Details Top

Internal ID UUID643fd954db677747910832
Scientific name Prosopis cineraria
Authority (L.) Druce
First published in Rep. Bot. Exch. Club Soc. Brit. Isles3: 422 (1913 publ. 1914)

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.

Prosopis cineraria enjoys wide recognition in arid-zone communities for several internal and topical preparations. In the Indian Aravalli Range, villagers prepare a mild bark decoction as a fever reducer and for stomach upset (Mertia et al., 2003). In Oman and southern Pakistan, healers have recorded aqueous bark infusions and decoctions for sore throat and cough, and a weak leaf infusion taken as a carminative (Batanouny et al., 1999). Among rural herbalists in the Syrian steppe, fresh leaf poultices are applied to swollen joints and old wounds, while a bark and leaf decoction is used for dysentery (Zohary, 1966). In the Arava Valley of Israel and Jordan, traditional practitioners mention a weak leaf tea taken for colds and as a digestive tonic (Orshan, 1986).

For preparation, a simple internal bark decoction begins by boiling 5–10 g of chopped dried Prosopis cineraria bark in 250–300 mL of water for 10–15 minutes, cooling, and straining; 150–200 mL is consumed warm once daily for 2–3 days. Use fresh, unblemished bark and avoid large or prolonged doses. The plant’s seed and pod oils contain linoleic acid and typical tocopherols (Duke, 1981; Gül et al., 2008), while its bark and wood include relatively high levels of flavonoids and condensed tannins (Haridas et al., 1985; Batanouny et al., 1999), consistent with the reported astringent and fever-reducing uses. This species remains a staple of desert agriculture and continues to appear in small-scale ethnomedicine, with interest in its extractives but no widely used commercial preparations (Duke, 1981; Gül et al., 2008; Haridas et al., 1985).

General Uses Top

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Common products:
The tree yields firewood and high-quality charcoal. Locally, the mature seed pods are processed as livestock fodder.

Industrial and craft applications:
Wood produces durable charcoal valued for consistent heat output. The heartwood is extremely hard and dense, suitable for small wooden implements and construction where wear resistance is required.

Food and beverages (non-medicinal):
Dried, mature seed pods (a characteristic Pods of Prosopis species) are ground into a coarse flour used as animal feed, particularly for camels and goats in arid regions where other fodder is scarce. This processing typically involves manual threshing and milling.

Colorants and tanning:
Tannins are present in the bark but there are no verified reports of their industrial use for leather tanning or dye production for Prosopis cineraria.

Wood and fiber:
The heartwood is hard, heavy, and durable. Specific documented uses include small construction timbers, posts, poles, and tool handles where durability and resistance to abrasion are critical. Fiber extracted from inner bark (bast fiber) has not been documented as an industrial textile fiber for this species.

Fragrance and cosmetics:
There are no documented uses of this plant's parts (such as flowers, leaves, or resins) in the fragrance or cosmetics industry.

Properties relevant to use:
* **Heartwood:** Extremely high density and hardness, providing dimensional stability and durability suitable for structural/timber applications where constant stress or abrasion occurs.
* **Seed Pod Flour:** High carbohydrate and protein content makes it a valuable livestock fodder source.
* **Wood:** Suitable for charcoal production due to its density and low moisture content when dry.

Standards and regulation:
Charcoal production and trade follow general regulations for biofuels and soil amendment (often as biochar) applicable in local/national markets. Wood used in construction adheres to national building codes specifying minimum structural properties (strength classes, durability classes).

Sustainability and sourcing:
* **Natural Habitat:** The tree is integral to the fragile arid agroforestry systems of the Thar Desert (India/Pakistan). Its slow growth rate necessitates responsible harvesting for timber and fodder.
* **Fodder:** Pod collection is a traditional practice; however, sustainable collection levels must balance livestock needs with natural regeneration to maintain ecosystem stability.
* **Timber/Charcoal:** Harvesting must be carefully managed to prevent over-exploitation. Its value in desert reclamation and soil stabilization provides an ecological counterbalance to resource extraction pressures.

