Details Top

Internal ID UUID644002331d0ea353485051
Scientific name Pedalium murex
Authority L.
First published in Syst. Nat. ed. 10 , 2: 1123 (1759)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Fresh leaves, harvested before flowering, are marketed as a leafy vegetable in local markets and are also exported as dried greens.
- Seed mucilage, extracted from mature seeds, is commercialized as a natural thickener, stabilizer, and binding agent.

Food and beverages (non-medicinal):
- Young leaves are cooked as a vegetable or added raw to salads, providing a neutral flavor, moderate protein (~15 % dry‑matter), and dietary fiber.
- The seed mucilage, when hydrated, forms a viscous gel used to thicken soups, sauces, bakery batters, and can be milled into a gluten‑free flour substitute.

Industrial and craft applications:
- The polysaccharide‑rich mucilage functions as a natural binder in the paper‑making process, improving pulp cohesion and reducing synthetic adhesive requirements.
- It is employed as a coating or sizing agent for textiles, imparting water‑retention and improving finish without altering handfeel.
- The material’s adhesive properties have been evaluated for eco‑friendly paper‑based packaging and as a binder in natural‑fiber composites; its viscosity can be tuned by pH adjustment, making it suitable for paint and ink formulations.

Properties relevant to use:
- Mucilage consists mainly of neutral polysaccharides (arabinose, galactose, rhamnose) with high molecular weight, giving strong water‑binding capacity and shear‑thinning rheology; 1–3 % (w/v) solutions typically exhibit viscosities of 200–800 cP at 25 °C.
- Leaves contain approximately 15 % protein on a dry‑matter basis, moderate fiber, and low levels of anti‑nutrients, facilitating direct culinary use.
- The mucilage’s gel strength and film‑forming ability are comparable to those of other plant hydrocolloids, enabling its use as a binder, thickener, or stabilizer.

Sustainability and sourcing:
- Pedalium murex is a drought‑tolerant herb native to semi‑arid regions of East Africa; it can be cultivated on marginal soils with minimal irrigation and incorporated into crop rotations with cereals.
- Harvesting of leaves and seed collection does not require land clearing; the plant regrows rapidly after cutting, supporting sustainable collection and providing an alternative income source for smallholder farmers.

Synonyms Top

Scientific name Authority First published in
Murex burmanni Kuntze Revis. Gen. Pl. 2: 481 (1891)
Pedalium muricatum Salisb. Prodr. Stirp. Chap. Allerton : 104 (1796)
Pedalium microcarpum Decne. Ann. Sci. Nat., Bot. , sér. 5, 3: 332 (1865)
Rogeria microcarpa Klotzsch Naturw. Reise Mossambique 6(1): 190 (1861)

Common names Top

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Language Common/alternative name
English common pedalium
English large caltrops
Bengali বিলাতি গোখুর
Hindi बड़ा गोखरू
Malayalam വലിയ ഞെരിഞ്ഞിൽ
Tamil ஆனை நெருஞ்சில்
Tamil பெரு நெருஞ்சில்

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Eritrea
      • Socotra
      • Somalia
      • Sudan
    • South Tropical Africa
      • Mozambique
    • West Tropical Africa
      • Benin
      • Ghana
      • Ivory Coast
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Central African Republic
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Myanmar
      • Vietnam
    • Malesia
      • Jawa

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000482113
UNII R1LMM9CVCD
Tropicos 24300021
INPN 807459
KEW urn:lsid:ipni.org:names:675880-1
The Plant List kew-2562876
Open Tree Of Life 857314
NCBI Taxonomy 642575
IPNI 675880-1
iNaturalist 355383
GBIF 5527253
EPPO PDUMU
EOL 2881659
USDA GRIN 431293

