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Abstract

A large proportion of the world’s population, especially in developing countries, relies on traditional systems of medicine. Humans have learned to seek therapy from the bark, leaves, fruits, flowers, and other parts of plants as a result of many years of struggle against illnesses. Gliricidia sepium (Jacq.) Kunth ex Walp. is one of the most important medicinal plants in pharmacognosy and medical fields because it serves as a reservoir of potent bioactive compounds. These include saponins, flavonoids, volatile oils, and other phytochemical constituents extracted from various parts of the plant. Gliricidia sepium shows numerous traditional applications, including the treatment of coughs, asthma, urticaria, skin rashes, burns, scabies, and dermatitis. It also acts as an antipruritic agent on the skin and is used in treating bacterial and protozoal infections. Over time, many medicinal properties of Gliricidia sepium have been reported, such as cytotoxic, antimicrobial, antibacterial, anti-inflammatory, antioxidant, thrombolytic, anti-sickling, wound healing, mosquitocidal, and anthelmintic activities.

Keywords

Gliricidia sepium, Phytochemical constituents, biological activities, Therapeutic uses.

Introduction

Medicinal plants have a long history of use, and their utilization is widespread in both developing and developed countries. According to reports of the World Health Organization (WHO), about 80% of the world’s population relies mainly on traditional therapies that involve the use of plant extracts or their active substances [1]. India is a country rich in natural resources and possesses a wide variety of medicinal plants.

In contrast to synthetic drugs, herbal drugs offer several advantages such as lower toxicity, better compatibility with the biological system, and affordability for all classes of people. In recent decades, herbs and medicinal plants have been extensively used as sources of therapeutic compounds in traditional medicinal systems. Medicinal plants play an important role not only in traditional health-care systems but also in international herbal and pharmaceutical markets. The most important bioactive constituents of plants include alkaloids, tannins, flavonoids, and phenolic compounds, which produce definite physiological actions on the human body.

Gliricidia sepium (Jacq.) Kunth ex Walp. is a multipurpose legume plant belonging to the family Fabaceae, which is a commercially and medicinally important family of flowering plants recognized by its fruit (legume). The Fabaceae family contains more than 700 genera and approximately 20,000 species, making it the third largest plant family after Orchidaceae and Asteraceae [2].

Gliricidia sepium (Leguminosae family) is a medium-sized tree introduced into India from the American continent. In Mexico, this tree is used as a shade plant for cocoa and coffee plantations and is therefore known as “Madrecacao” (mother of cocoa). It is also used as a hedge plant, and its flowers are consumed as food in some regions of Mexico [3].

In Panama, leaf decoctions of Gliricidia sepium are used to treat urticaria, skin rashes, burns, and erysipelas [4]. In Guatemala and Costa Rica, bark decoctions are used against bacterial and protozoal infections [5]. The branches of Gliricidia sepium are used to reduce fever in both children and adults. It has also been reported to treat infections caused by Microsporum canis, Trichophyton mentagrophytes, and Neisseria gonorrhoeae [6]. Sharma and Qadry investigated the larvicidal activity of Gliricidia sepium.

The larvicidal activity of the crude ethanol extract of Gliricidia sepium bark and leaves has also been reported [7]. Various phytochemicals such as flavonoids [8], triterpenoids, saponins [9], stigmasterol glucoside [10], rhamnogalactoside of kaempferol [11], coumarin, coumaric acid, and melilotic acid [12] have been isolated and characterized from different parts of this plant.

Allelochemicals present in the leaves of Gliricidia sepium were extracted, identified, and quantified using High Performance Liquid Chromatography (HPLC) [13].

2. RATIONALE OF WORK

2.1 Aim

To explore the potential medicinal properties, ecological benefits, and practical uses of Gliricidia sepium, a herbal plant. The study also focuses on the phytochemical constituents present in various parts of Gliricidia sepium.

2.2 Objectives

To evaluate and summarize existing literature on the medicinal uses, potential health benefits, and reported therapeutic properties of Gliricidia sepium.

