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Leionema coxii

Leionema coxii - 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 UUID644057ae8f604624536693
Scientific name Leionema coxii
Authority (F.Muell.) Paul G.Wilson
First published in Nuytsia 12: 272 (1998)

Description Top

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Leionema coxii is a unique shrub species found only in southern New South Wales, Australia. It has a distinct upright shape and dark green, narrow leaves. In the spring, it produces clusters of white flowers. The plant can grow up to 3 meters in height and 1 meter in width, with smooth and glandular stems. Its leaves are lance to narrowly-elliptic in shape with a shiny upper surface and sharp point at the end. The flowers are arranged in a corymb with 10-30 flowers on flattened branches. The species was first described in 1884 by Ferdinand von Mueller and was later renamed Leionema coxii in 1998 by Paul G. Wilson. It is named after James Charles Cox, a medical practitioner from Sydney who supported scientific endeavors. Leionema coxii is typically found in forests, brushland, and near water sources in the Budawang Range and surrounding areas of southern New South Wales.

Synonyms Top

Scientific name Authority First published in
Phebalium coxii (F.Muell.) Maiden & Betche Census N.S.W. Pl. : 116 (1916)
Eriostemon coxii F.Muell. Melbourne Chem. Druggist 7: 64 (1884)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001263512
Tropicos 50208826
KEW urn:lsid:ipni.org:names:1003739-1
The Plant List tro-50208826
Open Tree Of Life 5762591
IPNI 1003739-1
GBIF 3836185
Freebase /m/0dgnjg6
EOL 5624377
Wikipedia Leionema_coxii

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)!
Title Authors Publication Released IDs
Coumarins from Three Phebalium species Francoise Bevalot, James A. Armstrong, Alexander I. Gray, Peter G. Waterman Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(88)90076-2
6-methoxymurranganon derivatives from the aerial parts of Phebalium elatius subsp. Beckleri Jamila A. El-turbi, James A. Armstrong, Alexander I. Gray, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85386-T
Coumarins and their taxonomic value in the genus Phebalium Md.Abdul Quader, Jamila A. El-Turbi, James A. Armstrong, Alexander I. Gray, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83450-D

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
> Phenylpropanoids and polyketides / Coumarins and derivatives
(7-Methoxy-8-(1,2-dihydroxy-3-methyl-3-butenyl))coumarin 13917407 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1016/0305-1978(88)90076-2
[(1R)-1-(6,7-dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] 2-methylpropanoate 162850834 Click to see CC(C)C(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 374.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[(1R)-1-(6,7-dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] 3-methylbutanoate 163008424 Click to see CC(C)CC(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 388.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[(1R)-1-(6,7-dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] acetate 163097873 Click to see CC(=C)C(=O)C(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)OC(=O)C 346.30 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[(1R)-1-(6,7-dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobutyl] acetate 162851471 Click to see CC(C)C(=O)C(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)OC(=O)C 348.30 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[(1S,2S)-2-acetyloxy-1-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-3-enyl] acetate 13942381 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)OC(=O)C)OC(=O)C 360.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D
[(1S)-1-(6,7-dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] propanoate 163187118 Click to see CCC(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 360.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[(2S)-2-hydroxy-2-[(2S,3R)-3-(7-methoxy-2-oxochromen-8-yl)oxiran-2-yl]propyl] 3-methylbutanoate 162998468 Click to see CC(C)CC(=O)OCC(C)(C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D
[(2S)-3-hydroxy-1-(7-methoxy-2-oxochromen-8-yl)-3-methylbutan-2-yl] 3-methylbutanoate 13917412 Click to see CC(C)CC(=O)OC(CC1=C(C=CC2=C1OC(=O)C=C2)OC)C(C)(C)O 362.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D
[1-(6,7-Dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] 2-methylpropanoate 15730552 Click to see CC(C)C(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 374.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[1-(6,7-Dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] 3-methylbutanoate 15730553 Click to see CC(C)CC(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 388.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[1-(6,7-Dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] acetate 15730551 Click to see CC(=C)C(=O)C(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)OC(=O)C 346.30 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[1-(6,7-Dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobut-3-enyl] propanoate 15730554 Click to see CCC(=O)OC(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)C(=O)C(=C)C 360.40 unknown https://doi.org/10.1016/0031-9422(90)85386-T
[1-(6,7-Dimethoxy-2-oxochromen-8-yl)-3-methyl-2-oxobutyl] acetate 15730556 Click to see CC(C)C(=O)C(C1=C2C(=CC(=C1OC)OC)C=CC(=O)O2)OC(=O)C 348.30 unknown https://doi.org/10.1016/0031-9422(90)85386-T
2-(7-Methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal 179620 Click to see CC(=C(C=O)C1=C(C=CC2=C1OC(=O)C=C2)OC)C 258.27 unknown https://doi.org/10.1016/0305-1978(88)90076-2
2H-1-Benzopyran-2-one, 8-[(1E)-3-hydroxy-3-methyl-1-butenyl]-7-methoxy-; 8-[(1E)-3-Hydroxy-3-methyl-1-buten-1-yl]-7-methoxy-2H-1-benzopyran-2-one 78385338 Click to see CC(C)(C=CC1=C(C=CC2=C1OC(=O)C=C2)OC)O 260.28 unknown https://doi.org/10.1016/0031-9422(92)83450-D
7-Methoxy-8-(1-hydroxy-3-methyl-2-oxobutyl)-2H-1-benzopyran-2-one 5319956 Click to see CC(C)C(=O)C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O 276.28 unknown https://doi.org/10.1016/0031-9422(92)83450-D
7-Methoxy-8-[3-[1-hydroxy-1-[[(3-methylbutyryl)oxy]methyl]ethyl]oxiranyl]-2H-1-benzopyran-2-one 101632061 Click to see CC(C)CC(=O)OCC(C)(C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D
8-[(1R)-1-hydroxy-3-methyl-2-oxobutyl]-7-methoxychromen-2-one 76764423 Click to see CC(C)C(=O)C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O 276.28 unknown https://doi.org/10.1016/0031-9422(92)83450-D
Murrangatin diacetate 389004 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)OC(=O)C)OC(=O)C 360.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D
Murraol 15593213 Click to see CC(C)(C=CC1=C(C=CC2=C1OC(=O)C=C2)OC)O 260.28 unknown https://doi.org/10.1016/0031-9422(92)83450-D
Murrayatin 621354 Click to see CC(C)CC(=O)OC(CC1=C(C=CC2=C1OC(=O)C=C2)OC)C(C)(C)O 362.40 unknown https://doi.org/10.1016/0031-9422(92)83450-D

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