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Diospyros decandra

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440174956461584370957
Scientific name Diospyros decandra
Authority Lour.
First published in Fl. Cochinch. : 227 (1790)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Diospyros packmannii C.B.Clarke Fl. Brit. India 3: 564 (1882)

Common names Top

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Language Common/alternative name
Japanese カバイロクロガキ
Khmer ច័ន
Thai จัน-อิน
Thai จัน
Vietnamese thị
Chinese 金蘋柿
Chinese 黃柿
Chinese 法国香柿
Chinese 香水柿

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
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000648759
Tropicos 50179998
KEW urn:lsid:ipni.org:names:322304-1
The Plant List kew-2769607
Open Tree Of Life 3901747
IPNI 322304-1
iNaturalist 430945
GBIF 4070543
Freebase /m/0j249r1
EOL 5238601
USDA GRIN 14279
Wikipedia Diospyros_decandra

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)!
Title Authors Publication Released IDs
Novel 24-nor-, 24-nor-2,3-seco-, and 3,24-dinor-2,4-seco-ursane triterpenes from Diospyros decandra: evidences for ring A biosynthetic transformations Parichat Nareeboon, Wolfgang Kraus, Uwe Beifuss, Juergen Conrad, Iris Klaiber, Somyote Sutthivaiyakit Elsevier BV 13-Apr-2006
doi:10.1016/J.TET.2006.03.034

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 / Fatty Acyls / Fatty alcohols
methyl (Z)-2-[(1R)-1-hydroxy-2-oxopropyl]heptacos-2-enoate 102296374 Click to see 494.80 unknown https://doi.org/10.1016/J.TET.2006.03.034
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aS,9S,10R,12aS,14bS)-1,10-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11583677 Click to see 472.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
(1R,2R,4S,4aS,6aR,6aS,6bR,8aS,9S,10R,12aS,14bS)-1,4,10-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11562206 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5C)O)C)C)C2C1(C)O)C)C(=O)O)O 488.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
methyl (1R,2Z,4aR,4bS,6aS,7S,9R,10R,10aS,12aR)-7,10-dihydroxy-1-(2-methoxy-2-oxoethyl)-2-(1-methoxy-1-oxopropan-2-ylidene)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydrochrysene-6a-carboxylate 162971205 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC(=C(C)C(=O)OC)C4(C)CC(=O)OC)C)C2C1(C)O)C)C(=O)OC)O 560.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
(1R,2R,4aR,4bS,6aS,7S,9R,10R,10aS,12aR)-2-acetyl-1-(carboxymethyl)-7,10-dihydroxy-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 11569424 Click to see 490.60 unknown https://doi.org/10.1016/J.TET.2006.03.034
2-acetyl-1-(carboxymethyl)-7,10-dihydroxy-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 73010310 Click to see 490.60 unknown https://doi.org/10.1016/J.TET.2006.03.034
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(1R,2R,4S,4aS,6aS,6aS,6bR,12aS,14bS)-1,4,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-oxo-2,3,4,5,6,6a,7,8,13,14b-decahydropicene-4a-carboxylic acid 11591177 Click to see 484.60 unknown https://doi.org/10.1016/J.TET.2006.03.034
1,4,10-Trihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73007702 Click to see 488.70 unknown https://doi.org/10.1016/J.TET.2006.03.034
1,4,11-Trihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-oxo-2,3,4,5,6,6a,7,8,13,14b-decahydropicene-4a-carboxylic acid 73022005 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5=C(C(=O)C(=CC45C)O)C)C)C2C1(C)O)C)C(=O)O)O 484.60 unknown https://doi.org/10.1016/J.TET.2006.03.034
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
1,10-Dihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73019448 Click to see 472.70 unknown https://doi.org/10.1016/J.TET.2006.03.034

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