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Hesperozygis ringens

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 UUID64403e2a00791756566913
Scientific name Hesperozygis ringens
Authority (Benth.) Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 85: 134. 1936

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Glechon ringens Benth. Labiat. Gen. Spec. : 409 (1834)

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000981813
Tropicos 100203228
KEW urn:lsid:ipni.org:names:121021-2
The Plant List kew-98659
Open Tree Of Life 6082315
IPNI 447849-1
GBIF 3885141

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
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 / Menthane monoterpenoids
(2S,5R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-one 21630930 Click to see 170.25 unknown https://doi.org/10.1021/JF950653C
(3S,6R)-2,2,6-trimethyl-1-oxaspiro[2.5]octan-4-one 12280153 Click to see CC1CCC2(C(=O)C1)C(O2)(C)C 168.23 unknown https://doi.org/10.1021/JF950653C
2-Cyclohexen-1-one, 2-(1-hydroxy-1-methylethyl)-5-methyl-, (5R)- 11062797 Click to see CC1CC=C(C(=O)C1)C(C)(C)O 168.23 unknown https://doi.org/10.1021/JF950653C
2,2,6-Trimethyl-1-oxaspiro[2.5]octan-4-one 330109 Click to see CC1CCC2(C(=O)C1)C(O2)(C)C 168.23 unknown https://doi.org/10.1021/JF950653C
8-Hydroxy-p-menth-4-en-3-one 556628 Click to see 168.23 unknown https://doi.org/10.1021/JF950653C
8-Hydroxy-p-menthan-3-one 3014189 Click to see CC1CCC(C(=O)C1)C(C)(C)O 170.25 unknown https://doi.org/10.1021/JF950653C
p-Menth-4(8)-en-3-one 6988 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1021/JF950653C
p-Menthan-3-one, 4,8-epoxy-, cis- 6432045 Click to see 168.23 unknown https://doi.org/10.1021/JF950653C
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1021/JF950653C

Gallery Top

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Collections Top

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