Prosopis cineraria
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
Suggest a correction!
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
Suggest a correction!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
Add a new one! Suggest a correction!| 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 |
Germination/Propagation Top
Suggest a correction or add new data!
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
Suggest others/fix!| 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.
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.
If you wish to see all the related articles click here.
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
You can also contribute to this by clicking here.
| 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |