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Durio kutejensis

Durio kutejensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Durio kutejensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644018a21507c644888990
Scientific name Durio kutejensis
Authority (Hassk.) Becc.
First published in Malesia 3: 251 (1889)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lahia kutejensis Hassk. Hort. Bogor. Descr. : 100 (1858)

Common names Top

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Language Common/alternative name
English durian merah
English durian pulu
bjn pampakin
Persian خارگیل خونی
Indonesian pampakin
Indonesian pepaken
Indonesian lai
Japanese ドゥリオ・クテイェンシス
Malay durian nyekak
Chinese 古泰榴槤
Chinese 古泰榴梿

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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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-0000658073
Tropicos 100327442
KEW urn:lsid:ipni.org:names:559518-1
The Plant List kew-2779447
Open Tree Of Life 283637
NCBI Taxonomy 140964
IUCN Red List 34568
IPNI 559518-1
iNaturalist 191766
GBIF 4073117
Freebase /m/0b0t0q
EPPO DURKU
EOL 5406545
USDA GRIN 105575
Wikipedia Durio_kutejensis

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
Enhancing Attention and Interest in Plants to Mitigate Plant Awareness Disparity Prokop P, Fančovičová J Plants (Basel) 02-Jun-2023
PMCID:PMC10255336
doi:10.3390/plants12112201
PMID:37299180
A glycaemic index compendium of non-western foods Henry CJ, Quek RY, Kaur B, Shyam S, Singh HK Nutr Diabetes 06-Jan-2021
PMCID:PMC7791047
doi:10.1038/s41387-020-00145-w
PMID:33414403
Nutritional values of Baccaurea pubera and comparative evaluation of SHS treatment on its antioxidant properties Shaharuddin S, Husen R, Othman A J Food Sci Technol 27-Aug-2020
PMCID:PMC8076416
doi:10.1007/s13197-020-04748-0
PMID:33967332
Socialising over fruits and vegetables: the biocultural importance of an open-air market in Bandar Seri Begawan, Brunei Darussalam Franco FM, Chaw LL, Bakar N, Abas SN J Ethnobiol Ethnomed 31-Jan-2020
PMCID:PMC6995223
doi:10.1186/s13002-020-0356-6
PMID:32005124
Volatile sulfur compounds in tropical fruits Cannon RJ, Ho CT J Food Drug Anal 16-Feb-2018
PMCID:PMC9322215
doi:10.1016/j.jfda.2018.01.014
PMID:29567214
Antioxidant Activities, Metabolic Profiling, Proximate Analysis, Mineral Nutrient Composition of Salvadora persica Fruit Unravel a Potential Functional Food and a Natural Source of Pharmaceuticals Kumari A, Parida AK, Rangani J, Panda A Front Pharmacol 14-Feb-2017
PMCID:PMC5306401
doi:10.3389/fphar.2017.00061
PMID:28261096
Phytochemicals and Medicinal Properties of Indigenous Tropical Fruits with Potential for Commercial Development Khoo HE, Azlan A, Kong KW, Ismail A Evid Based Complement Alternat Med 31-May-2016
PMCID:PMC4906201
doi:10.1155/2016/7591951
PMID:27340420
The evolution of bat pollination: a phylogenetic perspective Fleming TH, Geiselman C, Kress WJ Ann Bot 29-Sep-2009
PMCID:PMC2766192
doi:10.1093/aob/mcp197
PMID:19789175
Secondary metabolites from the wood bark of Durio zibethinus and Durio kutejensis. Rudiyansyah, Garson MJ J Nat Prod 01-Aug-2006
doi:10.1021/NP050553T
PMID:16933881

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 / Triterpenoids
(1R,2S,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 16083171 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1C)C)C(=O)O 634.80 unknown https://doi.org/10.1021/NP050553T
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-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 7163260 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050553T
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-11-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 16083173 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1)C)C(=O)O)C 634.80 unknown https://doi.org/10.1021/NP050553T
10-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73236924 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1C)C)C(=O)O 634.80 unknown https://doi.org/10.1021/NP050553T
10-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-11-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 73236925 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1)C)C(=O)O)C 634.80 unknown https://doi.org/10.1021/NP050553T
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320146 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1021/NP050553T
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050553T
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1021/NP050553T
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050553T
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1021/NP050553T
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown https://doi.org/10.1021/NP050553T

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