Synonyms Top

Scientific name Authority First published in
Prosopis spicigera L. Mant. Pl.: 68 (1767)
Mimosa cineraria L. Syst. Nat. ed. 10, 2: 1311 (1759)
Adenanthera aculeata Roxb. Hort. Bengal. 90; Fl. Ind. ii. 37.
Prosopis aculeata J.Koenig ex Roxb. Asiat. Res.4: 405 (1795)
Acacia cineraria (L.) Willd. Sp. Pl., ed. 4, 4: 1057 (1806)
Prosopis spicata Burm.f. Fl. Indica: 102 (1768)
Mimosa cinerea L. Sp. Pl.: 517 (1753)
Adenanthera aculeata (J.Koenig ex Roxb.) W.Hunter Asiat. Res.6: 66 (1799)
Prosopis spicata Burm.
Mimosa cineraria L. Sp. Pl. : 517 (1753)

Common names Top

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Language Common/alternative name
English ghaf
English jand
Arabic غاف رمادي
Bengali শমী
Persian پرسپیس سینراریا
Gujarati ખીજડો
Gujarati શમી
Gujarati શમડી
Hebrew ינבוט מאפיר
Hindi खेजड़ी
Hindi मींझर
Hindi शमी
Italian ghaf
Kannada ಬನ್ನಿ
Malayalam വന്നി
Marathi शमी
Oriya ଶମୀ
Punjabi ਜੰਡ
Punjab جنڈ
sd ڪنڊي
Tamil வன்னி மரம்
Tamil வன்னி
Telugu జమ్మి చెట్టు
Telugu జమ్మిచెట్టు
Chinese 波斯牧豆樹

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185047
UNII 83X60L8I3S
USDA Plants PRCI4
Tropicos 13046207
KEW urn:lsid:ipni.org:names:515801-1
The Plant List ild-31185
Open Tree Of Life 847862
NCBI Taxonomy 364024
IPNI 515802-1
iNaturalist 131133
GBIF 5358521
Freebase /m/068_b6
EOL 643218
USDA GRIN 29749
Wikipedia Prosopis_cineraria
CMAUP NPO27221
PFAF Prosopis cineraria

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_029017545.1 ASM2901754v1 Scaffold UAE University 2023-03-06 213 659.36 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
An Alarming Decline in the Nutritional Quality of Foods: The Biggest Challenge for Future Generations’ Health Bhardwaj RL, Parashar A, Parewa HP, Vyas L Foods 14-Mar-2024
PMCID:PMC10969708
doi:10.3390/foods13060877
PMID:38540869
Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW Plants (Basel) 14-Mar-2024
PMCID:PMC10974405
doi:10.3390/plants13060832
PMID:38592859
Use of Medicinal Plants in the Process of Wound Healing: A Literature Review Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL Pharmaceuticals (Basel) 27-Feb-2024
PMCID:PMC10975678
doi:10.3390/ph17030303
PMID:38543089
Biocontrol potential of endophytic Pseudomonas strain IALR1619 against two Pythium species in cucumber and hydroponic lettuce Amaradasa BS, Mei C, He Y, Chretien RL, Doss M, Durham T, Lowman S PLoS One 26-Feb-2024
PMCID:PMC10896519
doi:10.1371/journal.pone.0298514
PMID:38408078
Incorporation of Prosopis cineraria Extract Improved the Mechanical, Barrier and Antioxidant Properties but Not the Antibacterial Activity of Tigertooth croaker Fish Scale Gelatin Film Kord Z, Taheri A, Ghaffari M, Sharifian S Foods 09-Feb-2024
PMCID:PMC10887683
doi:10.3390/foods13040538
PMID:38397514
Plant–soil feedback and plant invasion: effect of soil conditioning on native and invasive Prosopis species using the plant functional trait approach Ali HE, Al-Wahaibi AM, Shahid MS Front Plant Sci 16-Jan-2024
PMCID:PMC10824832
doi:10.3389/fpls.2024.1321950
PMID:38292912
Synergistic antibacterial mechanism of silver-copper bimetallic nanoparticles Hao Z, Wang M, Cheng L, Si M, Feng Z, Feng Z Front Bioeng Biotechnol 08-Jan-2024
PMCID:PMC10800703
doi:10.3389/fbioe.2023.1337543
PMID:38260749
Extracellular Self- and Non-Self DNA Involved in Damage Recognition in the Mistletoe Parasitism of Mesquite Trees López-García CM, Ávila-Hernández CA, Quintana-Rodríguez E, Aguilar-Hernández V, Lozoya-Pérez NE, Rojas-Raya MA, Molina-Torres J, Araujo-León JA, Brito-Argáez L, González-Sánchez AA, Ramírez-Chávez E, Orona-Tamayo D Int J Mol Sci 29-Dec-2023
PMCID:PMC10778891
doi:10.3390/ijms25010457
PMID:38203628
Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula Alrajhi K, Bibi S, Abu-Dieyeh M Saudi J Biol Sci 25-Dec-2023
PMCID:PMC10805673
doi:10.1016/j.sjbs.2023.103911
PMID:38268781
Insects, Plants, and Microorganisms from Dry Lands as Novel Sources of Proteins and Peptides for Human Consumption Ramírez-Guzmán N, Torres-León C, Aguillón-Gutiérrez D, Aguirre-Joya JA Foods 27-Nov-2023
PMCID:PMC10706450
doi:10.3390/foods12234284
PMID:38231705
Assembly, annotation and analysis of the chloroplast genome of the Algarrobo tree Neltuma pallida (subfamily: Caesalpinioideae) Caycho E, La Torre R, Orjeda G BMC Plant Biol 16-Nov-2023
PMCID:PMC10652460
doi:10.1186/s12870-023-04581-5
PMID:37974117
Heavy metals mitigation and growth promoting effect of endophytic Agrococcus terreus (MW 979614) in maize plants under zinc and nickel contaminated soil Shahzad A, Siddique A, Ferdous S, Amin MA, Qin M, Aslam U, Naeem M, Bashir T, Shakoor A Front Microbiol 09-Nov-2023
PMCID:PMC10668838
doi:10.3389/fmicb.2023.1255921
PMID:38029198
The Impact of Urbanization on Tree Growth and Xylem Anatomical Characteristics Gao X, Zhao B, Chen Z, Song W, Li Z, Wang X Biology (Basel) 27-Oct-2023
PMCID:PMC10669791
doi:10.3390/biology12111373
PMID:37997972
Aureobasidium pullulans Treatment Mitigates Drought Stress in Abies koreana via Rhizosphere Microbiome Modulation Mannaa M, Han G, Jung H, Park J, Kim JC, Park AR, Seo YS Plants (Basel) 23-Oct-2023
PMCID:PMC10610362
doi:10.3390/plants12203653
PMID:37896116
The complete chloroplast genome of Cicer reticulatum and comparative analysis against relative Cicer species Mehmetoğlu E, Kaymaz Y, Ateş D, Kahraman A, Tanyolaç MB Sci Rep 19-Oct-2023
PMCID:PMC10587350
doi:10.1038/s41598-023-44599-1
PMID:37857674

