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Ilex warburgii

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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 UUID6440219ff36b2944943298
Scientific name Ilex warburgii
Authority Loes.
First published in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 326 (1901)

Description Top

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Synonyms Top

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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-0000729947
Tropicos 50053599
KEW urn:lsid:ipni.org:names:83871-1
Open Tree Of Life 89485
NCBI Taxonomy 58299
IPNI 83871-1
GBIF 5534029
Elurikkus 539315
USDA GRIN 19792

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
Physcraper: a Python package for continually updated phylogenetic trees using the Open Tree of Life Sánchez-Reyes LL, Kandziora M, McTavish EJ BMC Bioinformatics 29-Jun-2021
PMCID:PMC8244228
doi:10.1186/s12859-021-04274-6
PMID:34187366
STRUCTURE OF A NEW CYANOGLUCOSIDE FROM <i>ILEX WARBURGII</i> LOESN. Katsuhiro Ueda, Kazuko Yasutomi, Iwao Mori Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1983.149

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
beta-Alnincanol 14633152 Click to see CC(C)C1(CCC(O1)(C)C2CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 458.80 unknown https://doi.org/10.1246/CL.1983.149
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2Z)-2-[(4R,5R,6S)-4,5-dihydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 16043519 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1246/CL.1983.149
(2Z)-2-[(4S,6R)-4-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 6440400 Click to see C1C(C=CC(=CC#N)C1OC2C(C(C(C(O2)CO)O)O)O)O 313.30 unknown https://doi.org/10.1246/CL.1983.149
(2Z)-2-[4,5-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 6079060 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1246/CL.1983.149

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Collections Top

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