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Eucalyptus camaldulensis subsp. obtusa

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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 UUID644075ba28a3e225487744
Scientific name Eucalyptus camaldulensis subsp. obtusa
Authority (Blakely) Brooker & M.W.McDonald
First published in Austral. Syst. Bot. 22: 277 (2009)

Description Top

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Common names Top

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Language Common/alternative name
Chinese 钝盖赤桉
Chinese 垂枝赤桉

Varieties (abbr. var.) 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
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • Western Australia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000912616
KEW urn:lsid:ipni.org:names:77101341-1
The Plant List kew-457535
NCBI Taxonomy 2780446
IPNI 77101341-1
GBIF 7505467

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
Spasmolytic constituents from Eucalyptus camaldulensis var. obtusa leaves. Begum S, Farhat F, Sultana I, Siddiqui BS, Shaheen F, Gilani AH J Nat Prod 01-Sep-2000
doi:10.1021/NP9902340
PMID:11000033
Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves. Siddiqui BS, Sultana I, Begum S Phytochemistry 01-Aug-2000
doi:10.1016/S0031-9422(00)00058-3
PMID:11014279

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
(1S,4R,5R,8R,10S,13R,14S,17S,18S,19R,20S)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 154497643 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-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 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(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]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP9902340

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Collections Top

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