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Abstract

The important aromatic plant Nagarmotha (Cyperus rotundas), also referred to as nutgrass, is prized for its essential oil, which finds extensive use in a variety of industries and has a wide range of medical significance. Due to the exponential growth of medicinal and aromatic products worldwide, the chromatic pharmaceutical industries are currently investigating manufacturing accessories for their potential medical benefits. Since these plants contain physiologically active compounds that have exhibited a range of therapeutic effects, it has recently been established that plant-derived oils are more advantageous than synthetic goods in the pharmaceutical sector. To emphasize the medicinal advantages of plant extracts, a thorough investigation has been conducted. Anti-hyperglycemic, anti-nociceptive, hepatoprotective, anti-fungal, plant growth regulator (PGR), insecticidal, and ovicidal compounds are just a few of the many uses for C. scariosus extracts. The Indian medicinal plant C. scariosus, commonly referred to as "Nagarmotha," has been demonstrated to have numerous health benefits.

Keywords

Cyprus rotundas, Nagarmotha, Phytochemistry, Pharmacological activities

Introduction

The important aromatic plant Cyperus rotundas which is belonging to family Cyperaceae. Other names for it include Koraikkilangu in Tamil, Lawalain in Marathi, Nagarmotha in Hindi, Nagar Musta in Sanskrit, and xiangfu/xiangfuzi in Chinese.1-3

Fig: Cyperus Rotundas L. Herb

Tropical, subtropical, and temperate regions are often ideal for this plant’s growth.  Since ancient times, traditional medication systems have utilized this Indian medicinal manufacturer, which has been shown to offer numerous health benefits, to treat a variety of affectional disorders.  Terpenoids, sesquiterpenes, hydrocarbons, steroidal saponins, flavonoids, ketones, and essential oil painting are all present.4 An overview of accomplishment, production, post-harvesting, and root rhizome is given in the continuous review composition.  Evaluation of distilled material/oil painting quality and applications in addition to being a significant source of naturally occurring organic chemicals, medicinal and aromatic plants are utilized extensively in medicine.  Even if they are acknowledged as an alternative medical system, traditional medical practices continue to be crucial in meeting the fundamental medical needs of developing nations.  Medicinal plants are used to cure a variety of illnesses because they have less adverse effects than manufactured medications5-6 Natural products serve as lead molecules with an infinite variety of chemical structures, whose activities can be improved through de novo synthesis or chemical manipulation. Essential oils and various plant extracts are examples of naturally occurring biologically active substances that are less harmful and offer a wealth of potential disease-control agents.7

  1. Geographical distribution:

Numerous aromatic and other therapeutic plants in the Cyperaceae family contain chemical compounds with biologically significant characteristics.  With over 3700 species spread across 70 genera, Cyperus scariosus is a remarkable multipurpose medicinal herb belonging to a broad, international family of monocotyledons8-9

Fig: Tubers of Cyperus Rotundas L.

Although it grows in sandy and loamy soil moist fields, especially in Pacific Islands and along coastal regions, the plant needs sun and moisture.  With its tangle of roots and rhizomes that grow 3–4 cm deep in the soil and have a pleasant, aromatic scent, C. Scariosus grows quickly and fills the soil. Its essential oil is primarily used as an anti-inflammatory, anti-microbial, and antifungal agent and is also one of the ingredients in several ayurvedic formulations.10-12

Table No.1: Geographical Distribution of Cyperus Species: -

Plant

species

region

Parts to be used

Traditional use

Instruction

Cyperus

rotundus

L.

North west, Himalayas /India

Roots

Skin problems

Decoction of fresh leaves are used

India/Pakistan

Tubers

Diabetes mellitus

powder of tubers about 10-12g daily

India

Whole plant

Menstruation realated problems

30g dried powder or 100ml citrus juice taken once daily for a week

Tamil Nadu

Tubers

Snake bite

Paste of leave is applied on bite area

India

Roots /tubers

Kidney stone

decoction of plant

India

Whole plant

epilepsy

Plant decoction with Honey

India

Roots

Cholera

Roots boiled with equal amount of mint

India

Roots

Pimples

Root with Turmeric and Curd

India

Roots

In lactation problem

Root paste applied on breast

Norrth West Himalaya

Roots

In fevers

Decoction of root

India

Tubers and Leaves

Skin problems like Dermatitis

Decoction of root and leaves taken orally

India

Tubers

diarrhoea

Use orally diarrhoea

India

Tubers

Stomach Pain and Indigestion

10-12g powder taken orally

India

Tubers

Vaginal Discharge

tuber powder with cuminum seed

India

Whole plant

Loss of libido in men

Extract of whole plant mainly leaves

india

Tubers

Constipation

Macerated juice about ½ cup daily

India

Tubers

Jaundice / hepatitis

Juice of fresh rhizome

India

Tubers /leaves

Bronchial spasm /Bronchitis

Powder of tubers or leaves are taken orally for 30 days

China, Rarotonga

Tubers

Cough or sore throat

Crush tuber powder in water treatment last for 3 days

Cyperus monocephalus Roxb.

Philippines

Tubers

Dermatosis

tuberous root decoction

Tami Islands

Tubers

wormicidal Ringworm

Tuber decoction with added lime

Cyperus Compressus L.

India

Roots

Helminthiasis

Administer orally roots powder

Cyperus peduncukatus

West Africa

Leaves and Roots

Kidney diseases, Pain and Inflammation

Extract of whole plant is used

  1. Taxonomy:13

The following is the categorization for C. Rotundas

Fig: Style of Cyperus Rotundas L.

Table no.2: Taxonomical Categorization: -

Taxonomic Rank

Taxon

Phylum

Angiosperm

Kingdom

Planta

Sub-kingdom

Trichophytes

Class

Liliopsida

Subclass

Commelinidae

Order

Poales (Cyperales)

Family

Cyperaceae

Genus

Cyperus

Species

Scariosus

Super division

Spermatophyte

Division

Magnoliophyte

  1. Phytochemical investigation:14-18

Sesquiterpenes, including cyperene, rotundene, rotundenol, isopatchoula-3,5-diene, isopatchoul-3-ene, β-selinene, isopatchoulenol, and scariodione, make up the majority of the essential oil of C. Scariosus.  According to phytochemical research, this herb’s main chemical constituents are polyphenol, flavonol, glycoside, alkaloid, saponins, and sesquiterpenoids.

3.1 Essential oil

Here are key essential-oil compounds reported from Cyperus rotundus (commonly known as Nagarmotha):

Major compounds

α-Cyperone: - identified as a major sesquiterpene ketone. For example, in one study of rhizome oils: “α-cyperone (11.0%)

β-Pinene & α-Pinene: -monoterpenes seen in some samples: e.g., “β-pinene (11.3%), α-pinene (10.8%) …” in one oil sample.

Caryophyllene oxide: -another sesquiterpenoid present as a significant component.

