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Durio zibethinus

Durio zibethinus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Durio zibethinus - 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 UUID644018a3c1581936116277
Scientific name Durio zibethinus
Authority L.
First published in Syst. Veg. ed. 13 : 581 (1774)

Description Top

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Synonyms Top

Scientific name Authority First published in
Durio acuminatissimus Merr. Philipp. J. Sci. 29: 393 (1926)
Durio stercoraceus Noronha Verh. Batav. Genootsch. Kunst. 5(Art. 4): 13. 1790

Common names Top

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Language Common/alternative name
English durian
Spanish durian
Spanish durián
Spanish durión
Arabic دوريان زبادي
bjn durian
Catalan dúrio
Czech durian cibetkový
German durianbaum
German stinkfrucht
German zibetbaum
German durian
Persian میوه های گرمسیری
Galician durián
Croatian durijan
Hungarian durián
Indonesian duren
Indonesian kadu
Indonesian durian
Icelandic dáraaldin
Japanese ドリアン
Kannada ಡ್ಯುರಿಯೊ ಜಿಬೆಥಿನಸ್
Korean 두리안
mad dhurin
Malayalam ഡുറിയാൻ
Malay durian kampung
Malay pokok durian kampung
Norwegian Bokmål duriantre
Dutch durian właściwy
Dutch doerian
Norwegian Nynorsk duriantre
Norwegian Nynorsk durian
Norwegian Nynorsk d. zibethinus
Polish durian właściwy
Portuguese durião
Russian Дурьян
Russian Дуриан цибетиновый
Slovak durian zapáchavý
Swedish stinkfrukt
Turkish durian
Ukrainian дуріан цібетиновий
Vietnamese sầu riêng
Chinese 麝香貓果
Chinese 麝香猫果
Chinese 榴槤
Chinese 假连翘叶
Chinese 榴莲
Chinese 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
  • Asia-tropical
    • Indian Subcontinent
      • India
    • Indo-China
      • Andaman Islands
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000658098
UNII S18I9G8Y6K
USDA Plants DUZI
Tropicos 3900624
INPN 447008
KEW urn:lsid:ipni.org:names:559531-1
The Plant List kew-2779470
Open Tree Of Life 236622
Observations.org 334653
NCBI Taxonomy 66656
IPNI 559531-1
iNaturalist 64443
GBIF 3152230
Freebase /m/0s96c4_
EPPO DURZI
EOL 483665
Elurikkus 365984
US Library of Congress sh97003546
USDA GRIN 14755
Wikipedia Durio_zibethinus
CMAUP NPO22133

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_002303985.1 Duzib1.0 Scaffold Thorn Biosystems 2017-09-15 153.0x 682.10 Mb

