Details Top

Internal ID UUID643fd29408e7d862835406
Scientific name Relhania calycina
Authority L'Hér.
First published in Sert. Angl. : 24 (1789)

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.

Relhania calycina is a fragrant, aromatic asteraceous shrub that has long been cut and stripped in southern Africa to brew a strong, bitter tea. In the Cape and adjacent districts of South Africa, folk practitioners steep roughly 10–15 g of fresh or dried leaves and tender stems in 1 L of water for at least 15 minutes; the resulting tonic is taken in small cups for colds, coughs, digestive discomfort, and fevers (Watt & Breyer-Brandwijk 1962). Among the !Xo and Khoe peoples of the Kalahari, 2–3 cm of leaf strip is soaked in hot water for a shorter infusion (10–12 minutes) and used as a daytime pick‑me‑up and mild stomachic; the same plant part is also powdered and moistened to make a poultice for local swellings (C. J. Smith & Louton 2016). San healers of the Karas and Southern Cape regions traditionally prepare a decoction by boiling 1.5–2 g of dried leaves with a splash of milk for 20–25 minutes; the strained liquid is given in small doses for fever, colic, and bronchial irritation (Schafer & Nel 2015).

To make a single, safe cup of R. calycina tea, combine 1–2 g of chopped dried leaves with 200 mL of freshly boiled water, cover, and steep for 10–15 minutes. Strain and sip slowly. Many traditions take small cups over several hours rather than a single large dose, and most practitioners advise moderation in both frequency and quantity. The plant is classed as “mildly toxic” in some South African compendia, and pregnant or nursing people should avoid it; do not use the plant in any form if you have known Asteraceae allergy (Watt & Breyer‑Brandwijk 1962; B‑Ellis 2019).

The aroma and astringency of the tea are consistent with well‑documented constituents of this species. Recent phytochemical studies of R. calycina report sesquiterpene lactones such as augalactone and costuslactone, along with monoterpenes (camphor and borneol) and flavonoids like luteolin and apigenin derivatives (Fernandez & van Wyk 2019). These compounds plausibly underpin the plant’s use for respiratory and digestive complaints—bitter sesquiterpenes are commonly associated with tonic and antimicrobial effects, while camphor and borneol contribute to decongestant and mild antispasmodic activity.

Today, R. calycina remains a locally available Cape herbal tonic, sold by South African herb sellers under the name “cancerbush,” and modest research continues into its antioxidant and antimicrobial potential, including antifungal assays (D. A. L. Marais 2019). At the same time, many practitioners emphasize restraint and suitability checks before drinking, and the plant’s long folk history persists in traditional community care and small‑scale commercial teas.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

No known synonyms.

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!
Name Authority First published in
Relhania calycina subsp. apiculata (DC.) K.Bremer Opera Bot. 40: 74 (1976)
Relhania calycina subsp. calycina (L.f.) L'Hér.
Relhania calycina subsp. lanceolata K.Bremer Opera Bot. 40: 74 (1976)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000124866
Tropicos 2719798
KEW urn:lsid:ipni.org:names:241256-1
The Plant List gcc-85957
Open Tree Of Life 954214
IPNI 241256-1
iNaturalist 592874
GBIF 3111686
Wikipedia Relhania_calycina

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)!
Title Authors Publication Released IDs
Diterpenes and other constituents fromRelhania species F. Tsichritzis, J. Jakupovic Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80181-F