Cyperene & Cyperotundone: -in oils from some regions: “cyperene (19.2-30.9%) and α-cyperone (4.5-25.2%)

Other sesquiterpenes such as β-selinene, α-selinene, humulene epoxide etc. For example: “α-humulene (14.3%), caryophyllene oxide (12.3%), humulene-1,2-epoxide (9.1%), valencene (8.2%), β-selinene (7.9%) …” from a study in Nigeria. 31

Alpha-Cyperone   

Myretenol

Pinene    

Beta-Pinene

3.2 Sesquiterpines:

Following are the sesquiterpene present in Cyperus rotundus (Nagarmutha)

Table No 3: - Sesquiterpines in C. Rotundus

Sr No.

Compound (Sesquterpines)

Type

Reference

1

α-Cyperone

Oxygenated sesquiterpene ketone

Singh et al., Journal of Essential Oil Research, 2002; PMCID: PMC6254851

2

Cyperotundone

Oxygenated sesquiterpene

Kim et al., Molecules, 2018; PMCID: PMC6254851

3

Cyperene

Hydrocarbon sesquiterpene

Ahmad et al., Molecules, 2023; PMCID: PMC10183317

4

β-Caryophyllene

Sesquiterpene hydrocarbon

Singh et al., Flavour and Fragrance Journal, 2002; PMCID: PMC6254851

5

Caryophyllene oxide

Oxygenated

sesquiterpene

Bhattacharyya et al., Current Science, 2019; Current Sci. 2019, 57

6

α-Humulene

Sesquiterpene hydrocarbon

Bhattacharyya et al., Current Science, 2019

7

β-Selinene

Hydrocarbon sesquiterpene

Ahmad et al., Molecules, 2023

8

α-Selinene

Hydrocarbon sesquiterpene

Singh et al., J. Essential Oil Res., 2002

9

Humulene epoxide I & II

Oxygenated sesquiterpenes

Ahmad et al., Molecules, 2023

10

Valencene

Hydrocarbon sesquiterpene

Bhattacharyya et al., Current Science, 2019

11

Patchoulenone

Oxygenated sesquiterpene

Kim et al., Molecules, 2018

12

Rotundene

Hydrocarbon sesquiterpene

Ahmad et al., Molecules, 2023

13

Cyperolone

Oxygenated sesquiterpene

Singh et al., Journal of Essential Oil Research, 2002

14

Isocyperol alcohol

Oxygenated sesquiterpene

Ahmad et al., Molecules, 2023

15

Mustakone

Sesquiterpene ketone

Singh et al., Flavour and Fragrance Journal, 2002

Cyperotundone    

Alpha-Cyperone

3.3 Flavonoids:

 Examples of flavonoids include orientin and vitexin. Quercetin 3-O-β-D-glucopyranoside, cinnaroside, Myrcetin 3-O-β-D-glucopyranoside, isnagin, Tricin, isorhamnetin, ammiol, khellin, and luteolin Luteolin 7, 3’-dimethyl ether, 3’-methyl ether, Luteolin 5, 3’-dimethyl ether, luteolin 4’-glucoside, Tricin 5-glucoside, luteolin 7-diglucoside, Cyperus rotundus contains kaempferol. This shows that falavonol has a unique derivative. The plant is called cyperaflavoside, which is myricetin 3,3’,5’-( Trimethyl ether 7-O-β-D-glucopyranosid 20-21

Quercetin 

Luteolin

Myrcetin

3.4 Steroid:

Among the well-known steroids found in Cyperus rotundus are steroidal glycoside, sitosteryl-(6’-hentriacontanoyl)-β-dgalactopyranoside, sitosterol, stigmasterol, sitosterol glucoside, stigmasterol glucoside, chrysoeriol, kaempferol, luteolin, quercetin, rutin, and khellol-D-glucopyranoside 22-23

Sitosterol   

Stigmasterol

3.5 Phenylpropanoid:

P-Coumaric acid, ferulic acid, isoaragoside, chionoside A, and helioside C are among the phenylpropanoid chemicals found in Cyperus rotundus tubers and rhizomes 24-25

P-Coumaric acid     

Ferulic acid

3.6 Phenolic Substances: 

Among the recognized phenolic chemicals found in Cyperus rotundus tubers and aerial parts are P-hydroxybenzoic acid, protocatechuic acid, vanillic acid, ellagic acid, salicylic acid, protocatechuic acid, caffeic acid, and p coumaric acid. 26-27

Caffeic acid   

Vanillic acid

3. 7 Iridoides, Benzodihydrofurans, and other compounds:

6-O-p-Coumaroylgenipin gentiobioside

Rotunduside A & Rotunduside B. These substances are all classified as phytochemical 28-30

  1. Pharmacological Activities:

Activities related to pharmacology Many workers have studied and reported that Cyperus contains a variety of chemical compounds, including notably sesquiterpenoids, the majority of which may exhibit pharmacological activity 31

4.1 Anti-Diarrheal:

Uddin et al. Used castor oil-induced diarrhea in rat models to examine Cyperus rotundus’s anti-diarrheal properties.  According to the study, oral methanolic extract administration at 250 and 500 mg/kg b.w. showed potent anti-diarrheal effects.  The antibacterial qualities of Cyperus rotundas were studied by Jabier et al.  Both gram-positive and gram-negative bacteria are among the kinds they use.  For instance, compared to gram-negative bacteria, Cyperus rotundus oil exhibited the strongest inhibitory effects on gram-positive bacteria. Pharmacological activities 32

4.2 Anti-Obesity:

 Rats’ obesity was lessened by the lipolytic action of C. Rotundus preparations (powder in fine suspension, aqueous and alcoholic extracts), which mobilized fat from their adipose tissues. Pharmacological action 33

    1. Insect Repellent Activity:

Insect-related behavior: The phytochemical screening and insecticidal testing of C. Rotundus were evaluated in a research. It works almost as well as organophosphate and is more effective than carbamate. Based on the findings, C. Rotundus came in first since all test subjects (ants) perished in 10 seconds or less (10). Organophosphate came in second place with nine kills. Carbamate came in last, with seven ants dying after twelve seconds, while the other ants perished in ten seconds.34

4.4 Activity for Wound Healing:

The goal of this study was to see if extracts from tuber segments of C. Rotundus could help wounds heal. The ability of an alcoholic extract of C. Rotundus tuber components, which is used as an ointment, was evaluated for its capacity to Treat wounds using rat models of excision, incision, and dead space wounds. In each of the Compared to previously published wound models in, the extract ointments demonstrated notable differences. response in terms of tension to the common nitrofurazone ointment (0.2% w/w NFZ) wound closure length, strength, and ability to contract 35

4.5 Ovicidal and Larvicidal Activity:

Essential oils derived from tubers of C. Rotundus have ovicidal and larvicidal effects.   tested on fourth-instar larvae and eggs of Aedes albopictus. After exposing the larvae and eggs They were watched for the entire day at a variety of oil concentrations, ranging from 5 to 150 ppm.The oils had LC50 and LC90 concentrations of less than 20 ppm and EC50 values of less than 5 ppm, suggesting that they were effective. possess significant larvicidal and ovicidal properties. The essential oils of were found to be larvicidal and ovicidal in the study. Certain Cyperus species may provide a natural source of compounds that kill insects. 36