Phytochemical Composition: To examine the chemical constituents of Gliricidia sepium and identify bioactive compounds contributing to its medicinal value.

Traditional Knowledge: To explore traditional uses and indigenous knowledge associated with Gliricidia sepium, providing insight into cultural practices and historical applications.

Future Research Directions: To propose areas for future research to bridge gaps in understanding and unlock the full potential of Gliricidia sepium in various domains.

3. GEOGRAPHICAL SOURCE [14]

Gliricidia sepium is native to tropical dry forests of Mexico and Central America. In addition to its native range, it is cultivated in many tropical and subtropical regions, including the Caribbean, northern parts of South America, Central Africa, parts of India, Sri Lanka, Myanmar, and Southeast Asia.

4. DESCRIPTION OF PLANT

Leaves

The alternate, pinnate leaves are 15–30 cm (6–12 in) long and show silky pubescence when young. There are 7–17 leaflet pairs and a terminal leaflet. The leaflets are elliptical to lanceolate, 3–6 cm (1.2–2.4 in) long and 1.5–3 cm (0.6–1.2 in) wide, short- to long-pointed at the tip and rounded to short-pointed at the base.

Stem

The plant may have a single or multiple stems with trunk diameters reaching up to 30 cm. The bark is grayish-brown to whitish and may be deeply furrowed in older trees. Leaves are pinnately compound, alternate in arrangement, and 20–30 cm long.     

4.1 Traditional Uses

Herbal medicine has long been used in ancient societies and civilizations. Gliricidia sepium is one such plant with several folkloric uses.

In Saint Lucia, leaves are brewed as tea to treat coughs and asthma and are also used for skin infections.

In Mexico, crushed fresh leaves are used as a poultice.

In Panama, a leaf decoction is used to treat urticaria, rashes, and burns.

In the Philippines, leaf juice or decoctions and bark decoctions are used for scabies, dermatitis, and as antipruritic agents; fresh leaves are applied as insect repellents.

In Guatemala and Costa Rica, bark decoctions are used to treat bacterial and protozoal infections.

4.2 Phytochemical Constituents

Various essential phytochemical constituents isolated from Gliricidia sepium include saponins, flavonoids, volatile oils, and other miscellaneous compounds.

a) Saponins

Three saponins were isolated from the fruits:

  • Hederagenin-3-O-(4-O-acetyl-β-D-xylopyranosyl)-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside
  • Hederagenin-3-O-(3,4-di-O-acetyl-β-D-xylopyranosyl)-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside
  • Hederagenin-3-O-(3,4-di-O-acetyl-α-L-arabinopyranosyl)-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside

The heartwood of the stem yielded stigmasterol glucoside, identified using IR, ¹H-NMR, and ¹³C-NMR techniques.

From the leaves and roots, two triterpene saponins (gliricidoside A and B) were isolated. Their structures were elucidated using 1D and 2D NMR techniques.

b) Flavonoids

The insecticidal dichloromethane extract of Gliricidia sepium heartwood contained:

  • Isoflavan (7,4′-dihydroxy-3′-methoxyisoflavan)
  • Isoflavonoids: isovestitol, formononetin, afrormosin
  • Pterocarpan (medicarpin)

Two isoflavones isolated include:

  • 2′,3′,7-trihydroxy-4′-methoxyisoflav-3-ene (sepiol)
  • 3′,7-dihydroxy-2′,4′-methoxyisoflavone

Table 4: Volatile Oils Content of Gliricidia sepium

Compound Name

Part Used

Reference

Safrole

Leaves

[25]

2′-Hydroxyacetophenone

Leaves

[25]

Pentadecanal

Leaves

[19, 23]

Z-phytol

Leaves

[26]

Methyl linoleate

Leaves

[26]

Nonanal

Leaves

[26]

Propylene glycol

Leaves

[20, 22]

(Z)-3-Hexenol

Leaves

[32]

β-Farnesene

Leaves

[20, 22]

(Z)-2-Hexeno

Leaves

[27]

Thymol

Leaves

[27]

Benzyl alcohol

Leaves

[27]

