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Salvia lavanduloides

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 UUID643febc53de28259914079
Scientific name Salvia lavanduloides
Authority Kunth
First published in Nov. Gen. Sp. [H.B.K.] 2: 287. 1818

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Essential oil obtained by hydrodistillation of the aerial parts (leaves and stems).
- Whole plants are cultivated as ornamental perennials for their aromatic foliage and compact growth habit.

Properties relevant to use:
- The volatile oil is dominated by camphor, 1,8‑cineole, α‑pinene and other monoterpenes, giving a fresh, herbaceous aroma characteristic of sage‑type oils.
- The oil is obtained in low yields, generally less than 1 % of dry weight, and its constituents are readily soluble in ethanol and typical fragrance solvents.

Sustainability and sourcing:
- Salvia lavanduloides occurs naturally in the southwestern United States and northern Mexico; the species is listed as locally common and not considered threatened.
- Commercial supply is primarily from cultivated ornamental plants, thereby limiting harvesting from wild populations.

Synonyms Top

Scientific name Authority First published in
Salvia fratrum Standl. Publ. Field Mus. Nat. Hist., Bot. Ser. 18: 1028. 1938
Salvia humboldtiana Schult. Mant. 1: 183 (1822)
Salvia lavanduloides var. hispida Benth. Prodr. 12: 303 (1848)
Salvia lavanduloides var. latifolia Benth. Prodr. 12: 303 (1848)
Salvia purpurina La Llave Naturaleza (Madrid) 7(App.): 82 (1885)

Common names Top

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Language Common/alternative name
English lavender leaf sage

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301406
Tropicos 17603323
KEW urn:lsid:ipni.org:names:30210332-2
The Plant List kew-183018
Open Tree Of Life 574342
NCBI Taxonomy 392669
IPNI 456537-1
iNaturalist 194529
GBIF 7308690
Wikipedia Salvia_lavanduloides
CMAUP NPO28083

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
Eupatorin and Salviandulin-A, with Antimicrobial and Anti-Inflammatory Effects from Salvia lavanduloides Kunth Leaves González-Cortazar M, Salinas-Sánchez DO, Herrera-Ruiz M, Román-Ramos DC, Zamilpa A, Jiménez-Ferrer E, Ble-González EA, Álvarez-Fitz P, Castrejón-Salgado R, Pérez-García MD Plants (Basel) 30-Jun-2022
PMCID:PMC9269164
doi:10.3390/plants11131739
PMID:35807691
Phylogenomics of Salvia L. subgenus Calosphace (Lamiaceae) Lara-Cabrera SI, Perez-Garcia MD, Maya-Lastra CA, Montero-Castro JC, Godden GT, Cibrian-Jaramillo A, Fisher AE, Porter JM Front Plant Sci 15-Oct-2021
PMCID:PMC8554000
doi:10.3389/fpls.2021.725900
PMID:34721456
In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L Molecules 02-Feb-2021
PMCID:PMC7867283
doi:10.3390/molecules26030766
PMID:33540716
Antinociceptive and anxiolytic-like effects of a neo-clerodane diterpene from Salvia semiatrata aerial parts Ortiz-Mendoza N, Zavala-Ocampo LM, Martínez-Gordillo MJ, González-Trujano ME, Peña FA, Bazany-Rodríguez IJ, Chávez JA, Dorazco-González A, Aguirre-Hernández E Pharm Biol 07-Jul-2020
PMCID:PMC7471977
doi:10.1080/13880209.2020.1784235
PMID:32633180
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227
Salvianduline C, a 5,6-secoclerodane diterpenoid fromSalvia lavanduloides Emma Maldonado, Jorge Ca´rdenas, Beatriz Salazar, Rube´n A. Toscano, Alfredo Ortega, Christophe K. Jankowski, Andre´ Aumelas, Marie R. Van Calsteren Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83039-N
Salviandulines A and B. Two secoclerodane diterpenoids from Salvia lavanduloides Alfredo Ortega, Jorge Cárdenas, Alfredo Toscano, Emma Maldonado, André Aumelas, Marie Rose Van Calsteren, Christopher Jankowski Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83209-4
Abietane and neo-clerodane diterpenoids from Salvia lavanduloides Emma Maldonado, Ma. de los Angeles Flores, Beatriz Salazar, Alfredo Ortega Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90438-2