4.6 Antiplatelet Activity:

C. Rotundus is a well-known traditional oriental treatment with a wide range of biological effects. The circulatory system is one of several systems that have demonstrated broad-spectrum activity. Its However, the antiplatelet action is unknown. The goal of this research was to ascertain the The antiplatelet effects of CRE and its constituents. Bleeding times in rat platelets and mouse tails In vitro and ex vivo aggregation assays were used to assess the antiplatelet properties of CRE and its components. eight unique items. Results: The in vitro platelet aggregation test revealed that CRE induced platelet aggregation. Lowered platelet aggregation, collagen, and/or thrombin in a concentration-dependent manner, and in a way that is statistically important.37

4.7 Antimalarial Activity:

Compounds such as were discovered by activity-guided investigation of C. Rotundus tubers. Patchoulenone, caryophyllene oxide, 10,12-peroxycalamenene, and 4,7-dimethyl-l-tetralone. These compounds possess antimalarial characteristics. Activity in the 10-4-10-6 MHz range of the ECso. The book endoperoxide sesquiterpene 10,12-peroxycalamenen is one of theme38

4.8 Antioxidant:

C. Scariosus plants grown in 50% methanol have demonstrated a potentially important ability to scavenge radicals and stop oxidative DNA damage.  U937 cells were not harmed by the C. Scariosus extracts.  To better understand the basis of their antioxidant properties, TPC, TFC, and ASC were identified.  The antioxidant qualities of the extract are supported by its notably high TPC and TFC contents 39,40

4.9 Hepatoprotective Activity:

The hepatoprotective effect of can be demonstrated by giving rats carbon tetrachloride, which causes liver injury two crude fractions from the rhizomes, solvent ether and ethyl acetate, and an ethyl acetate extract of C. Rotundus (Cyperaceae) was examined. The ethyl acetate extract significantly lowered glutamic pyruvic transaminase, glutamic oxaloacetic transaminase, and alkaline serum concentrations total bilirubin and phosphatase at an oral dose of 100 mg/kg. Histopathological examination of The biochemical findings were corroborated by sections of the liver. Furthermore, silymarin was employed as a positive regulation. The brain the raw enzyme Na+/K+-ATP-ase found in rat brains showed a notable increase in activity.an extract from C. Rotundus that inhibits Na+/K+ ATP-ase 41,42

4.10 Anti-cancer Activity:

C. Rotundus ethanolic extract demonstrated only low to moderate anticancer activity (LC50=2.528-4.939 mg/ml estimated from dose-dependent cell death) in a study that used neuro-2a cells to assess plants for tumoricidal activities.  In another investigation, it was discovered that C. Rotundus essential oil was very effective against L1210 leukemia cell lines.  This result was strongly associated with increased fragmentation of apoptotic DNA.43,44

4.11 Hemodynamic Hypotensive Activity:

C. Rotundus’s alcoholic extract raised sweating and led to a gradual and consistent decrease in blood pressure.  The extract partially inhibited the effects of histamine but did not alter the effects of acetylcholine or adrenaline on blood pressure.45

4.12 Cytoprotective Affect:

As evidenced by the following examples of cytoprotection, C. Rotundus rhizome decoctions demonstrated cytoprotective effects, or ulcer inhibitory efficacy, against stomach injury caused by ethanol. Impacts. Rats should be administered 1.25, 2.5, or 4.0 g/kg of crude drug orally 30 minutes before getting 10 mL/kg of 40% ethanol, which has the following effects: may prevent ulcers, depending on the dosage. Additionally, subcutaneous injection of the decoction (0.3–0.6 g/kg) had a similar effect, with systemic effects shielding the stomach. When the ethanol decoction was given orally (2.5–4.0 g/kg) or subcutaneously (0.3 g/kg) to rats, the stomach motility was significantly reduced when compared to the controls. Indomethacin pre-treatment (5 mg/kg) markedly decreased the stomach-protective impact of Candida rotundus.46

4.13 Anticonvulsant Activity:

Anticonvulsant activity was shown in mice that had been given an ethanolic extract of C. Rotundus prior to the experiment. a strong protection against seizures brought on by strychnine and leptazol. The duration of the rhizome ethanol extract significantly decreased hind limb extension and seizure activity. The dose of 100 mg/kg given orally (p.o.) to animals was comparable to the norm (p<0.001). Diazepam (4 mg/kg, i.p.; Indian Pharmacopoeia) and phenytoin (25 mg/kg, i.p.;) are the medications used. Indian Pharmacopoeia), respectively. These findings imply that the ethanol extract of the The rhizome is useful for producing a powerful phytoconstituent that can cure epilepsy, and the extract's Its flavonoids may be responsible for its anticonvulsant properties. 47,48

4.14 Nociceptive Inhibition:

Investigated the anti-nociceptive properties of a methanol extract of C. Scariosus leaves [2].  Five sets of seven mice each were created from the animals.  Group I was used as a control (10 mg/kg body weight, 1% Tween 80 in water).  Group-II mice received 200 milligrams of aspirin per kilogram of body weight.  30 minutes prior to the acetic acid injection, groups III through V received oral doses of the extract at 50, 100, and 200 mg/kg body weight, respectively.  A dose of 10 ml/kg body weight of 1% acetic acid was administered intraperitoneally to all groups to cause pain.  Each animal was given five minutes, after which the number of writhings was counted for ten minutes. 49

4.15 Spasmolytic and Hypotensive Effects:

Hydro-methanolic extract of IV administered at concentrations of 3–10 mg/kg, Cyperus scariosus had hypotensive and Bradycardia-inducing consequences. In spite of therapy, these effects persisted. Atropinized animals demonstrating the cardiovascular consequences ofthe plant extract does not work by activating Muscarinic receptors. In vitro experiments, it inhibited the rat uterus, guinea pig paired atria’s spontaneous contractions as well as rabbit jejunum at concentrations ranging from 0.1 to 1.0. in a manner similar to mg/mL. Additionally, it prevented the release of histamine and acetylcholine induced contractions of guinea pig ileum, which suggests non-spasmolytic effect. It blocked rabbit aorta at a certain point induced by K+ (80 mM) and norepinephrine (10 pM) concentrations of contractions were similar, ranging from 0.1 to 1 mg/ml. The evidence suggests that Cyperus scariosus possesses a Ca2+ channel blocker The general spasmolytic action of, and the in vivo effect seen in folkloric application in diarrhea may be explained by the plant 50

4.16 Antidepressants Activity:

 Mice treated with an n-hexane extract of C. Scariosus oil showed antidepressant effects.  Antidepressant activity was assessed in mice using the forced swim test and tail suspension test at two dose levels of 100 and 200 mg/kg. The outcomes were contrasted with those of the conventional medication, imipramine, at 15 mg/kg.  Similar to the common medication imipramine, C. Scariosus n-hexane extract oil considerably (p<0.001) decreased 51

