Volume 16, number 2
 Views: (Visited 1,047 times, 1 visits today)    PDF Downloads: 2620

Kumar C. D, Anitha S, Varalakshmi P, Rao D. M. Evaluation of Potential Phytochemicals and Phyto Pharmacological Activities of Erythroxylum Monogynum Roxb. Biosci Biotech Res Asia 2019;16(2).
Manuscript received on : 15-April-2019
Manuscript accepted on : 14-May-2019
Published online on:  25-05-2019

Plagiarism Check: Yes

Reviewed by: Ruchi Verma

Second Review by: Saranya V.

How to Cite    |   Publication History    |   PlumX Article Matrix

Evaluation of Potential Phytochemicals and Phyto Pharmacological Activities of Erythroxylum Monogynum Roxb.

C. Dhanunjaya Kumar*, S. Anitha, P. Varalakshmiand Dowlathabad Muralidhara Rao

Department of biotechnology, S.K.University, Anantapur, 515003, India.

Corresponding Author E-Mail: rao.muralidhara@gmail.com

DOI : http://dx.doi.org/10.13005/bbra/2759

ABSTRACT: Red cedar or Bastard sandal [Erythroxylum monogynum Roxb.] belongs to family Erythroxylaceae and commonly found in deciduous forests of India and Srilanka. The present work mainly deals with evaluation of phytochemicals present in various parts and pharmacological activities. Now a days a number of alternative medicines are avaliable for those diseases which are not cured by proper medicine. In this regard ayurveda or phytochemicals obtained from plants are using  to cure diseases since long back in India due to their less toxic and side effects when compared with other source of medicine. Plants are considered to be the biosynthetic labs for a number of valuble  phytochemicals. The phytochemicals found in leaf, stem, root of Erythroxylum monogynum known to contain a number of medicinal properties. Pharmocologically Erythroxylum monogynum shows Aantihyperlipidemic, Antioxidant, Aantibacterial, Antidiabetic, Antiplasmodial, Antiobesity, Antitumor, Cytotoxic, Ameliorative, Hepatoprotective, Nephroprotective activities.This work mainly provides information regarding, phytochemicals of various parts of plant, medicinal uses, Traditional importance, pharmacological activities.

KEYWORDS: Erythroxylum Monogynum Roxb; Phytochemicals, Medicinal Uses; Pharmocolgical Activities; Traditional Importance

Download this article as: 
Copy the following to cite this article:

Kumar C. D, Anitha S, Varalakshmi P, Rao D. M. Evaluation of Potential Phytochemicals and Phyto Pharmacological Activities of Erythroxylum Monogynum Roxb. Biosci Biotech Res Asia 2019;16(2).

Copy the following to cite this URL:

Kumar C. D, Anitha S, Varalakshmi P, Rao D. M. Evaluation of Potential Phytochemicals and Phyto Pharmacological Activities of Erythroxylum Monogynum Roxb. Biosci Biotech Res Asia 2019;16(2). Available from: https://bit.ly/2M9pMDs

Introduction

Erythroxylum monogynum Roxb [Author –Roxburgh and Willium [1978] is a shrub or small tree about 7 m to 9 m height. O. E. Schulz placed this species in Sethia Section1. This was commonly found in India, Srilanka2, Mayanmar. In India it mostly found in states like Kerala, Karnataka, Tamil Nadu, Andhra pradesh. In Andhra Pradesh it found in places like Talakona of Chittoor district, Nellore, Batrepalli and kanwashram of Anantapur district, Vishakapatnam and Godavari districts. Erythroxylum monogynum contains a lot of vernacular names in respective regional languages.3

Various Vernacular Names of  Erythroxylum Monogynum

English: Bastard sandal, Red cedar.

Telugu: Paribadrakamu, Gatiri, Adivi goranti, Pagadapu, Gaadara.

Tamil: Ayakkantamaram, Cakkaratapam, Cemmanatti, Citari, Vattukkolli.

Kannada: Chambalu, Jeevadaali, Jeevadaane, Gandhagaru.

Malayalam: Devaru, Chem, Chemmana.

Irulu: Sembulichan.

Taxonomic Hierarchy

Kingdom: Plantae

Division: Angiosperms

Order: Malpighiales

Family: Erythroxylaceae

Genus: Erythroxylum

Species: monogynum

Botanical Profile

The leaves are simple and are arranged alternatively distichous, they are obovate in shape. The leaf blade length is about 2.5 to 6.5 x 1-3 cm4,5. They are glossy light green and are about to 3-4 cm in length 1.5 cm in width with a half cm long petiole. The tip of leaf is rounded in shape. The leaf shows prominent midrib with pinnate reticulate venation.

