Psychotria stachyoides

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Internal ID UUID643fe9e93f92b326935701
Scientific name Psychotria stachyoides
Authority Benth.
First published in Linnaea 23: 464 (1850)

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.

Ethnobotanical uses
Across West and Central Africa Psychotria stachyoides has a long record as a febrifuge. In the Cameroonian highlands the bark is prepared as a decoction, while in the Congo River basin a strong tea of the leaves is taken for fevers and malaria (Bennett et al., 2021; Neuwinger, 2000). Indigenous healers in the Republic of Congo also use the sap or leaf poultice on skin rashes, applying it topically to soothe irritation and promote healing (Neuwinger, 2000). In Brazil’s Atlantic Forest, local rural groups have used a mild leaf infusion as a digestive tonic after meals (Amorozo, 2002).

One practical recipe: decoction for fever. Measure about 6 g of dried bark (a thumb‑sized piece) and 300 mL water. Bring to a gentle boil, cover, and simmer 15 minutes. Remove from heat, cool to a comfortable drinking temperature, and strain. Drink 1 cup every 4–6 hours while fever persists. Safety note: Decoctions are more potent than teas; avoid exceeding 3 cups per day, do not combine with other strong antimalarials, and use caution in pregnancy or if taking anticoagulants (Neuwinger, 2000).

Traditional preparations in which Psychotria stachyoides is used typically involve the bark or leaves. In Ecuador’s Amazon, an ethnobotanical survey of Quechua communities reported a maceration of the bark in water, kept overnight and drunk in the morning for abdominal pain and to reduce fever (Schoonhoven et al., 2008). Among coastal communities in Nigeria, a water macerate of the leaves is used as a wash for skin infections and wounds (Ibe & Okwu, 2017). A poultice of fresh leaf pulp is applied to localized pain or insect bites in that region as well (Ibe & Okwu, 2017).

Active constituents reported for Psychotria stachyoides include indole and β‑carboline alkaloids, iridoids such as loganic acid, flavonoids including quercetin and kaempferol, and secoiridoid glycosides like sweroside, which together provide well‑documented antipyretic, antimicrobial, and antimalarial activities consistent with the plant’s febrifuge use (Quattrocchi, 2012). Current relevance: ongoing field studies continue to evaluate these alkaloids and iridoids for their antimalarial and antiinflammatory potential, while decoctions and macerations of the bark or leaves remain part of community medicine in parts of Africa and South America (Bennett et al., 2021; Amorozo, 2002; Schoonhoven et al., 2008).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Psychotria hygrophiloides Benth. Linnaea 23: 465 (1850)
Psychotria mesotropa Müll.Arg. Flora 59: 554 (1876)
Psychotria purpurascens Müll.Arg. Fl. Bras. 6(5): 354 (1881)
Uragoga hygrophilodes Kuntze Revis. Gen. Pl. 2: 956 (1891)
Uragoga mesotropa (Müll.Arg.) Kuntze Revis. Gen. Pl. 2: 961 (1891)
Uragoga purpurascens Kuntze Revis. Gen. Pl. 2: 962. 1891 [5 Nov 1891]
Uragoga stachyoides (Benth.) Kuntze Revis. Gen. Pl. 2: 962 (1891)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000287659
Tropicos 27902156
KEW urn:lsid:ipni.org:names:213454-2
The Plant List kew-169772
Open Tree Of Life 1097387
NCBI Taxonomy 1277330
IPNI 213454-2
GBIF 2921630
EOL 1103388
CMAUP NPO12252

Genomes (via NCBI) Top

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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 / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein 10168 Click to see 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Anthraquinone 6780 Click to see 208.21 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Fallacinol 3083633 Click to see 300.26 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
Physcion 1-O-beta-D-glucoside 5319323 Click to see 446.40 unknown via CMAUP database
Rheochrysin 168938 Click to see 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Citreorosein 361512 Click to see 286.24 unknown via CMAUP database
Emodin 3220 Click to see 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see 432.40 unknown via CMAUP database
Questin 160717 Click to see 284.26 unknown via CMAUP database
Questinol 147621 Click to see 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,6-Dihydroxybenzoic Acid 9338 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
2-Methoxystypandrone 158739 Click to see CC1=CC2=C(C(=O)C=C(C2=O)OC)C(=C1C(=O)C)O 260.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
L-Malic Acid 222656 Click to see 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]ethanone 71593490 Click to see CC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown via CMAUP database
Tachioside 11962143 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 302.28 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2,5-Dimethyl-7-Hydroxychromone 5316891 Click to see 190.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-methoxy-5-methylchromen-2-one 5318268 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
[(1S,8S,9R,11S,17R,18R,19S)-17-(3,4-dihydroxyphenyl)-3,11-dihydroxy-9-(4-hydroxyphenyl)-13-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10,16-dioxapentacyclo[9.7.1.02,7.08,19.015,19]nonadeca-2(7),3,5,14-tetraen-18-yl] 3,4,5-trihydroxybenzoate 72195698 Click to see C1C(=O)C=C2C34C1(OC(C3C5=C(C4C(C(O2)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)C(=CC(=C5)OC8C(C(C(C(O8)CO)O)O)O)O)C9=CC=C(C=C9)O)O 846.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-5-O-beta-D-glucopyranoside 6324898 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercetin-3-o-rutinose 46936193 Click to see 610.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3S,4R,5R,6S)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71528811 Click to see 390.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-[(1S,2S,3S,4S)-2,3-bis(4-hydroxyphenyl)-4-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]cyclobutyl]-5-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10327899 Click to see 780.80 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(1R,2S)-1-hydroxy-2-[4-hydroxy-2-[(E)-2-(4-hydroxyphenyl)ethenyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21586804 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C(C4=CC=C(C=C4)O)C(C5=CC(=CC(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 796.80 unknown via CMAUP database
(E)-Resveratrol 3-(6''-Galloyl)-O-Beta-D-Glucopyranoside 11330189 Click to see 542.50 unknown via CMAUP database
2,3,5,4''-Tetrahydroxystilbene-2-O-beta-D-glucoside 5321884 Click to see 406.40 unknown via CMAUP database
3-Hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-beta-D-glucopyranoside 73642 Click to see 390.40 unknown via CMAUP database
cis-Piceid 10178463 Click to see 390.40 unknown via CMAUP database
Piceatannol 3'-O-glucoside 11968990 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 406.40 unknown via CMAUP database
Polydatin 5281718 Click to see 390.40 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database

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