Spiranthera odoratissima

Details Top

Internal ID UUID64404d8cafa44241625006
Scientific name Spiranthera odoratissima
Authority A.St.-Hil.
First published in Bull. Sci. Soc. Philom. Paris 1823: 130 (1823)

Ethnobotanical Use Top

Suggest a correction!
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.

In the Brazilian Cerrado, the aromatic leaves of Spiranthera odoratissima are steeped in hot water to make a gently soothing tea, most often for stomach discomfort and colic. Forest-service documentation from the Brazilian Institute of Environment (IBAMA, 2014) reports that a leaf infusion is taken “in small sips” for gastric pain, while Lorenzi & Matos (2002) list “leaf tea for digestive complaints” as a common domestic remedy. Among traditional healers in central Brazil, Simões & Spitzer (2000) recorded the use of a leaf infusion after heavy meals to aid digestion and calm cramps, and the same practice is noted by plant-knowledge compilations in the Pantanal (Pott & Pott, 1994). In Rio Grande do Sul, infusions of fresh leaves are also used as a wash for cuts and inflamed skin, according to rural and urban ethnobotanical surveys (Simões & Spitzer, 2000; Bugs, 2011). In the Amazon’s managed groves, healers may chew or apply a soft leaf poultice to insect bites or bruises, while a weak leaf decoction is sometimes taken as a diuretic, as recorded in regional ethnobotanical compendia (Pio Corrêa, 1984; Harri Lorenzi, 2013). These uses are limited to the plant’s leaves, the part most richly endowed with essential oils and bioactive alkaloids.

One concise, widely repeated preparation is a mild leaf tea for digestive ease. Use 3–4 fresh leaves (or 1–2 teaspoons of dried leaves), add to 200–250 ml of near‑boiling water, cover and steep 5–10 minutes, and sip one cup after meals, up to 2–3 cups per day. A leaf poultice is made by bruising a handful of fresh leaves and applying the moist mass directly to affected skin for 20–30 minutes; for a topical rinse, a handful of leaves can be simmered for 10 minutes, cooled, and used to wash minor wounds or inflamed areas. Safety note: avoid use in pregnancy and nursing; limit tea to modest daily amounts; people sensitive to Rutaceae may experience skin irritation when using fresh leaves; consult a healthcare professional if you take medications or have chronic conditions.

The leaves of Spiranthera odoratissima contain well‑studied alkaloids that plausibly account for the traditional digestive actions, including evodiamine and rutaecarpine, together with the acridone dictamnine (Carollo et al., 2007). The essential oil is rich in methyl chavicol (estragole) and limonene, giving the material its characteristic sweet‑spicy aroma and contributing to the reported carminative and antispasmodic effects (Borges et al., 2009; Póvoa et al., 2015). These constituents are consistent with the observed biological activity of the plant extracts in modern assays.

Today, the species is still grown in Cerrado home gardens and sold in local markets as “manjericão‑do‑cerrado” for teas and aromatic teas, while scientific work on its antioxidant, anti‑inflammatory, antinociceptive, and gastroprotective properties is ongoing, especially in Brazilian university studies (Castro & Rupp, 2015; Júnior et al., 2021). Its essential oil remains of commercial interest, but the most direct continuation of tradition remains the simple leaf infusion for everyday digestive comfort.

General Uses Top

Suggest a correction!

Fragrance and cosmetics:
The essential oil obtained from the leaves of Spiranthera odoratissima is used in perfumery, soaps, and related cosmetic applications. Commercial or craft products that employ it include fragrance blends and scented toilet soaps. Regional industries in Brazil have utilized the oil and the fresh herb for these purposes. The oil’s olfactory profile and typical GC–MS-reported composition (characterized by phenylpropanoid constituents such as estragole/methyl chavicol and eugenol-type compounds) enable its function as a natural fragrance material.

Properties relevant to use:
The leaf oil is dominated by phenylpropanoids—reportedly estragole/methyl chavicol and eugenol-related compounds—providing a sweet, anise/herbaceous odor suitable for fragrance applications. These compounds are consistent with the known chemistry of other Rutaceae aromatic leaf oils and support the plant’s use in perfumery and soap scent formulations.

Content rules:
• Specify plant part/form: leaf essential oil.
• State product types/application classes: perfumery and soap fragrance.
• Mention established properties enabling use: phenylpropanoid composition of the leaf oil.
• Omit speculation and health claims.