Caryophyllene

Leaves

[27]

α-Farnesene

Leaves

[27]

Coumarin

Leaves, Flower, Bark

[20, 21, 22, 26, 32]

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Reference

  1. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q8(R2): Pharmaceutical Development. Geneva; 2009.
  2. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q9: Quality Risk Management. Geneva; 2005.
  3. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q10: Pharmaceutical Quality System. Geneva; 2008.
  4. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q11: Development and Manufacture of Drug Substances (Chemical Entities and Biotechnological/Biological Entities). Geneva; 2012.
  5. Grangeia HB, Silva C, Simões SP, Reis MS. Quality by design in pharmaceutical manufacturing: A systematic review of current status, challenges and future perspectives. European Journal of Pharmaceutics and Biopharmaceutics [Internet]. 2020 Feb 1 [cited 2025 Nov 11];147:19–37. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0939641119313189
  6. Yang S, Hu X, Zhu J, Zheng B, Bi W, Wang X, et al. Aspects and Implementation of Pharmaceutical Quality by Design from Conceptual Frameworks to Industrial Applications. Pharmaceutics 2025, Vol 17, Page 623 [Internet]. 2025 May 8 [cited 2025 Nov 11];17(5):623. Available from: https://www.mdpi.com/1999-4923/17/5/623/htm
  7. Ding B. Pharma Industry 4.0: Literature review and research opportunities in sustainable pharmaceutical supply chains. Process Safety and Environmental Protection. 2018 Oct;119:115–30.
  8. Chen Y, Yang O, Sampat C, Bhalode P, Ramachandran R, Ierapetritou M. Digital Twins in Pharmaceutical and Biopharmaceutical Manufacturing: A Literature Review. Processes 2020, Vol 8, Page 1088 [Internet]. 2020 Sep 2 [cited 2025 Nov 11];8(9):1088. Available from: https://www.mdpi.com/2227-9717/8/9/1088/htm
  9. Maharjan R, Kim NA, Kim KH, Jeong SH. Transformative roles of digital twins from drug discovery to continuous manufacturing: pharmaceutical and biopharmaceutical perspectives. Int J Pharm X. 2025 Dec;10:100409.
  10. Soori M, Arezoo B, Dastres R. Digital twin for smart manufacturing, A review. Sustainable Manufacturing and Service Economics [Internet]. 2023 Apr 1 [cited 2025 Nov 11];2:100017. Available from: https://www.sciencedirect.com/science/article/pii/S2667344423000099
  11. Sajadieh SMM, Noh S Do. From Simulation to Autonomy: Reviews of the Integration of Artificial Intelligence and Digital Twins. International Journal of Precision Engineering and Manufacturing-Green Technology 2025 12:5 [Internet]. 2025 May 3 [cited 2025 Nov 11];12(5):1597–628. Available from: https://link.springer.com/article/10.1007/s40684-025-00750-z
  12. Bloor M, Ahmed A, Kotecha N, Mercangöz M, Tsay C, del Río-Chanona EA. Control-Informed Reinforcement Learning for Chemical Processes. Ind Eng Chem Res. 2025 Mar 5;64(9):4966–78.
  13. Devarakonda VS, Sun W, Tang X, Tian Y. Recent Advances in Reinforcement Learning for Chemical Process Control. Processes. 2025 Jun 5;13(6):1791.
  14. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q12: Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management. Geneva; 2019.
  15. Wahlich J. Review: Continuous Manufacturing of Small Molecule Solid Oral Dosage Forms. Pharmaceutics. 2021 Aug 22;13(8):1311.
  16. Vermeer NS, Straus SMJM, Mantel-Teeuwisse AK, Domergue F, Egberts TCG, Leufkens HGM, et al. Traceability of Biopharmaceuticals in Spontaneous Reporting Systems: A Cross-Sectional Study in the FDA Adverse Event Reporting System (FAERS) and EudraVigilance Databases. Drug Saf. 2013 Aug 15;36(8):617–25.
