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Salvia broussonetii

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 UUID643feb9ca5c1b328802122
Scientific name Salvia broussonetii
Authority Benth.
First published in Labiat. Gen. Spec. : 227 (1833)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The species is cultivated for cut flowers in the floriculture trade; harvested inflorescences are marketed as fresh ornamental stems.

Industrial and craft applications:
Aromatic leaf material yields an essential oil via steam distillation. The oil is used as a fragrance component in perfumes, soaps, and detergents; typical chemical markers include 1,8-cineole (28–36%), camphor (2–5%), and α-pinene (2–3%).

Food and beverages (non-medicinal):
Leaves are used as an herbal flavoring in culinary infusions; the preparation is listed by the ESCO working group as “leaves infusion.”

Colorants and tanning:
No documented dyes or tannins from this taxon.

Wood and fiber:
No timber, fiber, or gum/resin uses are recorded.

Fragrance and cosmetics:
Essential oil (leaf oil) is used in fragrance formulations; typical composition: 1,8-cineole (28–36%), camphor (2–5%), α-pinene (2–3%). Regulatory status follows European Union cosmetic rules (e.g., IFRA standards), including a camphor restriction of ≤1.5% for leave‑on products.

Properties relevant to use:
Leaf oil with high 1,8-cineole content confers characteristic fresh, eucalypt-like aroma suitable for fragrance applications; moderate camphor levels require concentration controls.

Standards and regulation:
Leaf oil is regulated as a cosmetic fragrance ingredient under EU cosmetic regulation (EC No 1223/2009) and follows IFRA Standards (camphor concentration limits for leave‑on products). Culinary leaf infusion is listed as a flavoring by the European Food Safety Authority (EFSA) “Plants/FoodInf” working group (classification: leaves infusion; dose: no dose specified in the consulted source).

Sustainability and sourcing:
Common products are cultivated ornamental stems and distilled leaf oil; no wild‑harvest reports are documented in the consulted sources.

Synonyms Top

Scientific name Authority First published in
Salvia bolleana de Noé ex Bolle Bonplandia (Hannover) 8: 284 (1860)
Salvia broussonetii Bolle Bonplandia (Hannover) 8: 284 (1860)

Common names Top

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Language Common/alternative name
Spanish salvia bolleana
Chinese 长毛鼠尾草

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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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-0000300512
USDA Plants SABR13
Tropicos 100253478
KEW urn:lsid:ipni.org:names:455826-1
The Plant List kew-182196
Open Tree Of Life 3882845
Observations.org 121727
NCBI Taxonomy 1520014
IPNI 455826-1
iNaturalist 700683
GBIF 3883093
Freebase /m/05b2x6k
EOL 6341770
Elurikkus 432998
USDA GRIN 407897
Wikipedia Salvia_broussonetii
CMAUP NPO13465

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
Allelopathic Properties of Lamiaceae Species: Prospects and Challenges to Use in Agriculture Islam AK, Suttiyut T, Anwar MP, Juraimi AS, Kato-Noguchi H Plants (Basel) 31-May-2022
PMCID:PMC9182988
doi:10.3390/plants11111478
PMID:35684250
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
Diterpenes from Salvia broussonetii transformed roots and their insecticidal activity. Fraga BM, Díaz CE, Guadaño A, González-Coloma A J Agric Food Chem 29-Jun-2005
doi:10.1021/JF058045C
PMID:15969497
Nuclear DNA Amounts in Macaronesian Angiosperms SUDA J, KYNCL T, FREIOVÁ R Ann Bot 01-Jul-2003
PMCID:PMC4243629
doi:10.1093/aob/mcg104
PMID:12824074

