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Bothriocline amplifolia

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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 UUID643fcc5d07036022031037
Scientific name Bothriocline amplifolia
Authority (O.Hoffm. & Muschl.) M.G.Gilbert
First published in Kew Bull. 36(3): 593 (1981)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erlangea amplifolia var. aberdarica R.E.Fr. Acta Horti Bergiani 9: 113 1929
Erlangea amplifolia O.Hoffm. & Muschl. Bot. Jahrb. Syst. 46(1-2): 64 (1911)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • West-central Tropical Africa
      • Cameroon

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000061862
Tropicos 2727114
KEW urn:lsid:ipni.org:names:908452-1
The Plant List gcc-18881
Open Tree Of Life 7052512
NCBI Taxonomy 2507393
IPNI 908452-1
iNaturalist 861249
GBIF 3089770

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Two new genera, Hoffmannanthus and Jeffreycia, mostly from East Africa (Erlangeinae, Vernonieae, Asteraceae) Robinson H, Keeley SC, Skvarla JJ, Chan R PhytoKeys 18-Jul-2014
PMCID:PMC4152891
doi:10.3897/phytokeys.39.7624
PMID:25197225
A 5-methylcoumarin and glaucolides from Bothriocline amplifolia Muniruddin Ahmed, Jasmin Jakupovic, Ferdinand Bohlmann, M.G. Mungai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85154-R

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 lactones
[(1S,2R,4R,11R,13S)-8-acetyl-15-(acetyloxymethyl)-4,11-dimethyl-9,16-dioxo-3,10,17-trioxatetracyclo[12.3.0.02,4.07,11]heptadeca-7,14-dien-13-yl] 2-(hydroxymethyl)prop-2-enoate 15689667 Click to see CC(=O)C1=C2CCC3(C(O3)C4C(=C(C(=O)O4)COC(=O)C)C(CC2(OC1=O)C)OC(=O)C(=C)CO)C 504.50 unknown https://doi.org/10.1016/0031-9422(91)85154-R
[(1S,2R,4R,8R,10S)-8-acetyloxy-12-(acetyloxymethyl)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-11-en-10-yl] 2-(hydroxymethyl)prop-2-enoate 15689663 Click to see CC(=O)OCC1=C2C(CC(C(=O)CCC3(C(C2OC1=O)O3)C)(C)OC(=O)C)OC(=O)C(=C)CO 480.50 unknown https://doi.org/10.1016/0031-9422(91)85154-R
[8-Acetyl-15-(acetyloxymethyl)-4,11-dimethyl-9,16-dioxo-3,10,17-trioxatetracyclo[12.3.0.02,4.07,11]heptadeca-7,14-dien-13-yl] 2-(hydroxymethyl)prop-2-enoate 162897789 Click to see CC(=O)C1=C2CCC3(C(O3)C4C(=C(C(=O)O4)COC(=O)C)C(CC2(OC1=O)C)OC(=O)C(=C)CO)C 504.50 unknown https://doi.org/10.1016/0031-9422(91)85154-R
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)85154-R
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)85154-R
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)85154-R
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[6-(Acetyloxymethyl)-10-hydroxy-11-methoxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 162969965 Click to see CC(=O)OCC1=C2C(CC(C3(CCC(O3)(C=C2OC1=O)C)OC)(C)O)OC(=O)C(=C)CO 452.50 unknown https://doi.org/10.1016/0031-9422(91)85154-R
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
2-(3,3-dimethyloxiran-2-yl)-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 14464536 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C4C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/0031-9422(91)85154-R

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