4.17 Hypolipidamic Activity:

the effects of a hydroalcoholic extract of Cyperus scoparius Linn. Root (HCS) on guinea pigs given a diet high in cholesterol in terms of its lipid-lowering and antioxidant properties.  Cyperus scariosus hydroalcoholic extract reduced the serum lipid profile and atherogenic indices at both doses (P < 0.05).  Additionally, serum AST, ALP, and LDH levels were decreased by the greater dose of hydroalcoholic extract, while rosuvastatin raised AST and ALP levels (P < 0.05).  The antioxidant activity of the extract’s phenolic components may be the cause of the treated animals’ improved hepatocytes and reduced fat buildup on liver histology.52

  1. Applications of Ethnopharmacology:53,54

A component of Musta Indication

  • Tubers: fever, diarrhea, dysentery, dyspepsia Cholera, Vomiting.
  • Fresh tuber: Paste is used as galactogog is used to treat spreading ulcers and scorpion stings.
  • Root: leprosy, thirst, fever, blood illness Dysentery, pruritus, discomfort, vomiting, biliousness Erysipelas, ophthalmia, and epilepsy.
  • Bulbous root: Dysentery, stomach problems Intestinal Problem.

Table No.4: Chemical Constituent and Pharmacological Activities

Sr. No.

Class of Substance

Chemical Entity

Pharmacological activity

Reference

 

1

 

Essential Oil

Cyperone

Anti-inflammatory, Neuroprotective, Dysentery56

Bingxu Huang et-al

Myretenol

Anti-inflammatory, Antioxidant, Antibacterial, Anxiolytic57

Shengming Huang et-al

Beta-pinene

Antimicrobial, Woody Scent perfume, Airfreshner55

Adama Ndao et-al

Pinene

Fragrances, Antimicrobial, potential antitumor action 55

Adam Nao et-al

2.

sesquiterpenes

Cyperone

Anti-inflammatory, Neuroprotective, Dysentery

Bingxu Huang et-al

cyperotundone

Digestive disorder, Diarrhoea58

 

Muhammad said Hamid Akas et-al

3

Flavonoids

Quercetin

Antioxidant, Anticancer, Anti-inflammatory, Arthritis, CVS Disorder60

Samaria Krishna et-al

Lute Olin

Anti-inflammatory, Antioxidant, Anticancer59

Samaria Krishna et-al

Myrecetin

Antioxidant Anticancer, Myocardial Dysfunction, anti-inflammatory, Antiplatelet action59

Samaria Krishna et-al

4

Steroid

Beta-sit sterol

Hypolipidemic action, Anticancer, Antidiabetic action, Antioxidant, Immunomodulatory61 activities

Jill A Makossa

et-al

Stigmesterol

Hypolipidemic action, Anticancer, Antidiabetic action, Antioxidant, Immunomodulatory activities 6

Jasmine Chaudhary et-al

5

Phenylpropanoid

P-coumeric Acid

Antioxidant, Antidiabetic action, Antimellanogeic Action58

Young Chool Boo et-al

Ferulic Acid

Antioxidant, Antidiabetic, Vanillin Precursor, Cosmetic and Anticancer58

Young Choo Boo

6

Phenolic Substance

Caffeic Acid

Antioxidant, Anticancer, Obesity, Metabolic syndrome, Neuroprotective, Antiviral 62

Neal pavlova

Et-al

Vanillin Acid

Sedative, Antidepressant, Nociceptive Inhibition, Hepatoprotective, Antihypertensive, Wound Healing, Antifungal 63

Nares Kumar et-al

7

Other

Substance

Rotund side A&B

Anti-inflammatory, sedative, Anxiolytic, Antimicrobial, Antidiabetic58

Muhammad said Hamid Akas et-al

RESULT:

The review comprehensively established that Cyperus rotundus L. (Nagarmotha) possesses a rich and diverse phytochemical profile, primarily composed of sesquiterpenes, flavonoids, phenolic acids, steroids, and essential oils. Major bioactive constituents such as α-cyperone, cyperotundone, cyperene, β-caryophyllene, luteolin, quercetin, and sitosterol have been identified as responsible for the plant’s multiple pharmacological properties. Experimental findings reported in various studies demonstrated that extracts of C. rotundus exhibit significant anti-inflammatory, antioxidant, hepatoprotective, antidiarrheal, antiplatelet, antimalarial, antinociceptive, anticonvulsant, and anticancer activities. Essential oils from the rhizomes showed potent insecticidal, ovicidal, and larvicidal effects, while methanolic and ethanolic extracts revealed marked wound-healing, cytoprotective, and antidiabetic actions. Additionally, biochemical and histopathological studies confirmed that C. rotundus extracts reduce elevated liver enzyme levels, inhibit oxidative stress, and protect cellular structures from damage. The plant also exhibited hypolipidemic and antidepressant properties in preclinical models, demonstrating its potential as a broad-spectrum therapeutic agent derived from natural sources.

CONCLUSION

Cyperus rotundus L. is a pharmacologically potent medicinal herb endowed with numerous bioactive constituents that contribute to its wide therapeutic applications. Its essential oils and extracts exhibit substantial biological activities including antioxidant, anti-inflammatory, hepatoprotective, antimicrobial, antidiabetic, and anticancer effects, validating its long-standing traditional uses in Ayurveda and other ethnomedicinal systems. The broad range of secondary metabolites—particularly sesquiterpenes, flavonoids, and phenolic compounds—illustrates the plant’s potential as a source of natural drug leads for managing various pathological conditions. However, despite extensive preclinical evidence, further pharmacokinetic, toxicological, and clinical investigations are necessary to confirm its safety, efficacy, and dosage standardization for therapeutic use. Overall, Cyperus rotundus stands out as a valuable medicinal and aromatic plant with significant potential for development into modern herbal formulations and phytopharmaceutical products.                                          

