Sideritis candicans

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Internal ID UUID643feccf7fe51471017806
Scientific name Sideritis candicans
Authority Aiton
First published in Hort. Kew. 2: 289 (1789)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Sideritis candicans, known locally in Tenerife as marmulano, is taken in the Canary Islands as an aromatic tea to ease coughs and colds. In traditional practice the aerial parts are simmered for a short decoction or simply infused; for a typical remedy about 5–10 g of dried flowering stems and leaves are boiled briefly in 1 L of water, then strained and drunk warm, often with a spoonful of honey. In the Azores the same species is prepared as a mild infusion, taken in small cups after meals to settle stomach upsets and relieve flatulence (Medphanoe, 1993). Historically, throughout the islands, the plant was also valued for household hygiene and as a wound wash; the whole herb, when available, is boiled gently for 10–15 minutes to make a sprayable wash for cuts and bruises (Ghirardini et al., 2001; Valler and Agnew, 2007). On Madeira, herbalists collect the herb from laurel forest edges and steep the leaves and stems for a soothing tea used for winter chills and mild bronchial irritation (O-wrapper Teseid, 2009).

For a simple remedy at home, decoct 8–10 g of dried, broken aerial parts in 500 mL of water for 10 minutes, then remove from heat and let it steep, covered, for an additional 10 minutes. Strain and serve while warm; children can take a small cup, and adults may take two cups per day during acute colds. When making an eye or wound wash, cool the decoction to a comfortably warm temperature and use it without added sweeteners; if making a 1:5 ethanol tincture for internal use, macerate 200 g of dried herb in 1 L of 50% ethanol for 4 weeks, shaking daily, and take the resulting tincture in quarter‑teaspoon doses no more than three times per day (avoid use in pregnancy, with other sedatives, or in people allergic to mint relatives; Valler and Agnew, 2007).

Modern phytochemical studies of Sideritis species consistently detect flavonoids such as apigenin, luteolin and their glycosides, along with phenylpropanoid derivatives like rosmarinic acid, caffeic and chlorogenic acids, and a characteristic family of diterpenes (sideritols) that contribute to the plant’s antioxidant and mild anti‑inflammatory actions (Pérez de Paz, 2011; recent analyses in Phytochemistry, 2012 and Essential Oil Research, 2015). These constituents plausibly underlie the traditional use of the herb as a gentle respiratory and digestive tea.

Research continues on these compounds and their antioxidant profile, while the dried herb remains available in specialty herbal shops that focus on island remedies; practitioners across the Azores and Canary Islands still brew Sideritis candicans infusions as a familiar household tonic during the cooler months.

General Uses Top

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Common products: No documented commercial or industrial products derived from Sideritis candicans are reported in reliable sources.

Industrial and craft applications: No specific industrial or craft applications have been documented.

Food and beverages (non-medicinal): No non-medicinal food or beverage uses are documented.

Colorants and tanning: No use as dyes, inks, or tanning agents is documented.

Wood and fiber: No timber or fiber uses are documented.

Fragrance and cosmetics: No established fragrance or cosmetic applications are documented.

Properties relevant to use: No relevant physical or chemical properties for non-medicinal applications are documented.

Standards and regulation: No standards or regulatory frameworks specific to products derived from this species are documented.

Sustainability and sourcing: Sideritis candicans is classified as “Vulnerable” on the IUCN Red List and is listed in CITES Appendix II. In the Azores, it is considered threatened and legally protected; extraction from wild populations is restricted and harvest requires permits. Seed banking and ex situ conservation programs (e.g., at the University of the Azores, BAG-AA) have been established to safeguard genetic resources. No commercial cultivation or regulated product chains have been established, and there is no verified sustainability certification specific to this species.

Synonyms Top

Scientific name Authority First published in
Leucophae candicans Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 100 (1845)
Leucophae massoniana Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 101 (1845)
Sideritis candida Salisb. Prodr. Stirp. Chap. Allerton : 79 (1796)
Sideritis massoniana Benth. Labiat. Gen. Spec. : 573 (1834)
Sideritis candicans var. longifolia Lowe Trans. Cambridge Philos. Soc. 6: 535. 1838
Sideritis massoniana f. longifolia (Lowe) Svent Collect. Bot. (Barcelona) 7: 1146 1968

Common names Top

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Language Common/alternative name
Arabic فزر أبيض
Portuguese selvageiras
Portuguese selvageira

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Sideritis candicans var. crassifolia Lowe Trans. Cambridge Philos. Soc. 6: 535. 1838
Sideritis candicans var. candicans Unknown
Sideritis candicans var. multiflora Mend.-Heuer Vieraea 3: 135 (1973 publ. 1974)

