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Endiandra baillonii

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 UUID644019a52851a501013133
Scientific name Endiandra baillonii
Authority (Pancher & Sebert) Guillaumin
First published in Bull. Soc. Bot. France 71: 1106 (1924 publ. 1925)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Beilschmiedia baillonii Pancher & Sebert Rev. Marit. Colon. 40: 562 (1874)
Endiandra parviflora Kosterm. Reinwardtia 7: 142 (1965)
Endiandra novocaledonensis Kamik. Trans. Nat. Hist. Soc. Kagoshima Imp. Coll. Agric. 3: 128 (1935)
Endiandra micrantha Schltr. Bot. Jahrb. Syst. 39: 110 (1906)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000667571
Tropicos 17805446
INPN 673374
KEW urn:lsid:ipni.org:names:464360-1
The Plant List kew-2788812
Open Tree Of Life 6026196
IPNI 464360-1
GBIF 4178823

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
Constituents of Some Species of Beilschmiedia and Endiandra (Lauraceae): New Endiandric Acid and Benzopyran Derivatives Isolated From B. oligandra JE Banfield, DS Black, DJ Collins, BPM Hyland, JJ Lee, SR Pranowo CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9940587

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 / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1071/CH9940587
(1R,5S,6R,8S,9R,10R)-5,6,9-trimethyltetracyclo[7.2.1.01,6.08,10]dodecane 163009190 Click to see CC1CCCC23C1(CC4C(C2)C4(C3)C)C 204.35 unknown https://doi.org/10.1071/CH9940587
(1S,2S,6S,7R,8S)-1,3,6-trimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 162899675 Click to see CC1=CCC2(C3C1C2(CCC3C(C)C)C)C 218.38 unknown https://doi.org/10.1071/CH9940587
1,3,6-Trimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 162899674 Click to see 218.38 unknown https://doi.org/10.1071/CH9940587
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1071/CH9940587
Calamenene, cis-(+)- 11298625 Click to see 202.33 unknown https://doi.org/10.1071/CH9940587
Calamenene, trans-(+)- 6429022 Click to see 202.33 unknown https://doi.org/10.1071/CH9940587
Ishwarane 14619932 Click to see 204.35 unknown https://doi.org/10.1071/CH9940587
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see 450.80 unknown https://doi.org/10.1071/CH9940587

Gallery Top

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Collections Top

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