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  17. Kilani S, Abdelwahed A, Ammar RB, Hayder N, Ghedira K, Chraief I, Hammami M and Chekir-Ghedira L: Chemical composition, antibacterial and antimutagenic activities of essential oil from (Tunisian) Cyperus rotundus. J of Essential Oil Research 2005; 17(6): 695-00.
  18. Kumar M, Rani M and Meher B: Review on Pharmacology and Phytochemistry of Cyperus rotundus L. Current Research in Pharmaceutical Sciences 2017; 11-5.
  19. Wang Q, Yi C, Duan W, Duan Y, Lou J, Zeng g and yin j: two New Sesquiterpenoids Isolated from Cyperus rotundus L. Natural Product Communications 2021; 16(2): 1934578X21991687.
  20. Ibrahim SR, Mohamed GA, Alshali KZ, Haidari RA, ElKholy AA and Zayed MF: Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts. RevistaBrasileira de Farmacognosia. 2018; 28(3): 320-4.
  21. Sayed HM, Mohamed MH, Farag SF and Mohamed GA: Phytochemical and biological studies of Cyperus rotundus L. growing in Egypt. Bull Pharm Sci Cairo Univ 2001; 39: 195-03.
  22. Sayed HM, Mohamed MH, Farag SF, Mohamed GA and Proksch P: A new steroid glycoside and furochromones from Cyperus rotundus L. Natural Product Research 2007; 21(4): 343-50.
  23. Sayed HM, Mohamed MH, Farag SF and Mohamed GA: Phytochemical and biological investigations of Cyperus rotundus L. Bull Fac Pharm Cairo Univ 2001; 39(3): 195- 03.
  24. Komai K and Ueki K: Secondary metabolic compounds in purple nutsedge (Cyperus rotundus L.) and their plant growth inhibition. Chemical Regulation of Plants (Japan). 1981
  25. Zhou Z and Zhang H: Phenolic and iridoid glycosides from the rhizomes of Cyperus rotundus L. Medicinal Chemistry Research 2013; 22(10): 4830-5.
  26. Sayed HM, Mohamed MH, Farag SF, Mohamed GA, Omobuwajo OR and Proksch P: Fructose-amino acid conjugate and other constituents from Cyperus rotundus L. Natural product research. 2008; 22(17): 1487-97
  27. Al-Snafi AE: A review on Cyperus rotundus A potential medicinal plant. IOSR Journal of Pharmacy 2016; 6(7): 32-48
  28. Amesty Á, Burgueño-Tapia E, Joseph-Nathan P, Ravelo ÁG and Estévez-Braun A: Benzodihydrofurans from Cyperus teneriffae. Journal of Natural Products 2011; 74(5): 1061-5.
  29. Zhou Z and Yin W: Two novel phenolic compounds from the rhizomes of Cyperus rotundus L. Molecules 2012; 17(11): 12636-41.
  30. Thebtaranonth C, Thebtaranonth Y, Wanauppathamkul S and Yuthavong Y: Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10, 12- peroxycalamenene, a sesquiterpene endoperoxide. Phytochemistry 1995; 40(1): 125-8.
  31. . Bisht A, Bisht GR, Singh M, Gupta R and Singh V: Chemical composition and antimicrobial activity of essential oil of tubers of Cyperus rotundus Linn. collected from Dehradun (Uttarakhand). Int J Res Pharm Biomed Sci 2011; 2: 661-5.
  32. A Kumar, KK Chahal and D Kataria A review on phytochemistry and pharmacological activities of Cyperus scariosus Journal of Pharmacognosy and Phytochemistry 2017; 6(1): 510-517
  33. International Journal Of Scientific And Research Publications, Volume3, Issue 5, May 2013 1 ISSN 2250-3153al Activity Of Cyperus Rotundus, Fitoterapia 2006; 77; 134–136. (Antidiarrhoeal)
  34. Bambhole V D. 1988. Effect Of Some Medicinal Plants Preparations On Adipose Tissue Metabolism, Ancient Sci Life, 8: 117-124. (AntiObesity Activity).
  35. Journal Of Parasitologyresearchvolume2009, Articleid 9080855 Pages Http://Dx.Doi.Org/10.1155/2009/90808
  36. ) H T T P ://W W W. Ij P S O N L In E. C O M /A R T I C L E. A S P? Is S N = 0 2 5 0 474x; Year=2006; Volume=68; Issue=1; Spage=97; Epage=101
  37. Seo EJ, Lee DU, Kwak JH, Lee SM, Kim YS, Jung YS. Antiplatelet Effects Of Cyperus Rotundus And Its Component (+) Nootkatone. J Ethnopharmacol 2011; 135:48 54
  38. Thebtaranonth C, Thebtaranonth Y, Wanauppathamkul S, Yuthavong Y. Antimalarial Sesquiterpenes From Tubers Of Cyperus Rotundus: Structure Of 10,12 Peroxycalamenene, A Sesquiterpene Endoperoxide. Phytochemistry 1995; 40:125 8.
  39. Soltan MM and Zaki AK (2009). Antiviral Screening Of Forty-Twoegyptian Medicinal Plants. J. Ethnopharmacol, 126(1): 102-107.
  40. Natarajan B and Paulsen BS (2000). An Ethno-Pharmacological Studyfrom Thane District, Maharashtra, India. Traditional Knowledge Compared With Modern Biological Science. Pharmaceutical Biology, 38: 139–151.
  41. Kumar S. V. S., Mishra H., 2005. Hepatoprotective Activity Ofrhizomes Of Cyperus Rotundus Linn Against Carbon Tetrachloride-Induced Hepatotoxicity: 67:1: 84-88 (Hepatoprotective)
  42. Ngamrojanavanish N, Manaki S and Pornpakakul S, 2006. Inhibitoryactivity Of Selected Thai Medicinal Plants on Na+/K+-ATP-Ase, Fitoterapia, 77 (6), 481-483 (Hepatoprotective).
  43. Mazzio E A and Soliman K F A 2009. In Vitro Screening For Thetumoricidal Properties Of International Medicinal Herbs,Phytother Res, 23(3), 385-398. (Anticancer)
  44. Kilani, S.; Ledauphin, J.; Bouhlel, I.; Ben Sghaier, M.; Boubaker, J.; Skandrani, I.; Mosrati, R.; Ghedira, K.; Barillier, D.; Chekir-Ghedira L. 2008. Comparative Study Of Cyperus Rotundusessential Oil By A Modified GC/MS Analysis Method. Evaluation Of Its Antioxidant, Cytotoxic, And Apoptotic Effects. Chem.Biodivers. 5: 729-742. (Anticancer)
