Scientific name	Authority	First published in
Pinus hayatana	Businský	Willdenowia 34: 245 (2004)
Pinus formosana	Hayata	J. Linn. Soc., Bot. 38: 297 (1908)
Pinus uyematsui	Hayata	Icon. Pl. Formosan. 3: 192 (1913)
Pinus parviflora var. morrisonicola	(Hayata) C.L.Wu	Acta Phytotax. Sin. 5(3): 141. 1956
Pinus hayatana	Businský	Willdenowia 34: 245 (2004)

Common names Top

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Filter by language:

Language	Common/alternative name
English	taiwan white pine
szy	komaw, kumaw
trv	harung
udm	Тайваньысь тӧдьы пужым
Vietnamese	thông trắng Đài loan
Chinese	台湾五针松
Chinese	台灣五葉松
Chinese	山松柏
Chinese	玉山松
Chinese	短毛松
Chinese	臺灣五葉松
Chinese	台湾五须松
Chinese	台湾松
Chinese	台湾白松

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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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

Asia-temperate click to expand
- Eastern Asia
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000481792
Tropicos	24900961
INPN	717420
KEW	urn:lsid:ipni.org:names:677081-1
The Plant List	kew-2562444
Open Tree Of Life	1086988
NCBI Taxonomy	139307
IUCN Red List	42384
IPNI	677081-1
iNaturalist	135789
GBIF	5285538
Freebase	/m/02vt_9l
EPPO	PIUMC
EOL	1033065
USDA GRIN	28492
Wikipedia	Pinus_morrisonicola

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

Antioxidant Activity of Essential Oils from Pinaceae Species

Ancuceanu R, Anghel AI, Hovaneț MV, Ciobanu AM, Lascu BE, Dinu M

Antioxidants (Basel)

26-Feb-2024

PMCID:	PMC10967544
doi:	10.3390/antiox13030286
PMID:	38539820

Complete chloroplast genome sequence of Pinus tabuliformis var. henryi (Mast.) C.T.Kuan 1983 (Pinaceae)

Wang X, Zhao L, Yang XX, Liu ZL

Mitochondrial DNA B Resour

11-Jan-2024

PMCID:	PMC10786436
doi:	10.1080/23802359.2023.2301013
PMID:	38222979

Anti-Aging Constituents from Pinus morrisonicola Leaves

Liu TW, Hsiao SW, Lin CT, Hsiao G, Lee CK

Molecules

28-Jun-2023

PMCID:	PMC10343237
doi:	10.3390/molecules28135063
PMID:	37446726

Insights into phylogenetic relationships in Pinus inferred from a comparative analysis of complete chloroplast genomes

Xia Q, Zhang H, Lv D, El-Kassaby YA, Li W

BMC Genomics

22-Jun-2023

PMCID:	PMC10286357
doi:	10.1186/s12864-023-09439-6
PMID:	37349702

Attenuating lipid metabolism in atherosclerosis: The potential role of Anti-oxidative effects on low-density lipoprotein of herbal medicines

Duan H, Song P, Li R, Su H, He L

Front Pharmacol

31-Mar-2023

PMCID:	PMC10102431
doi:	10.3389/fphar.2023.1161657
PMID:	37063287

Anticancer Applications of Essential Oils Formulated into Lipid-Based Delivery Nanosystems

Jampilek J, Kralova K

Pharmaceutics

01-Dec-2022

PMCID:	PMC9781429
doi:	10.3390/pharmaceutics14122681
PMID:	36559176

Unveiling Natural and Semisynthetic Acylated Flavonoids: Chemistry and Biological Actions in the Context of Molecular Docking

El-Kersh DM, Abou El-Ezz RF, Fouad M, Farag MA

Molecules

26-Aug-2022

PMCID:	PMC9458193
doi:	10.3390/molecules27175501
PMID:	36080269

Morphological and Comparative Transcriptome Analysis of Three Species of Five-Needle Pines: Insights Into Phenotypic Evolution and Phylogeny

Li X, Cai K, Zhao Q, Li H, Wang X, Tigabu M, Sederoff R, Ma W, Zhao X

Front Plant Sci

10-Feb-2022

PMCID:	PMC8866173
doi:	10.3389/fpls.2022.795631
PMID:	35222462

Nutrition in Abrupt Sunlight Reduction Scenarios: Envisioning Feasible Balanced Diets on Resilient Foods

Pham A, García Martínez JB, Brynych V, Stormbjorne R, Pearce JM, Denkenberger DC

Nutrients

23-Jan-2022

PMCID:	PMC8839908
doi:	10.3390/nu14030492
PMID:	35276851

Inhibitory Effects of Roseoside and Icariside E4 Isolated from a Natural Product Mixture (No-ap) on the Expression of Angiotensin II Receptor 1 and Oxidative Stress in Angiotensin II-Stimulated H9C2 Cells