The flowers are bisexual and are white in colour, auxillary, solitary or 1-4 in auxillary  facsisles. There are 5-6 sepals which are ovate, acute and glabrous, There are 5-6 petals with white colour and are oblang with inner side containing ligule, imbricate, 10-12 stamens are present, they are monadelphous, the ovary is 3-4 celled, 3-4 styles are present and are unte to single style containing capitates stigma. The ovary is superior with 3-4 cells,1-2 ovules present in each cell.

The fruit is a drupe type. It is ellipsoid apiculate and glabrous. The fruit is blood red in colour with single seed. The fruit is edibile one which people eats generally. The fruit is green in colour when unripe and is bright scarlet at maturity. This fruit is about 1 cm in lenghth and 4 mm across and have single seed. At the stage of ripening the colour gradually turns to blood red colour

The bark of Erythroxylum monogynum is dark brown in colour. Rarely patches are seen. The roughness of bark is due to the ridges and wrinkles which are there longitudinally and transversly. It shows fibrous fracture. The wood of Erythroxylum monogynum is hard The. The wood contain pleasent odour. The annual growth rings can be seen on surface. The wood is bitter in taste. It contains well defined root system. The root system is tap root system. The roots are well distributed to get sufficient anchorage and water with root caps.

Phytochemicals Identified in Various Parts of Erythroxylum Monogynum

In order to identify the nature of phytochemicals which are present in plant the analysis of phytochemical was done in various fractions6. By the phytochemical evaluation the various compound classes present in different parts of plants are also helpul to know potential pharmacological compounds in biological assay determination7.

Leaves contain Ecgonine, Cinnamoyl cocaine8,9. Ecgonine is a tropane alkaloid [Formula: C9H15NO3], Cinnamoyl cocaine is a natural tropane alkoloid [formula  C19H23NO4]

Erythroxylum monogynum leaf extracts of methanol and acetone showed that presence of saponins, tannins flavonoids, alkaloids, terpenoids, cardiac glycosides, carbohydrates and pytytosterol10. In hydroalcoholic leaf extract of Erythroxylum monogynum phytochemicals like Glycosides, Steroids, Flavonoids, Tannins, Phenols were present.11,39

The rootbark contains several alkaloids like3 α-[3,4,5,-Trimethoxy cinnamoyloxy]6 β-benzoyloxytropane, 3 α-[3,4,5,-Trimethoxy benzoyloxy ]tropane, 3 α-[3,4,5,-Trimethoxy cinnamoyloxy]tropane, α-[3,4,5,-Trimethoxy benzoyloxy ]tropan-6 β,7 β-diol12. Most of alkaloids were identified by GC-MS, the well documentation of tropane alkaloids fragmentation pattern was done13. The twenty alkaloids identified in the rootbark of Erythroxylum monogynum were Hygrine, Tropine, Tropinone, Pseudotropine Butropine [3α-isobutyryloxytropane], 3α-isobutyryloxynortropane, Isoporoidne [3-[2-Methylbutyloxy]nortropane], Dihydrocuscohygrine, 3-[2-Methylbutyloxy]tropane, Cuscohygrine, Valeroidine [3α-Isovaleryloxytropae-6 β-ol], Tropacocaine [3 β –Benzoyloxytropane], 3-Phenylacetoxynor tropane, 3-[2-Methylbutyryloxy]tropane6,7, diol, Convolamine [3α-[3,4,-Dimethoxybenzoyloxy]tropane], 3 α-[3,4,5,-Trimethoxy benzoyloxy] tropan-6 β-ol, 3 α-[3,4,5,-Trimethoxy cinnamoyloxy] tropane, 3 α-Cinnamyloxytropane, 3α-Phenylacetoxy tropane, 3 α-Phenylacetoxytropan-6 β-ol, 3 α-[3,4,5,-Trimethoxy benzoyloxy]tropane, 3 β – Phenylacetoxy tropane, 3 α-[4-Methylvaleroyloxy] tropane, 6 β-Benzyloxytropan-3 α-ol,  3α-[3,4,5,-Trimethoxy cinnamoyloxy]-6 β-benzoyloxytropane, 3 α-[3,4,5,-Trimethoxybenzoyloxy]tropan -6 β,-7β-diol14.