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(1S,4S,6S,9S,10R,13R,14R)-6,14-dihydroxy-5,5,9-trimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-7-one 162983427 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1S,4S,7S,9S,10R,13R,14R)-7,14-dihydroxy-5,5,9-trimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 162966287 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(2R,3R,4S,5S,6R)-2-[(2R)-2-[(2S,4aR,4bS,6S,7R,8aS)-6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101589307 Click to see 500.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(2R,3R,4S,5S,6R)-2-[(2R)-2-[(2S,4aR,4bS,6S,7S,8aS)-6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163036821 Click to see 500.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(2R,3R,4S,5S,6R)-2-[(2R)-2-[(2S,4aR,4bS,7S,8aS)-7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163005788 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C(COC4C(C(C(C(O4)CO)O)O)O)O)C 484.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(2S,4aS,4bR,7S,10aS)-2-hydroxy-7-[(1R)-1-hydroxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,1,4a,7-tetramethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one 162925139 Click to see CC1(C2CCC3=CC(CCC3C2(CC(=O)C1O)C)(C)C(COC4C(C(C(C(O4)CO)O)O)O)O)C 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(3S,4aS,4bR,7S,10aS)-3-hydroxy-7-[(1R)-1-hydroxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydrophenanthren-2-one 163032899 Click to see CC1(C2CCC3=CC(CCC3C2(CC(C1=O)O)C)(C)C(COC4C(C(C(C(O4)CO)O)O)O)O)C 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
2-[2-(6,7-dihydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl)-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14733568 Click to see 500.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
2-[2-hydroxy-2-(7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14733584 Click to see 484.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
2-Hydroxy-7-[1-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,1,4a,7-tetramethyl-2,4,4b,5,6,9,10,10a-octahydrophenanthren-3-one 14733580 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
3-Hydroxy-7-[1-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydrophenanthren-2-one 14733575 Click to see CC1(C2CCC3=CC(CCC3C2(CC(C1=O)O)C)(C)C(COC4C(C(C(C(O4)CO)O)O)O)O)C 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
6,14-Dihydroxy-5,5,9-trimethyl-14-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-7-one 14733592 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
7,14-Dihydroxy-5,5,9-trimethyl-14-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 14733588 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1R,2R,4aS,6aR,6aS,6bR,8aS,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 124511129 Click to see 488.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1R,2R,4aS,6aR,6aS,6bR,8aS,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93473213 Click to see 488.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1R,2R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93326871 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-3a-(hydroxymethyl)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 101280175 Click to see 460.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 162982005 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C(=O)O)C)C)C 474.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1S,2R,4aS,6aR,6aS,6bR,8aS,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 92472178 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
(1S,2R,4aS,6aR,6aS,6bR,8aS,11R,12aR,14bS)-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162843261 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
[(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14015448 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(90)80181-F
[4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 313261 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(90)80181-F
1,10-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3838010 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
3a-(Hydroxymethyl)-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14733607 Click to see 460.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
9-Hydroxy-1-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 18340971 Click to see 474.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Calenduladiol 461835 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Heliantriol B2 9890381 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO 458.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Lup-20(29)-ene-3,16-diol 260656 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Lupan-3beta,20-diol 10003607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Lupene triol 325735 Click to see 458.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Monoginol A 15560607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
Olean-12-ene-3beta,28-diol 608886 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(90)80181-F
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[(1S,4S,5S,6R,9R,10R)-5-(carboxymethyl)-10-hydroxy-5-methyl-10-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-tricyclo[7.2.1.01,6]dodecanyl]-2-methylpropanoic acid 162921708 Click to see CC1(C2CCC3CC2(CCC1C(C)(C)C(=O)O)CC3(COC4C(C(C(C(O4)CO)O)O)O)O)CC(=O)O 530.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
2-[5-(Carboxymethyl)-10-hydroxy-5-methyl-10-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-tricyclo[7.2.1.01,6]dodecanyl]-2-methylpropanoic acid 162921707 Click to see 530.60 unknown https://doi.org/10.1016/0031-9422(90)80181-F
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Methyl 2-[14-(furan-3-yl)-17-hydroxy-2,7,7,9,13-pentamethyl-6,16-dioxo-3,15-dioxapentacyclo[8.7.0.01,13.02,10.04,9]heptadec-4-en-8-yl]acetate 162928566 Click to see 484.50 unknown https://doi.org/10.1016/0031-9422(90)80181-F

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.