  17. Murphy RM, Klopotowska JE, de Keizer NF, Jager KJ, Leopold JH, Dongelmans DA, et al. Adverse drug event detection using natural language processing: A scoping review of supervised learning methods. PLoS One. 2023 Jan 3;18(1):e0279842.
  18. Li M, Chen S, Lai Y, Liang Z, Wang J, Shi J, et al. Integrating Real-World Evidence in the Regulatory Decision-Making Process: A Systematic Analysis of Experiences in the US, EU, and China Using a Logic Model. Front Med (Lausanne). 2021 May 31;8.
  19. Yu LX, Amidon G, Khan MA, Hoag SW, Polli J, Raju GK, et al. Understanding Pharmaceutical Quality by Design. AAPS J. 2014 Jul 23;16(4):771–83.
  20. Zineh I. Quantitative Systems Pharmacology: A Regulatory Perspective on Translation. CPT Pharmacometrics Syst Pharmacol. 2019 Jun 11;8(6):336–9.
  21. Reusch D, Tejada ML. Fc glycans of therapeutic antibodies as critical quality attributes. Glycobiology. 2015 Dec;25(12):1325–34.
  22. Wang P, Li T, Yu L, Zhou L, Yan T. Towards an effective framework for integrating patient-reported outcomes in electronic health records. Digit Health. 2022 Jan 13;8:205520762211121.
  23. Cil AY, Abdurahman D, Cil I. Internet of Things enabled real time cold chain monitoring in a container port. Journal of Shipping and Trade. 2022 Dec 5;7(1):9.
  24. Aljohani A. Predictive Analytics and Machine Learning for Real-Time Supply Chain Risk Mitigation and Agility. Sustainability. 2023 Oct 20;15(20):15088.
  25. Wong WP, Saw PS, Jomthanachai S, Wang LS, Ong HF, Lim CP. Digitalization enhancement in the pharmaceutical supply network using a supply chain risk management approach. Sci Rep. 2023 Dec 15;13(1):22287.
  26. Abdallah S, Nizamuddin N. Blockchain-based solution for Pharma Supply Chain Industry. Comput Ind Eng. 2023 Mar;177:108997.
  27. Alqarni MA, Alkatheiri MS, Chauhdary SH, Saleem S. Use of Blockchain-Based Smart Contracts in Logistics and Supply Chains. Electronics (Basel). 2023 Mar 11;12(6):1340.
  28. Constable DJC, Curzons AD, Cunningham VL. Metrics to ‘green’ chemistry—which are the best? Green Chem. 2002;4(6):521–7.
  29. Jimenez-Gonzalez C, Ponder CS, Broxterman QB, Manley JB. Using the Right Green Yardstick: Why Process Mass Intensity Is Used in the Pharmaceutical Industry To Drive More Sustainable Processes. Org Process Res Dev. 2011 Jul 15;15(4):912–7.
  30. Koenig SG, Bee C, Borovika A, Briddell C, Colberg J, Humphrey GR, et al. A Green Chemistry Continuum for a Robust and Sustainable Active Pharmaceutical Ingredient Supply Chain. ACS Sustain Chem Eng. 2019 Oct 21;7(20):16937–51.
  31. Roschangar F, Sheldon RA, Senanayake CH. Overcoming barriers to green chemistry in the pharmaceutical industry – the Green Aspiration LevelTM concept. Green Chemistry. 2015;17(2):752–68.
  32. Rose HB, Kosjek B, Armstrong BM, Robaire SA. Green and sustainable metrics: Charting the course for green-by-design small molecule API synthesis. Current Research in Green and Sustainable Chemistry. 2022;5:100324.
  33. Satta M, Passarini F, Cespi D, Ciacci L. Advantages and drawbacks of life cycle assessment application to the pharmaceuticals: a short critical literature review. Environmental Science and Pollution Research. 2024 Jun 19;
  34. Sneddon H. Embedding Sustainable Practices into Pharmaceutical R&D: What are the Challenges? Future Med Chem. 2014 Aug 20;6(12):1373–6.