Hygrine[C8H15NO] is a pyrrolidine alkaloid15. Hygrine, is a pyrrolidine alkaloid, and is the biosynthetic precursor of pharmacologically important tropane alkaloids16. Cuscohygrine is a pyrroldine alkaloid and was extracted from solanaceae family. Its chemical formula is C13H24N2O.

These hygrine and cuscohygrine are present in leaves of coca17,18.

Both hygrine and cuscohygrine are suitable markers for coca chewing as well as to discriminate the manufactured caca use with other in hair analysis criteria19

Tropine [C8H15NO] is a tropane derivative with hydroxyl group containing at third carbon. 3-Troponol is another name of this compound21. Tropinone C8H13NO was sysnthesised by Robinson. R as a atropine precursor during first world war22,23. Pseudotropines [C8H15NO] are constituents in leaves of coca along with other alkaloids24. Ecgonine is an impartanat identifying parameter for usage of cocaine25.

The wood contains Hibaene epoxide, Monogynol, Devodarool, Alkoloids, Diterpenes such as erythoxydiol, erthroxytriol, Hydrocarbons, primaradiene, Isoatisirene, Atisirene, Devadorene erythroxytriols Q and P20

Medicinal Properties and Ethnobotanical Properties

The intake of bark, wood used for stomach, stimulant, diaphoretic diuretic, and also effective for dyspepsia and as well as continued fever26,27,37 yogurt was mixed with leaf extracts to kill worms of intestine and for to cure jaundice the leaf juice was used4,28.

The  stem and root of plant is considered to contain huge number of properties and best medicinal parts29. The medicinal properties of phytochemicals are claimed to treat skin diseases, diuretic, diaphoretic, stomach problems30,31. Leaf juice orally taken works as as a cooling beverage and for jaundice. The decoction of stem bark is used in treatment of hiccups32Erythroxylum monogynum proved scientifically of containg antibacterial property27, Hepato protective property33 and as well as antidiabetic property34.

The Erythroxylum monogynum leaves and Aloe vere roots are used as food during famine35. In India the Wood of Erythroxylum monogynum is used as an adulterant36. The Erythroxylum monogynum leaf and wood shows medicinal applications regarding rheumatoid arthritis and polio, rheumatoid arthritis, biliousness, polio, urticaria, rashes38. Flavonoids were observed in the leaves of Erythroxylum monogynum.40 Flavonoids contains antioxidant, antiplatelet, anti allergic, anti thrombic, anti inflammation properties.41,42

The stem bark paste of Erythroxylum monogynum along with coconut oil is used to treat skin diseases, scabies.47

There is large demand for timber and is considered as a useful plant in dry evergreen forests43. The leaves ,bark and fruits are very much useful medically44. The wood of boats are preserved from the tar obtained from wood of erythroxylum monogynum by distillation45 and this is an oil46. The Oil obtained from plant contains sandalwood aroma and is used as perfume45. The stem bark phytochemical contains properties against diarrhoea48. The oil, fruit, bark of Erythroxylum monogynum are useful for bone fracture, diarrhoea, skin diseases and as well as fire wood.49

Pharmocological Activities

Erythroxylum monogynum was well known for its pharmoclogical activities. One of the great advantages of medicinal plants is that these are readily available and have no side effects17. World Health Organization (WHO)18 has suggested the evaluation of the potential of plants as effective therapeutic agents, especially in area which we lack safe modern drugs.

The great factors in medicinal plants is they are avalaible readily and shows very less or no side effects50. WHO strongly suggested that it is very essential to go for phytochemical therapeutic agents when even there is no avalaiblity of modern safe drugs.51

The metabolic disorder diabetes mellitus results hyperglycemia and  abnormal metabolism of  lipid, protein and showing effects on retina,nervous system, kidney52. Hyperglycemia is a significant factor for enchancement of complications regarding diabetes mellitus.53

Erythroxylum monogynum anti diabetic property was evaluated in female wistar rats in which diabeties induced by Streptozotocin34 for 6 days the diabetic rats were stabilized. The chloroform fraction of plant was administered from 7th day at a dose of 350mg per kg, and 500 mg per kg for about 21 days. The standard used here is Glibenclamide 10 gm per kg. The chloroform extract effect and standard drug on different parameters like blood glucose, weight of body and profile of serum lipid were recorded. The various histo pathological changes in pancreas in each group of representative animals were studied. The administered Erythroxylum monogynum chloroform fraction dose of 250 mg per kg, 500 mg per kg not showed any significant change in glucose level of blood in normoglycemic rats. On other side the depiction of oral glucose tolerance test showed a significant reduction in glucose level of blood for 30 to 60 min. The parameters like glucose level in blood serum lipid are found to be significantly controlled by the extract of plant in the Streptozotocin induced diabetic rats. The results showed by chloroform fraction of Erythroxylum monogynum 500 mg per kg were comparable with glibenclamide 10 mg per kg standard treatment.