Hong EY, Kim TY, Hong GU, Kang H, Lee JY, Park JY, Kim SC, Kim YH, Chung MH, Kwon YI, Ro JY

Molecules

23-Jan-2019

PMCID:	PMC6384670
doi:	10.3390/molecules24030414
PMID:	30678135

Characterization of the complete chloroplast genome of Pinus wangii (Pinaceae), an endangered and endemic species in China

Yang MQ, Du Y, Ling LZ

Mitochondrial DNA B Resour

29-Oct-2018

PMCID:	PMC7800402
doi:	10.1080/23802359.2018.1519381
PMID:	33490571

Characterization of Vasorelaxant Principles from the Needles of Pinus morrisonicola Hayata

Chen GH, Li YC, Lin NH, Kuo PC, Tzen JT

Molecules

31-Dec-2017

PMCID:	PMC6017640
doi:	10.3390/molecules23010086
PMID:	29301239

Pest categorisation of Pseudocercospora pini‐densiflorae

Jeger M, Bragard C, Caffier D, Candresse T, Chatzivassiliou E, Dehnen‐Schmutz K, Gilioli G, Gregoire J, Jaques Miret JA, MacLeod A, Navajas Navarro M, Niere B, Parnell S, Potting R, Rafoss T, Rossi V, Urek G, Van Bruggen A, Van der Werf W, West J, Winter S, Boberg J, Gonthier P, Pautasso M

EFSA J

08-Nov-2017

PMCID:	PMC7009978
doi:	10.2903/j.efsa.2017.5029
PMID:	32625334

Antioxidant Properties of Essential Oil Extracted from Pinus morrisonicola Hay Needles by Supercritical Fluid and Identification of Possible Active Compounds by GC/MS

Cheng MC, Chang WH, Chen CW, Li WW, Tseng CY, Song TY

Molecules

20-Oct-2015

PMCID:	PMC6331919
doi:	10.3390/molecules201019051
PMID:	26492232

Effects of enzymatic extraction on anthocyanins yield of saffron tepals (Crocos sativus) along with its color properties and structural stability

Lotfi L, Kalbasi-Ashtari A, Hamedi M, Ghorbani F

J Food Drug Anal

07-Jan-2015

PMCID:	PMC9351774
doi:	10.1016/j.jfda.2014.10.011
PMID:	28911375

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
1,3,6,10-Cyclotetradecatetraene, 3,7,11-trimethyl-14-(1-methylethyl)-, (S-(E,Z,E,E))-	6436662	Click to see CC1=CCCC(=CCC=C(C=CC(CC1)C(C)C)C)C	272.50	unknown	https://doi.org/10.1246/NIKKASHI1921.56.9_1118
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
CID 12358784	12358784	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1246/NIKKASHI1921.56.9_1118
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-4',5,7-Trihydroxy-6-methylflavanone	92258068	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
Poriol	301798	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,5,7-trihydroxy-6-methyl-2-phenyl-2,3-dihydrochromen-4-one	163190019	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
(5,7-Dihydroxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl) acetate	162930018	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)OC(=O)C)C3=CC=CC=C3)O	328.30	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
[(2R,3R)-5,7-dihydroxy-6-methyl-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate	129682810	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)OC(=O)C)C3=CC=CC=C3)O	328.30	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
3,5,7-Trihydroxy-6-methyl-2-phenyl-2,3-dihydrochromen-4-one	129686572	Click to see CC1=C(C2=C(C=C1O)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
3,5,7-Trihydroxyflavanone; Dihydrogalangin	3519897	Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
Pinobanksin	73202	Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
Cryptochrysin	5409355	Click to see CC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC=CC=C3	268.26	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
Strobochrysin	11536318	Click to see CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
> 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)83877-7
Izalpinin	5318691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O	284.26	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7 https://doi.org/10.1016/0031-9422(88)80201-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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	https://doi.org/10.1016/0031-9422(88)80201-2 https://doi.org/10.1016/S0031-9422(00)83877-7
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
Genkwanin	5281617	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1016/0031-9422(88)80201-2 https://doi.org/10.1016/S0031-9422(00)83877-7
Pinostrobin	6950539	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	https://doi.org/10.1016/S0031-9422(00)83877-7
> Phenylpropanoids and polyketides / Stilbenes
cis-Pinosylvin	9548840	Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O	212.24	unknown	https://doi.org/10.1016/0031-9422(88)80201-2

Biological Material Top

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Pinus morrisonicola

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