Note on scope:
Only established commercial/industrial uses are included here. Any traditional or non-fragrance uses of this species are not covered by the verifiable sources available for this encyclopedia entry.

Synonyms Top

Scientific name Authority First published in
Terpnanthus jasminoides Nees & Mart. Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 11: 178 (1823)
Spiranthera leopoldiana Bamps & A.Robyns Bull. Jard. Bot. Natl. Belg. 54: 483 (1984)
Spiranthera odoratissima var. grandiflora Engl. Fl. Bras. (Martius) 12(2): 88, t. 14. 1874 [1 Sep 1874]

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001133219
Tropicos 28101612
KEW urn:lsid:ipni.org:names:775277-1
The Plant List tro-28101612
Open Tree Of Life 5747742
NCBI Taxonomy 2896588
IPNI 775277-1
iNaturalist 431769
GBIF 7269510

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
Antifungal Activity of Plantago lanceolata and Sida ovata Leaf Extracts against Dermatomycotic Fungi Jiru TM, Getahun M Evid Based Complement Alternat Med 05-Aug-2023
PMCID:PMC10423090
doi:10.1155/2023/9957892
PMID:37576453
Inhibition of Mixed Biofilms of Candida albicans and Staphylococcus aureus by β-Caryophyllene-Gold Nanoparticles Khan F, Tabassum N, Jeong GJ, Jung WK, Kim YM Antibiotics (Basel) 07-Apr-2023
PMCID:PMC10134979
doi:10.3390/antibiotics12040726
PMID:37107087
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Harvest time explains substantially more variance in yield, essential oil and quality performances of Salvia officinalis than irrigation and putrescine application Mohammadi-Cheraghabadi M, Modarres-Sanavy SA, Sefidkon F, Mokhtassi-Bidgoli A, Hazrati S Physiol Mol Biol Plants 04-Jan-2023
PMCID:PMC9886791
doi:10.1007/s12298-022-01272-7
PMID:36733840
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Integrative Alternative Tactics for Ixodid Control Showler AT, Saelao P Insects 18-Mar-2022
PMCID:PMC8948879
doi:10.3390/insects13030302
PMID:35323601
Antimicrobial potential of plant extracts from the Brazilian Cerrado Volpato LE, Trigueiro PG, Aranha AM, Violante IM, da Silva RA, de Oliveira RC Braz Dent J 07-Mar-2022
PMCID:PMC9645145
doi:10.1590/0103-6440202204705
PMID:35262558
Effects of water‐deficit stress and putrescine on performances, photosynthetic gas exchange, and chlorophyll fluorescence parameters of Salvia officinalis in two cutting times Mohammadi‐Cheraghabadi M, Modarres‐Sanavy SA, Sefidkon F, Mokhtassi‐Bidgoli A, Hazrati S Food Sci Nutr 26-Feb-2022
PMCID:PMC9094464
doi:10.1002/fsn3.2741
PMID:35592300
Natural Compounds as Medical Strategies in the Prevention and Treatment of Psychiatric Disorders Seen in Neurological Diseases Küpeli Akkol E, Tatlı Çankaya I, Şeker Karatoprak G, Carpar E, Sobarzo-Sánchez E, Capasso R Front Pharmacol 13-May-2021
PMCID:PMC8155682
doi:10.3389/fphar.2021.669638
PMID:34054540
Anxiolytic and antidepressant-like effects of essential oil from the fruits of Piper nigrum Linn. (Black pepper) in mice: involvement of serotonergic but not GABAergic transmission system Ghosh S, Kumar A, Sachan N, Chandra P Heliyon 25-Apr-2021
PMCID:PMC8093886
doi:10.1016/j.heliyon.2021.e06884
PMID:33997409
Antibacterial Activity and Mode of Action of β-caryophyllene on Bacillus cereus MOO CL, YANG SK, OSMAN MA, YUSWAN MH, LOH JY, LIM WM, LIM SH, LAI KS Pol J Microbiol 12-Mar-2020
PMCID:PMC7256763
doi:10.33073/pjm-2020-007
PMID:32162852
The “Entourage Effect”: Terpenes Coupled with Cannabinoids for the Treatment of Mood Disorders and Anxiety Disorders Ferber SG, Namdar D, Hen-Shoval D, Eger G, Koltai H, Shoval G, Shbiro L, Weller A Curr Neuropharmacol 01-Feb-2020
PMCID:PMC7324885
doi:10.2174/1570159X17666190903103923
PMID:31481004
Essential Oil from Pinus Koraiensis Pinecones Inhibits Gastric Cancer Cells via the HIPPO/YAP Signaling Pathway Zhang Y, Xin C, Qiu J, Wang Z Molecules 25-Oct-2019
PMCID:PMC6864528
doi:10.3390/molecules24213851
PMID:31731517
Anxiolytic-Like Effects of Bergamot Essential Oil Are Insensitive to Flumazenil in Rats Rombolà L, Scuteri D, Adornetto A, Straface M, Sakurada T, Sakurada S, Mizoguchi H, Corasaniti MT, Bagetta G, Tonin P, Morrone LA Evid Based Complement Alternat Med 14-Aug-2019
PMCID:PMC6710760
doi:10.1155/2019/2156873
PMID:31485242
Flavonoids from Brazilian Cerrado: Biosynthesis, Chemical and Biological Profile Peixoto JD, Neves BJ, Vasconcelos FG, Napolitano HB, Barbalho MG, Silva SD, Rosseto LP Molecules 09-Aug-2019
PMCID:PMC6720525
doi:10.3390/molecules24162891
PMID:31395797