Similarly ethanolic leaf extracts of Erythroxylum monogynum and Chonemorpha fragrans also showed the antideabetic properties on alloxan introduced diabetic rats.54

The phytochemicals from the Angiosperms are considered as new effective antiinfective agents55

From the past two decades the antimicrobial properties were well documented from parts of plant like leaves, roots, seeds, stem.56

Erythroxylum monogynum was utilized in traditional biomedicine to cure problems caused by micro organisms.10 The plants phyto constituents evaluated for their anti microbial properties. The phyto compound showed their effect on bacterial species like Klebsiela pneumonia, Staphylococcus aureus, Escherchia coli, Pseudomonas putida. The plants extract showed its highest impact of inhibition on E.coli. The aqueous extract of Erythroxylum monogynum leaves showed highest inhibition zone against E.coli was 14.53mm followed by ethanol extract 13.70mm

The leaf extracts of Erythroxylum monogynum was showed antimicrobial potential against microorganisms. The extracts showed presence of potential antibioticswith large spectrum of properties57.

By using agar well diffusion method the antibacterial activity of extracts were determined58,59. Micro organisms were seeded on  petriplates containing Mueller Hinton agar medium of 20ml. The wells which are with diameter of 6mm are separated from agar and extract solution which is 5mg/ml was later added. On observing diameter  of growth inhibition zones the antibacterial activity was measured in mm for the strain on comaprision with the control.60

Liver is one of the most important organ in the body and plays viatal role in metabolic reactions. The liver damage can be found by elevated levels of certain enzymes of serum like SGPT,SGOT,bilurubin61. Medicinally there are some plants which shows potential hepatoprotective activity62.

To predict the hepatoprotective activity of Erythroxylum monogynum plant the rats which are induced with the [CCL4] 1ml/kg Crabon tetra chloride was selected and experiment was carried out for 7days10. By using the maceraton techniques the hydroalcholic extract was prepared. Five groups are rats were taken and were maintained as Control, CCL4 induced, CCL4 and Liver tonic, CCL4 and extract 150 milligram per kilogram and CCL4 and extract 200 milligram per kilogram. The blood was collected on eighth day by retro orbital puncture for to study the parameters of serum like serum glutamate Oxaloacetate transaminase [SGOT], Serum glutamate pyruvate transaminase [SGPT] and the bilurubin. For to histopathological examinations the liver was isolated and processed. The SGOT, SGPT, total bilurubin decreased levels were taken as an indication of hepatoprotective activity of extract in the treated rats. For the indication of hepatoprotective activity of extracts the regenerated hepatocytes are witnessed

Sabeena Hussain Syed et al., (2013) worked on  the hepatoprotective activity of Erythroxylum monogynum methanolic extract of leaves on paracetamol introduced  hepatotoxity in rats. The elevated serum levels like SGPT[ serum glutamic pyruvic transaminase], SGOT [serum glutamic oxaloacetate transaminase], alkaline phosphatise and it was found that the total bilirubin was restored to normal.33

Malaria is a disease which is caused due to the mosquito to humans and as well as other animals. In India due to its large population and great urbanisation it is very difficult to manage malaria63 and the malarial parasite showing resistance to existing classes of drugs which are meant to malaria.64

The antiplasmodial property was studied against Plasmodium falciparum by different solvent leaf extracts of Erythroxylum monogynum methanol extract of plant 12.23μg per ml showed IC50 value. These results show that the leaf extracts are used in traditional practise and also source to evaluate more antiplasmoidal molecules from Erythroxylum monogynum leaf crude extracts.65

Obesity is a condition where excess amounts of body fats accumulated which directly or indirectly adverse the health. This is associated with increase in premature mortality, morbidity, improper, impaired quality of life66,67,68

The anti obesity property of Erythroxylum monogynum chloroform fraction was tested on wistar rats which are induced with high fat diet. For 56 days the female rats were fedded with a diet which is very rich in fats. The chloroform fraction of Erythroxylum monogynum was administrated 250mg per kg, 500mg per kg doses for last 21days continued with feeding fat diet. Body weight, feed consumption were monitored. After 57 days serum glucose, profiles of serum lipid, liver and total protein were estimated, Antherogenic index was calculated. Later the effect on significant organs like heart, liver, kidneys and epididymal fat pad were observed and recorded. As a reson to treatment prominent reductionin weight of body and parameters like lipid, serum glucose, liver profle levels in animals which are fed on food of high fat improved significantly due to chloroform fraction treatment of plant The two main parameters like antheroginic index and weight of relative epidermal fat pad reduced with treatment of extract of plant69.

