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Syzygium siamense

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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 UUID643fee65b5078335348748
Scientific name Syzygium siamense
Authority (Craib) Chantar. & J.Parn.
First published in Kew Bull. 48: 609 (1993)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eugenia jambos var. sylvatica Gagnep. Fl. Indo-Chine 2: 835. 1921
Syzygium jambos var. sylvaticum (Gagnep.) Merr. & L.M.Perry J. Arnold Arbor. 19: 114 1938
Eugenia rubida Ridl. J. Fed. Malay States Mus. 10: 90 (1920)
Eugenia siamensis Craib Bull. Misc. Inform. Kew 1912: 153 (1912)
Eugenia javanica var. balansae Gagnep. Fl. Indo-Chine 2: 838. 1920

Common names Top

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Language Common/alternative name
Thai ชมพู่น้ำ

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
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000319421
Tropicos 100264642
KEW urn:lsid:ipni.org:names:973191-1
The Plant List kew-200298
Open Tree Of Life 3935188
IPNI 973191-1
iNaturalist 1046776
GBIF 3182011
EOL 5590085

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
New cytotoxic steroids from the fruits of Syzygium siamense. Chumkaew P, Kato S, Chantrapromma K J Asian Nat Prod Res 01-May-2010
doi:10.1080/10286021003762028
PMID:20496200

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
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] formate 15864211 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC=O)C)C)C(C)C 442.70 unknown https://doi.org/10.1080/10286021003762028
Stigmast-5-EN-3-beta-YL formate 4125345 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC=O)C)C)C(C)C 442.70 unknown https://doi.org/10.1080/10286021003762028
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9S,10R,13S,14S,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-diol 46223557 Click to see CCC(CCC(C)C1(CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O)C(C)C 430.70 unknown https://doi.org/10.1080/10286021003762028
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol 5318414 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown https://doi.org/10.1080/10286021003762028
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-diol 75154147 Click to see CCC(CCC(C)C1(CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O)C(C)C 430.70 unknown https://doi.org/10.1080/10286021003762028
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 6743 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1080/10286021003762028
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/10286021003762028
3-Oxo-24-ethyl-cholest-5-ene 4358735 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10286021003762028
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/10286021003762028
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10286021003762028
CID 10837035 10837035 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)OC)C)C(C)C 444.70 unknown https://doi.org/10.1080/10286021003762028
Ikshusterol 161816 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown https://doi.org/10.1080/10286021003762028
Schleicheol 2 75048827 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)OC)C)C(C)C 444.70 unknown https://doi.org/10.1080/10286021003762028
Stigmastanol 241572 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1080/10286021003762028

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