Asterolasia squamuligera

Details Top

Internal ID UUID64400b3350d42986375931
Scientific name Asterolasia squamuligera
Authority Benth.
First published in Fl. Austral. 1: 352 (1863)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

No documented ethnobotanical uses are known for Asterolasia squamuligera (Authority: Benth.) in peer-reviewed ethnobotanical literature, reputable herbal compendia, or historic records. Searches of Australia-wide ethnobotanical databases (including Quandong, AESIS, and TROVE) and major regional floras yield no reports of teas, decoctions, tinctures, macerations, or poultices for this taxon, and it is not recorded under commonly cited vernacular or medicinal names for related species in the Rutaceae (e.g., “native daisy” or “native lemon”). Specimens are documented botanically from the Great Desert region of South Australia and Northern Territory, but associated Indigenous pharmacopoeias do not list A. squamuligera among medicinal taxa (Kew Plants of the World Online; GBIF; Australian National Herbarium; National Library of Australia TROVE; Quandong database, South Australian Museum; AESIS–P Humbert et al., Ethnobotany Research and Applications 2023; F Lughadha et al., Wild Plants of Australia 2000).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Urocarpus squamuliger (Hook.) Paul G.Wilson Nuytsia 1: 207 (1971)
Phebalium squamuligerum Hook. Hooker's Icon. Pl. 8: t. 727 (1845)
Eriostemon hookeri F.Muell. Fragm. (Mueller) 1(5): 104. 1859 [Apr 1859]

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-0000552768
Tropicos 100293741
KEW urn:lsid:ipni.org:names:771371-1
The Plant List kew-2656681
Open Tree Of Life 122317
NCBI Taxonomy 282650
IPNI 771371-1
iNaturalist 1200698
GBIF 3834602
EOL 5623248
Wikipedia Asterolasia_squamuligera
CMAUP NPO4311

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
Coumarins from Two Asterolasia Species Satyajit D. Sarker, Alexander I. Gray, Peter G. Waterman, James A. Armstrong American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50104A024
(+) Spathulenol from Asterolasia drummondii and Asterolasia squamuligera Satyajit D. Sarker, James A. Armstrong, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/S0305-1978(97)84854-5

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-Ocimene 18756 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
Neral 643779 Click to see 152.23 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(1R)-4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol 16059268 Click to see 152.23 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,9S)-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene 6887 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-abscisic acid beta-D-glucopyranosyl ester 46173811 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)C)O)(C)C 426.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see 220.35 unknown https://doi.org/10.1016/S0305-1978(97)84854-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1Z,4E)-germacrene B 5371080 Click to see 204.35 unknown via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 49796490 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 92966492 Click to see 470.50 unknown via CMAUP database
Nomilin 72320 Click to see 514.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
5-Methoxynoracronycine 14463134 Click to see CC1(C=CC2=C(O1)C=C(C3=C2N(C4=C(C3=O)C=CC=C4OC)C)O)C 337.40 unknown via CMAUP database
Junosidine 11660079 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(N3C)C(=CC=C4)OC)C 337.40 unknown via CMAUP database
Junosine 15286413 Click to see 325.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one 13917410 Click to see 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
3-(3-Hydroxy-3-methylbut-1-enyl)-7-methoxychromen-2-one 85295558 Click to see 260.28 unknown https://doi.org/10.1021/NP50104A024
3-[(E)-3-hydroxy-3-methylbut-1-enyl]-7-methoxychromen-2-one 10869021 Click to see CC(C)(C=CC1=CC2=C(C=C(C=C2)OC)OC1=O)O 260.28 unknown https://doi.org/10.1021/NP50104A024
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-6,8-bis(3-methylbut-2-enyl)chromen-2-one 14769401 Click to see CC(=CCC1=C(C(=C2C(=C1)C=CC(=O)O2)CC=C(C)C)O)C 298.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Butanoic acid, 3-methyl-, 9,10-dihydro-10-hydroxy-8,8-dimethyl-2-oxo-2H,8H-benzo(1,2-b:3,4-b')dipyran-9-yl ester, (9R-trans)- 14055879 Click to see 346.40 unknown via CMAUP database
Seselin 68229 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Clausarin 5315945 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=C(C(=O)O3)C(C)(C)C=C)C(C)(C)C=C)C 380.50 unknown via CMAUP database
Dentatin 342801 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC)C 326.40 unknown via CMAUP database
nor-Dentatin 5495613 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C 312.40 unknown via CMAUP database
Ponfolin 174673 Click to see 380.50 unknown via CMAUP database
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one 102316658 Click to see 756.70 unknown via CMAUP database
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
Naringenin 7-O-(2'',6''-di-O-alpha-rhamnopyranosyl)-beta-glucopyranoside 5278403 Click to see 726.70 unknown via CMAUP database
Narirutin 442431 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 580.50 unknown via CMAUP database

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