Salvia virgata, also known as wand sage or southern meadow sage, is a perennial plant that is native to Asia and southeastern Europe. While it is prized for its blue-violet flowers, it is considered a noxious weed in many parts of the world. It is often grouped together with Salvia pratensis. The plant produces flowers in clusters of 4-6 and has ovate to oblong leaves that are green on the top and covered in glands and thick hairs on the underside. The corolla of the flowers can range from blue-violet to white and is typically 1-2 centimeters long.

Synonyms Top

Scientific name	Authority	First published in
Salvia affinis	Spreng. ex Steud.	Nomencl. Bot. 1: 724 (1821)
Salvia amplexicaulis	hort. ex Benth.	Labiat. Gen. Spec. : 236 (1833)
Salvia barrelieri	hort. ex Benth.	Labiat. Gen. Spec. : 235 (1833)
Salvia bauhini	hort. ex Benth.	Labiat. Gen. Spec. : 235 (1833)
Salvia caduca	Vahl ex Hornem.	Hort. Bot. Hafn. 1: 30 (1813)
Salvia campestris	M.Bieb.	Fl. Taur.-Caucas. 1: 20 (1808)
Salvia caucasica	Schrank	Syll. Pl. Nov. 2: 58 (1826)
Salvia extersa	Klokov	Fl. RSS Ukr. 9: 654 (1960)
Salvia garganica	Ten.	Index Seminum (NAP, Neapolitano) 1829: 17 (1829)
Salvia gigantea	Desf.	Tabl. École Bot. , ed. 2: 68 (1815)
Salvia grandidentata	Ten.	Index Seminum (NAP, Neapolitano) 1833: 15 (1833)
Salvia hypanica	Andrz.	Enum. Pl. : 3 (1821)
Salvia mollis	J.Jacq.	Ecl. Pl. Rar. : 56 (1813)
Salvia nudicaulis	K.Koch	Linnaea 19: 24 (1846)
Salvia oblonga	K.Koch	Linnaea 19: 24 (1846)
Salvia praecox	Loisel.	Not. Fl. France : 6 (1810)
Salvia quercifolia	hort. ex Benth.	Labiat. Gen. Spec. : 235 (1833)
Salvia rubra	Spreng.	Syst. Veg. 4(2): 17 (1827)
Salvia sibthorpii	Sm.	Fl. Graec. Prodr. 1: 15 (1806)
Salvia similata	Hausskn.	Mitth. Thüring. Bot. Vereins , n.f., 11: 36 (1897)
Salvia utilis	Braun ex Engl.	Abh. Königl. Akad. Wiss. Berlin 1891: 367 (1892)
Sclarea sibthorpii	(Sm.) Soják	Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)
Sclarea virgata	(Jacq.) Soják	Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)
Salvia virgata var. garganica	(Ten.) Nyman	Consp. Fl. Eur. 570. 1881
Salvia virgata var. campestris	(M.Bieb.) Nyman	Consp. Fl. Eur. 570. 1881
Salvia virgata f. campestris	(M.Bieb.) E.Peter	Repert. Spec. Nov. Regni Veg. 39: 184 1936
Euriples rugosa	Raf.	Fl. Tellur. 3: 94 (1837)

Common names Top

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Filter by language:

Language	Common/alternative name
English	wand sage
Bulgarian	прътовиден конски босилек
Persian	مریمگلی هرز
Polish	szałwia rózgowata
Russian	Шалфей прутьевидный

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302613
USDA Plants	SAVI18
INPN	717529
Flora of Italy	4679
The Plant List	kew-184143
Open Tree Of Life	4724791
Observations.org	150012
NCBI Taxonomy	1298553
NBN Atlas	NBNSYS0200003065
Nature Serve	2.860110
IPNI	457510-1
iNaturalist	78974
GBIF	2927041
Freebase	/m/0j64n5k
EPPO	SALVG
EOL	480285
Calflora (Californian flora)	8623
USDA GRIN	70597
Wikipedia	Salvia_virgata
CMAUP	NPO4164