  45. Singh N, Kulshrestha VK, Gupta MB And Bhargava K P, 1970. Apharmacological Study Of Cyperus Rotundus, Indian J Med, Res, 103-109. (Haemodynamic (Hypotensive) Activity)
  46. Zhu M.; Luk H. H.; Fung H. S.; Luk C. T. 1997. Cytoprotectiveeffects Of Cyperus Rotundus Against Ethanol Induced Gastric Ulceration In Rats PTR. Phytotherapy Research ISSN 0951-418X Vol. 11, Pp. 392-394. (Cytoprotective Effects).
  47. Pal D, Dutta S and Sarkar 2009. An Evaluation Of CNS Activities Ofethanol Extract Of Roots And Rhizomes Of Cyperus Rotundus In Mice, Acta Poloniae Pharmaceut Drug Res. 66(5), 535-541. (Anticonvulsant Activity)
  48. Shivakumar S I, Suresh H M, Hallikeri C S, Hatapakki B C, Handiganurj S, Kuber S And Shivakumar B. 2009. Anticonvulsant Effect Of Cyperus Rotundus Linn. Rhizomes In Rats, J Nat Rened, 9(2), 192-196. (Anticonvulsant Activity)
  49. Alam MA, Jahan R, Rahman S, Das AK, Rahmatullah M. Antinociceptive and anti-hyperglycemic activity of methanol extract of Cyperus scariosus. Pakistan journal Pharmaceutical Science 2011; 24(1):53-56.
  50. Shamkuwar PB, Hoshamani AH, Indrajeet D. Antispasmodic Effect Of Cyperus Rotundus L. (Cyperaceae) In Diarrhoea. Der Pharm Lettre 2012; 4:522 4.
  51. Ramesh S, Maruthirao B, Mahesh V, Prabhakar T, Swamy P, Nagaraju P. Pharmacological study of antidepressant like activity of Cyperus scariosus oil in mice International Research Journal of Pharmaceutical Applied Sciences. 2012; 2:139-142.
  52. Chawda HM, Mandavia DR, Parmar PH, Baxi SN, Tripathi CR. Hypolipidemic activity of a hydroalcoholic extract of Cyperus scariosus Linn. root in guinea pigs fed with a high cholesterol diet. Chinese Journal of Natural Medicines. 2014; 12(11):819-82
  53. Kirtikar & Basu, Indian Medicinal Plants, second edition Vol-1, Vol-III. International Book distributors & publishers, Dehradun.P.2638- 2640
  54. AK Nadkarni, Indian Materia Medica, Vol-1, Edition: 1976. Popular Prakashan, Mumbai. P.428-430
  55. Adama Nadao and KOkou Adjalle Overview of the Biotransformation of Limonene and α-Pinene from Wood and Citrus Residues by Microorganisms National Institute of Scientific Research Oct 2023
  56. Bingux Huang, Juxiong Liu, Shouprng Fu et-al Alpha-Cyperone Attenuates H2O2-Induced Oxidative Stress and Apoptosis in SH-SY5Y Cells via Activation of Nrf2 Carlos Alberto Manssour Fraga, Federal University of Rio de Janeiro Brazil April 2020
  57. Shengming Huang, Zhanguo Tan, Jirui Cai, Zhiping Wang and Yuejun Tiana, Myrtenol improves brain damage and promotes angiogenesis in rats with cerebral infarction by activating the ERK1/2 signalling pathway, Tylor and Francis Vol 59 No 1,582-591 Year2021
  58. Muhammad Sajid Hamid Akash1?, Ammara Afzaal1, Kanwal Rehman2, Amjad Hussain3?, Muhammad Ibrahim4, Syed Muhammad Shoaib5, Mudassar Shahid6, and Bushra Sadaf Identification of Secondary Metabolites of Cyperus rotundus L. and Dose-dependent Effects on Antioxidant Activity and Carbohydrate Digestion Enzymes Dose Respone An Internationl journal Oct-Dec 2024 DOI: 10.1177/15593258241308724
  59. Samariya Krishna* and Sarin Reno Isolation And Identification Of Flavonoids From Cyperus Rotundus Linn. In Vivo And In Vitro, Journal of Drug Delivery & Therapeutics; 2013, 3(2), 109-113
  60. Foteini Ntalouka* and Athina Tsirivakou Luteolin: A promising natural agent in management of pain in chronic conditions, fortienrs in pain research March 2023 | DOI 10.3389/fpain.2023.1114428
  61. Jasmine Chaudhary, Akashi Jain, Navpreet Kaur, Lalit Kishor Stigmasterol: A Comprehensive Review International Journal of Pharmaceutical Sciences and Research · January 2011 VOL2 Issue 9
  62. Nela Pavlíková Caffeic Acid and Diseases—Mechanisms of Action International Journal of Molecular Sciences Int. J. Mol. Sci. 2023, 24, 588 https://doi.org/10.3390/ijms24010588.
  63. Ashwini S. Ingole, Megha P. Kadam, Aishwarya P. Dalu, Shital M. Kute, Piyusha R. Mange, Vaishali D. Theng, Om R. Lahane, Aniket P. Nikas, Yash V. Kawal, Shatrughna U. Nagrik , Prashant A. Patil A Review of the Pharmacological Characteristics of Vanillic Acid Journal of Drug Delivery & Therapeutics. 2021; 11(2-s):200-204 http://dx.doi.org/10.22270/jddt.v11i2-s.4823
  64. Raina, A. P., Verma, S. K., & Abraham, Z. (2014). Volatile constituents of essential oils isolated from Alpinia galanga Willd. (L.) and A. officinarum Hance rhizomes from North East India. Journal of Essential Oil Research, 26(1), 24–28. https://doi.org/10.1080/10412905.2013.822430
  65. Simorangkir, D., Masfria, M., Harahap, U., & Satria, D. (2019). Activity anticancer n-hexane fraction of Cyperus rotundus L. rhizome to breast cancer MCF-7 cell line. Open Access Macedonian Journal of Medical Sciences, 7(22), 3904–3906. https://doi.org/10.3889/oamjms.2019.530
  66. Xue, B.-X., He, R.-S., Lai, J.-X., Mireku-Gyimah, N.A., Zhang, L.-H., & Wu, H.-H. (2023). Phytochemistry, data mining, pharmacology, toxicology and the analytical methods of Cyperus rotundus L. (Cyperaceae): a comprehensive review. Frontiers in Pharmacology,14:1178233. DOI: 10.3389/fphar.2023.1178233.

