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Kippistia suaedifolia

Kippistia suaedifolia - 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 UUID643fd3d11806e755914323
Scientific name Kippistia suaedifolia
Authority F.Muell.
First published in Rep. Pl. Babbage's Exped. : 13 (1859)

Description Top

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Synonyms Top

Scientific name Authority First published in
Minuria suaedifolia F.Muell. ex Benth. Fl. Austral. 3: 499 (1867)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Victoria
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000135160
Tropicos 2734069
KEW urn:lsid:ipni.org:names:227302-1
The Plant List gcc-95919
Open Tree Of Life 895472
NCBI Taxonomy 119775
IPNI 227302-1
iNaturalist 634240
GBIF 5389440
Freebase /m/06zp0__
CMAUP NPO22467

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
Phylogenetic relationships and generic delimitation of Eurasian Aster (Asteraceae: Astereae) inferred from ITS, ETS and trnL-F sequence data Li WP, Yang FS, Jivkova T, Yin GS Ann Bot 19-Apr-2012
PMCID:PMC3359916
doi:10.1093/aob/mcs054
PMID:22517812
The volatile herb oil of Kippistia suaedifolia Joseph J. Brophy, Terence M. Flynn, Erich V. Lassak, John Pickard Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83205-6

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Cilinaphthalide B 10476659 Click to see COC1=C(C=C(C=C1)C2=C3C(=C(C4=CC(=C(C=C42)OC)OC)OC)COC3=O)OC 410.40 unknown via CMAUP database
Diphyllin 100492 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2O)COC3=O)C4=CC5=C(C=C4)OCO5)OC 380.30 unknown via CMAUP database
Justicidin A 159982 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown via CMAUP database
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown via CMAUP database
Justicidin C 493173 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2OC)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown via CMAUP database
Justicidin D 5318737 Click to see COC1=C2C(=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6)COC2=O 378.30 unknown via CMAUP database
Prostalidin A 443016 Click to see COC1=C2C(=CC3=C(C4=C(C=C31)C(=O)OC4)C5=CC6=C(C=C5O)OCO6)OCO2 394.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Justin B 10672178 Click to see CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C(=C3)OC)O)OC)COC(=O)C 474.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Tuberculatin 10391676 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)O)COC3=O)C5=CC6=C(C=C5)OCO6)OC 512.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
https://doi.org/10.1016/0031-9422(82)83205-6
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
(+)-cis-Carveol 443177 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/0031-9422(82)83205-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83205-6
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(82)83205-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Euscaphic Acid 471426 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
[(3S)-1-(furan-3-yl)-4-methylpentan-3-yl] acetate 163048723 Click to see CC(C)C(CCC1=COC=C1)OC(=O)C 210.27 unknown https://doi.org/10.1016/0031-9422(82)83205-6
[1-(Furan-3-yl)-4-methylpentan-3-yl] acetate 163048722 Click to see CC(C)C(CCC1=COC=C1)OC(=O)C 210.27 unknown https://doi.org/10.1016/0031-9422(82)83205-6
> Organoheterocyclic compounds / Naphthofurans / Furanonaphthodioxoles
9-(1,3-Benzodioxol-5-yl)-5-methoxy-[1]benzofuro[6,5-f][1,3]benzodioxol-8-one 5321603 Click to see COC1=C2C(=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6)C(=O)CO2 378.30 unknown via CMAUP database

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