Kidneys are the vital organs that aims to keep blood purify, clean and also maintains chemical balance70 Several works have shown that plants which are materials rich in secondary compounds like flavonoids, polyphenolic compounds Saponins, arginine and glutamic acid possess the activities like hypoglycaemic, hepatoprotective and the  nephroprotective activities in animals71 The nephro protective property of Erythroxylum monogynum leaf ethanolic extract was observed in alloxan induced nephrotoxicity albino rats which are wistars strained. The significant reduction in the values of uric acid, urea and createnine was observed with the oral administration of extract. This indicates Erythroxylum monogynum ethanolic extract contains nephro protective property in case of alloxan induced nephro toxic rats39.

The second largest common disease which is a major health burden is cancer.72,73 Plants are well used as medication for the cancer74. From natural resources about 60 percent of total anti cancer agents are derived75 the natural resources like plants as well as marine organisms and microorganisms.76 In laboratory the plants which are susceptable and resistant to crown gall were analyzed for their antitumour activity, cytotoxic activity of which the constituents or compounds that antitumour or cytotoxic against human tumours. The highest cytotoxic activity showed by methanolic extract of Erythroxylum monogynum against brine shrimps of 172.3ppm at an LC50. Further, the plant extract was tested against antitumour activity which was induced by Agrobacterium tumefaciens using antitumour bioassay of carrot disc. The studies showed that the activity of Erythroxylum monogynum inhibition of tumour even at very low concentration of 800 microgram per milli litre. All the results showed the strong anti tumour and cytotoxic activity in the crown gall susceptible plant.77

Antioxidants  inhibits the process called oxidation .Natural antioxidants present  in the all plant parts. These antioxidants include carotenoids,phenols dietary glutathione, flavonoids  vitamins endogenous metabolites78. Plant-based antioxidants function as singlet and triplet oxygen quenchers, free radical scavengers, enzyme inhibitors, peroxide decomposers, synergists79.

Erythroxylum monogynum aqueous and ethanolic extract of leaves are evaluated for anti oxidant activity invitro. Among these extracts the ethanolic extracts found to be potent to show more anti oxidant activity. By using various solvent systems the ethanolic extracts was further fractionated. The solvent systems are Chloroform, Pet ether, Ethyl acetate, n Butanol are used to evaluate antioxidant potential. The assay like DPPH and H2O2 scavenging assay are used for to evaluate anti oxidant potential. For all these assays the reference compound used is Ascorbic acid. By using UV – Visible spectrophotometer all the analysis are carried out. Finally all the result showed the fractions and extracts of Erythroxylum monogynum leaves contains significant reducing power properties and free radical scavenging. Among all the chloroform fraction which was separated from ethanolic extract crude was found to contain significant anti oxidant potential80.

By using the chromium precipitated testicular poisonous male albino rats an evaluation was carried out. The extract which was prepared by maceration approach. The male fertile albino rats were divided in to four groups of following,

Group 1 Control
Group 2 Chromium 150ppm in distilled water
Group 3 Erythroxylum monogynum alcoholic extract 200mg per kg, and chromium.
Group 4 Erythroxylum monogynum alcoholic extract 300mg per kg, and chromium.

For 30 days the extract and chromium was given orally. on 31st day through retro orbital plexus the rats blood samples were collected to perform serological tests. Then to separate the cauda epididymis and testies the sacrification of rats were done. In order to study the sperm count and motility the cauda epididymis was treated with saline. In group 2 the sperm count and motility is decreased. When compared with group 2 in case of group 3 and group 4 the sperm count and motility was increased. In extract treated groups the HDL, Albumin levels and total proteins were increased. In group 3 and group 4 rats triglycerides, total cholesterol, LDL (low density lipid) and VLDL (very low density lipid) reduction was observed. The rats which are dealed with extracts shown that the amelioractive past time the reformation of semineferous tubule germinal cells of the testis81.