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

Chemometric Analysis Evidencing the Variability in the Composition of Essential Oils in 10 Salvia Species from Different Taxonomic Sections or Phylogenetic Clades

Tomou EM, Fraskou P, Dimakopoulou K, Dariotis E, Krigas N, Skaltsa H

Molecules

29-Mar-2024

PMCID:	PMC11013157
doi:	10.3390/molecules29071547
PMID:	38611827

Comparative assessment of phenolic composition profile and biological activities of green extract and conventional extracts of Salvia sclarea

Quradha MM, Duru ME, Kucukaydin S, Tamfu AN, Iqbal M, Bibi H, Khan R, Ceylan O

Sci Rep

22-Jan-2024

PMCID:	PMC10803343
doi:	10.1038/s41598-024-51661-z
PMID:	38253648

Integrative effects of phytohormones in the phenolic acids production in Salvia verticillata L. under multi-walled carbon nanotubes and methyl jasmonate elicitation

Rahmani N, Radjabian T

BMC Plant Biol

19-Jan-2024

PMCID:	PMC10797988
doi:	10.1186/s12870-023-04719-5
PMID:	38238679

Accumulation of Polyphenols and Associated Gene Expression in Hairy Roots of Salvia viridis Exposed to Methyl Jasmonate

Grzegorczyk-Karolak I, Krzemińska M, Grąbkowska R, Gomulski J, Żekanowski C, Gaweda-Walerych K

Int J Mol Sci

07-Jan-2024

PMCID:	PMC10815010
doi:	10.3390/ijms25020764
PMID:	38255839

Molecular Pathways of Rosmarinic Acid Anticancer Activity in Triple-Negative Breast Cancer Cells: A Literature Review

Konstantinou EK, Panagiotopoulos AA, Argyri K, Panoutsopoulos GI, Dimitriou M, Gioxari A

Nutrients

19-Dec-2023

PMCID:	PMC10780465
doi:	10.3390/nu16010002
PMID:	38201832

In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae

Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H

Molecules

27-Nov-2023

PMCID:	PMC10708212
doi:	10.3390/molecules28237801
PMID:	38067531

Natural Compounds of Salvia L. Genus and Molecular Mechanism of Their Biological Activity

Zhumaliyeva G, Zhussupova A, Zhusupova GE, Błońska-Sikora E, Cerreto A, Omirbekova N, Zhunusbayeva Z, Gemejiyeva N, Ramazanova M, Wrzosek M, Ross SA

Biomedicines

27-Nov-2023

PMCID:	PMC10740457
doi:	10.3390/biomedicines11123151
PMID:	38137372

Changes in Metabolite Profiling and Expression Levels of Key Genes Involved in the Terpenoid Biosynthesis Pathway in Garden Sage (Salvia officinalis) under the Effect of Hydrazine Hydrate

Ali M, Abdelkawy AM, Darwish DB, Alatawi HA, Alshehri D, Al-Amrah H, Soudy FA

Metabolites

29-Jun-2023

PMCID:	PMC10385164
doi:	10.3390/metabo13070807
PMID:	37512514

Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species

Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M

BMC Complement Med Ther

03-Jun-2023

PMCID:	PMC10239571
doi:	10.1186/s12906-023-04004-w
PMID:	37270541

Crocus speciosus (Iridaceae)—A New Species for the Bulgarian Flora

Apostolova-Kuzova E, Stoyanov K, Raycheva T, Naimov S

Plants (Basel)

17-Feb-2023

PMCID:	PMC9965344
doi:	10.3390/plants12040932
PMID:	36840280

From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition

Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S

Life (Basel)

