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Sphaeranthus bullatus

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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 UUID643fd2bb84e10671721598
Scientific name Sphaeranthus bullatus
Authority Mattf.
First published in Notizbl. Bot. Gart. Berlin-Dahlem 13: 290 (1936)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Ethiopia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000126189
Tropicos 50075954
KEW urn:lsid:ipni.org:names:250503-1
The Plant List gcc-87232
Open Tree Of Life 5921008
NCBI Taxonomy 1548657
IPNI 250503-1
iNaturalist 182150
GBIF 3094712
EPPO SPSBU
USDA GRIN 450227

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
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Compounds from African Medicinal Plants with Activities Against Selected Parasitic Diseases: Schistosomiasis, Trypanosomiasis and Leishmaniasis Simoben CV, Ntie-Kang F, Akone SH, Sippl W Nat Prod Bioprospect 09-May-2018
PMCID:PMC5971035
doi:10.1007/s13659-018-0165-y
PMID:29744736
Carvotacetone derivatives and eudesman-12,6β-olides from Sphaeranthus species J. Jakupovic, M. Grenz, F. Bohlmann, G.M. Mungai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85431-E

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
> Acetylides
Trideca-1,3,5,7,9-pentayne 139646581 Click to see CCCC#CC#CC#CC#CC#C 164.20 unknown https://doi.org/10.1016/0031-9422(90)85431-E
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol isobutyrate 228738 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C(C)C 220.31 unknown https://doi.org/10.1016/0031-9422(90)85431-E
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(4S,5S,6R)-4,6-dihydroxy-2-(hydroxymethyl)-5-propan-2-ylcyclohex-2-en-1-one 14589114 Click to see CC(C)C1C(C=C(C(=O)C1O)CO)O 200.23 unknown https://doi.org/10.1016/0031-9422(90)85431-E
[(1S,5R,6R)-5-hydroxy-3-(hydroxymethyl)-2-oxo-6-propan-2-ylcyclohex-3-en-1-yl] (E)-2-methylbut-2-enoate 162924687 Click to see CC=C(C)C(=O)OC1C(C(C=C(C1=O)CO)O)C(C)C 282.33 unknown https://doi.org/10.1016/0031-9422(90)85431-E
[(3S,4S,5R)-5-acetyloxy-3-[(E)-2-methylbut-2-enoyl]oxy-6-oxo-4-propan-2-ylcyclohexen-1-yl]methyl (E)-2-methylbut-2-enoate 14589112 Click to see CC=C(C)C(=O)OCC1=CC(C(C(C1=O)OC(=O)C)C(C)C)OC(=O)C(=CC)C 406.50 unknown https://doi.org/10.1016/0031-9422(90)85431-E
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85431-E
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(90)85431-E
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Chrysosplenol C 189065 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC)O 360.30 unknown https://doi.org/10.1016/0031-9422(90)85431-E

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