  35. Arden NS, Fisher AC, Tyner K, Yu LX, Lee SL, Kopcha M. Industry 4.0 for pharmaceutical manufacturing: Preparing for the smart factories of the future. Int J Pharm. 2021 Jun;602:120554.
  36. Mastrantonas A, Kokkas P, Chatzopoulos A, Papoutsidakis M, Stergiou C, Vairis A, et al. Identifying the effects of Industry 4.0 in the pharmaceutical sector: achieving the sustainable development goals. Discover Sustainability. 2024 Dec 3;5(1):460.
  37. McDermott O, Wojcik AM, Trubetskaya A, Sony M, Antony J, Kharub M. Pharma industry 4.0 deployment and readiness: a case study within a manufacturer. The TQM Journal. 2024 Dec 16;36(9):456–76.
  38. Schaber SD, Gerogiorgis DI, Ramachandran R, Evans JMB, Barton PI, Trout BL. Economic Analysis of Integrated Continuous and Batch Pharmaceutical Manufacturing: A Case Study. Ind Eng Chem Res. 2011 Sep 7;50(17):10083–92.
  39. Narayanan H, von Stosch M, Feidl F, Sokolov M, Morbidelli M, Butté A. Hybrid modeling for biopharmaceutical processes: advantages, opportunities, and implementation. Frontiers in Chemical Engineering. 2023 May 15;5.
  40. Tsopanoglou A, Jiménez del Val I. Moving towards an era of hybrid modelling: advantages and challenges of coupling mechanistic and data-driven models for upstream pharmaceutical bioprocesses. Curr Opin Chem Eng [Internet]. 2021 Jun 1 [cited 2025 Nov 10];32:100691. Available from: https://www.sciencedirect.com/science/article/pii/S221133982100023X
  41. Matsunami K, Martin Salvador P, Naranjo Gómez LN, Comoli GS, Charmchi I, Kumar A. Mechanistic modelling in pharmaceutical product and process development: A review of distributed and discrete approaches. Chemical Engineering Research and Design [Internet]. 2025 Jun 1 [cited 2025 Nov 10];218:8–24. Available from: https://www.sciencedirect.com/science/article/abs/pii/S0263876225001789
  42. Coveney P, Highfield R, Stahlberg E, Vázquez M. Digital twins and Big AI: the future of truly individualised healthcare. NPJ Digit Med. 2025 Aug 1;8(1):494.
  43. Li X, Loscalzo J, Mahmud AKMF, Aly DM, Rzhetsky A, Zitnik M, et al. Digital twins as global learning health and disease models for preventive and personalized medicine. Genome Med. 2025 Feb 7;17(1):11.
  44. Silva A, Vale N. Digital Twins in Personalized Medicine: Bridging Innovation and Clinical Reality. J Pers Med. 2025 Oct 22;15(11):503.
  45. Vallée A. Envisioning the Future of Personalized Medicine: Role and Realities of Digital Twins. J Med Internet Res. 2024 May 13;26:e50204.
  46. Fischer RP, Volpert A, Antonino P, Ahrens TD. Digital patient twins for personalized therapeutics and pharmaceutical manufacturing. Front Digit Health [Internet]. 2024 [cited 2025 Nov 10];5:1302338. Available from: https://pmc.ncbi.nlm.nih.gov/articles/PMC10796488/
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Mayur Patil
Corresponding author

KCT’s R.G. Sapkal Institute of Pharmacy, Nashik, Maharashtra, India

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Mustafa Deshmukh
Co-author

KCT’s R.G. Sapkal Institute of Pharmacy, Nashik, Maharashtra, India

Photo
Tejas Patil
Co-author

Smt. SharadhChandrika Suresh Patil College of Pharmacy, Chopda

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Durgesh Zope
Co-author

KCT’s R.G. Sapkal Institute of Pharmacy, Nashik, Maharashtra, India

Mayur Patil, Mustafa Deshmukh, Tejas Patil, Durgesh Zope, A Review on Beneficial Properties of Gliricidian sepium Plant, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 1, 1906-1912. https://doi.org/10.5281/zenodo.18303545

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