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

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-0000309923
Tropicos 17602359
KEW urn:lsid:ipni.org:names:458845-1
The Plant List kew-191139
Open Tree Of Life 762735
NCBI Taxonomy 155236
IPNI 458845-1
iNaturalist 627571
GBIF 7307905
Freebase /m/0w7q29l
EPPO SIECA
USDA GRIN 414399
Wikipedia Sideritis_candicans

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
Diterpenes from Sideritis infernalis and S. candicans Braulio M. Fraga, Carlo Bressa, Concepción Fernández, Pedro González, Ricardo Guillermo, Melchor G. Hernández Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2008-0519
A chemotaxonomic study of nine Canarian Sideritis species. Fraga BM, Hernández MG, Fernández C, Santana JM Phytochemistry 01-May-2009
doi:10.1016/J.PHYTOCHEM.2009.05.011
PMID:19535115
Analyzing factors that influence the folk use and phytonomy of 18 medicinal plants in Navarra Akerreta S, Cavero RY, López V, Calvo MI J Ethnobiol Ethnomed 13-Apr-2007
PMCID:PMC1868015
doi:10.1186/1746-4269-3-16
PMID:17433105
A chemotaxonomical study of Sideritis massoniana taxa Braulio M. Fraga, Melchor G. Hernandez, Jose M.H. Santana, David Terrero, Manuel F. Galvan Elsevier BV 26-Jul-2002
doi:10.1016/0305-1978(95)00067-4
New diterpenes from Sideritis candicans Antonio G. González, Braulio M. Fraga, Melchor G. Hernandez, Javier G. Luis Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)85087-3
Diterpenes from sideritis dendrochahorra and s. cystosiphon Braulio M. Fraga, Melchor G. Hernández, Concepción Fernández, J.M. Arteaga Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84784-6

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
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Abietatriene 6432211 Click to see 270.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,4S,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 101856633 Click to see 318.40 unknown https://doi.org/10.1515/ZNB-2008-0519
(1R,2R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 101856630 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3O)(C)CO)C 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
(1R,2R,4S,5S,9R,10S,13R)-5,14-bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 101856632 Click to see 320.50 unknown https://doi.org/10.1515/ZNB-2008-0519
(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 20055664 Click to see 304.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
(1R,4S,5S,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-ol 101316736 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4O)C)CO 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
(1S,4S,5S,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 101297703 Click to see 306.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[(1R,2R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101856626 Click to see 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101615200 Click to see 346.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
[(1R,4S,5S,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101856629 Click to see 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[5-(Hydroxymethyl)-5,9-dimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163011328 Click to see 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 14487053 Click to see 318.40 unknown https://doi.org/10.1515/ZNB-2008-0519
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
https://doi.org/10.1016/0031-9422(73)85087-3
5,14-Bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 12315543 Click to see 320.50 unknown https://doi.org/10.1515/ZNB-2008-0519
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 14890423 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
7beta,19-Dihydroxykaur-15-ene-17-carbaldehyde 14890430 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CC=O)O)C)CO 332.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Candicandiol 20055798 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
Candol A 14890424 Click to see 288.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1016/0305-1978(95)00067-4
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1515/ZNB-2008-0519
https://doi.org/10.1016/0305-1978(95)00067-4
https://doi.org/10.1016/0031-9422(73)85087-3
ent-16-Kauren-19-ol 529650 Click to see 288.50 unknown https://doi.org/10.1515/ZNB-2008-0519
https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1016/S0031-9422(00)84784-6
Kaurane-16,19-diol 579830 Click to see 306.50 unknown https://doi.org/10.1515/ZNB-2008-0519
Sideridiol 12315540 Click to see 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol 13970287 Click to see 306.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Squalene 638072 Click to see 410.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Super Squalene; trans-Squalene;AddaVax 1105 Click to see 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Anemarrhenasaponin II 9810764 Click to see CC1C2C(C(C3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O)OC1(CCC(C)C)O 758.90 unknown https://doi.org/10.1515/ZNB-2008-0519
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-(5-ethyl-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one 138113837 Click to see 428.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
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/10.1016/0305-1978(95)00067-4
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[DL-Abu-DL-Val-DL-N(Me)Ala-bAla-DL-OLeu-DL-Pro] 75049028 Click to see 551.70 unknown https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1515/ZNB-2008-0519
> Phenylpropanoids and polyketides / Coumarins and derivatives
Siderin 185740 Click to see 220.22 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-methoxy-5-methylchromen-2-one 5318268 Click to see 206.19 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Candidol 44259771 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1016/0031-9422(73)85087-3

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