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Elaeocarpus nitidus

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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 UUID64401923c6eb1214769383
Scientific name Elaeocarpus nitidus
Authority Jack
First published in Malayan Misc. 1(5): 41 (1820)

Description Top

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Synonyms Top

Scientific name Authority First published in
Elaeocarpus gracilipes R.Knuth Repert. Spec. Nov. Regni Veg. 49: 70 (1940)
Elaeocarpus nigropunctatus Merr. J. Straits Branch Roy. Asiat. Soc. 77: 196 (1917)
Elaeocarpus parvifolius Wall. Numer. List [Wallich] n. 2662. 1831

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Elaeocarpus nitidus var. macrophyllus Coode Kew Bull. 56: 526 (2001)
Elaeocarpus nitidus var. pseudovelutinus Coode Kew Bull. 56: 525 (2001)
Elaeocarpus nitidus var. velutinus Ng Gard. Bull. Singapore 41: 44 (1988 publ. 1989)

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-tropical
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000664560
Tropicos 50202355
KEW urn:lsid:ipni.org:names:833892-1
The Plant List kew-2785817
Open Tree Of Life 5748799
NCBI Taxonomy 1504432
IPNI 833892-1
iNaturalist 427571
GBIF 7291075
EOL 5408139

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)!
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Title Authors Publication Released IDs
Anti-babesial ellagic acid rhamnosides from the bark of Elaeocarpus parvifolius. Elkhateeb A, Subeki, Takahashi K, Matsuura H, Yamasaki M, Yamato O, Maede Y, Katakura K, Yoshihara T, Nabeta K Phytochemistry 01-Nov-2005
doi:10.1016/J.PHYTOCHEM.2005.08.020
PMID:16226774
Ellagic acid derivatives and cytotoxic cucurbitacins from Elaeocarpus mastersii. Ito A, Chai HB, Lee D, Kardono LB, Riswan S, Farnsworth NR, Cordell GA, Pezzuto JM, Kinghorn AD Phytochemistry 01-Sep-2002
doi:10.1016/S0031-9422(02)00232-7
PMID:12169311

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
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2S,3R,4R,5S,6S)-2-[(6,14-dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 11706077 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)OC(=O)C)O 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
[(2S,3R,4R,5S,6S)-3-acetyloxy-2-[(6,14-dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-5-hydroxy-6-methyloxan-4-yl] acetate 11763306 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)OC(=O)C)OC(=O)C)O 546.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
https://doi.org/10.1016/S0031-9422(02)00232-7
[(2S,3R,4S,5R,6S)-6-[(6,14-dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-4,5-dihydroxy-2-methyloxan-3-yl] acetate 11562454 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)O)OC(=O)C 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
[2-[(6,14-Dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-3,5-dihydroxy-6-methyloxan-4-yl] acetate 73068118 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)OC(=O)C)O 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
[3-Acetyloxy-2-[(6,14-dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-5-hydroxy-6-methyloxan-4-yl] acetate 21159147 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)OC(=O)C)OC(=O)C)O 546.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
[6-[(6,14-Dihydroxy-13-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-7-yl)oxy]-4,5-dihydroxy-2-methyloxan-3-yl] acetate 73007787 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)O)OC(=O)C 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
6,14-Dihydroxy-13-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 73048562 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020
6,14-dihydroxy-13-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 11669821 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C4=C2OC(=O)C5=CC(=C(C(=C54)OC3=O)O)OC)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.020

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