Salvia dorisiana is a perennial shrub native to Honduras. It grows 1–1.3 m tall and is heavily branched, with large magenta-pink flowers that bloom in winter. The leaves have a fruity scent when brushed, and the entire plant is covered in hairs that release a pineapple-grapefruit scent. It was first described in 1950 and has become popular as a greenhouse plant. It was named after Doris Zemurray Stone, an archaeologist and ethnographer, though some sources incorrectly attribute the name to Doris, daughter of Oceanus and Tethys.

Synonyms Top

No known synonyms.

Common names Top

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Language	Common/alternative name
German	frucht-salbei

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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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-0000300892
Tropicos	17607722
KEW	urn:lsid:ipni.org:names:226562-2
The Plant List	kew-182544
Open Tree Of Life	497988
NCBI Taxonomy	933131
IPNI	311018-2
iNaturalist	543227
GBIF	3903741
Freebase	/m/05b61mb
Wikipedia	Salvia_dorisiana

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

Comparative transcriptomics of two Salvia subg. Perovskia species contribute towards molecular background of abietane-type diterpenoid biosynthesis

Bielecka M, Stafiniak M, Pencakowski B, Ślusarczyk S, Jastrzębski JP, Paukszto Ł, Łaczmański Ł, Gharibi S, Matkowski A

Sci Rep

06-Feb-2024

PMCID:	PMC10847172
doi:	10.1038/s41598-024-53510-5
PMID:	38321199

Edible Flower Species as a Promising Source of Specialized Metabolites

Dujmović M, Radman S, Opačić N, Fabek Uher S, Mikuličin V, Voća S, Šic Žlabur J

Plants (Basel)

27-Sep-2022

PMCID:	PMC9570977
doi:	10.3390/plants11192529
PMID:	36235395

Editorial: Edible flowers: Understanding the effect of genotype, preharvest, and postharvest on quality, safety, and consumption

Scariot V, Ferrante A, Romano D

Front Plant Sci

13-Sep-2022

PMCID:	PMC9513602
doi:	10.3389/fpls.2022.1025196
PMID:	36176674

Valorization of a Waste Product of Edible Flowers: Volatile Characterization of Leaves

Najar B, Pistelli L, Marchioni I, Pistelli L

Molecules

27-Mar-2022

PMCID:	PMC9000653
doi:	10.3390/molecules27072172
PMID:	35408571

Phytonutritional Content and Aroma Profile Changes During Postharvest Storage of Edible Flowers

Marchioni I, Pistelli L, Ferri B, Copetta A, Ruffoni B, Pistelli L, Najar B

Front Plant Sci

27-Nov-2020

PMCID:	PMC7731506
doi:	10.3389/fpls.2020.590968
PMID:	33329654

Identification of phytochemicals from North African plants for treating Alzheimer’s diseases and of their molecular targets by in silico network pharmacology approach

Raafat K

J Tradit Complement Med

12-Aug-2020

PMCID:	PMC8116716
doi:	10.1016/j.jtcme.2020.08.002
PMID:	34012873

Salvia Spp. Essential Oils against the Arboviruses Vector Aedes albopictus (Diptera: Culicidae): Bioactivity, Composition, and Sensorial Profile—Stage 1

Najar B, Pistelli L, Venturi F, Ferroni G, Giovanelli S, Cervelli C, Bedini S, Conti B

Biology (Basel)

04-Aug-2020

PMCID:	PMC7463507
doi:	10.3390/biology9080206
PMID:	32759742

Toxic, Radical Scavenging, and Antifungal Activity of Rhododendron tomentosum H. Essential Oils

Judzentiene A, Budiene J, Svediene J, Garjonyte R

Molecules

05-Apr-2020

PMCID:	PMC7181133
doi:	10.3390/molecules25071676
PMID:	32260539

Essential Oils Extracted from Different Species of the Lamiaceae Plant Family as Prospective Bioagents against Several Detrimental Pests

Ebadollahi A, Ziaee M, Palla F

Molecules

28-Mar-2020

PMCID:	PMC7180760
doi:	10.3390/molecules25071556
PMID:	32231104

Novel routes towards bioplastics from plants: elucidation of the methylperillate biosynthesis pathway from Salvia dorisiana trichomes