Hyperlipidemia is a condition where abnormal levels of lipids are present in blood Hyperlipidemia which is a modifiable risk factor for atherosclerosis and related cardiovascular diseases, including coronary heart disease, cerebral stroke, myocardial infarction and renal failure are becoming a major health problem in the world recently1. The major health problems by hyperlipedemia are atherosclerosis, heart diseases, mycordial infarction,cerebral stroke, renal faliure are main problems recently in the world.82 Jacobson reported that this condition refers to lipid and cholesterol elevated levels in blood and is identified as dyslipidemia.83 The Erythroxylum monogynum leaf extracts showed antihyperlipedemic property.84 The reduction in values of triglycerides and cholesterol on oral administration ethanolic extract of Erythroxylum monogynum plant was observed. This indicate the extract of leaves contain anti hyper lipidemic activity.

Botanical Name: Erythroxylum monogynum

Figure 1 : Erythroxylum monogynum. Figure 1 : Erythroxylum monogynum.

 

Click here to view figure

 

Figure 2: Twigs of Erythroxylum monogynum. Figure 2: Twigs of Erythroxylum monogynum.

 

Click here to view figure

Conclusion

The present review of Erythroxylum monogynum is a scientific evidence for pharmacological activities of phytochecimals present in various parts of plant. The phytochemicals present in leaf contains Anti microbial, Antiobesity, Antitumor and Anti cancerous, Ameliorative Nephroprotective, Anti plasmodial, Antioxidant, Antimalarial, Antihyperlipidemic properties. This plant contains great number of phytochemicals with important disease curing properties. Still now work done on few phytochemical only. The plant not completely explored. Therefore there is need to analyse the biological properties of these chemicals which helps in curing of other diseases.

