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Pappobolus stuebelii

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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 UUID643fca5249fc0958829544
Scientific name Pappobolus stuebelii
Authority (Hieron.) Panero
First published in Syst. Bot. Monogr. 36: 129 (1992)

Description Top

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Synonyms Top

Scientific name Authority First published in
Helianthus stuebelii Hieron. Bot. Jahrb. Syst. 21(3): 349 (1895)
Helianthopsis bishopii H.Rob. Phytologia 54: 52 (-53), fig (1983)
Helianthopsis stuebelii (Hieron.) H.Rob. Phytologia 44: 266 (1979)

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-0000037414
Tropicos 2739056
KEW urn:lsid:ipni.org:names:969064-1
The Plant List gcc-136183
Open Tree Of Life 234530
NCBI Taxonomy 1048912
IPNI 969064-1
iNaturalist 1063022
GBIF 3093666
EOL 5120703

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
A further geranylnerol derivative from Helianthopsis species Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83199-4
Sesquiterpene lactones and benzofurans in glandular trichomes of three Pappobolus species Otmar Spring, David Vargas, Nikolaus H. Fischer Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85029-Y

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 / Diterpenoids / Kaurane diterpenoids
(1S,4S,5S,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 11722476 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
4,10-Dimethylidene-7-(propan-2-yl)cyclodec-5-en-1-ol 71370041 Click to see CC(C)C1CCC(=C)C(CCC(=C)C=C1)O 220.35 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
5-cyclodecen-1-ol, 4,10-bis(methylene)-7-(1-methylethyl)-, (1R,5E,7S)- 643709 Click to see CC(C)C1CCC(=C)C(CCC(=C)C=C1)O 220.35 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2,11-Dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl) 2-methylbut-2-enoate 500211 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)83199-4
15-deoxybudlein A 14314511 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/0031-9422(91)85029-Y
https://doi.org/10.1016/S0031-9422(00)83199-4
Atripliciolidtiglate 14314512 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/0031-9422(91)85029-Y
Budlein A 5281430 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(=CC3C1C(=C)C(=O)O3)CO)C 374.40 unknown https://doi.org/10.1016/0031-9422(91)85029-Y
Niveusin C 5281488 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(91)85029-Y

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