Dacrycarpus dacrydioides - Unknown
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Internal ID UUID64401596e56cd742359692
Scientific name Dacrycarpus dacrydioides
Authority (A.Rich.) de Laub.
First published in J. Arnold Arbor. 50: 337 (1969)

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Synonyms Top

Scientific name Authority First published in
Nageia dacrydioides F.Muell. Select Pl. , ed. 2: 138 (1876)
Nageia excelsa Kuntze Revis. Gen. Pl. 2: 800 (1891)
Podocarpus excelsus Druce Rep. Bot. Soc. Exch. Club Brit. Isles 1916: 640 (1917)
Podocarpus thujoides R.Br. Pl. Jav. Rar. : 41 (1838)
Podocarpus dacrydioides A.Rich. Voy. Astrolabe 1: 358 (1832)
Dacrydium excelsum D.Don Descr. Pinus , ed. 2(App.): 143 (1828)
Dacrydium ferrugineum Van Houtte ex Gordon Pinetum : 200 (1858)
Nageia excesla (D.Don) Kuntze Revis. Gen. Pl. 2: 800 1891

Common names Top

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Language Common/alternative name
English kahika
English white pine
Spanish kahikatea
Arabic صنوبر أبيض
German kahikatea
German neuseeländische warzeneibe
Estonian kahikatea
Estonian kahitkatea
Estonian kõrge kivijugapuu
Estonian kõrge pisarviljak
Japanese ダクリカルプス・ダクリディオイデス
Japanese ポドカルプス・ダクリディオイデス
Japanese スイシスギマキ
Lithuanian paprastasis dakridenis
mi kahikatea
Norwegian Nynorsk kahikatea
Russian Кахикатеа
Russian Ногоплодник дакридиевидный
Chinese 紐西蘭雞毛松

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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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-0000636634
USDA Plants DADA2
Tropicos 25600137
KEW urn:lsid:ipni.org:names:687947-1
The Plant List kew-2755036
PFAF Dacrycarpus dacrydioides
PaleoBotany 52244
Open Tree Of Life 54153
NCBI Taxonomy 56888
IUCN Red List 42443
IPNI 687947-1
iNaturalist 52390
GBIF 2687859
Freebase /m/04x4tv
EPPO PODDA
EOL 1033665
USDA GRIN 101861
Wikipedia Dacrycarpus_dacrydioides
CMAUP NPO27642

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
Differential Etching of Rays at Wood Surfaces Exposed to an Oxygen Glow Discharge Plasma Cheng KJ, Ma W, Evans PD Materials (Basel) 22-Jan-2024
PMCID:PMC10818692
doi:10.3390/ma17020521
PMID:38276461
Detailed Seed Cone Morpho-Anatomy Provides New Insights into Seed Cone Origin and Evolution of Podocarpaceae; Podocarpoid and Dacrydioid Clades Khan R, Hill RS, Dörken VM, Biffin E Plants (Basel) 19-Nov-2023
PMCID:PMC10674377
doi:10.3390/plants12223903
PMID:38005800
Characterization of Colletotrichum Species Infecting Litchi in Hainan, China Cao X, Li F, Xu H, Li H, Wang S, Wang G, West JS, Wang J J Fungi (Basel) 24-Oct-2023
PMCID:PMC10672147
doi:10.3390/jof9111042
PMID:37998848
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
Pest categorisation of Platypus apicalis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 20-Jun-2022
PMCID:PMC9208325
doi:10.2903/j.efsa.2022.7398
PMID:35765383
A field test of forest canopy structure measurements with the CanopyCapture smartphone application Lusk CH PeerJ 13-May-2022
PMCID:PMC9109689
doi:10.7717/peerj.13450
PMID:35586134
Colletotrichum Species Associated with Peaches in China Tan Q, Schnabel G, Chaisiri C, Yin LF, Yin WX, Luo CX J Fungi (Basel) 18-Mar-2022
PMCID:PMC8950351
doi:10.3390/jof8030313
PMID:35330315
Assessing Two Different Aerial Toxin Treatments for the Management of Invasive Rats O’Malley TD, Stanley MC, Russell JC Animals (Basel) 27-Jan-2022
PMCID:PMC8833531
doi:10.3390/ani12030309
PMID:35158633
Extreme bill dimorphism leads to different but overlapping isotopic niches and similar trophic positions in sexes of the charismatic extinct huia Tomotani BM, Salvador RB, Sabadel AJ, Miskelly CM, Brown JC, Delgado J, Boussès P, Cherel Y, Waugh SM, Bury SJ Oecologia 29-Nov-2021
PMCID:PMC8803797
doi:10.1007/s00442-021-05082-8
PMID:34842996
Colletotrichum Species Causing Anthracnose of Citrus in Australia Wang W, de Silva DD, Moslemi A, Edwards J, Ades PK, Crous PW, Taylor PW J Fungi (Basel) 12-Jan-2021
PMCID:PMC7828153
doi:10.3390/jof7010047
PMID:33445649
Exploiting the Biosynthetic Potency of Taxol from Fungal Endophytes of Conifers Plants; Genome Mining and Metabolic Manipulation El-Sayed AS, El-Sayed MT, Rady AM, Zein N, Enan G, Shindia A, El-Hefnawy S, Sitohy M, Sitohy B Molecules 30-Jun-2020
PMCID:PMC7412027
doi:10.3390/molecules25133000
PMID:32630044
Commodity risk assessment of Acer spp. plants from New Zealand Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Mosbach‐Schulz O, Gonthier P EFSA J 20-May-2020
PMCID:PMC10464684
doi:10.2903/j.efsa.2020.6105
PMID:37649508
Fungal diversity in canopy soil of silver beech, Nothofagus menziesii (Nothofagaceae) Nilsen AR, Teasdale SE, Guy PL, Summerfield TC, Orlovich DA PLoS One 24-Jan-2020
PMCID:PMC6980614
doi:10.1371/journal.pone.0227860
PMID:31978185
Leaf functional trait variation in a humid temperate forest, and relationships with juvenile tree light requirements Lusk CH PeerJ 08-May-2019
PMCID:PMC6511228
doi:10.7717/peerj.6855
PMID:31119078
The palaeoenvironment of the Upper Cretaceous (Cenomanian–Turonian) portion of the Winton Formation, Queensland, Australia Fletcher TL, Moss PT, Salisbury SW PeerJ 07-Sep-2018
PMCID:PMC6130253
doi:10.7717/peerj.5513
PMID:30210941