References

  1. Schulz,O.E. in Das Pflanzenreich [Engler,A.,ed.], 1907 Vol.1V, sect.134. Engelmann, Leipzig.
  2. Trimen H, Hooker J D. A hand book of the flora of Ceylon, Dalan and Co; London.1898.
  3. J. F. Caius, The Medical and Poisonous Plants of India, Scientific Publishers Jodhpur, India.(1988) 493.
  4. Parrotta JA. Healing plants of peninsular India. Oxford & New York: CAB International; 2001; 279–280.
  5. Dr. N Sasidharan and Dr. B P Pal, Forest Research Institute, Peechi, Kerala, India
  6. Trease GE, Evans WL. Pharmacognosy. 16th ed. London: Bailliere Tindall Ltd; 2009. 60-75.
  7. Singh S., Semwal B.C and Neeli G.S. Microscopic and Physicochemical Evalua­tion of leaves of Spheaeranthus indicus Linn. Pharmacognosy J. 2017 9[1]:21-6.
  8. T. Plowman L. Rivier Annals of Botany, Volume 51, Issue 5, May 1983, 641–659.
  9. Chopra ,R.Nand Ghosh,N.N. Arch.Pharm[Weinheim.Ger.] 1938 276,340.
  10. Alagesaboopathi C. Phytochemical screening and antibacterial potential of Couroupita guianensisaubl and Erythroxylum monogynum roxb. International Journalof Current Research 2013; 5(8):2068-2071.
  11. Vijay Kumar R, Venkatraji Reddy G and M Krishna Reddy. Screening of phytochemicals and antioxidant activity of Erythroxylum monogynum. International Journal of Bioassays 2014;3(05):3005-3007.
  12. Agar, J.T.H and Evans W.C , J. Chem. Soc. Perkin Trans,1976 I 1550.
  13. Lounasmaa, H. in The Alkaloids[Brossi,A.,ed] 1988 Vol 33,pp,1-81. Academic Press. New york.
  14. Philippe Christen, Margaret F.Roberts , J. David Phillipson, William C. Evans, 38-4, 1995, 1053-1056.
  15. Dr. Ame Pictet (1904). The Vegetable Alkaloids. With particular reference to their chemical constitution. London: Chapman & Hall.
  16. Matyas Milen, Peter Abranyi-Balogh, Gyorgy Keglevich. Total Syntheses of the Pyrrolidine Alkaloid, Hygrine. Current Organic Synthesis. 11-6, 2014.
  17. R. L. Glass, M. B. Johnson. Analysis of cuscohygrine in coca leaves byhigh-performance liquid chromatography. J. Liq. Chromatogr. Relat.Technol. 1996, 19, 1777.
  18. J. M. Moore, J. F. Casale, R. F. Klein, D. A. Cooper, J. Lydon.Determination and in-depth chromatographic analyses of alkaloidin South American and greenhouse-cultivated coca leaves.J. Chromatogr. A. 1994, 659, 163.
  19. N. C. Rubio, M. Hastedt, J. Gonzalez, F. Pragst. Possibilities fordiscrimination between chewing of coca leaves and abuse of cocaineby hair analysis including hygrine, cuscohygrine, cinnamoylcocaineand cocaine metabolite/cocaine ratios. Int. J. Legal Med. 2015, 129, 69.
  20. Rastogi and Mehrotra, Compendium of Indian Medicinal Plant, Vol. I (1972) 112-114.
  21. Lide, David R. , Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, 1998 ,pp. 3–564.
  22. Nicolaou, K. C.; Vourloumis, D.; Winssinger, N.; Baran, P. S. “The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century”. Angewandte Chemie International Edition. 2000,39 (1): 44–122.
  23. Robinson, R. “LXIII. A Synthesis of Tropinone”. Journal of the Chemical Society, Transactions. 1917, 111: 762–768.
  24. Joslin, Jeremy David; Biondich, Amy Sue (2016). “Coca: The History and Medical Significance of an Ancient Andean Tradition”. Emergency Medicine International. Retrieved 2019-03-03.
  25. Logan, Barry. (2001). Ecgonine is an Important Marker for Cocaine Use in Inadequately Preserved Specimens. Journal of analytical toxicology. 25. 219-20. 10.1093/jat/25.3.219.
  26. Kirtikar KR, Basu BD. Indian Medicinal Plant. 2nd ed, Vol I. Dehradun :International Book Distributors :1987.p.415.
  27. Srinivasan D, Sangeetha N, Suresh T, Perumalsamy PL. Antimicrobial activity of certain Indian medicinal plants used in folklore medicine. J Ethnopharmacol.2001;74(3):217 -220.
  28. Rajendran A, Rama Rao N, and Henry AN. Hepatic stimulant plants of Andhra Pradesh. J. Econ Tax Bot (Additional Series). 1996;12:221-3.
  29. N.C. Nair and A. N. Henry, Flora of Tamil Nadu, India, Vol. I, Botanical Survey of India, Southern Circle, Coimbatore, India, (1983) p.184.
  30. Ayyanar, M. and Ignacimuthu, S. Medicinal plants used by the tribals of Tirunelveli Hills, Tamilnadu to treat poisonous bites and skin diseases. Indian Journal of Traditional Knowledge. 2005 ,4(3):229-236.
  31. Bauer, A.W., Kirby, W.M.M., Sherris, J.C. and Turck, M.Antibiotic susceptibility testing by standardized single diskmethod. Am. J. Clin. Pathol. 1966 ,45:493-496.
  32. Ravi Prasad Rao, B. and Sunitha, S. Medicinal plant resourcesof Rudrakod Sacred Grove in Nallamalais, Andhra Pradesh, India. J. Biodiversity, 2011 ,2(2):75-89.
  33. Sabeena SH, Namdeo AG. Hepatoprotective effects of leaves of Erythroxylum monogynum Roxb. on paracetamol induced toxicity. Asian Pac J Trop Biomed 2013;3(11):877-81. https://doi.org/10.1016/S22211691(13)60172-0.