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
Investigation on the insecticidal activities of cyanobacterial extracts as an alternative source for the management of fall armyworm, Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae) C.H. S, M B, A P, Naik HR, Naik NM, Rao SN, Moussa IM, Alsubki RA, Ullah F, Elansary HO, B K Heliyon 03-Apr-2024
PMCID:PMC11016625
doi:10.1016/j.heliyon.2024.e29060
PMID:38623187
Subgenome-aware analyses reveal the genomic consequences of ancient allopolyploid hybridizations throughout the cotton family Sun P, Lu Z, Wang Z, Wang S, Zhao K, Mei D, Yang J, Yang Y, Renner SS, Liu J Proc Natl Acad Sci U S A 03-Apr-2024
PMCID:PMC11009661
doi:10.1073/pnas.2313921121
PMID:38568968
BnAP2-12 overexpression delays ramie flowering: evidence from AP2/ERF gene expression Zhang X, Peng W, Chen H, Xing H Front Plant Sci 25-Mar-2024
PMCID:PMC10999622
doi:10.3389/fpls.2024.1367837
PMID:38590749
Characterization of leucine aminopeptidase (LAP) activity in sweet pepper fruits during ripening and its inhibition by nitration and reducing events Muñoz-Vargas MA, Taboada J, González-Gordo S, Palma JM, Corpas FJ Plant Cell Rep 11-Mar-2024
PMCID:PMC10927865
doi:10.1007/s00299-024-03179-x
PMID:38466441
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
RNA Sequencing Analysis and Verification of Paeonia ostii ‘Fengdan’ CuZn Superoxide Dismutase (PoSOD) Genes in Root Development Wang J, Song Y, Wang Z, Shi L, Yu S, Xu Y, Wang G, He D, Jiang L, Shang W, He S Plants (Basel) 31-Jan-2024
PMCID:PMC10856844
doi:10.3390/plants13030421
PMID:38337954
Genome-Wide Association Study for Agronomic Traits in Gamma-Ray-Derived Mutant Kenaf (Hibiscus cannabinus L.) Kim WJ, Yang B, Lee YJ, Kim JH, Kim SH, Ahn JW, Kang SY, Kim SH, Ryu J Plants (Basel) 16-Jan-2024
PMCID:PMC10819814
doi:10.3390/plants13020249
PMID:38256802
Single molecule real-time sequencing data sets of Hypericum perforatum L. plantlets and cell suspension cultures Selvakesavan RK, Nuc M, Kolarčik V, Krajewski P, Franklin G Sci Data 06-Jan-2024
PMCID:PMC10771467
doi:10.1038/s41597-023-02878-6
PMID:38184679
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Comparative Physiological and Transcriptome Analyses of Tolerant and Susceptible Cultivars Reveal the Molecular Mechanism of Cold Tolerance in Anthurium andraeanum Dou N, Li L, Fang Y, Fan S, Wu C Int J Mol Sci 23-Dec-2023
PMCID:PMC10779044
doi:10.3390/ijms25010250
PMID:38203421
Moringa oleifera leaf alleviates functional constipation via regulating the gut microbiota and the enteric nervous system in mice Gao X, Yang W, Li S, Liu S, Yang W, Song S, Sheng J, Zhao Y, Tian Y Front Microbiol 20-Dec-2023
PMCID:PMC10773919
doi:10.3389/fmicb.2023.1315402
PMID:38192287
A chromosome-level genome assembly of Agave hybrid NO.11648 provides insights into the CAM photosynthesis Yang Z, Yang Q, Liu Q, Li X, Wang L, Zhang Y, Ke Z, Lu Z, Shen H, Li J, Zhou W Hortic Res 19-Dec-2023
PMCID:PMC10848310
doi:10.1093/hr/uhad269
PMID:38333731
Comprehensive Analysis of NAC Transcription Factors Reveals Their Evolution in Malvales and Functional Characterization of AsNAC019 and AsNAC098 in Aquilaria sinensis Yang Z, Mei W, Wang H, Zeng J, Dai H, Ding X Int J Mol Sci 12-Dec-2023
PMCID:PMC10744133
doi:10.3390/ijms242417384
PMID:38139213
Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses Bejerman N, Dietzgen R, Debat H Viruses 10-Dec-2023
PMCID:PMC10747219
doi:10.3390/v15122402
PMID:38140643
Overexpression and knockdown of cotton GhdadD gene reveals its drought and salt stress tolerance role Zhang Y, Zheng J, Linyerera SM, Magwanga RO, Hou Y, Wang Y, Xu Y, Khan A, Yu S, Zhou Z, Liu F, Cai X iScience 07-Dec-2023
PMCID:PMC10788213
doi:10.1016/j.isci.2023.108664
PMID:38226165

