Syzygium formosanum

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Details Top

Internal ID	UUID643fee285b5c3644431329
Scientific name	Syzygium formosanum
Authority	(Hayata) Mori
First published in	Trans. Nat. Hist. Soc. Formosa 28: 439 (1938)

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Synonyms Top

Scientific name	Authority	First published in
Syzygium acutisepalum	(Hayata) Mori	Trans. Nat. Hist. Soc. Formosa 28: 438 (1938)
Eugenia acutisepala	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30(1): 112 (1911)
Eugenia formosana	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30(1): 113 (1911)

Common names Top

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Language	Common/alternative name
Chinese	台湾蒲桃
Chinese	臺灣赤楠
Chinese	台湾赤楠

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

Asia-temperate click to expand
- Eastern Asia
  - Taiwan

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000318647
Tropicos	22103370
KEW	urn:lsid:ipni.org:names:601695-1
The Plant List	kew-199593
Open Tree Of Life	3934591
NCBI Taxonomy	1609897
IPNI	601695-1
iNaturalist	133606
GBIF	3182768
EOL	2890222

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

Analysis of Four Solvatomorphs of Betulin by TG–DTA–EI/PI–MS System Equipped with the Skimmer-Type Interface

Yuan PH, Bi YC, Su B, Yang DZ, Gong NB, Zhang L, Lu Y, Du GH

Nat Prod Bioprospect

15-May-2020

PMCID:	PMC7253561
doi:	10.1007/s13659-020-00243-3
PMID:	32415420

In Search of Panacea—Review of Recent Studies Concerning Nature-Derived Anticancer Agents

Przystupski D, Niemczura MJ, Górska A, Supplitt S, Kotowski K, Wawryka P, Rozborska P, Woźniak K, Michel O, Kiełbik A, Bartosik W, Saczko J, Kulbacka J

Nutrients

25-Jun-2019

PMCID:	PMC6627480
doi:	10.3390/nu11061426
PMID:	31242602

High-Content Screening of a Taiwanese Indigenous Plant Extract Library Identifies Syzygium simile leaf Extract as an Inhibitor of Fatty Acid Uptake

Yen CH, Chang HS, Yang TH, Wang SF, Wu HC, Chen YC, Lin KJ, Wang S

Int J Mol Sci

22-Jul-2018

PMCID:	PMC6073993
doi:	10.3390/ijms19072130
PMID:	30037134

Tree mortality in response to typhoon-induced floods and mudslides is determined by tree species, size, and position in a riparian Formosan gum forest in subtropical Taiwan

Tzeng HY, Wang W, Tseng YH, Chiu CA, Kuo CC, Tsai ST

PLoS One

05-Jan-2018

PMCID:	PMC5755898
doi:	10.1371/journal.pone.0190832
PMID:	29304149

Effect of 3, hydroxy-lup- 20(29)-en-28-oic acid on 7,12-Dimethylbenz(a) anthracene impaired cellular homeostasis in extrahepatic organs of Sprague Dawley rats

Kaur P, Kaur R, Arora R, Arora S

J Xenobiot

28-Apr-2017

PMCID:	PMC6325307
doi:	10.4081/xeno.2017.6475
PMID:	30701057

INVITED SPEAKERS’ ABSTRACTS

N/A

J Carcinog

07-Apr-2016

PMCID:

PMC6460989

Classification of Tree Species in Overstorey Canopy of Subtropical Forest Using QuickBird Images

Lin C, Popescu SC, Thomson G, Tsogt K, Chang CI

PLoS One

15-May-2015

PMCID:	PMC4433356
doi:	10.1371/journal.pone.0125554
PMID:	25978466

New Betulinic Acid Derivatives as Potent Proteasome Inhibitors

Qian K, Kim SY, Hung HY, Huang L, Chen CH, Lee KH

Bioorg Med Chem Lett

26-Jul-2011

PMCID:	PMC3171619
doi:	10.1016/j.bmcl.2011.07.072
PMID:	21856154

Hypericum lanceolatum (Hypericaceae) as a potential source of new anti-malarial agents: a bioassay-guided fractionation of the stem bark

Zofou D, Kowa TK, Wabo HK, Ngemenya MN, Tane P, Titanji VP

Malar J

17-Jun-2011

PMCID:	PMC3131257
doi:	10.1186/1475-2875-10-167
PMID:	21682873

Immunomodulatory effects of betulinic acid from the bark of white birch on mice

Yi JE, Obminska-Mrukowicz B, Yuan LY, Yuan H

J Vet Sci

03-Dec-2010

PMCID:	PMC2998741
doi:	10.4142/jvs.2010.11.4.305
PMID:	21113099

Betulinic Acid Suppresses STAT3 Activation Pathway Through Induction of Protein Tyrosine Phosphatase SHP-1 in Human Multiple Myeloma Cells

Pandey MK, Sung B, Aggarwal BB

Int J Cancer

15-Jul-2010

PMCID:	PMC2877157
doi:	10.1002/ijc.25059
PMID:	19937797

Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents

Kuo RY, Qian K, Morris-Natschke SL, Lee KH

Nat Prod Rep

13-Aug-2009

PMCID:	PMC3773821
doi:	10.1039/b810774m
PMID:	19779642

Cancer Preventive Agents 9. Betulinic Acid Derivatives as Potent Cancer Chemopreventive Agents

Nakagawa-Goto K, Yamada K, Taniguchi M, Tokuda H, Lee KH

Bioorg Med Chem Lett

18-May-2009

PMCID:	PMC2747314
doi:	10.1016/j.bmcl.2009.05.050
PMID:	19481937

Betulinic Acid Suppresses Constitutive and TNFα-induced NF-κB Activation and Induces Apoptosis in Human Prostate Carcinoma PC-3 Cells

Rabi T, Shukla S, Gupta S

Mol Carcinog

01-Dec-2008

PMCID:	PMC2864721
doi:	10.1002/mc.20447
PMID:	18444250

Terpenoids of Syzygium formosanum.

Chang CW, Wu TS, Hsieh YS, Kuo SC, Chao PD

J Nat Prod

01-Feb-1999

doi:	10.1021/NP980313W
PMID:	10075776

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 / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol	145386	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/NP980313W
3,7,11,15-Tetramethyl-2-hexadecen-1-OL	5366244	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/NP980313W
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/NP980313W
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/NP980313W
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/NP980313W
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/NP980313W
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1021/NP980313W
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1021/NP980313W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	293273	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1021/NP980313W
(3S,4aR,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol	162949682	Click to see CC1(CCC2(CCC3(C4CCC5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	428.70	unknown	https://doi.org/10.1021/NP980313W
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/NP980313W
2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carbaldehyde	586214	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C	440.70	unknown	https://doi.org/10.1021/NP980313W
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/NP980313W
4,4,6a,6b,8a,11,11,14a-Octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol	162949681	Click to see CC1(CCC2(CCC3(C4CCC5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	428.70	unknown	https://doi.org/10.1021/NP980313W
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP980313W
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP980313W
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1021/NP980313W
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP980313W
Canophyllal	12302400	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C	440.70	unknown	https://doi.org/10.1021/NP980313W
Epifriedelin	15559350	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Friedelan-3-one	244297	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Glutinol	9932254	Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Lup-20(29)-ene-3beta,28-diol	221023	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1021/NP980313W
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/NP980313W
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/NP980313W
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP980313W
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1021/NP980313W
Uvaol	92802	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1021/NP980313W

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Syzygium formosanum

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