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Electranthera parvifolia

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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 UUID64405e22ca8cd845856505
Scientific name Electranthera parvifolia
Authority (S.F.Blake) Mesfin, D.J.Crawford & Pruski
First published in Phytoneuron 2015-68: 15 (2015)

Description Top

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Synonyms Top

Scientific name Authority First published in
Coreopsis parvifolia S.F.Blake Proc. Amer. Acad. Arts 49: 338 (1913)
Electra parvifolia (S.F.Blake) Mesfin & D.J.Crawford Nordic J. Bot. 32(1): 89 (2013)

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-0001330567
Tropicos 100438207
KEW urn:lsid:ipni.org:names:60472676-2
Open Tree Of Life 7602281
IPNI 60472676-2
iNaturalist 973549
GBIF 9097999

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
Polyacetylenverbindungen, 243. Über die Inhaltsstoffe von <i>Coreopsis parvifolia</i> Blake Ferdinand Bohlmann, Christa Zdero Wiley 29-Jun-2007
doi:10.1002/CBER.19771100209

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
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(10R)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 182352 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1002/CBER.19771100209
(6Z,10R)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 6442684 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1002/CBER.19771100209
(6Z,10S)-3,6,10-trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 13996861 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1002/CBER.19771100209
3,6,10-Trimethyl-5,8,9,10-tetrahydrobenzo[8]annulen-2-ol 78410270 Click to see CC1CCC=C(CC2=C1C=C(C(=C2)C)O)C 216.32 unknown https://doi.org/10.1002/CBER.19771100209
> Benzenoids / Phenols / Methoxyphenols
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enyl 3-methylbutanoate 163009099 Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C=C1)O)OC 264.32 unknown https://doi.org/10.1002/CBER.19771100209
Coniferyl isovalerate 92006833 Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C=C1)O)OC 264.32 unknown https://doi.org/10.1002/CBER.19771100209
> Organosulfur compounds / Sulfonyls / Sulfones
(7E)-7-methylsulfonyltrideca-1,7-dien-3,5,9,11-tetrayne 92034542 Click to see CC#CC#CC=C(C#CC#CC=C)S(=O)(=O)C 242.29 unknown https://doi.org/10.1002/CBER.19771100209
7-Methylsulfonyltrideca-1,7-dien-3,5,9,11-tetrayne 71383625 Click to see CC#CC#CC=C(C#CC#CC=C)S(=O)(=O)C 242.29 unknown https://doi.org/10.1002/CBER.19771100209
> Organosulfur compounds / Sulfoxides
(7E)-7-[(R)-methylsulfinyl]trideca-1,7-dien-3,5,9,11-tetrayne 162969535 Click to see CC#CC#CC=C(C#CC#CC=C)S(=O)C 226.30 unknown https://doi.org/10.1002/CBER.19771100209
(7Z)-7-[(R)-methylsulfinyl]trideca-1,7-dien-3,5,9,11-tetrayne 162969536 Click to see CC#CC#CC=C(C#CC#CC=C)S(=O)C 226.30 unknown https://doi.org/10.1002/CBER.19771100209
7-Methylsulfinyltrideca-1,7-dien-3,5,9,11-tetrayne 71383626 Click to see CC#CC#CC=C(C#CC#CC=C)S(=O)C 226.30 unknown https://doi.org/10.1002/CBER.19771100209
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 173954 Click to see COC1=C(C=CC(=C1)C=CCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 356.40 unknown https://doi.org/10.1002/CBER.19771100209
Coniferyl ferulate 6441913 Click to see COC1=C(C=CC(=C1)C=CCOC(=O)C=CC2=CC(=C(C=C2)O)OC)O 356.40 unknown https://doi.org/10.1002/CBER.19771100209

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