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Beyeria lechenaultii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff17face34708834701
Scientific name Beyeria lechenaultii
Authority (DC.) Baill.
First published in Adansonia 6: 307. 1866

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Beyeria backhousei Hook.f. Fl. Tasman. 1: 339 (1857)
Beyeria drummondii F.Muell. Linnaea 34: 58 (1865)
Beyeria ledifolia Sond. Linnaea 28: 565 (1857)
Beyeria ledifolia var. angustifolia Mull.Arg. Prodr. 15(2): 203 (1866)
Beyeria ledifolia var. backhousei (Hook.f.) Mull.Arg. Prodr. 15(2): 203 (1866)
Beyeria lechenaultii var. backhousei (Hook.f.) Gruning Pflanzenr. , IV, 147: 70 (1913)
Beyeria lechenaultii var. drummondii (Mull.Arg.) Gruning Pflanzenr. , IV, 147: 70 (1913)
Beyeria lechenaultii f. eloeagnoides Baill. Adansonia 6: 308 (1866)
Beyeria lechenaultii f. genuina Baill. Adansonia 6 1866
Beyeria lechenaultii var. latifolia Gruning Pflanzenr. , IV, 147: 71 (1913)
Beyeria lechenaultii var. ledifolia (Klotzsch) Gruning Pflanzenr. , IV, 147: 70 (1913)
Beyeria lechenaultii f. myrtoides Baill. Adansonia 6: 308 (1866)
Beyeria lechenaultii f. pernettioides Baill. Adansonia 6: 307 (1866)
Beyeria lechenaultii var. rosmarinoides Gruning Pflanzenr. , IV, 147: 70 (1913)
Beyeria lechenaultii f. rosmarinoides Baill. Adansonia 6: 308 (1866)
Beyeria lechenaultii f. salsoloides Baill. Adansonia 6: 308 (1866)
Beyeria lechenaultii f. vaccinioides Baill. Adansonia 6: 308 (1866)
Beyeria opaca var. linearis Benth. Fl. Austral. 6: 65 (1873)
Beyeriopsis drummondii Müll.Arg. Linnaea 34: 58 (1865)
Calyptrostigma ledifolium Klotzsch Pl. Preiss. 1: 176 (1845)
Beyeria viscosa var. angustifolia F.Muell. & Tate Trans. & Proc. Roy. Soc. South Australia 16: 341. 1896
Hemistemma lechenaultii DC. Syst. Nat. [Candolle] 1: 414. 1817 [1818 publ. 1-15 Nov 1817]
Beyeria lechenaultii var. genuina Gruning Pflanzenr. , IV, 147: 70 (1913)
Beyeria ledifolia var. genuina Mull.Arg. Prodr. 15(2): 203 (1866)
Beyeria leschenaultii var. latifolia Ewart
Beyeria leschenaultii var. genuina (Baill.) Grüning

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000338369
Tropicos 50003465
KEW urn:lsid:ipni.org:names:166283-3
The Plant List kew-21868
Open Tree Of Life 5787083
Open Tree Of Life 526463
Observations.org 323555
NCBI Taxonomy 316915
IPNI 166283-3
iNaturalist 708652
GBIF 5380396
Elurikkus 531080
Wikipedia Beyeria_lechenaultii

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
Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms Saad B, Kmail A, Haq SZ Evid Based Complement Alternat Med 18-Jul-2022
PMCID:PMC9313926
doi:10.1155/2022/2276094
PMID:35899227
Exploring the anti-diabetic potential of Australian Aboriginal and Indian Ayurvedic plant extracts using cell-based assays Gulati V, Gulati P, Harding IH, Palombo EA BMC Complement Altern Med 05-Feb-2015
PMCID:PMC4328078
doi:10.1186/s12906-015-0524-8
PMID:25652009
The chemistry of the Euphorbiaceae. XX. Further compounds from Beyeria leschenaultii 12β,17-Dihydroxy-16α-( - )-kauran-19-oic acid PR Jefferies, RW Retallack CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9682085
The chemistry of the Euphorbiaceae. VI. A triterpene from Beyeria leschenaultii GV Baddeley, AJ Bealing, PR Jefferies, RW Retallack CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9640908
The complete nucleotide sequence of the cassava (Manihot esculenta) chloroplast genome and the evolution of atpF in Malpighiales: RNA editing and multiple losses of a group II intron Daniell H, Wurdack KJ, Kanagaraj A, Lee SB, Saski C, Jansen RK Theor Appl Genet 24-Jan-2008
PMCID:PMC2587239
doi:10.1007/s00122-007-0706-y
PMID:18214421
Biosynthesis of diterpenes in Beyeria leschenaultii H.J. Bakker, E.L. Ghisalberti, P.R. Jefferies Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88381-8

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 / Diterpenoids
[(1R,4S,5R,9S,10S,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 22210606 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)88381-8
Monogynol 500043 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)88381-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5R,6R,9S,10R,13R,14R)-5,14-bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,14-diol 101289603 Click to see 338.50 unknown https://doi.org/10.1071/CH9682085
(1S,4S,6R,9S,10R,13R,14R)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,14-diol 26196128 Click to see 322.50 unknown https://doi.org/10.1071/CH9682085
5,14-Bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,14-diol 76372163 Click to see 338.50 unknown https://doi.org/10.1071/CH9682085
Ent-kaurane-3,16,17-triol 14019139 Click to see CC1(C2CCC34CC(CCC3C2(CCC1O)C)C(C4)(CO)O)C 322.50 unknown https://doi.org/10.1071/CH9682085
methyl (1R,4S,5R,9S,10R,12R,13R,14R)-12-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162987412 Click to see 350.50 unknown https://doi.org/10.1071/CH9682085
methyl (1S,4S,5R,9S,10R,13R,14R)-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 163194974 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)OC 334.50 unknown https://doi.org/10.1071/CH9682085
methyl (1S,4S,5R,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylate 162875235 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)C(=O)OC)C)CO 334.50 unknown https://doi.org/10.1071/CH9682085
Methyl 12-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162987411 Click to see CC12CCCC(C1CCC34C2CC(C(C3)C(C4)CO)O)(C)C(=O)OC 350.50 unknown https://doi.org/10.1071/CH9682085
Methyl 14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 13994832 Click to see 334.50 unknown https://doi.org/10.1071/CH9682085
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Calenduladiol 461835 Click to see 442.70 unknown https://doi.org/10.1071/CH9640908
Lup-20(29)-ene-3,16-diol 260656 Click to see 442.70 unknown https://doi.org/10.1071/CH9640908
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1R,4R,5R,9R,10S,13R)-13-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-6-one 163048018 Click to see 288.40 unknown https://doi.org/10.1016/S0031-9422(00)88381-8
13-(Hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-6-one 163048017 Click to see 288.40 unknown https://doi.org/10.1016/S0031-9422(00)88381-8
> Organoheterocyclic compounds / Furofurans
(3aR,5R,6aR)-5,6a-diethyl-5-[(E,2R)-2-ethylhex-3-enyl]-3a,6-dihydro-3H-furo[3,2-b]furan-2-one 21778532 Click to see CCC=CC(CC)CC1(CC2(C(O1)CC(=O)O2)CC)CC 294.40 unknown https://doi.org/10.1071/CH9682085

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