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Cassinia laevis

Cassinia laevis - 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 UUID643fca016e11e972547298
Scientific name Cassinia laevis
Authority R.Br.
First published in Observ. Compositae : 127 (1817)

Description Top

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Cassinia laevis, also known as cough bush, dead finish, curry bush, or rosemary bush, is a flowering plant found in south-eastern continental Australia. It is a shrub with a curry-like scent, linear leaves, and creamy-white flowers arranged in panicles. It was first described in 1818 and is widespread in Queensland, New South Wales, and eastern South Australia, with some records in the Northern Territory. It can be found in various habitats, including stony ridges and mallee.

Synonyms Top

Scientific name Authority First published in
Cassinia rosmarinifolia A.Cunn. ex DC. Prodr. 6: 156 (1838)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000034990
Tropicos 100399244
KEW urn:lsid:ipni.org:names:189570-1
The Plant List gcc-133842
Open Tree Of Life 721925
NCBI Taxonomy 1284871
IPNI 189570-1
iNaturalist 856226
GBIF 5390390
EPPO CSALA
EOL 6265432
USDA GRIN 411180
Wikipedia Cassinia_laevis

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
Trace Elements in Gluten-free Pastas and Flours from Markets Located in the Las Vegas, Nevada Area Collumb CJ, Delelegn AA, Fernandez GM, Hudson AC, Kimberley KW, Sims DB, Walton DJ J Food Res 14-Aug-2019
PMCID:PMC7731072
doi:10.5539/jfr.v8n5p59
PMID:33312318
Sesquiterpene lactones and other constituents from Cassinia, actinobole and an axeton species J. Jakupovic, L. Lehmann, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83027-9

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 / Sesquiterpenoids
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
(1R)-4,7-Dimethyl-1-(propan-2-yl)-1,2-dihydronaphthalene 71353669 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/0031-9422(88)83027-9
(2,8-Dimethyl-5-propan-2-yl-7-tricyclo[4.4.0.02,8]decanyl) acetate 163017328 Click to see CC(C)C1CCC2(C3C1C(C2(CC3)C)OC(=O)C)C 264.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
[(1S,2R,5S,6S,7R,8S)-2,8-dimethyl-5-propan-2-yl-7-tricyclo[4.4.0.02,8]decanyl] acetate 163017329 Click to see CC(C)C1CCC2(C3C1C(C2(CC3)C)OC(=O)C)C 264.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/0031-9422(88)83027-9
alpha-Calacorene 12302243 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
(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)83027-9
1,1,4,7-Tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene 89532 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
beta-Diploalbicene 177445 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/0031-9422(88)83027-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Methyl 2-(7-hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate 162870454 Click to see CC12CCC(CC1C(=C)C(CC2)O)C(=C)C(=O)OC 264.36 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-(8-formyl-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)prop-2-enoate 162892099 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)OC)C=O 262.34 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-[(2R,4aR,8aR)-8-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 163186567 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)OC)COC(=O)C=CC3=CC=C(C=C3)O 410.50 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-[(2R,4aR,8aR)-8-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 163195072 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)OC)COC(=O)C=CC3=CC=C(C=C3)O 410.50 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-[(2R,4aR,8aR)-8-formyl-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 162892100 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)OC)C=O 262.34 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-[(2R,4aS,7S,8aR)-7-hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 162870455 Click to see CC12CCC(CC1C(=C)C(CC2)O)C(=C)C(=O)OC 264.36 unknown https://doi.org/10.1016/0031-9422(88)83027-9
methyl 2-[8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 14707117 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)OC)CO 264.36 unknown https://doi.org/10.1016/0031-9422(88)83027-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18|A)-Oleanolic acid 7048528 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
(1R,3aS,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 12358875 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(88)83027-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Mikanin 15560536 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/0031-9422(88)83027-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
kaempferol-3-O-alpha-L-rhamnoside 15558501 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(88)83027-9

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