Salvia candidissima is a perennial herb found in western Greece, Turkey, Iraq, and Iran at elevations between 2000 and 6500 feet. It grows up to 3 feet in height and width, with light green leaves covered in hairs and notches on the edges. The leaves become lighter in color in hot weather. The plant produces 8-12 inch inflorescences with creamy white flowers that may have a yellow lip. It is closely related to six other salvias and can easily hybridize with them, leading to a wide variety of the species.

Synonyms Top

Scientific name	Authority	First published in
Salvia argentea	hort. ex Benth.	Labiat. Gen. Spec. : 223 (1833)
Salvia crassifolia	Sm.	Fl. Graec. Prodr. 1: 17 (1806)
Sclarea candidissima	(Vahl) Soják	Cas. Nár. Mus., Odd. Prír. 152: 21 (1983)
Salvia albida	Spreng.	Index Seminum (HAL, Halensis) 1807: 53 (1807)

Common names Top

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Language	Common/alternative name
German	reinweißblütiger salbei
Chinese	银灰鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Salvia candidissima subsp. candidissima		Unknown
Salvia candidissima subsp. occidentalis	Hedge	Notes Roy. Bot. Gard. Edinburgh 38: 48 (1980)

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Western Asia
  - Iran
  - Iraq
  - Turkey

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000300581
Tropicos	17600573
KEW	urn:lsid:ipni.org:names:455875-1
The Plant List	kew-182258
Open Tree Of Life	582961
Observations.org	121733
NCBI Taxonomy	268896
IPNI	455875-1
iNaturalist	513850
GBIF	7306544
Freebase	/m/05b4b0b
EPPO	SALCD
EOL	6341823
Elurikkus	661886
Wikipedia	Salvia_candidissima

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

Diterpenoids from Roots of Salvia lachnocalyx; In-silico and In-vitro Toxicity against Human Cancer Cell Lines

Hadavand Mirzaei H, Firuzi O, Jassbi AR

Iran J Pharm Res

01-Sep-2020

PMCID:	PMC8019878
doi:	10.22037/ijpr.2019.15429.13095
PMID:	33841524

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

A New Ferula (Apiaceae) Species from Southwest Anatolia: Ferula pisidica Akalın & Miski

Akalın E, Tuncay HO, Olcay B, Miski M

Plants (Basel)