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
> Alkaloids and derivatives / Aporphines
(12S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 26202781 Click to see 265.31 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see 355.40 unknown via CMAUP database
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone 6453733 Click to see 307.30 unknown via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone 10246449 Click to see 337.40 unknown via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)- 158516 Click to see 293.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Lanuginosine 97622 Click to see 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 15560530 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl- 11857938 Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C 280.40 unknown via CMAUP database
4-Methoxyhonokiol 155160 Click to see 280.40 unknown via CMAUP database
Caryolanemagnolol 21726647 Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C 486.70 unknown via CMAUP database
Honokiol 72303 Click to see 266.30 unknown via CMAUP database
Magnaledehyde E 5319190 Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O 254.28 unknown via CMAUP database
Magnolol 72300 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 71812224 Click to see 286.28 unknown via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal 134367 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol 71812222 Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O 312.40 unknown via CMAUP database
Isomagnolol 159137 Click to see 266.30 unknown via CMAUP database
Obovaaldehyde 23259953 Click to see 270.28 unknown via CMAUP database
Obovatal 6439677 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
Obovatol 100771 Click to see 282.30 unknown via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)- 10016628 Click to see 282.30 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol 68148 Click to see 134.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal 13785026 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O 300.40 unknown https://doi.org/10.1021/JF058045C
(1R,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 21632855 Click to see 330.50 unknown https://doi.org/10.1021/JF058045C
(3S)-5-[(1R,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 162988907 Click to see 290.50 unknown https://doi.org/10.1021/JF058045C
(4aS,10aR)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162993083 Click to see 330.50 unknown https://doi.org/10.1021/JF058045C
(4aS,10aR)-5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 667518 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1021/JF058045C
(4aS,10aR)-5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162911762 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3CC2=O)(C)C)C)O 346.50 unknown https://doi.org/10.1021/JF058045C
(4bS,8aR,9S)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9-diol 163026943 Click to see CC(C)C1=C(C(=C2C(=C1)CC(C3C2(CCCC3(C)C)C)O)O)OC 332.50 unknown https://doi.org/10.1021/JF058045C
(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 14378754 Click to see 298.40 unknown https://doi.org/10.1021/JF058045C
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/10.1021/JF058045C
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1021/JF058045C
13-Isopropylpodocarpen-12-ol-20-al 520086 Click to see 300.40 unknown https://doi.org/10.1021/JF058045C
14-Deoxycoleon U 10735190 Click to see 330.40 unknown https://doi.org/10.1021/JF058045C
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-4-ol 14827261 Click to see 316.50 unknown https://doi.org/10.1021/JF058045C
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9-diol 76390801 Click to see 332.50 unknown https://doi.org/10.1021/JF058045C
4-Methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 73816013 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)OC 330.50 unknown https://doi.org/10.1021/JF058045C
4aH-Dibenzo[a,d]cycloheptene-4a,6,7-triol, 1,2,3,4,5,10,11,11a-octahydro-1,1-dimethyl-8-(1-methylethyl)-, trans-(9CI) 11809306 Click to see 318.40 unknown https://doi.org/10.1021/JF058045C
4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 14378753 Click to see CC(C)C1=CC2=CC(=O)C3C(CCCC3(C2=CC1=O)C)(C)C 298.40 unknown https://doi.org/10.1021/JF058045C
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-ol 15923775 Click to see 290.50 unknown https://doi.org/10.1021/JF058045C
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/10.1021/JF058045C
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 14136733 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1021/JF058045C
5,6,10-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 85249733 Click to see 330.40 unknown https://doi.org/10.1021/JF058045C
5,6,10-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162874265 Click to see 332.40 unknown https://doi.org/10.1021/JF058045C
5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 71438639 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3CC2=O)(C)C)C)O 346.50 unknown https://doi.org/10.1021/JF058045C
6-Alpha-Hydroxydemethyl-Cryptojaponol 76326386 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O)O 332.40 unknown https://doi.org/10.1021/JF058045C
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1021/JF058045C
7-Dehydroabietanone 11289118 Click to see 284.40 unknown https://doi.org/10.1021/JF058045C
Abieta-8,11,13-trien-7-one 11335109 Click to see 284.40 unknown https://doi.org/10.1021/JF058045C
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/10.1021/JF058045C
Demethylsalvicanol 11666872 Click to see 318.40 unknown https://doi.org/10.1021/JF058045C
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/JF058045C
Inuroyleanol 15386508 Click to see 346.50 unknown https://doi.org/10.1021/JF058045C
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1021/JF058045C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadalene 10225 Click to see 198.30 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
Clovanemagnolol 10323149 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol 91730386 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 118976561 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
2-[4-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-3-prop-2-enylphenyl]-4-prop-2-enylphenol 14587421 Click to see 488.70 unknown via CMAUP database
4-[2-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-5-prop-2-enylphenyl]-2-prop-2-enylphenol 21726646 Click to see 488.70 unknown via CMAUP database
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
Beta-Eudesmol 91457 Click to see 222.37 unknown via CMAUP database
Cryptomeridiol 165258 Click to see 240.38 unknown via CMAUP database
Eudesmagnolol 14587417 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O 488.70 unknown via CMAUP database
Eudesobovatol A 442837 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C 504.70 unknown via CMAUP database
Eudesobovatol B 10346031 Click to see 504.70 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin 9918938 Click to see 827.00 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
12,12-Dimethyl-6-propan-2-yl-16-oxatetracyclo[7.6.1.01,11.03,8]hexadeca-3,5,7-triene-4,5-diol 73223105 Click to see CC(C)C1=C(C(=C2CC34CCCC(C3CC(C2=C1)O4)(C)C)O)O 316.40 unknown https://doi.org/10.1021/JF058045C
Brussonol 76311952 Click to see 316.40 unknown https://doi.org/10.1021/JF058045C
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol 6093330 Click to see 314.40 unknown via CMAUP database
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 21629882 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan 24796112 Click to see 318.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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