We don't have an image yet. Upload an image!

Details Top

Internal ID UUID643ff7d474041263374108
Scientific name Perrottetia arisanensis
Authority Hayata
First published in Icon. Pl. Formosan. 5: 26 (1915)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 佩羅特木
Chinese 台湾核子木

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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-0000394766
Tropicos 50003038
KEW urn:lsid:ipni.org:names:162338-1
The Plant List kew-2408411
Open Tree Of Life 5748376
NCBI Taxonomy 1609888
IPNI 162338-1
iNaturalist 717306
GBIF 8201816
EOL 2907682

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
Genera of phytopathogenic fungi: GOPHY 4 Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW Stud Mycol 02-Jun-2022
PMCID:PMC9365048
doi:10.3114/sim.2022.101.06
PMID:36059898
Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds Sousa JL, Freire CS, Silvestre AJ, Silva AM Molecules 19-Jan-2019
PMCID:PMC6359067
doi:10.3390/molecules24020355
PMID:30669472
Compounds From Celastraceae Targeting Cancer Pathways and Their Potential Application in Head and Neck Squamous Cell Carcinoma: A Review Hernandes C, Pereira AM, Severino P Curr Genomics 01-Feb-2017
PMCID:PMC5321769
doi:10.2174/1389202917666160803160934
PMID:28503090
New Bioactive Lupane Triterpene Coumaroyl Esters Isolated from Buxus cochinchinensis Pan L, Acuña UM, Chai H, Park HY, Ninh TN, Van Thanh B, Merino EF, Cassera MB, Rakotondraibe LH, Carcache de Blanco EJ, Soejarto DD, Kinghorn AD Planta Med 01-Jul-2015
PMCID:PMC4545412
doi:10.1055/s-0035-1546118
PMID:26132853
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
Lupane-type triterpenoids from Microtropis fokienensis and Perrottetia arisanensis and the apoptotic effect of 28-hydroxy-3-oxo-lup-20(29)-en-30-al. Chen IH, Du YC, Lu MC, Lin AS, Hsieh PW, Wu CC, Chen SL, Yen HF, Chang FR, Wu YC J Nat Prod 01-Aug-2008
doi:10.1021/NP800093A
PMID:18590313

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 / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 473112 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/NP800093A
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-3a-(hydroxymethyl)-1-[1-(hydroxymethyl)vinyl]-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 473110 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)CO)C)C)C 458.70 unknown https://doi.org/10.1021/NP800093A
(1R,4R,5R,8R,10R,13R,14R,17R,18S,19R,20S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-21-oxahexacyclo[18.2.1.01,18.04,17.05,14.08,13]tricosan-22-one 102476281 Click to see CC(=C)C1C2CC3(C1C4CCC5C6(CCC(C(C6CCC5(C4(CC3)C)C)(C)C)O)C)C(=O)O2 454.70 unknown https://doi.org/10.1021/NP800093A
(1R,4R,5R,8R,10S,13R,14R,17R,18S,19R,20S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-21-oxahexacyclo[18.2.1.01,18.04,17.05,14.08,13]tricosan-22-one 101281392 Click to see CC(=C)C1C2CC3(C1C4CCC5C6(CCC(C(C6CCC5(C4(CC3)C)C)(C)C)O)C)C(=O)O2 454.70 unknown https://doi.org/10.1021/NP800093A
30-Hydroxylup-20(29)-en-3-one 15038289 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 440.70 unknown https://doi.org/10.1021/NP800093A
Hennadiol 489919 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1021/NP800093A
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/NP800093A
Thurberogenone 572464 Click to see CC(=C)C1C2CC3(C1C4CCC5C6(CCC(=O)C(C6CCC5(C4(CC3)C)C)(C)C)C)C(=O)O2 452.70 unknown https://doi.org/10.1021/NP800093A

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.