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1021/NP50018A003
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
12-(5-Hydroxy-6-methylpiperidin-2-yl)dodecanoic acid 85832317 Click to see CC1C(CCC(N1)CCCCCCCCCCCC(=O)O)O 313.50 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
12-[(2R,5S,6S)-5-hydroxy-6-methylpiperidin-2-yl]dodecanoic acid 101680810 Click to see 313.50 unknown https://doi.org/10.1016/0031-9422(80)83112-8
12-[(2S,5R,6S)-5-hydroxy-6-methylpiperidin-2-yl]dodecanoic acid 162878983 Click to see 313.50 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-14-oxo-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 102480386 Click to see 780.90 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6bR,8aR,10S,12aR,14bS)-2,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate 21625902 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)O 751.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,4S,5R,8R,10S,13R,14R,17R,18R)-10-hydroxy-5,9,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 102480384 Click to see 442.70 unknown via CMAUP database
(1S,2R,4S,4aS,6aR,6aR,6bR,8aR,12aR,14bS)-4-hydroxy-1,2,6b,9,9,12a-hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 102480385 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C(=O)O)C(=O)O)O 500.70 unknown via CMAUP database
Quinovic acid 120678 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)89105-0
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 / Alcohols and polyols / Cyclic alcohols and derivatives
(4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 12314810 Click to see 442.70 unknown via CMAUP database
3beta-Hydroxy-27-norolean-13-en-28-oic acid ethyl ester 101682287 Click to see CCOC(=O)C12CCC3=C(C1CC(CC2)(C)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C 470.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid 7067333 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
Mitraphylline 94160 Click to see 368.40 unknown via CMAUP database
Uncarine A 188999 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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 https://doi.org/10.1021/NP50018A003
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin 5281678 Click to see 332.26 unknown https://doi.org/10.1021/NP50018A003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one 5318763 Click to see 432.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercetin-3-O-rhamnoside 15939939 Click to see 448.40 unknown via CMAUP database
Quercetin-3-o-rutinose 46936193 Click to see 610.50 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
Neohesperidin 442439 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O 610.60 unknown via CMAUP database
Patulitrin 5320435 Click to see 494.40 unknown https://doi.org/10.1021/NP50018A003
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
4H-1-Benzopyran-4-one, 6,7-dihydroxy-2-(3,4,5-trimethoxyphenyl)- 5488683 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=CC(=C(C=C3O2)O)O 344.30 unknown https://doi.org/10.1021/NP50018A003
https://doi.org/10.1016/S0031-9422(00)89105-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Prosogerin A 44257586 Click to see 312.27 unknown https://doi.org/10.1016/0031-9422(79)80104-1
Prosogerin D 44257587 Click to see 358.30 unknown https://doi.org/10.1016/0031-9422(80)83112-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Prosogerin B 42607554 Click to see COC1=C(C=C(C(=C1)C(=O)C=CC2=CC3=C(C=C2)OCO3)O)O 314.29 unknown https://doi.org/10.1016/0031-9422(79)80104-1

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