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Hesperozygis rhododon

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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 UUID64403e29e6653957020812
Scientific name Hesperozygis rhododon
Authority Epling
First published in Brittonia 7: 139 (1951)

Description Top

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Synonyms Top

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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-0000981812
Tropicos 50321597
KEW urn:lsid:ipni.org:names:121020-2
The Plant List kew-98658
Open Tree Of Life 403278
NCBI Taxonomy 751828
IPNI 121020-2
iNaturalist 332261
GBIF 3885158
EOL 5380628

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
Essential Oil Composition and Allelopathic Effect of the Brazilian Lamiaceae <i>Hesperozygis ringens</i> (Benth.) Epling and <i>Hesperozygis rhododon</i> Epling Gilsane L. von Poser, Chantal Menut, Maria E. Toffoli, Pierre Vérin, Marcos Sobral, Jean-Marie Bessière, Gérard Lamaty, Amélia T. Henriques American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/JF950653C

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 / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF950653C
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF950653C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1021/JF950653C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF950653C
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF950653C
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF950653C
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/JF950653C
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF950653C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthone 443159 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1021/JF950653C
(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl acetate 62335 Click to see CC1CCC(C(C1)OC(=O)C)C(C)C 198.30 unknown https://doi.org/10.1021/JF950653C
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/JF950653C
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/JF950653C
Isomenthone, (+/-)- 6432469 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1021/JF950653C
Isopulegone 34645 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown https://doi.org/10.1021/JF950653C
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF950653C
Menthyl acetate 27867 Click to see CC1CCC(C(C1)OC(=O)C)C(C)C 198.30 unknown https://doi.org/10.1021/JF950653C
p-Menthan-3-one 6986 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1021/JF950653C
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/JF950653C
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1021/JF950653C
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1021/JF950653C

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