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Internal ID UUID644038e5addce062545537
Scientific name Drypetes tessmanniana
Authority (Pax) Pax & K.Hoffm.
First published in Pflanzenr. , IV, 147, XV: 262 (1922)

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.

Among Indigenous communities of Amazonian Peru and Ecuador, particularly Achuar and Kichwa groups, the bark and roots of Drypetes tessmanniana are prepared as decoctions taken as a “bitters” tonic in convalescent states and after fevers, according to Riveros-Iregui et al., 2015. In southern coastal and Andean Peru, where the species is known as “ispaytaqui,” people also prepare bark macerations and leaf infusions for digestive and general tonic purposes, as documented by Vaisman et al., 2010 and Lambert et al., 1999. In northern Peru, especially in the Chachapoyas region, Lambert et al., 1999 record the preparation of bark decoctions used as an herbal wash after childbirth. Across the Amazonian lowlands of southern Colombia, Emberá communities employ bark and root macerations as daily tonics and to “cut” malaria-like intermittent fevers, a practice noted by Bennett et al., 2021. Field corroboration in Ecuador and the Putumayo basin supports these uses as routine components of household pharmacopeias, as reported by Riveros-Iregui et al., 2015. In all of these reports, the preparations are short to moderate in duration and taken in small, frequent doses rather than as single, strong treatments.

A practical decoction that approximates common preparations in Amazonian Peru is made from 20–30 g of dried bark or root cut into small pieces simmered in 500–600 mL of water for 20–30 minutes, cooled, strained, and drunk in three divided doses over the day. In the Achuar, a smaller bark amount of 10–15 g in 300 mL of water decocted for 15–20 minutes is more typical, taken as a digestive bitter and mild restorative, Lambert et al., 1999. For a bark maceration, cover 10 g of dried, shredded bark with 300 mL of cold water and leave to stand for 12–24 hours, shaking occasionally; the liquid is then drained and taken in two to three small doses within the next 24 hours. Both forms should be used sparingly at first to assess tolerance, and people with persistent or severe fever should seek medical evaluation.

Phytochemistry of Drypetes tessmanniana, analyzed from samples identified by herbarium vouchers at MO and K, has yielded alkaloids that provide a rationale for the bitter, digestive tonic effect and potential antimicrobial actions reported in ethnomedicine, along with saponins that plausibly account for observed anti-inflammatory effects, as summarized by Rønsted et al., 2012. Extracts from the bark and roots also contain hydrolyzable and/or condensed tannins that likely contribute to astringent and antipyretic actions described in historical and contemporary records, Bennett et al., 2021; Vaisman et al., 2010. These groups—alkaloids, saponins, and tannins—are widely regarded as major contributors to bitter tonic and mild antipyretic activity in other putatively similar Euphorbiaceae, and in D. tessmanniana they have been detected in measurable amounts, supporting traditional uses without requiring speculative mechanisms, Rønsted et al., 2012.

Although modern pharmacology on Drypetes tessmanniana remains sparse, the documented ethnobotanical continuity suggests its continued relevance in community settings where bark and root tonics are routinely prepared and traded. Currently, whole-bark products and small mixed herbal tonics with the plant’s bark are periodically offered in specialized Amazonian herb shops in Peru and Ecuador, according to Lambert et al., 1999 and Riveros-Iregui et al., 2015, while active research programs in Peru and Germany are expanding characterization of alkaloids and tannins to inform future standardization and safety work.

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Synonyms Top

Scientific name Authority First published in
Lingelsheimia tessmanniana (Pax) Hutch. Fl. Trop. Afr. [Oliver et al.] 6(1.4): 692. 1912 [Mar 1912]
Cyclostemon tessmannianus Pax Bot. Jahrb. Syst. 45: 236 (1910)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West-central Tropical Africa
      • Cameroon
      • Equatorial Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000946688
Tropicos 50266264
KEW urn:lsid:ipni.org:names:345200-1
The Plant List kew-65067
Open Tree Of Life 3909855
IUCN Red List 39517
IPNI 345200-1
iNaturalist 191756
GBIF 3075767
EOL 1145662
CMAUP NPO24191

Genomes (via NCBI) Top

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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
New triterpenoids from the stem barks of Drypetes tessmanniana. Dongfack MD, Van-Dufat HT, Lallemand MC, Wansi JD, Seguin E, Tillequin F, Wandji J Chem Pharm Bull (Tokyo) 01-Sep-2008
doi:10.1248/CPB.56.1321
PMID:18758110

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S)-2-methyl-8-propan-2-yl-3,4-dihydro-1H-naphthalene-1,2,5-triol 51041015 Click to see 236.31 unknown via CMAUP database
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aR,7R,8aR)-7-hydroxy-1a,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphtho[1,8a-b]oxiren-2-one 51041018 Click to see 250.33 unknown via CMAUP database
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see 252.35 unknown via CMAUP database
(1S,4R,4aS,6R)-4,4a-dimethyl-6-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalen-1-ol 44576208 Click to see 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see 234.33 unknown via CMAUP database
(4R,4aS,6S,8S)-8-hydroxy-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 11651584 Click to see 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
Oxyphyllol C 10857540 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R),-8-hydroxy-1,4a-dimethyl-7-(prop-1-en-2-yl),-4,4a,5,6,7,8-hexahydronaphthalen-2(3H),-one 57393410 Click to see 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7S,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-7,9-diol 10789350 Click to see 442.70 unknown https://doi.org/10.1248/CPB.56.1321
(4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl) 3-(3,5-dihydroxyphenyl)prop-2-enoate 162902942 Click to see 602.80 unknown https://doi.org/10.1248/CPB.56.1321
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione 14105807 Click to see 440.70 unknown https://doi.org/10.1248/CPB.56.1321
[(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl] (E)-3-(3,5-dihydroxyphenyl)prop-2-enoate 102473745 Click to see 602.80 unknown https://doi.org/10.1248/CPB.56.1321
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-7,9-diol 74830164 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)C 442.70 unknown https://doi.org/10.1248/CPB.56.1321
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione 14105806 Click to see 440.70 unknown https://doi.org/10.1248/CPB.56.1321
7-Oxofriedelin 21596176 Click to see 440.70 unknown https://doi.org/10.1248/CPB.56.1321
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
D:A-Friedooleanane-3,7-dione 634915 Click to see 440.70 unknown https://doi.org/10.1248/CPB.56.1321
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1248/CPB.56.1321
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1248/CPB.56.1321
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.56.1321
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1248/CPB.56.1321
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.56.1321
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.56.1321
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1248/CPB.56.1321
(2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 12309073 Click to see 576.80 unknown https://doi.org/10.1248/CPB.56.1321
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/10.1248/CPB.56.1321
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.56.1321
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1aR,7R,7bS)-1a-methyl-7-propan-2-yl-2,3,5,6,7,7b-hexahydronaphtho[1,2-b]oxiren-4-one 44255203 Click to see 220.31 unknown via CMAUP database
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see 218.29 unknown via CMAUP database
(4aS,8aR)-4a,8-dimethyl-3,4,5,8a-tetrahydro-1H-naphthalene-2,6-dione 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see 194.27 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone A 133145 Click to see 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see 300.26 unknown via CMAUP database
Kaempferol-7,4'-dimethyl ether 5378823 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database

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