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1021/NP050553T
> Lignans, neolignans and related compounds
3-[4-[(1R,2S)-1-hydroxy-1-(3-hydroxy-4-methoxyphenyl)-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxypropan-2-yl]oxy-3-methoxyphenyl]propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163188172 Click to see COC1=C(C=C(C=C1)C(C(COC(=O)C=CC2=CC(=C(C=C2)O)OC)OC3=C(C=C(C=C3)CCCOC(=O)C=CC4=CC(=C(C=C4)O)OC)OC)O)O 730.80 unknown https://doi.org/10.1021/NP050553T
3-[4-[1-Hydroxy-1-(3-hydroxy-4-methoxyphenyl)-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propan-2-yl]oxy-3-methoxyphenyl]propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162951238 Click to see COC1=C(C=C(C=C1)C(C(COC(=O)C=CC2=CC(=C(C=C2)O)OC)OC3=C(C=C(C=C3)CCCOC(=O)C=CC4=CC(=C(C=C4)O)OC)OC)O)O 730.80 unknown https://doi.org/10.1021/NP050553T
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
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 via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lanosta-7,24-dienol 12302189 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-9-hydroxy-5b,8,8,11a-tetramethyl-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-carboxylate 102242317 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C=CC6=CC(=C(C=C6)O)O)C)(C)C)O)C)C(=O)OC 648.90 unknown https://doi.org/10.1021/NP050553T
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-[[(Z)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-9-hydroxy-5b,8,8,11a-tetramethyl-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-carboxylate 101408484 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C=CC6=CC(=C(C=C6)O)O)C)(C)C)O)C)C(=O)OC 648.90 unknown https://doi.org/10.1021/NP050553T
Methyl 5a-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxymethyl]-9-hydroxy-5b,8,8,11a-tetramethyl-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-carboxylate 73236923 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C=CC6=CC(=C(C=C6)O)O)C)(C)C)O)C)C(=O)OC 648.90 unknown https://doi.org/10.1021/NP050553T
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4H-1-Benzopyran-4-one, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-5,7-dihydroxy- 5488575 Click to see CC1C(C(C(C(O1)OC2=COC3=CC(=CC(=C3C2=O)O)O)O)O)O 340.28 unknown https://doi.org/10.1021/NP050553T
5,7-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 14214024 Click to see CC1C(C(C(C(O1)OC2=COC3=CC(=CC(=C3C2=O)O)O)O)O)O 340.28 unknown https://doi.org/10.1021/NP050553T
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-Dihydroxy-6,7-dimethoxyxanthone 101631689 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O)OC 288.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Brasilixanthone B 5324261 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4C=CC(O5)(C)C)O)C 392.40 unknown via CMAUP database
Brasillixanthone 11668301 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=C(C(=C4)O)OC(C=C5)(C)C)O)C 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
3-Methyl-4,8-dihydroxy-3,4-dihydroisocoumarin 169539 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown https://doi.org/10.1021/NP050553T
trans-4-Hydroxymellein 10262028 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown https://doi.org/10.1021/NP050553T
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-[(2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 160107987 Click to see COC1=CC(=CC2=C1OC(C2COC(=O)C=CC3=CC(=C(C=C3)O)OC)C4=CC(=C(C=C4)O)OC)CCCOC(=O)C=CC5=CC(=C(C=C5)O)OC 712.70 unknown https://doi.org/10.1021/NP050553T
3-[2-(4-Hydroxy-3-methoxyphenyl)-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxymethyl]-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 53439689 Click to see COC1=CC(=CC2=C1OC(C2COC(=O)C=CC3=CC(=C(C=C3)O)OC)C4=CC(=C(C=C4)O)OC)CCCOC(=O)C=CC5=CC(=C(C=C5)O)OC 712.70 unknown https://doi.org/10.1021/NP050553T
Boehmenan 5274624 Click to see COC1=CC(=CC2=C1OC(C2COC(=O)C=CC3=CC(=C(C=C3)O)OC)C4=CC(=C(C=C4)O)OC)CCCOC(=O)C=CC5=CC(=C(C=C5)O)OC 712.70 unknown https://doi.org/10.1021/NP050553T
> Phenylpropanoids and polyketides / Macrolides and analogues
(R)-De-O-methyllasiodiplodin 14562694 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)O)C(=O)O1 278.34 unknown https://doi.org/10.1021/NP050553T
14,16-Dihydroxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one 14562693 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)O)C(=O)O1 278.34 unknown https://doi.org/10.1021/NP050553T
> Phenylpropanoids and polyketides / Stilbenes
4-[(2S)-3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propyl]-2-methoxyphenol 163060312 Click to see COC1=C(C=CC(=C1)CC(CO)C2=CC(=C(C=C2)O)OC)O 304.34 unknown https://doi.org/10.1021/NP050553T
4-[3-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)propyl]-2-methoxyphenol 13908507 Click to see COC1=C(C=CC(=C1)CC(CO)C2=CC(=C(C=C2)O)OC)O 304.34 unknown https://doi.org/10.1021/NP050553T

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Collections Top

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