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Salvia willeana

Salvia willeana - 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 UUID643fec0352692634843153
Scientific name Salvia willeana
Authority (Holmboe) Hedge
First published in Notes Roy. Bot. Gard. Edinburgh 23: 47 (1959)

Description Top

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Synonyms Top

Scientific name Authority First published in
Salvia grandiflora subsp. willeana Holmboe Stud. Veg. Cyprus 157. 1914 (1914)

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-0000302637
Tropicos 100254393
KEW urn:lsid:ipni.org:names:457535-1
The Plant List kew-184166
Open Tree Of Life 6083687
Observations.org 454892
IPNI 457535-1
iNaturalist 814284
GBIF 3883740
Elurikkus 433101

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
Contribution to the Study of the Essential Oils from Three Species of Salvia Growing Wild in the Eastern Mediterranean Region B. Bellomaria, N. Arnold, G. Valentini, H. J. Arnold Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1992.9698143
Terpenoids from Salvia willeana and S. Virgata Maria C. de la Torre, Maurizio Bruno, Franco Piozzi, Giuseppe Savona, Benjamin Rodriguez, Nelly Apostolides Arnold Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85143-4

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
(4aR,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 36689575 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
Carnosic acid 65126 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
Carnosicacid 5024746 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698143
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1016/0031-9422(90)85143-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,9R,10R)-3,4,9-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 38349676 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
3,4,9-Trihydroxy-11,11-dimethyl-5-(propan-2-yl)-16-oxatetracyclo[6.6.2.0^{1,10}.0^{2,7}]hexadeca-2(7),3,5-trien-15-one 11996616 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
Isorosmanol 13820511 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/0031-9422(90)85143-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14R,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-3,14-diol 21669100 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14R,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-3,14-diol 14487121 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
11alpha-Hydroxy-beta-amyrin 13918522 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,14-diol 13918523 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-3,14-diol 14487118 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)O)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/0031-9422(90)85143-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/0031-9422(90)85143-4

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