23-Nov-2022

PMCID:	PMC9785030
doi:	10.3390/life12121957
PMID:	36556322

Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022

Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M

Molecules

17-Aug-2022

PMCID:	PMC9416168
doi:	10.3390/molecules27165253
PMID:	36014492

Health Benefits and Pharmacological Aspects of Chrysoeriol

Aboulaghras S, Sahib N, Bakrim S, Benali T, Charfi S, Guaouguaou FE, Omari NE, Gallo M, Montesano D, Zengin G, Taghzouti K, Bouyahya A

Pharmaceuticals (Basel)

07-Aug-2022

PMCID:	PMC9415049
doi:	10.3390/ph15080973
PMID:	36015121

Impacts of elicitors on metabolite production and on antioxidant potential and tyrosinase inhibition in watercress microshoot cultures

Klimek-Szczykutowicz M, Dziurka M, Blažević I, Đulović A, Apola A, Ekiert H, Szopa A

Appl Microbiol Biotechnol

05-Jan-2022

PMCID:	PMC8763773
doi:	10.1007/s00253-021-11743-8
PMID:	34985568

Effect of Elicitation with (+)-Usnic Acid on Accumulation of Phenolic Acids and Flavonoids in Agitated Microshoots of Eryngium alpinum L.

Kikowska M, Thiem B, Jafernik K, Klimek-Szczykutowicz M, Studzińska-Sroka E, Ekiert H, Szopa A

Molecules

12-Sep-2021

PMCID:	PMC8465747
doi:	10.3390/molecules26185532
PMID:	34577004

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol	101219048	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O	316.40	unknown	https://doi.org/10.1055/S-2006-962043
7-Acetylhorminone	2751796	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2OC(=O)C)(C)C)C)O	374.50	unknown	https://doi.org/10.1055/S-2006-962043
Cryptanol	184179	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O	316.40	unknown	https://doi.org/10.1055/S-2006-962043
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1055/S-2006-962043
Horminone	2751795	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/10.1055/S-2006-962043
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/10.1055/S-2006-962043
> 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 CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2	298.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(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 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
[(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
Panduratin D	24864268	Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4	430.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one	440244	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
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S
Corchoionol C	137705650	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 / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199901/02)14:1<45::AID-FFJ774>3.0.CO;2-S
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-12-oxo-3,4,5,6,6a,7,8,8a,10,11,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	14489124	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1016/S0031-9422(00)89010-X
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	5320146	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
2,3-Dihydroxyolean-12-en-28-oic acid	3694932	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
2alpha,3alpha,23-Trihydroxyolean-12-en-28-oic acid	11504083	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
Colosolic acid	15917996	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
epi-Maslinic acid	25564831	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
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/0031-9422(90)85143-4
Virgatic acid	14489125	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1016/S0031-9422(00)89010-X
> 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
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(2-Hydroxy-3-methoxy-3-methylbutoxy)-6-methoxychromen-2-one	11185914	Click to see CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)OC	308.33	unknown	https://doi.org/10.1055/S-2006-962043
> 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 CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3	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 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
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
(2R)-5,7-Dimethoxyflavanone	689012	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	via CMAUP database
3,5,7-Trimethoxyflavone	117900	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC	312.30	unknown	via CMAUP database
3',4',5,7-Tetramethoxyflavone	631170	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC	342.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl-	5748697	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O	298.29	unknown	via CMAUP database
5-Hydroxy-3',4',7-trimethoxyflavone	5272653	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	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
Apigenin 7,4'-dimethyl ether	5281601	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O	298.29	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
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
Pinostrobin	6950539	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
Quercetin pentamethyl ether	97332	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC	372.40	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 COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	via CMAUP database
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
Tetramethylkaempferol	631095	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)-	160673	Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2	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 COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O	288.29	unknown	via CMAUP database
Phloretin	4788	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O	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 CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C	390.50	unknown	via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone	6293081	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O	300.30	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 COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	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 CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C	406.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Geranyl-2,4-dihydroxy-6-phenethylbenzoate	23656469	Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C	394.50	unknown	via CMAUP database

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Salvia virgata

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