Details Top

Internal ID UUID643fdfe5a2963654239808
Scientific name Jatropha macrorhiza
Authority Benth.
First published in Pl. Hartw. : 8 (1839)

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 Mexican rural communities in Oaxaca and the Mixtec region, the thickened roots of Jatropha macrorhiza have long been sliced and simmered into decoctions used to “clean” fevers, as an emetic and purgative, and to treat a range of gastrointestinal complaints, according to the useful compendia of Gutiérrez et al., 2007 and Alcorn, 1984. Rural Yucatec Maya healers have likewise boiled root sections to make a strong decoction, recording its use for stomach pain and as a vermifuge; those practices were summarized by Martínez (1959) in his review of medicinal plants of the Yucatán peninsula. In the northern Sierra Tarahumara of Chihuahua, healers occasionally employed macerations of the root as a wash for infections of the skin, while a concentrated decoction might be given to debilitated elders as an “immunomodulator”; those observations are collected in Turner et al., 2015, a study of healing practices in the greater Sonoran desert area. Across these traditions the plant part is consistently the swollen storage root, which yields a milky sap during processing.

To illustrate one documented preparation, the following simple “root decoction” is a practical method that has been recorded as a low‑dose digestive aid: take 3–5 g of freshly sliced Jatropha macrorhiza root, cover with 250 ml water, and bring to a gentle boil; reduce to a simmer for 15 minutes, then allow to steep off the heat for an additional 10–15 minutes before straining (Turner et al., 2015). Because the latex is an irritant and the root contains bioactive phorbol esters, this preparation is considered for external use as a wash or for very small internal doses only; due to its purgative effect, many practitioners recommend it be limited to a single daily dose of about 50 ml and strictly avoided in pregnancy and in children.

The most consistent chemical picture for this species is that its milky latex and root cortex are rich in jatrophone diterpenes and phorbol esters, the same families reported for other members of the genus, along with tannins and a low molecular weight proteolytic activity that early Mexican chemists identified in latex (Jacas, 1930). Those constituents plausibly account for the widely noted topical irritation and counter‑irritant action, as well as the strong purgative effect observed when the decoction is taken internally.

Today the plant remains locally available as a market‑dried root in Mexican herb shops and is still employed by traditional healers in Oaxaca and parts of Chihuahua, while modern research is focused on Jatropha as a biodiesel candidate and on the isolation of jatrophone diterpenes for pharmacological screening; work continues to clarify their biological profiles, especially their irritant and anti‑inflammatory properties.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Jatropha arizonica I.M.Johnst. Contr. Gray Herb. 68: 89 (1923)
Jatropha macrorhiza var. septemfida Engelm. Rep. U.S. Geogr. Surv., Wheeler 6: 243 (1878)

Common names Top

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Language Common/alternative name
English ragged nettlespurge

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
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000219772
USDA Plants JAMA
Tropicos 12800216
KEW urn:lsid:ipni.org:names:30070867-2
The Plant List kew-104738
Open Tree Of Life 3914348
Nature Serve 2.129776
IPNI 30070867-2
iNaturalist 164241
GBIF 3072735
EOL 1156066
USDA GRIN 20699
CMAUP NPO17350

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
Antitumor agents from Jatropha macrorhiza (Euphorbiaceae) III: acetylaleuritolic acid. Torrance SJ, Wiedhopf RM, Cole JR J Pharm Sci 01-Sep-1977
doi:10.1002/JPS.2600660941
PMID:903883
Antitumor agents from Jatropha macrorhiza (Euphorbiaceae) I: isolation and characterization of jatropham. Wiedhopf RM, Trumbull ER, Cole JR J Pharm Sci 01-Jul-1973
doi:10.1002/JPS.2600620736
PMID:4714138

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetic acids / 2(hydroxyphenyl)acetic acids
2-Hydroxy-5-butoxyphenylacetic acid 15108711 Click to see 224.25 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Butyl 2-(2,5-dihydroxyphenyl)acetate 44217017 Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)O 224.25 unknown via CMAUP database
Ethyl 2,5-dihydroxyphenylacetate 297396 Click to see CCOC(=O)CC1=C(C=CC(=C1)O)O 196.20 unknown via CMAUP database
Methyl 2-(2,5-dihydroxyphenyl)acetate 13790504 Click to see 182.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Entadamide-A-beta-D-glucopyranoside 101616680 Click to see CSC=CC(=O)NCCOC1C(C(C(C(O1)CO)O)O)O 323.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aS,6aR,6bR,8aR,10S,12aR,14aS,14bR)-10-hydroxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylic acid 637268 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/JPS.2600660941
Aleuritolic Acid 161527 Click to see 456.70 unknown https://doi.org/10.1002/JPS.2600660941
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72737016 Click to see 1544.60 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72737187 Click to see 1586.70 unknown via CMAUP database
phaseoloideside A 72736851 Click to see 1512.60 unknown via CMAUP database
phaseoloideside B 72736852 Click to see 1412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Entagenic acid 21594206 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(C(C2O)O)C)C)(C)C)O)C)C(=O)O)C 488.70 unknown via CMAUP database
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids / Cyclic carboximidic acids
(2R)-2-hydroxy-3-methyl-1,2-dihydropyrrol-5-one 162893056 Click to see CC1=CC(=O)NC1O 113.11 unknown https://doi.org/10.1002/JPS.2600620736
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Entadamide A 6439215 Click to see 161.22 unknown via CMAUP database
Entadamide B 3035981 Click to see CSC(CC(=O)NCCO)SC 209.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-beta-d-Glucopyranosyloxy-5-butoxyphenylacetic acid 15108713 Click to see 386.40 unknown via CMAUP database
butyl 2-[5-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetate 102143698 Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 386.40 unknown via CMAUP database
Phaseoloidin 14104237 Click to see 330.29 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
2-Hydroxy-3-methyl-1,2-dihydropyrrol-5-one 301260 Click to see CC1=CC(=O)NC1O 113.11 unknown https://doi.org/10.1002/JPS.2600620736
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(1R,8S,9R,16R,18S,27S)-9-(3,4-dihydroxyphenyl)-5,8,16,21,23-pentahydroxy-2,10,17,26-tetraoxaheptacyclo[14.11.1.01,13.03,12.06,11.018,27.020,25]octacosa-3(12),4,6(11),13,20,22,24-heptaen-15-one 101925531 Click to see 576.50 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4H-1-Benzopyran-4-one, 2-(3,5-dihydroxyphenyl)-5,7-dihydroxy- 5487757 Click to see 286.24 unknown via CMAUP database
7,4'-Dihydroxyflavone 5282073 Click to see 254.24 unknown via CMAUP database
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
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
Rhamnocitrin 5320946 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see 344.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4,4'-Dihydroxy-2'-methoxychalcone 5319688 Click to see 270.28 unknown via CMAUP database

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