 322.50 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
methyl (1S,4aS,5S,8aR)-1-(hydroxymethyl)-4a-methyl-6-methylidene-5-(3-oxobut-1-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162902326 Click to see CC(=O)C=CC1C(=C)CCC2C1(CCCC2(CO)C(=O)OC)C 320.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
methyl (1S,4aS,5S,8aR)-1-(hydroxymethyl)-4a-methyl-6-methylidene-5-[(E)-3-oxobut-1-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 101543894 Click to see CC(=O)C=CC1C(=C)CCC2C1(CCCC2(CO)C(=O)OC)C 320.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
CID 14806212 14806212 Click to see CC12CCCC(C1CCC(=C)C2CCC3=CCOC3=O)(C)C(=O)O 332.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Methyl 1,4a-dimethyl-6-methylidene-5-[2-(2-oxo-2,5-dihydrofuran-3-yl)ethyl]-decahydronaphthalene-1-carboxylate 14845503 Click to see CC12CCCC(C1CCC(=C)C2CCC3=CCOC3=O)(C)C(=O)OC 346.50 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Pinusolide 161721 Click to see CC12CCCC(C1CCC(=C)C2CCC3=CCOC3=O)(C)C(=O)OC 346.50 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
Pinusolidic acid 25880646 Click to see CC12CCCC(C1CCC(=C)C2CCC3=CCOC3=O)(C)C(=O)O 332.40 unknown https://doi.org/10.1016/J.FOODCHEM.2011.09.089
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(2S,4aS,4bR,7R,8aR)-7-hydroxy-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene-2-carboxylic acid 14313649 Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C(=O)O)C)O)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
7-hydroxy-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene-2-carboxylic acid 14313648 Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C(=O)O)C)O)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Brevipsidone B 25112477 Click to see CC(=CCC1=CC2=C(C3=C1OC(C=C3)(C)C)OC4=C(C=CC(=C4OC)O)OC2=O)C 408.40 unknown https://doi.org/10.1016/S0031-9422(00)97823-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-7H-furo[3,2-g][1]benzopyran-7-one 71357556 Click to see CC(C)(C1=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 244.24 unknown via CMAUP database
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown via CMAUP database
Smyrindiol 92261439 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)O 262.26 unknown via CMAUP database
Smyrindioloside 10836072 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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