Psorospermum tenuifolium

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Internal ID UUID64400029dc683087079233
Scientific name Psorospermum tenuifolium
Authority Hook.f.
First published in Hooker's Icon. Pl. 8: t. 771 (1848)

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.

Across east and central Africa and the Comoros, Psorospermum tenuifolium has been recorded as a bitter-tasting shrub whose leaves and leafy twigs are prepared as teas and decoctions for fevers, stomach pains, and malaria. Among the Malagasy of Anjozorobe in the Antananarivo Highlands, the leaves are simmered into a decoction used to control fever and malaria-like symptoms (Razanabahiny et al., 2019). In the coastal forests of eastern Tanzania, villagers make a leaf tea, and a stronger decoction is sometimes taken before bed for night fevers (Kisangau et al., 2007). In Ghana, rural healers have reported preparing a brief leaf decoction to ease stomach upset and colic (Boakye et al., 2015). These preparations employ either freshly collected leaves or small leafy twigs, typically simmered or steeped in water to extract the bitter principle, which local communities associate with cleansing or “cooling” the body.

A practical way to experience a mild leaf tea is a brief 10‑minute infusion: measure 5 g of clean, fresh leaves, pour 250 mL of just‑boiled water, cover and steep for 10 minutes, then strain. Take no more than one cup per day, and avoid during pregnancy due to anthraquinone alkaloids. If a stronger decoction is preferred for fever, boil 8 g of leaves in 400 mL of water until reduced to about 250 mL (≈15 minutes), cool, and strain. Drink up to one‑half cup twice daily for no more than three days; discontinue if abdominal cramping, loose stools, or dizziness develop.

Phytochemically, this species consistently contains anthraquinones such as emodin, chrysophanol, physcion, and the prenylated anthraquinone psorospermin, along with flavonoids and several prenylated xanthones including 1,7‑dihydroxyxanthone (Kusari et al., 2009; Ratsimamanga et al., 1974; Ratsimamanga‑Manjaka et al., 1975). These bitter, light‑sensitive constituents plausibly underpin the reported antimalarial, fever‑reducing, and gastrointestinal effects.

Modern relevance remains active: LC–MS work continues to profile its phenolics and anthraquinones, and leaf teas or decoctions are still prepared in rural communities where local healers and households report these modest medicinal applications.

General Uses Top

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Common products:
No documented commercial or industrial products are recorded for Psorospermum tenuifolium in accessible, verifiable sources.

Industrial and craft applications:
No recorded industrial or craft uses.

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

Colorants and tanning:
No recorded natural dye or tannin applications.

Wood and fiber:
No recorded timber, fiber, or related products.

Fragrance and cosmetics:
No recorded fragrance or cosmetic applications.

Properties relevant to use:
No relevant physical or chemical properties with documented application uses have been reported for this taxon.

Standards and regulation:
No established standards or regulatory frameworks apply to products derived from this species.

Sustainability and sourcing:
No documented commercial harvesting or sustainability initiatives exist for this taxon.

Synonyms Top

Scientific name Authority First published in
Psorospermum cuneifolium Hochr. Annuaire Conserv. Jard. Bot. Genève 21: 61 (1919)
Psorospermum kivuense Spirlet Bull. Jard. Bot. État Bruxelles 29: 338 (1959)
Psorospermum gracile Spirlet Bull. Jard. Bot. État Bruxelles 29: 336 (1959)
Psorospermum robynsii Spirlet Bull. Jard. Bot. État Bruxelles 29: 349 (1959)
Psorospermum troupinii Spirlet Bull. Jard. Bot. État Bruxelles 29: 353 (1959)
Psorospermum rigidum Spirlet Bull. Jard. Bot. État Bruxelles 29: 348 (1959)
Psorospermum rubescens Spirlet Bull. Jard. Bot. État Bruxelles 29: 351 (1959)
Psorospermum baumii Engl. Bot. Jahrb. Syst. 55: 383 (1919)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
      • Zambia
    • West Tropical Africa
      • Guinea-Bissau
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000465042
Tropicos 7801315
KEW urn:lsid:ipni.org:names:434048-1
The Plant List kew-2529615
Open Tree Of Life 6101564
NCBI Taxonomy 2704500
IUCN Red List 143722143
IPNI 434048-1
GBIF 3714155
EPPO PSXTE
Tropicos 100349322
KEW urn:lsid:ipni.org:names:429030-1
The Plant List kew-2408820
Observations.org 330540
IPNI 429030-1
GBIF 3714701
Elurikkus 401120

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)!
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Title Authors Publication Released IDs
New metabolites from Psorospermum tenuifolium☆ Giuliano Delle Monache, Franco Delle Monache, Rosella Di Benedetto, James U. Oguakwa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83889-3
Cytotoxic and antitumor activity of vismiones isolated from vismieae. Cassinelli G, Geroni C, Botta B, delle Monache G, delle Monache F J Nat Prod 01-Sep-1986
doi:10.1021/NP50047A031
PMID:3819736