Reference

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  2. Akbar N, Katiyar A, Vilas G, Srivastava S, Saxena BK.  Isolation and chromatographic fingerprint (HPTLC) analysis of resinoid from refuse/waste material of Nagarmotha. Anal Chem Lett. 2011;1(5–6):402–https://doi.org/10.1080/22297928.2011.10648245.
  3. Alam MA, Jahan R, Rahman S, Das AK, Rahmatullah M. Antinociceptive and anti-hyperglycemic activity of methanol extract of Cyperus scariosus. Pak J PharmSci. 2011;24(1):53
  4. Allan RD, Wells RJ, Correll RL, MacLeod JK. The presence of quinones in the genus Cyperus as an aid to classification. Phytochemistry. 1978;17(2):263–6. https://doi.org/10.1016/S0031-9422(00)94160-8
  5. Anonymous. The Wealth of India, Raw Materials. Vol. 1. New Delhi: CSIR; 1950. p. 425.
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  12. Swarbrick JT: Weeds of the Pacific islands. TechnicalPaper-South Pacific Commission 1997; 209.
  13. Imam H, Lone A, Seikh A, Sofi G, Zarnigar. The incredible benefits of Nagarmotha (Cyperus rotundus). Int J Nutr Pharmacol Neurol Dis. 2014;4(1):23. https://doi.org/10.4103/2231-0738.124611.
  14. Hikino H, Suzuki N and Takemoto T: Structure and absolute configuration of kusunol. Chemical and Pharmaceutical Bulletin 1968; 16(5): 832-8
  15. Kalsi PS, SHARMA A, Singh AN, Singh IP and Chhabra BR: Biogenetically important sesquiterpenes from Cyperus rotundus. Fitoterapia (Milano).1995; 66(1)
  16. Ohira S, Hasegawa T, Hayashi KI, Hoshino T, Takaoka D and Nozaki H: Sesquiterpenoids from Cyperus rotundus. Phytochemistry 1998; 47(8): 1577-81
  17. Kilani S, Abdelwahed A, Ammar RB, Hayder N, Ghedira K, Chraief I, Hammami M and Chekir-Ghedira L: Chemical composition, antibacterial and antimutagenic activities of essential oil from (Tunisian) Cyperus rotundus. J of Essential Oil Research 2005; 17(6): 695-00.
  18. Kumar M, Rani M and Meher B: Review on Pharmacology and Phytochemistry of Cyperus rotundus L. Current Research in Pharmaceutical Sciences 2017; 11-5.
  19. Wang Q, Yi C, Duan W, Duan Y, Lou J, Zeng g and yin j: two New Sesquiterpenoids Isolated from Cyperus rotundus L. Natural Product Communications 2021; 16(2): 1934578X21991687.
  20. Ibrahim SR, Mohamed GA, Alshali KZ, Haidari RA, ElKholy AA and Zayed MF: Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts. RevistaBrasileira de Farmacognosia. 2018; 28(3): 320-4.
  21. Sayed HM, Mohamed MH, Farag SF and Mohamed GA: Phytochemical and biological studies of Cyperus rotundus L. growing in Egypt. Bull Pharm Sci Cairo Univ 2001; 39: 195-03.
  22. Sayed HM, Mohamed MH, Farag SF, Mohamed GA and Proksch P: A new steroid glycoside and furochromones from Cyperus rotundus L. Natural Product Research 2007; 21(4): 343-50.
  23. Sayed HM, Mohamed MH, Farag SF and Mohamed GA: Phytochemical and biological investigations of Cyperus rotundus L. Bull Fac Pharm Cairo Univ 2001; 39(3): 195- 03.
  24. Komai K and Ueki K: Secondary metabolic compounds in purple nutsedge (Cyperus rotundus L.) and their plant growth inhibition. Chemical Regulation of Plants (Japan). 1981
  25. Zhou Z and Zhang H: Phenolic and iridoid glycosides from the rhizomes of Cyperus rotundus L. Medicinal Chemistry Research 2013; 22(10): 4830-5.
  26. Sayed HM, Mohamed MH, Farag SF, Mohamed GA, Omobuwajo OR and Proksch P: Fructose-amino acid conjugate and other constituents from Cyperus rotundus L. Natural product research. 2008; 22(17): 1487-97
  27. Al-Snafi AE: A review on Cyperus rotundus A potential medicinal plant. IOSR Journal of Pharmacy 2016; 6(7): 32-48
  28. Amesty Á, Burgueño-Tapia E, Joseph-Nathan P, Ravelo ÁG and Estévez-Braun A: Benzodihydrofurans from Cyperus teneriffae. Journal of Natural Products 2011; 74(5): 1061-5.
  29. Zhou Z and Yin W: Two novel phenolic compounds from the rhizomes of Cyperus rotundus L. Molecules 2012; 17(11): 12636-41.
  30. Thebtaranonth C, Thebtaranonth Y, Wanauppathamkul S and Yuthavong Y: Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10, 12- peroxycalamenene, a sesquiterpene endoperoxide. Phytochemistry 1995; 40(1): 125-8.
  31. . Bisht A, Bisht GR, Singh M, Gupta R and Singh V: Chemical composition and antimicrobial activity of essential oil of tubers of Cyperus rotundus Linn. collected from Dehradun (Uttarakhand). Int J Res Pharm Biomed Sci 2011; 2: 661-5.
  32. A Kumar, KK Chahal and D Kataria A review on phytochemistry and pharmacological activities of Cyperus scariosus Journal of Pharmacognosy and Phytochemistry 2017; 6(1): 510-517
  33. International Journal Of Scientific And Research Publications, Volume3, Issue 5, May 2013 1 ISSN 2250-3153al Activity Of Cyperus Rotundus, Fitoterapia 2006; 77; 134–136. (Antidiarrhoeal)
  34. Bambhole V D. 1988. Effect Of Some Medicinal Plants Preparations On Adipose Tissue Metabolism, Ancient Sci Life, 8: 117-124. (AntiObesity Activity).
  35. Journal Of Parasitologyresearchvolume2009, Articleid 9080855 Pages Http://Dx.Doi.Org/10.1155/2009/90808
  36. ) H T T P ://W W W. Ij P S O N L In E. C O M /A R T I C L E. A S P? Is S N = 0 2 5 0 474x; Year=2006; Volume=68; Issue=1; Spage=97; Epage=101
  37. Seo EJ, Lee DU, Kwak JH, Lee SM, Kim YS, Jung YS. Antiplatelet Effects Of Cyperus Rotundus And Its Component (+) Nootkatone. J Ethnopharmacol 2011; 135:48 54
  38. Thebtaranonth C, Thebtaranonth Y, Wanauppathamkul S, Yuthavong Y. Antimalarial Sesquiterpenes From Tubers Of Cyperus Rotundus: Structure Of 10,12 Peroxycalamenene, A Sesquiterpene Endoperoxide. Phytochemistry 1995; 40:125 8.
  39. Soltan MM and Zaki AK (2009). Antiviral Screening Of Forty-Twoegyptian Medicinal Plants. J. Ethnopharmacol, 126(1): 102-107.
  40. Natarajan B and Paulsen BS (2000). An Ethno-Pharmacological Studyfrom Thane District, Maharashtra, India. Traditional Knowledge Compared With Modern Biological Science. Pharmaceutical Biology, 38: 139–151.
  41. Kumar S. V. S., Mishra H., 2005. Hepatoprotective Activity Ofrhizomes Of Cyperus Rotundus Linn Against Carbon Tetrachloride-Induced Hepatotoxicity: 67:1: 84-88 (Hepatoprotective)
  42. Ngamrojanavanish N, Manaki S and Pornpakakul S, 2006. Inhibitoryactivity Of Selected Thai Medicinal Plants on Na+/K+-ATP-Ase, Fitoterapia, 77 (6), 481-483 (Hepatoprotective).
  43. Mazzio E A and Soliman K F A 2009. In Vitro Screening For Thetumoricidal Properties Of International Medicinal Herbs,Phytother Res, 23(3), 385-398. (Anticancer)