Jongedijk E, Müller S, van Dijk AD, Schijlen E, Champagne A, Boutry M, Levisson M, van der Krol S, Bouwmeester H, Beekwilder J

J Exp Bot

24-Feb-2020

PMCID:	PMC7260718
doi:	10.1093/jxb/eraa086
PMID:	32090266

Essential oils sensory quality and their bioactivity against the mosquito Aedes albopictus

Bedini S, Flamini G, Ascrizzi R, Venturi F, Ferroni G, Bader A, Girardi J, Conti B

Sci Rep

14-Dec-2018

PMCID:	PMC6294827
doi:	10.1038/s41598-018-36158-w
PMID:	30552358

Methyl Perillate as a Highly Functionalized Natural Starting Material for Terephthalic Acid

Jongedijk E, van der Klis F, de Zwart R, van Es DS, Beekwilder J

ChemistryOpen

08-Feb-2018

PMCID:	PMC5803525
doi:	10.1002/open.201700178
PMID:	29450122

Composition of the Essential Oil of Salvia ballotiflora (Lamiaceae) and Its Insecticidal Activity

Cárdenas-Ortega NC, González-Chávez MM, Figueroa-Brito R, Flores-Macías A, Romo-Asunción D, Martínez-González DE, Pérez-Moreno V, Ramos-López MA

Molecules

05-May-2015

PMCID:	PMC6272514
doi:	10.3390/molecules20058048
PMID:	25951002

Toxicity of Amorphigenin from the Seeds of Amorpha fruticosa against the Larvae of Culex pipiens pallens (Diptera: Culicidae)

Liang Y, Li X, Gu Z, Qin P, Ji M

Molecules

16-Feb-2015

PMCID:	PMC6272459
doi:	10.3390/molecules20023238
PMID:	25690287

The Essential Oil of<i>Salvia dorisiana</i>Standley

Arthur O. Tucker, Michael J. Maciarello

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1994.9698330

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
3-Methyl-5-phenylpentanoic acid	13570487	Click to see CC(CCC1=CC=CC=C1)CC(=O)O	192.25	unknown	https://doi.org/10.1080/10412905.1994.9698330
5-Methylhexanoic acid	12344	Click to see CC(C)CCCC(=O)O	130.18	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid	264	Click to see CCCC(=O)O	88.11	unknown	https://doi.org/10.1021/JF60199A051
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Octanol	20083	Click to see CCCCCCC(C)O	130.23	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
3-Octanol	11527	Click to see CCCCCC(CC)O	130.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
5,9-Dimethyl-4,8-decadienoic acid	6365434	Click to see CC(=CCCC(=CCCC(=O)O)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1994.9698330
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene, (E)-(-)-	6429302	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Pinocamphone	6427105	Click to see CC1C2CC(C2(C)C)CC1=O	152.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF60199A051
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Methyl perillate	14159029	Click to see CC(=C)C1CCC(=CC1)C(=O)OC	180.24	unknown	https://doi.org/10.1021/JF60199A051
Perilla alcohol	369312	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	https://doi.org/10.1021/JF60199A051
Perillaldehyde	16441	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Perillyl acetate	61780	Click to see CC(=C)C1CCC(=CC1)COC(=O)C	194.27	unknown	https://doi.org/10.1021/JF60199A051
Perillyl alcohol	10819	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	https://doi.org/10.1021/JF60199A051
Perillyl butyrate	10398645	Click to see CCCC(=O)OCC1=CCC(CC1)C(=C)C	222.32	unknown	https://doi.org/10.1021/JF60199A051
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
(+)-Nerolidol	5356544	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1021/JF60199A051
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1021/JF60199A051
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1021/JF60199A051
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1021/JF60199A051
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698330
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330 https://doi.org/10.1021/JF60199A051
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF60199A051 https://doi.org/10.1080/10412905.1994.9698330
trans-Nerolidol	5284507	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1021/JF60199A051
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1021/JF60199A051
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene	10123	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol	5991	Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O	296.40	unknown	https://doi.org/10.1080/10412905.1994.9698330
> Organic oxygen compounds / Organic oxides
beta-Cyclocitral	9895	Click to see CC1=C(C(CCC1)(C)C)C=O	152.23	unknown	https://doi.org/10.1080/10412905.1994.9698330

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Salvia dorisiana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top