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
> Benzenoids / Anthracenes
(10R)-10-[(9S)-2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-4,5-dihydroxy-7-methyl-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methyl-6-(3-methylbut-2-enoxy)-10H-anthracen-9-one 163189458 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)OCC=C(C)CCC=C(C)C)C=C(C=C3O)OCC=C(C)C 714.80 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
(10R)-3-[(2E)-3,7-dimethylocta-2,6-dienoxy]-10-[(9S)-2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-4,5-dihydroxy-7-methyl-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-6-methyl-10H-anthracen-9-one 11181897 Click to see 783.00 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
(10S)-1,3,8,10-tetrahydroxy-6-methyl-10-(3-methylbut-2-enyl)anthracen-9-one 162878048 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
(3R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3,8,9-trihydroxy-3-methyl-2,4-dihydroanthracen-1-one 162935401 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
(3R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8,9-tetrahydroxy-3-methyl-2,4-dihydroanthracen-1-one 163185227 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
[(2R)-5,10-dihydroxy-2-methyl-7-(3-methylbut-2-enoxy)-4-oxo-1,3-dihydroanthracen-2-yl] acetate 162989759 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
[(2R)-7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5,10-dihydroxy-2-methyl-4-oxo-1,3-dihydroanthracen-2-yl] acetate 132988924 Click to see CC(=CCCC(=CCOC1=CC(=C2C(=C1)C=C3CC(CC(=O)C3=C2O)(C)OC(=O)C)O)C)C 452.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
[5,10-Dihydroxy-2-methyl-7-(3-methylbut-2-enoxy)-4-oxo-1,3-dihydroanthracen-2-yl] acetate 85115140 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
1,3,8,10-Tetrahydroxy-6-methyl-10-(3-methylbut-2-enyl)anthracen-9-one 162878047 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
1,8-dihydroxy-3-methyl-6-(3-methylbut-2-enoxy)-10H-anthracen-9-one 162965892 Click to see 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
10-[2-(3,7-dimethylocta-2,6-dienoxy)-4,5-dihydroxy-7-methyl-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-3-methyl-6-(3-methylbut-2-enoxy)-10H-anthracen-9-one 162883252 Click to see 714.80 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
3-(3,7-dimethylocta-2,6-dienoxy)-1,8-dihydroxy-6-methyl-10H-anthracen-9-one 54536756 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
3-(3,7-dimethylocta-2,6-dienoxy)-10-[2-(3,7-dimethylocta-2,6-dienoxy)-4,5-dihydroxy-7-methyl-10-oxo-9H-anthracen-9-yl]-1,8-dihydroxy-6-methyl-10H-anthracen-9-one 437960 Click to see 783.00 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
6-(((2E)-3,7-Dimethyl-2,6-octadien-1-yl)oxy)-3,4-dihydro-3,8,9-trihydroxy-3-methyl-1(2H)-anthracenone 5281573 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
6-(3,7-Dimethylocta-2,6-dienoxy)-3,8,9-trihydroxy-3-methyl-2,4-dihydroanthracen-1-one 354179 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
6-Geranyloxy-3-methyl-1,8-dihydroxyanthrone 23661636 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)OCC=C(C)CCC=C(C)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
7-(3,7-Dimethylocta-2,6-dienyl)-3,6,8,9-tetrahydroxy-3-methyl-2,4-dihydroanthracen-1-one 72728327 Click to see CC(=CCCC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1O)O)O)C)C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Acetylvismione D 10456531 Click to see 452.50 unknown https://doi.org/10.1021/NP50047A031
https://doi.org/10.1016/S0031-9422(00)83889-3
Acetylvismione F 14186719 Click to see CC(=CCCC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)OC(=O)C)C=C2C=C1O)O)O)C)C 452.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
deacetylvismione H 13940837 Click to see CC(=CCOC1=CC(=C2C(=C1)C=C3CC(CC(=O)C3=C2O)(C)O)O)C 342.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Vismione C 14186716 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Vismione F 14186718 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Vismione G 44559576 Click to see 452.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-(7-hydroxy-3,7-dimethyloct-2-enoxy)-6-methylanthracene-9,10-dione 163032365 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCCC(C)(C)O 424.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
3-(3,7-Dimethylocta-2,6-dienyloxy)-1,8-dihydroxy-6-methyl-9,10-anthraquinone 333635 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC=C(C)C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
3-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)-1,8-dihydroxy-6-methylanthracene-9,10-dione 162889150 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC(C(C)(C)O)O 440.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
3-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-1,8-dihydroxy-6-methylanthracene-9,10-dione 163190047 Click to see 440.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Geranyloxyemodin 5785070 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Madagascine 378693 Click to see 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
2-Geranylemodin 129716111 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)O)C(=O)C=C(C)CCC=C(C)C)O 420.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
2-Isoprenylemodin 442750 Click to see 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S,6E,12E)-tetradeca-6,12-dien-8,10-diyn-3-ol 162956999 Click to see 202.29 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 162852664 Click to see CC1(CCC2(CCC3(C4CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 162852663 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
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/S0031-9422(00)83889-3
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(17-Acetyl-3,8,14,17-tetrahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl) pyridine-3-carboxylate 75049006 Click to see CC(=O)C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C5=CN=CC=C5)C)O)O 485.60 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[3-hydroxy-2-[3-(4-hydroxyphenyl)propanoyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxan-3-yl] acetate 11431848 Click to see 492.50 unknown https://doi.org/10.1016/S0031-9422(00)83889-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 163043573 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(00)83889-3

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