12-Jun-2020

PMCID:	PMC7355485
doi:	10.3390/plants9060740
PMID:	32545501

Effect-Directed Analysis for the Antioxidant Compound in Salvia verticillata

Nickavar B, Rezaee J, Nickavar A

Iran J Pharm Res

01-Jan-2016

PMCID:	PMC4986120
PMID:	27610164

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

Terpenoids and flavonoids from the aerial parts of Salvia candidissima

G. Topcu, N. Tan, A. Ulubelen, D. Sun, W.H. Watson

Elsevier BV

23-Apr-2003

doi:	10.1016/0031-9422(95)00245-3

Terpenoids from Salvia candidissima subsp. candidissima

Ayhan Ulubelen, Nur Tan, Gülaçti Topcu

Elsevier BV

25-Mar-2003

doi:	10.1016/S0031-9422(97)00146-5

Diterpenoids from Salvia candidissima

Ayhan Ulubelen, Gülaçti Topcu, Nur Tan

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4039(00)60883-3

Composition of essential oils from turkish Salvia species

Ali Bayrak, Attila Akgül

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)84802-5

Rearranged abietane diterpenes from Salvia candidissima

A. Ulubelen, G. Topcu, N. Tan

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)83745-K

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2,4-Dimethoxybenzoic acid	7052	Click to see COC1=CC(=C(C=C1)C(=O)O)OC	182.17	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
> Benzenoids / Naphthalenes
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione	10495322	Click to see CC1=C2C(=O)CCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)C)(C)O	312.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(1S)-1-hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one	163016674	Click to see CC1=C2CCCC(=C)CC3(C2=C(C=C1)C=C(C3=O)C(C)C)O	296.40	unknown	https://doi.org/10.1016/S0040-4039(00)60883-3
1-Hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one	102011357	Click to see CC1=C2CCCC(=C)CC3(C2=C(C=C1)C=C(C3=O)C(C)C)O	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/S0040-4039(00)60883-3
Microstegiol	403772	Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C	298.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/0031-9422(92)83745-K
> Benzenoids / Naphthalenes / Naphthoquinones
1-Ketoaethiopinone	11983338	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)C(=O)CCC(=C)C	310.40	unknown	https://doi.org/10.1016/0031-9422(92)83745-K
4-Hydroxy-7-methyl-8-(4-methyl-3-oxopent-4-enyl)-3-propan-2-ylnaphthalene-1,2-dione	101931842	Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCC(=O)C(=C)C	326.40	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
4-Hydroxy-7-methyl-8-(4-methylpent-4-enyl)-3-propan-2-ylnaphthalene-1,2-dione	821448	Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCCC(=C)C	312.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/0031-9422(92)83745-K
Aethiopinone	157301	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C	296.40	unknown	https://doi.org/10.1016/S0040-4039(00)60883-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,10aS)-10a-hydroxy-1,4a-dimethyl-4-oxo-7-propan-2-yl-2,3,9,10-tetrahydrophenanthrene-1-carboxylic acid	101712284	Click to see CC(C)C1=CC2=C(C=C1)C3(C(=O)CCC(C3(CC2)O)(C)C(=O)O)C	330.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(1R,8R,10R)-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol	138113902	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)O	316.40	unknown	https://doi.org/10.1016/S0040-4039(00)60883-3
(4aR,10aR)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	162993082	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(4aR)-5,6,8-trihydroxy-4a-(methoxymethyl)-1,1-dimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one	101712283	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3=CC2=O)(C)C)COC)O	360.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(4aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one	162958596	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)OC	328.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(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/10.1016/0031-9422(92)83745-K
(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione	15241261	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
10a-Hydroxy-1,4a-dimethyl-4-oxo-7-propan-2-yl-2,3,9,10-tetrahydrophenanthrene-1-carboxylic acid	163009620	Click to see CC(C)C1=CC2=C(C=C1)C3(C(=O)CCC(C3(CC2)O)(C)C(=O)O)C	330.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
11-Hydroxy-12-methoxyabietatriene	14827262	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C)O)OC	316.50	unknown	https://doi.org/10.1016/0031-9422(92)83745-K https://doi.org/10.1016/S0031-9422(97)00146-5
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-4-ol	14827261	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C)O)OC	316.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/0031-9422(92)83745-K
4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione	73189945	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one	162958595	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)OC	328.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	5316143	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one	10935937	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)O	314.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5,6,8-trihydroxy-4a-(methoxymethyl)-1,1-dimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one	162878892	Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3=CC2=O)(C)C)COC)O	360.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
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/10.1016/0031-9422(92)83745-K
Abieta-9(11),8(14),12-trien-12-ol	521330	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
cis-Ferruginol	91747538	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
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/10.1016/0031-9422(92)83745-K
Cryptojaponol	11724205	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC	330.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/0031-9422(92)83745-K https://doi.org/10.1016/S0031-9422(97)00146-5
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/10.1016/0031-9422(92)83745-K
Manool	3034394	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
Salvinolone	11723174	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)O	314.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
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/10.1016/0031-9422(92)83745-K
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)84802-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,4aR,6aS,10aS,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-1-ol	101931843	Click to see CC1(CCCC2(C1CCC3(C2C(CC(O3)(C)C=C)O)C)C)C	306.50	unknown	https://doi.org/10.1016/0031-9422(95)00245-3 https://doi.org/10.1016/S0031-9422(97)00146-5
(3S,4aS,6aS,10aS,10bR)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	98133973	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
[(3R,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] hexadecanoate	101712285	Click to see CCCCCCCCCCCCCCCC(=O)OC1CC2=CCC3C4CCC(C4(CCC3C2(C(=O)C1)C)C)C(C)C=CC(CC)C(C)C	665.10	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
[17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] hexadecanoate	85741702	Click to see CCCCCCCCCCCCCCCC(=O)OC1CC2=CCC3C4CCC(C4(CCC3C2(C(=O)C1)C)C)C(C)C=CC(CC)C(C)C	665.10	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-1-ol	162987617	Click to see CC1(CCCC2(C1CCC3(C2C(CC(O3)(C)C=C)O)C)C)C	306.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/0031-9422(95)00245-3
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	518574	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/0031-9422(95)00245-3 https://doi.org/10.1016/S0031-9422(97)00146-5
Labd-14-ene, 8,13-epoxy-, (13S)-	6432025	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5 https://doi.org/10.1016/S0040-4039(00)60883-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(3R)-3-[(1R,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-4-en-1-ol	163006519	Click to see CC1(CCCC2(C1CCC(=C)C2C(C)(CCO)C=C)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
3-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-4-en-1-ol	163006518	Click to see CC1(CCCC2(C1CCC(=C)C2C(C)(CCO)C=C)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,2R,4aS,8aS)-1-[(3R)-5-hydroxy-3-methylpent-1-en-3-yl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	162935254	Click to see CC1(CCCC2(C1CCC(C2C(C)(CCO)C=C)(C)O)C)C	308.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
1-(5-hydroxy-3-methylpent-1-en-3-yl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	162935253	Click to see CC1(CCCC2(C1CCC(C2C(C)(CCO)C=C)(C)O)C)C	308.50	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1Z,5S,12Z)-5-hydroxy-12-methyl-7-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-1(14),2,9(15),12-tetraen-4-one	162871303	Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(CC1)CC(=C)C3)O)C(C)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
(5S)-5-hydroxy-6,6,11-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-1(13),2,9(14),11-tetraen-4-one	163093447	Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(C1)CCC3(C)C)O)C(C)C	298.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5-Hydroxy-12-methyl-7-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-1(14),2,9(15),12-tetraen-4-one	162871302	Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(CC1)CC(=C)C3)O)C(C)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
5-Hydroxy-6,6,11-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-1(13),2,9(14),11-tetraen-4-one	163093446	Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(C1)CCC3(C)C)O)C(C)C	298.40	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
4-Hydroxy-trans-cinnamic acid icosyl ester	15139446	Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	444.70	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Mikanin	15560536	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	https://doi.org/10.1016/S0031-9422(97)00146-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/0031-9422(95)00245-3
> 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/S0031-9422(97)00146-5 https://doi.org/10.1016/0031-9422(95)00245-3

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Salvia candidissima

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