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Internal ID UUID643fdd060e379681250373
Scientific name Cajanus trinervius
Authority (DC.) Maesen
First published in Agric. Univ. Wageningen Pap.85(4): 199 (1985 publ. 1986)

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.

Cajanus cajan (L.) Millsp. has been used in traditional medicine primarily as an aqueous decoction or tisane, with leaves being the dominant plant part. Across Southeast Asia, leaves are boiled to make a bitter drink believed to promote lactation in postpartum women and to support digestion. In parts of Sri Lanka, the same preparation is taken as a febrifuge, while in coastal India and coastal regions of Kenya and Tanzania, decoctions are used to treat dysentery and related digestive complaints (Mohan et al., 2014; Jayaweera, 1981–1982; Oduor et al., 2018). In coastal Ecuador, healers prepare a leaf infusion for “fiebre” and to “bajar el seguro” (reduce stubborn fevers), applying poultices of crushed leaves to head or joints (Bennett et al., 2021). These fluid preparations are commonly taken daily, while compresses are applied externally as needed.

To illustrate how practitioners often prepare the decoction: place 15–20 g of fresh leaves (or 3–5 g dried) in 500 mL water, bring to a boil, then simmer for 15–20 minutes; strain and cool before drinking one cup, 1–2 times daily for acute digestive or febrile complaints. Practitioners emphasize short-term use—generally a 5–7 day course—since long-term diuretic effects can be draining and may aggravate gastric sensitivity. Because pigeonpea is a member of Fabaceae, people with known legume (peanut) allergies should avoid internal preparations or take only under medical supervision; pregnant women generally limit this use to very small amounts and short durations (Alabi et al., 2020; Bennett et al., 2021).

Phytochemistry supports these uses: the leaves and young stems contain alkaloids (such as cajanin) and several flavonoids (apigenin, luteolin) along with moderate tannins, saponins, and phenolics that are plausibly antispasmodic, anti-inflammatory, and astringent (Oduor et al., 2018; Anantharaman & Shivakumar, 2021). Modern analytical work has also identified stilbenes and phenolic acids associated with antioxidant and antimicrobial activity, which may underlie the febrifuge and antidysenteric actions (Mohan et al., 2014). These compounds are well reported for C. cajan and provide a plausible mechanistic link to traditional decoction practice.

Today, research continues on the anti-inflammatory, antimicrobial, and gastroprotective activities of C. cajan extracts, particularly the phenolic-rich leaf preparations, and the plant is still used in household teas and poultices in rural Southeast Asia and East Africa (Alabi et al., 2020; Oduor et al., 2018).

General Uses Top

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**Common products:**
* Mature dry seeds (dried peas) are used as a culinary legume. These are hulled and may be split to produce "dal" (split peas).
* The seed is processed into flour.

**Food and beverages (non-medicinal):**
* Dried mature seeds are a significant food source, cooked and eaten whole or split (dal).
* Split dried seeds (dal) are cooked into curries, soups, stews, and dals, commonly consumed across South Asia, Southeast Asia, and parts of Africa and the Caribbean. Forms include yellow, red, or green dal depending on the variety and processing.
* Green immature seeds are consumed as a vegetable, similar to green peas, often cooked in curries or stir-fries.
* Mature seed flour is used as an ingredient in various food preparations, including traditional breads, batters, and as a gluten-free flour substitute in some regions. This is enabled by its starch (high amylose content in some varieties) and protein composition.

**Fragrance and cosmetics:**
* None documented beyond the food uses above.

**Sustainability and sourcing:**
* As a nitrogen-fixing legume used in intercropping systems (e.g., with cereals), it contributes to sustainable soil fertility management, reducing the need for synthetic nitrogen fertilizers.
* Its drought tolerance makes it a reliable protein source in rainfed agricultural systems.
* Sourcing primarily occurs through established agricultural supply chains for pulses and vegetables in its cultivation regions.

Synonyms Top

Scientific name Authority First published in
Atylosia candollei Wight & Arn. Prodr. Fl. Ind. Orient.1: 257 (1834)
Atylosia major Wight & Arn. Prodr. Fl. Ind. Orient.1: 257 (1834)
Atylosia trinervia (DC.) Gamble Fl. Madras: 368 (1918)
Atylosia trinervia var. major (Wight & Arn.) Gamble
Cantharospermum trinervium (DC.) Taub.
Collaea trinervia DC. Mém. Légum.: 247 (1826)
Odonia trinervia (DC.) Spreng. Syst. Veg. ed. 16, 4(2): 279 (1827)
Cantharospermum trineurum (DC.) Taub. H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam.3(3): 373 (1894)
Rhynchosia wightiana Graham Numer. List : n.° 5500 (1831)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000203791
Tropicos 13072606
KEW urn:lsid:ipni.org:names:942605-1
The Plant List ild-50111
Open Tree Of Life 3921338
IPNI 942605-1
GBIF 2960338
EOL 661621
USDA GRIN 470542
CMAUP NPO11558

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
An antibacterial biphenyl derivative and other constituents of Atylosia trinervia V.D. Tripathi, S.K. Agarwal, R.P. Rastogi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88751-8

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
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2-Methoxy-3-(3-methylbut-2-enyl)-5-phenylphenol 101324778 Click to see 268.30 unknown https://doi.org/10.1016/S0031-9422(00)88751-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E)-tetradec-5-en-1-ol 6431325 Click to see CCCCCCCCC=CCCCCO 212.37 unknown via CMAUP database
6-Tetradecen-1-ol, (E) 6431327 Click to see 212.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Trachelosperogenin A1, >=95% (LC/MS-ELSD) 21637743 Click to see 680.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,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]chrysen-9-ol 11876093 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/10.1016/S0031-9422(00)88751-8
(2R,3R,4R,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101673896 Click to see 680.80 unknown via CMAUP database
(5R,8R,9S,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 12309262 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown via CMAUP database
[(3R,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-yl] acetate 13688749 Click to see 470.80 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown via CMAUP database
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
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/10.1016/S0031-9422(00)88751-8
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)88751-8
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)88751-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3R,8R,9R,10S,13R,14R,17S)-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-ol 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)88751-8
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/10.1016/S0031-9422(00)88751-8
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol 441437 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R,4R)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 13831071 Click to see 746.60 unknown via CMAUP database
Benzoic acid, 3,4,5-trihydroxy-, (2R,2'R,3R,3'R,4R)-2-(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-5,5',7,7'-tetrahydroxy-2'-(3,4,5-trihydroxyphenyl)(4,8'-bi-2H-1-benzopyran)-3,3'-diyl ester 11622083 Click to see 898.70 unknown via CMAUP database
Epicatechin-(4beta->8)-epigallocatechin 3'-gallate 11513300 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
Procyanidin B3 3,3'-digallate 12795892 Click to see 882.70 unknown via CMAUP database
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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 / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 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
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see 824.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see 824.70 unknown via CMAUP database
Kaempferol 3-(2'',6''-di-(E)-p-coumarylglucoside) 10439991 Click to see 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Epi-castalagin 12302512 Click to see 934.60 unknown via CMAUP database
Castalagin 12302513 Click to see 934.60 unknown via CMAUP database

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