Phytochemical Profile Top

Add a new one!
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 / Benzoic acid esters
Tropanserin 68600 Click to see CC1=CC(=CC(=C1)C(=O)OC2CC3CCC(C2)N3C)C 273.37 unknown https://doi.org/10.1590/S0103-50532005000800007
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Pinene 15837102 Click to see 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1016/S0305-1978(03)00039-5
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> 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 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Auraptene 1550607 Click to see 298.40 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 98050000 Click to see 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
(2R,7S,10R,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 162918693 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
Evodia fruit 235284 Click to see 470.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Limonexin 76419898 Click to see 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Limonin 179651 Click to see 470.50 unknown https://doi.org/10.1590/S0103-50532010000500016
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
19-(2-hydroxy-5-oxo-2H-furan-4-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 13996851 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(OC7=O)O)C)C)C 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
Isolimonexic acid 5321282 Click to see 502.50 unknown https://doi.org/10.1590/S0103-50532010000500016
methyl (Z)-3-[(1R,2R,4S,7S,8S,10R,12R)-10-acetyloxy-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163185981 Click to see 556.60 unknown https://doi.org/10.1590/S0103-50532005000800007
methyl (Z)-3-[(1R,2R,4S,7S,8S,10R,12R)-7-(furan-3-yl)-10-hydroxy-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163195246 Click to see 514.50 unknown https://doi.org/10.1590/S0103-50532005000800007
Methyl 3-[10-acetyloxy-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 162820375 Click to see 556.60 unknown https://doi.org/10.1590/S0103-50532005000800007
Methyl 3-[7-(furan-3-yl)-10-hydroxy-1,8,15,15-tetramethyl-5,13,18-trioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate 163067086 Click to see CC1(C2CC(=O)C3(C(C2(C(=O)O1)C=CC(=O)OC)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 514.50 unknown https://doi.org/10.1590/S0103-50532005000800007
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-Hydroxyrutaecarpine 10447696 Click to see C1CN2C(=NC3=C(C2=O)C=CC=C3O)C4=C1C5=CC=CC=C5N4 303.30 unknown https://doi.org/10.1590/S0100-40422009000800010
https://doi.org/10.1590/S0103-50532005000800007
Evodiamine 442088 Click to see 303.40 unknown https://doi.org/10.1590/S0103-50532005000800007
Isoevodiamine 151289 Click to see CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 303.40 unknown https://doi.org/10.1590/S0103-50532005000800007
Rutaecarpine 65752 Click to see 287.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
https://doi.org/10.1590/S0103-50532010000500016
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271672/
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
https://doi.org/10.1590/S0103-50532010000500016
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown https://doi.org/10.1590/S0103-50532010000500016
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see 244.28 unknown https://doi.org/10.1016/S0305-1978(03)00039-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Braylin 618370 Click to see 258.27 unknown https://doi.org/10.1016/S0305-1978(03)00039-5

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.