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Asteriscus daltonii subsp. vogelii

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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
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Details Top

Internal ID UUID64406e08ef768824678163
Scientific name Asteriscus daltonii subsp. vogelii
Authority (Webb) Greuter
First published in Fl. Medit. 7: 46 (1997)

Description Top

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Common names Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Asteriscus vogelii subsp. vogelii var. darwinii (Webb) Walp. Ann. Bot. Syst. 2: 845 (1852)

Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000093639
KEW urn:lsid:ipni.org:names:999895-1
GBIF 5705517

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
Bioactive humulene derivatives from Asteriscus vogelii. Rauter AP, Branco I, Bermejo J, González AG, García-Grávalos MD, Feliciano AS Phytochemistry 01-Jan-2001
doi:10.1016/S0031-9422(00)00304-6
PMID:11219809

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Icosa-2,4,6-trienoic acid 157667 Click to see CCCCCCCCCCCCCC=CC=CC=CC(=O)O 306.50 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,4,8-Trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylic acid 162942647 Click to see CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
methyl (1Z,5E,8E)-4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate 163189799 Click to see CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)OC 262.34 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
methyl (1Z,5E,8Z)-4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate 21724965 Click to see CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)OC 262.34 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
Methyl 4,4,8-trimethyl-7-oxocycloundeca-1,5,8-triene-1-carboxylate 73831179 Click to see CC1=CCCC(=CCC(C=CC1=O)(C)C)C(=O)OC 262.34 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3E,4aR,5S,8aR)-3-(1-hydroxypropan-2-ylidene)-4a,5-dimethyl-4,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one 101849880 Click to see CC1CCCC2C1(CC(=C(C)CO)C(=O)C2)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(16R,17S,18S,21S)-6-[(16R,17S,18S,21S)-17-carboxy-18-hydroxy-17,21-dimethyl-10-azapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1,3(11),4,6,8,12-hexaen-10-yl]-18-hydroxy-17,21-dimethyl-10-azapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1,3(11),4(9),5,7,12-hexaene-17-carboxylic acid 73058386 Click to see CC12CCC(C(C1CCC3=CC4=C(C=C23)C5=C(N4)C=CC(=C5)N6C7=CC=CC=C7C8=C6C=C9CCC1C(C9=C8)(CCC(C1(C)C(=O)O)O)C)(C)C(=O)O)O 724.90 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4E,7E,10R)-5,9,9-trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 92977572 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
(4E,7E,10S)-5,9,9-Trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 13919627 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
(4Z,7E,10R)-5,9,9-trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 98086581 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
(4Z,7E,10S)-5,9,9-trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 13919626 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
(5R,10R)-5,9,9-trimethyl-11-oxabicyclo[8.2.1]tridec-1(13)-ene-6,12-dione 162923215 Click to see CC1CCCC2=CC(C(CCC1=O)(C)C)OC2=O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
11-Oxabicyclo[8.2.1]tridec-1(13)-ene-6,12-dione, 5,9,9-trimethyl- 10562648 Click to see CC1CCCC2=CC(C(CCC1=O)(C)C)OC2=O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
5,9,9-Trimethyl-11-oxabicyclo[8.2.1]trideca-1(13),4,7-triene-6,12-dione 44511055 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6
Asteriscunolide A 13919624 Click to see CC1=CCCC2=CC(C(C=CC1=O)(C)C)OC2=O 246.30 unknown https://doi.org/10.1016/S0031-9422(00)00304-6

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