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Efficacy and safety of the Ayurvedic herbal preparation Maharishi Amrit Kalash: a systematic review of randomized controlled trials Koch AK, Patel M, Gupta S, Wullenkord R, Jeitler M, Kessler CS Front Med (Lausanne) 16-Apr-2024
PMCID:PMC11058942
doi:10.3389/fmed.2024.1325037
PMID:38690176
Unveiling the antibacterial and antifungal potential of biosynthesized silver nanoparticles from Chromolaena odorata leaves Bishoyi AK, Sahoo CR, Samal P, Mishra NP, Jali BR, Khan MS, Padhy RN Sci Rep 29-Mar-2024
PMCID:PMC10980689
doi:10.1038/s41598-024-57972-5
PMID:38553574
Biosynthesis and assessment of antibacterial and antioxidant activities of silver nanoparticles utilizing Cassia occidentalis L. seed Arya A, Tyagi PK, Bhatnagar S, Bachheti RK, Bachheti A, Ghorbanpour M Sci Rep 27-Mar-2024
PMCID:PMC10973378
doi:10.1038/s41598-024-57823-3
PMID:38538702
Formulation of Mentha piperita-Based Nanobiopesticides and Assessment of the Pesticidal and Antimicrobial Potential Jahan N, Hussain N, Touqeer SI, KU, Shamshad H, Abbas N Life (Basel) 19-Jan-2024
PMCID:PMC10817515
doi:10.3390/life14010144
PMID:38276273
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Green Synthesis of Silver Nanoparticles Using Jacobaea maritima and the Evaluation of Their Antibacterial and Anticancer Activities Althubiti AA, Alsudir SA, Alfahad AJ, Alshehri AA, Bakr AA, Alamer AA, Alrasheed RH, Tawfik EA Int J Mol Sci 20-Nov-2023
PMCID:PMC10671674
doi:10.3390/ijms242216512
PMID:38003704
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532
Bovine reproductive immunoinfertility: pathogenesis and immunotherapy Gupta VK, Mohanty TK, Bhakat M, Dewry RK, Katiyar R, Nain D, Shah N, Sethi M, Rautela R, Singh M, Deori S Front Vet Sci 05-Oct-2023
PMCID:PMC10585041
doi:10.3389/fvets.2023.1248604
PMID:37869494
Antioxidant activities of thermally treated Sesamum indicum L. leaf extracts and their inhibitory effects against growth and metastatic properties of human colon cancer cells Kim S, Lee HJ, Ju J Food Sci Biotechnol 23-Sep-2023
PMCID:PMC10541370
doi:10.1007/s10068-023-01408-9
PMID:37781062
Acute and Repeated Dose 28-Day Oral Toxicity Study of the Aqueous Extracts from the Leafy Stem and Fruit of Pedalium murex D.Royen EX.L in Wistar Rats Dossou-Agoin GB, Sangaré-Oumar MM, Sacramento TI, Sindété M, Hougbénou-Houngla EJ, Tossavi ND, Azonbakin S, Gbankoto A J Toxicol 21-Jul-2023
PMCID:PMC10382242
doi:10.1155/2023/2962905
PMID:37520119
Phytochemical-Mediated Biosynthesis of Silver Nanoparticles from Strobilanthes glutinosus: Exploring Biological Applications Javed R, Ijaz S, Hameed H, Nazish M, Sharif MS, Afreen A, Alarjani KM, Elshikh MS, Mehboob S, Abdul Razak S, Waheed A, Ahmed R, Tariq M Micromachines (Basel) 04-Jul-2023
PMCID:PMC10386440
doi:10.3390/mi14071372
PMID:37512683
Facile synthesis of efficient Co3O4 nanostructures using the milky sap of Calotropis procera for oxygen evolution reactions and supercapacitor applications Bhatti AL, Tahira A, Kumar S, Ujjan ZA, Bhatti MA, Kumar S, Aftab U, Karsy A, Nafady A, Infantes-Molina A, Ibupoto ZH RSC Adv 16-Jun-2023
PMCID:PMC10273030
doi:10.1039/d3ra02555a
PMID:37333727
Biogenic Fabrication of Silver Nanoparticles Using Calotropis procera Flower Extract with Enhanced Biomimetics Attributes Nagime PV, Singh S, Shaikh NM, Gomare KS, Chitme H, Abdel-Wahab BA, Alqahtany YS, Khateeb MM, Habeeb MS, Bakir MB Materials (Basel) 30-May-2023
PMCID:PMC10254777
doi:10.3390/ma16114058
PMID:37297192
Comparative assessment of green and chemically synthesized glutathione capped silver nanoparticles for antioxidant, mosquito larvicidal and eco-toxicological activities Yadav R, Preet S Sci Rep 19-May-2023
PMCID:PMC10198023
doi:10.1038/s41598-023-35249-7
PMID:37208391
A combined approach of DNA metabarcoding collectively enhances the detection efficiency of medicinal plants in single and polyherbal formulations Travadi T, Shah AP, Pandit R, Sharma S, Joshi C, Joshi M Front Plant Sci 15-May-2023
PMCID:PMC10225634
doi:10.3389/fpls.2023.1169984
PMID:37255553

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 / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/0031-9422(83)85033-X
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1016/0031-9422(92)83667-N
Pentatriacontane 12413 Click to see 492.90 unknown https://doi.org/10.1016/0031-9422(83)85033-X
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1016/0031-9422(92)83667-N
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Tetratriacontanyl octacosanoate 129664425 Click to see 901.60 unknown https://doi.org/10.1016/0031-9422(83)85033-X
Triacontyl dotriacontanoate 85667894 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 901.60 unknown https://doi.org/10.1016/0031-9422(92)83667-N
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hentriacontanoic acid 37982 Click to see 466.80 unknown https://doi.org/10.1016/0031-9422(83)85033-X
Hexatriacontanoic acid 5282596 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 537.00 unknown https://doi.org/10.1016/0031-9422(83)85033-X
Triacontanoic acid 10471 Click to see 452.80 unknown https://doi.org/10.1016/0031-9422(92)83667-N
Tritriacontanoic acid 181572 Click to see 494.90 unknown https://doi.org/10.1016/0031-9422(92)83667-N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(83)85033-X
(4aS,6aR,6aR,6bR,7R,8aR,10S,12aS,14bS)-7,10-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-carboxylic acid 101297651 Click to see CC1(CCC2(CCC3(C(=CCC4C3(C(CC5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/0031-9422(92)83667-N
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(83)85033-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)85033-X
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/10.1016/0031-9422(83)85033-X
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/10.1016/0031-9422(92)83667-N
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 https://doi.org/10.1016/0031-9422(92)83667-N
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)85033-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Heptatriacontan-4-one 123635263 Click to see 535.00 unknown https://doi.org/10.1016/0031-9422(83)85033-X
> 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/10.1016/0031-9422(92)83667-N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 17981428 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
DiosMetin 7-O-beta-D-Glucuronide 74977725 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
DiosMetin 7-O-beta-D-Glucuronide 54462250 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
Hispidulin 7-glucuronide 5318059 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
Nepetin 5317284 Click to see 316.26 unknown https://doi.org/10.1016/S0031-9422(00)90057-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Isoetin 5,7-dimethyl ether 44258304 Click to see 330.29 unknown https://doi.org/10.1016/0031-9422(92)83667-N

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