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Podocarpa-8,11,13-trien-16-oic acid, 12-hydroxy- 220357 Click to see CC12CCCC(C1CCC3=C2C=C(C=C3)O)(C)C(=O)O 274.35 unknown https://doi.org/10.1016/0031-9422(75)85047-3
Podocarpic acid 93017 Click to see CC12CCCC(C1CCC3=C2C=C(C=C3)O)(C)C(=O)O 274.35 unknown https://doi.org/10.1016/J.PHYMED.2008.02.020
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 101855692 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.42B-0462
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
(2S)-6-Geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.42B-0462
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 2''-O-rhamnoside 5282151 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
Vitexin-2"-O-rhamnoside 5874704 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[3,4-Dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-5,7-dihydroxy-3-methoxychromen-4-one 74978437 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(CO4)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
2-[3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5,7-dihydroxy-3-methoxychromen-4-one 163029051 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(CO4)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-Dihydroxy-2-[3-hydroxy-4-methoxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxychromen-4-one 74978440 Click to see COC1=C(C=C(C=C1OC2C(C(C(CO2)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)OC)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-dihydroxy-2-[3-hydroxy-4-methoxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3-methoxychromen-4-one 162985704 Click to see COC1=C(C=C(C=C1OC2C(C(C(CO2)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)OC)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-Dihydroxy-2-[4-hydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxychromen-4-one 74978417 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(CO4)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3-methoxychromen-4-one 38360299 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(CO4)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-dihydroxy-2-[4-hydroxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]chromen-4-one 102154331 Click to see C1=C(C=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=O)C5=C(C=C(C=C5O4)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5,7-Dihydroxy-2-[4-hydroxy-3,5-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]chromen-4-one 74977740 Click to see C1=C(C=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=O)C5=C(C=C(C=C5O4)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
delphinidin 3-O-beta-D-glucoside betaine 165559 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=O)C=C3O2)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.42B-0462
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)84944-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978415 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C=C4)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
2-(3,4-dihydroxyphenyl)-5-hydroxy-3-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163039616 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C=C4)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
2-[3,4-Dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-5-hydroxy-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978439 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
2-[3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-3-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162888167 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-Hydroxy-2-[3-hydroxy-4-methoxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978441 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)OC)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-hydroxy-2-[3-hydroxy-4-methoxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102153774 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)OC)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-Hydroxy-2-[4-hydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978420 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C=C4)O)OC5C(C(C(CO5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102145124 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C=C4)O)OC5C(C(C(CO5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-Hydroxy-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 74978436 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
5-hydroxy-3-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162865053 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)84944-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 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
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Geranyl-2,4-dihydroxy-6-phenethylbenzoate 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

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