  44. Kilani, S.; Ledauphin, J.; Bouhlel, I.; Ben Sghaier, M.; Boubaker, J.; Skandrani, I.; Mosrati, R.; Ghedira, K.; Barillier, D.; Chekir-Ghedira L. 2008. Comparative Study Of Cyperus Rotundusessential Oil By A Modified GC/MS Analysis Method. Evaluation Of Its Antioxidant, Cytotoxic, And Apoptotic Effects. Chem.Biodivers. 5: 729-742. (Anticancer)
  45. Singh N, Kulshrestha VK, Gupta MB And Bhargava K P, 1970. Apharmacological Study Of Cyperus Rotundus, Indian J Med, Res, 103-109. (Haemodynamic (Hypotensive) Activity)
  46. Zhu M.; Luk H. H.; Fung H. S.; Luk C. T. 1997. Cytoprotectiveeffects Of Cyperus Rotundus Against Ethanol Induced Gastric Ulceration In Rats PTR. Phytotherapy Research ISSN 0951-418X Vol. 11, Pp. 392-394. (Cytoprotective Effects).
  47. Pal D, Dutta S and Sarkar 2009. An Evaluation Of CNS Activities Ofethanol Extract Of Roots And Rhizomes Of Cyperus Rotundus In Mice, Acta Poloniae Pharmaceut Drug Res. 66(5), 535-541. (Anticonvulsant Activity)
  48. Shivakumar S I, Suresh H M, Hallikeri C S, Hatapakki B C, Handiganurj S, Kuber S And Shivakumar B. 2009. Anticonvulsant Effect Of Cyperus Rotundus Linn. Rhizomes In Rats, J Nat Rened, 9(2), 192-196. (Anticonvulsant Activity)
  49. Alam MA, Jahan R, Rahman S, Das AK, Rahmatullah M. Antinociceptive and anti-hyperglycemic activity of methanol extract of Cyperus scariosus. Pakistan journal Pharmaceutical Science 2011; 24(1):53-56.
  50. Shamkuwar PB, Hoshamani AH, Indrajeet D. Antispasmodic Effect Of Cyperus Rotundus L. (Cyperaceae) In Diarrhoea. Der Pharm Lettre 2012; 4:522 4.
  51. Ramesh S, Maruthirao B, Mahesh V, Prabhakar T, Swamy P, Nagaraju P. Pharmacological study of antidepressant like activity of Cyperus scariosus oil in mice International Research Journal of Pharmaceutical Applied Sciences. 2012; 2:139-142.
  52. Chawda HM, Mandavia DR, Parmar PH, Baxi SN, Tripathi CR. Hypolipidemic activity of a hydroalcoholic extract of Cyperus scariosus Linn. root in guinea pigs fed with a high cholesterol diet. Chinese Journal of Natural Medicines. 2014; 12(11):819-82
  53. Kirtikar & Basu, Indian Medicinal Plants, second edition Vol-1, Vol-III. International Book distributors & publishers, Dehradun.P.2638- 2640
  54. AK Nadkarni, Indian Materia Medica, Vol-1, Edition: 1976. Popular Prakashan, Mumbai. P.428-430
  55. Adama Nadao and KOkou Adjalle Overview of the Biotransformation of Limonene and α-Pinene from Wood and Citrus Residues by Microorganisms National Institute of Scientific Research Oct 2023
  56. Bingux Huang, Juxiong Liu, Shouprng Fu et-al Alpha-Cyperone Attenuates H2O2-Induced Oxidative Stress and Apoptosis in SH-SY5Y Cells via Activation of Nrf2 Carlos Alberto Manssour Fraga, Federal University of Rio de Janeiro Brazil April 2020
  57. Shengming Huang, Zhanguo Tan, Jirui Cai, Zhiping Wang and Yuejun Tiana, Myrtenol improves brain damage and promotes angiogenesis in rats with cerebral infarction by activating the ERK1/2 signalling pathway, Tylor and Francis Vol 59 No 1,582-591 Year2021
  58. Muhammad Sajid Hamid Akash1?, Ammara Afzaal1, Kanwal Rehman2, Amjad Hussain3?, Muhammad Ibrahim4, Syed Muhammad Shoaib5, Mudassar Shahid6, and Bushra Sadaf Identification of Secondary Metabolites of Cyperus rotundus L. and Dose-dependent Effects on Antioxidant Activity and Carbohydrate Digestion Enzymes Dose Respone An Internationl journal Oct-Dec 2024 DOI: 10.1177/15593258241308724
  59. Samariya Krishna* and Sarin Reno Isolation And Identification Of Flavonoids From Cyperus Rotundus Linn. In Vivo And In Vitro, Journal of Drug Delivery & Therapeutics; 2013, 3(2), 109-113
  60. Foteini Ntalouka* and Athina Tsirivakou Luteolin: A promising natural agent in management of pain in chronic conditions, fortienrs in pain research March 2023 | DOI 10.3389/fpain.2023.1114428
  61. Jasmine Chaudhary, Akashi Jain, Navpreet Kaur, Lalit Kishor Stigmasterol: A Comprehensive Review International Journal of Pharmaceutical Sciences and Research · January 2011 VOL2 Issue 9
  62. Nela Pavlíková Caffeic Acid and Diseases—Mechanisms of Action International Journal of Molecular Sciences Int. J. Mol. Sci. 2023, 24, 588 https://doi.org/10.3390/ijms24010588.
  63. Ashwini S. Ingole, Megha P. Kadam, Aishwarya P. Dalu, Shital M. Kute, Piyusha R. Mange, Vaishali D. Theng, Om R. Lahane, Aniket P. Nikas, Yash V. Kawal, Shatrughna U. Nagrik , Prashant A. Patil A Review of the Pharmacological Characteristics of Vanillic Acid Journal of Drug Delivery & Therapeutics. 2021; 11(2-s):200-204 http://dx.doi.org/10.22270/jddt.v11i2-s.4823
  64. Raina, A. P., Verma, S. K., & Abraham, Z. (2014). Volatile constituents of essential oils isolated from Alpinia galanga Willd. (L.) and A. officinarum Hance rhizomes from North East India. Journal of Essential Oil Research, 26(1), 24–28. https://doi.org/10.1080/10412905.2013.822430
  65. Simorangkir, D., Masfria, M., Harahap, U., & Satria, D. (2019). Activity anticancer n-hexane fraction of Cyperus rotundus L. rhizome to breast cancer MCF-7 cell line. Open Access Macedonian Journal of Medical Sciences, 7(22), 3904–3906. https://doi.org/10.3889/oamjms.2019.530
  66. Xue, B.-X., He, R.-S., Lai, J.-X., Mireku-Gyimah, N.A., Zhang, L.-H., & Wu, H.-H. (2023). Phytochemistry, data mining, pharmacology, toxicology and the analytical methods of Cyperus rotundus L. (Cyperaceae): a comprehensive review. Frontiers in Pharmacology,14:1178233. DOI: 10.3389/fphar.2023.1178233.

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Manoj Bhad
Corresponding author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Photo
Manoj Garad
Co-author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Photo
Rushikesh Sanap
Co-author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Photo
Ishwar Araj
Co-author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Photo
Ramdas Darade
Co-author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Photo
Vikram Sarukh
Co-author

Student of S N D College of Pharmacy, Babhulgaon, Yeola

Manoj Bhad*, Manoj Garad, Rushikesh Sanap, Ishwar Araj, Ramdas Darade, Vikram Sarukh, A Comprehensive Review on Phytochemistry and Pharmacological Activities of Cyperus Rotundus L., Int. J. Sci. R. Tech., 2025, 2 (11), 351-364. https://doi.org/10.5281/zenodo.17605637

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