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Vittadinia gracilis

Vittadinia gracilis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcc2a45bd6788781367
Scientific name Vittadinia gracilis
Authority (Hook.f.) N.T.Burb.
First published in Brunonia 5(1): 54 (1982): (1982)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aster humilis Banks & Sol. ex Hook.f. Fl. Nov.-Zel. 1: 125 (1852)
Eurybiopsis gracilis Hook.f. Hooker's London Journal of Botany 6 1847
Vittadinia lobata hort. ex E.Vilm. Fl. Pleine Terre : 959 (1863)
Vittadinia scabra Hook.f. Fl. Tasman. i. 181
Aster behrii Schltdl. Linnaea 21: 446 (1848)
Eurybiopsis hookeri F.Muell. Linnaea 25: 453 (1853)

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
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000059431
Tropicos 50154861
KEW urn:lsid:ipni.org:names:911620-1
The Plant List gcc-16519
Open Tree Of Life 395885
NCBI Taxonomy 119808
IPNI 911620-1
iNaturalist 406989
GBIF 3138899
Wikipedia Vittadinia_gracilis

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)!
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Title Authors Publication Released IDs
Nerylgeraniol derivatives and two clerodanes from Vittadinia gracilis C. Zdero, F. Bohlmann, R.M. King, L. Haegi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80136-5

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 alcohols
(2R)-2-[(2R,5Z)-5-[(E)-6-hydroxy-4-methylhex-4-enylidene]oxan-2-yl]-6-methylhept-5-enal 14138927 Click to see CC(=CCCC(C=O)C1CCC(=CCCC(=CCO)C)CO1)C 320.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
(2S)-2-[(2R,5Z)-5-[(E)-6-hydroxy-4-methylhex-4-enylidene]oxan-2-yl]-6-methylhept-5-enal 14138926 Click to see CC(=CCCC(C=O)C1CCC(=CCCC(=CCO)C)CO1)C 320.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
2-[5-(6-Hydroxy-4-methylhex-4-enylidene)oxan-2-yl]-6-methylhept-5-enal 162855496 Click to see CC(=CCCC(C=O)C1CCC(=CCCC(=CCO)C)CO1)C 320.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
3-[(1R,3S,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-8-(5,7-dihydroxy-4-oxochromen-2-yl)-1-hydroxy-11-methoxy-5-methyl-2-oxatricyclo[6.3.1.04,12]dodeca-5,10-dien-9-one 44557355 Click to see CC1=CCC2(C3C1C(OC3(C(=CC2=O)OC)O)C4C(=C)C(CC5C4(CCCC5(C)C)C)O)C6=CC(=O)C7=C(C=C(C=C7O6)O)O 618.70 unknown https://doi.org/10.1016/0031-9422(88)80136-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
12-Hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal 129686335 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)C=O)C 320.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
18-Oxo-19-hydroxynerylgeraniol 14138924 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)C=O)C 320.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
18,19-Dihydroxynerylgeraniol 14138921 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)CO)C 322.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
6-(Hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-triene-1,12-diol 162920589 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)CO)C 322.50 unknown https://doi.org/10.1016/0031-9422(88)80136-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(88)80136-5
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(88)80136-5
> Organoheterocyclic compounds / Furofurans
(1S,4R,7S,9S,11S,12S)-9-(furan-3-yl)-6,8,18-trioxapentacyclo[10.7.0.01,16.04,11.07,11]nonadec-15-ene-5,17-dione 14138932 Click to see C1CC2C3(CCC4C25CC(OC5OC4=O)C6=COC=C6)COC(=O)C3=C1 356.40 unknown https://doi.org/10.1016/0031-9422(88)80136-5
9-(Furan-3-yl)-6,8,18-trioxapentacyclo[10.7.0.01,16.04,11.07,11]nonadec-15-ene-5,17-dione 14138931 Click to see C1CC2C3(CCC4C25CC(OC5OC4=O)C6=COC=C6)COC(=O)C3=C1 356.40 unknown https://doi.org/10.1016/0031-9422(88)80136-5
> Organoheterocyclic compounds / Naphthopyrans
(1S,4R,7S,9R,10R,12S)-7-(furan-3-yl)-12-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-13-ene-5,15-dione 162965640 Click to see CC12CC(OC(=O)C1CCC34C2CC(C=C3C(=O)OC4)O)C5=COC=C5 358.40 unknown https://doi.org/10.1016/0031-9422(88)80136-5
7-(Furan-3-yl)-12-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-13-ene-5,15-dione 14138933 Click to see CC12CC(OC(=O)C1CCC34C2CC(C=C3C(=O)OC4)O)C5=COC=C5 358.40 unknown https://doi.org/10.1016/0031-9422(88)80136-5

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