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 / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see 156.31 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Horminone 2751795 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate 24864449 Click to see 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(6-hydroxy-4-methoxy-1-benzofuran-7-yl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 24864268 Click to see 430.50 unknown via CMAUP database
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 101855692 Click to see 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see 1237.30 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid 163059045 Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O 786.80 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R)-2-[(3aS,7aR)-1,4-dioxo-7,7a-dihydro-3H-2-benzofuran-3a-yl]-1-[(2R)-2-(furan-3-yl)-4-methyl-6-oxo-2,3-dihydropyran-5-yl]ethyl] acetate 101615681 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(91)83209-4
[2-(1,4-dioxo-7,7a-dihydro-3H-2-benzofuran-3a-yl)-1-[2-(furan-3-yl)-4-methyl-6-oxo-2,3-dihydropyran-5-yl]ethyl] acetate 73811610 Click to see 414.40 unknown https://doi.org/10.1016/0031-9422(91)83209-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
(3aS,7aR)-3a-[(2S)-2-[(2R)-2-(furan-3-yl)-4-methyl-6-oxo-2,3-dihydropyran-5-yl]-2-hydroxyethyl]-7,7a-dihydro-3H-2-benzofuran-1,4-dione 101615682 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(91)83209-4
3a-[2-[2-(furan-3-yl)-4-methyl-6-oxo-2,3-dihydropyran-5-yl]-2-hydroxyethyl]-7,7a-dihydro-3H-2-benzofuran-1,4-dione 162922383 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(91)83209-4
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones / Phthalides
[(2S,3S)-3-[(2S,3R,5R)-5-(furan-3-yl)-2-hydroxy-3-(1-oxo-3H-2-benzofuran-4-yl)oxolan-3-yl]butan-2-yl] acetate 101618886 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(91)83039-N
3-[5-(furan-3-yl)-2-hydroxy-3-(1-oxo-3H-2-benzofuran-4-yl)oxolan-3-yl]butan-2-yl acetate 162958342 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(91)83039-N
> Organoheterocyclic compounds / Naphthofurans
14-(Furan-3-yl)-12,16-dimethyl-7,13,17-trioxapentacyclo[12.2.1.01,9.05,9.012,16]heptadec-4-en-6-one 163192259 Click to see CC12CCC34COC(=O)C3=CCCC45C1(CC(O2)(O5)C6=COC=C6)C 342.40 unknown https://doi.org/10.1016/S0031-9422(00)90438-2
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see 420.50 unknown via CMAUP database
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
(2S)-6-Geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2R)-5,7-Dimethoxyflavanone 689012 Click to see 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see 284.31 unknown via CMAUP database
3,5,7,4'-Tetramethoxyflavone 631095 Click to see 342.30 unknown via CMAUP database
5-Hydroxy-3,7-dimethoxyflavone 5748697 Click to see 298.29 unknown via CMAUP database
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
5,7,3',4'-Tetramethoxyflavone 631170 Click to see 342.30 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Galangin 3,5,7-trimethyl ether 117900 Click to see 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pentamethylquercetin 97332 Click to see 372.40 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
7,8-Dihydro-5,6-dehydrokawain 160673 Click to see 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see 288.29 unknown via CMAUP database
Phloretin 4788 Click to see 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see 390.50 unknown via CMAUP database
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Cardamonin 641785 Click to see 270.28 unknown via CMAUP database
Flavokawain C 6293081 Click to see 300.30 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one 23656471 Click to see 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Geranyl-2,4-dihydroxy-6-phenethylbenzoate 23656469 Click to see 394.50 unknown via CMAUP database

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