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Salvia vermifolia

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 UUID643fec011a1bc261459079
Scientific name Salvia vermifolia
Authority Hedge & Hub.-Mor.
First published in Notes Roy. Bot. Gard. Edinburgh 22: 185 (1957)

Ethnobotanical Use Top

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General Uses Top

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Scientific and model use:
* Salvia vermifolia is cultivated in botanical gardens and referenced in the literature as a taxon within the *Salvia* genus for comparative morphological and phylogenetic studies. It is not a standard model organism but serves as a reference in taxonomic research.

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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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-0000302599
Tropicos 100254372
KEW urn:lsid:ipni.org:names:457499-1
The Plant List kew-184130
Open Tree Of Life 6083670
NCBI Taxonomy 1933764
IPNI 457499-1
GBIF 3884111

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
Composition of the Essential Oils of Salvia vermifolia from Turkey Sengul Nacar, Ahmet Ilcim Informa UK Limited 17-Feb-2003
doi:10.1076/PHBI.40.1.67.5852

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 / Olefins / Cyclic olefins / Azulenes
Azulene 9231 Click to see 128.17 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1076/PHBI.40.1.67.5852
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1076/PHBI.40.1.67.5852

Gallery Top

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Contributors Top

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Collections Top

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