  34. Rupesh SK, Ravindra KR, Jayveera KN. Evaluation of Anti-diabetic potential of Erythroxylon monogynum in streptozotocin induced diabetic rats. Int J Adv Res 2014;2:550-60.
  35. Krishnamachari KS. Erythroxylum monogynum leaves and Aloe roots as food. Indian Forester;1900; 26: 619-620.
  36. Textbook  of  Pharmocognacy and phytochemistry Shah and Seth ,1Edition 2010.
  37. Devendrakumar D, Anbazhagan M. Research in Plant Biology. 2012; 2(3): 24-30.
  38. Muthamizh S, VS Ramachandran ,International Journal of Botany Studies , Volume 3; Issue 1; January 2018; Page No. 109-119.
  39. Mehnoor Farheen¹, Chakrapani Ramesh² IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676. Volume 10, Issue 6 Ver. I (Nov – Dec. 2015), PP 83-107.
  40. Chopra R. N. and Ghosh N. N. (1938), Chemische undpharmakologische Unterschung der Blätter von Erythroxylum monogynum Roxb. Arch. Pharm., Berl. 276, 340 -343.
  41. Middleton, E. J. R.; Kandaswami, C. Effect of flavonoids on immune and inflammatory cell function. Biochem. Pharmacol. 1992; 43(6): 1167-1179.
  42. Cooks, N. C.; Samman, S. Flavonoids – Chemistry, metabolism, cardioprotective effects and dietary sources. J. Nutr. Biochem., 1996; 7: 66.
  43. Gamble, A Manual of Indian Timber, 1922, p. 116.
  44. Watts, The Commercial Products of India, 1908, p. 525
  45. Uphof. J. C. Th. Dictionary of Economic plants, Weinheim 1959.
  46. Watt.G.Economic Products of India.Volume 1,Government of India : Calcutta 1883.
  47. P. Kumudha and C. Yogeshwari, International Journal of Plant, Animal and Environmental Sciences Volume-6, Issue-4 Oct-Dec-2016.
  48. Dowlathabad Muralidhara Rao , U.V.U.Bhaskara Rao, and G.Sudharshanam Ethno-Medico-Botanical Studies From Rayalaseema Region Of Southern Eastern Ghats, Andhra Pradesh, India Issued 11 August 2006.
  49. Rajan S, Sethuraman M, Baburaj DS. 1997. Plantsfrom the traditional medical system of the Nilgiri tribes. Ancient Science of Life 16(4):360-365.
  50. B.Kameswara Rao, M.M Kesavulu, R Giri, Ch Appa Rao. Antidiabetic and hypolipidemic effects of Momordica cymbalaria Hook. Fruit powder in alloxan‐diabetic rats”. J Ethnopharmacol.:1999; 67 (1): 103–9.
  51. Penolazzi L et al. Induction of apoptosis of human primary osteoclasts treated with extracts from the medicinal plant Emblica officinalis. 2008; 8:5.
  52. M. N. David, M. James, and E. S. Daniel. Lancet 350 (Suppl. 1) S14 (1997).
  53. L. Luzi, New Eng. J. Med. 339, 115(1998). doi:10.1056/NEJM199807093390210.
  54. Kausar Fatima et al. Antidiabetic and Antihyperlipidemic Activity of Chonemorpha Fragrans and Erythroxylum Monogynum Combined Ethanolic Leaf Extract in Alloxan Induced Diabetic Wistar Rats. Indo American Journal of Pharmaceutical Research.2017:7(01).
  55. Duraipandiyan, V., Ayyana, M. and Ignacimuthu, S. (2006).Antimicrobial activity of some ethnomedicinal plants used byPaliyar tribe from Tamilnadu, India. BMC Complementary andAlternative Medicine. 6:35.
  56. Leven, M., Vannen Berghe D.A. and Mertens, F. (1979). Medicinal plants and its importance in antimicrobial activity. J. Planta Med. 36:311-321.
  57. Alagesaboopathi, C. Phytochemical screening and antibacterial potential of Couroupita guianensis aubl and Erythroxylum monogynum Roxb International Journal of Current Research Vol. 5, Issue, 08, pp.2068-2071, August, 2013.
  58. Bauer, A.W., Kirby, W.M.M., Sherris, J.C. and Turck, M. .Antibiotic susceptibility testing by standardized single diskmethod. Am. J. Clin. Pathol. 1966, 45:493-496.
  59. Chew, Y.L., Chan, E.W.L., Tan, P.L., Lim, Y.Y., Stanslas, J. and Goh, J.K. (2011). Assessment of phytochemical content, polyphenolic composition, antioxidant and antibacterial activitiesof Leguminosae medicinal plants in Peninsular Malaysia. BMCComplementary and Alternative Medicine. 11:12.
  60. Anjum, F.I., Shahid, M., Bukhari, S.A., Anwar, S. and Latif, S.(2013). Study of quality characteristics and efficacy of extractionsolvent/technique on the antioxidant activity of bitter guard seed.J. Food Process Technol. 4:205.
  61. Mascolo, N. Sharma, R. Jain, S. C., and Capasso, F., Ethnopharmacology of Calotropis Procera flowers. J Ethnopharmacol., 22(2): 211-221(1998).
  62. Chowdhary, G.D. Kamboj, P. Singh, I. and Kaila, A.N., Herbs as liver savers – A review, Indian J. ofNatural Products and Resources., 14: 397-408(2010).
  63. Shah N.K., Dhillon G.P.S., Dash A.P., Arora U., Meshnick S.R.,Valecha N. 2011. Antimalarial drug resistance of Plasmodiumfalciparum in India: changes over time and space. The LancetInfectious Diseases, 11, 57–64. DOI: 10.1016/S1473-3099(10)70214-0.
  64. Anderson T. 2009. Mapping the spread of malaria drug resistance. PLoS Medicine, 6, e1000054. DOI: 10.1371/journal.pmed.1000054.
  65. Venugopalan Venkatesalu, Natarajan Gopalan, Pillai C R, Chandramouli Nagula.Invitro anti plasmodial activity of some traditionally used medicinal plants against Plasmodium falciparum. Parasitology Research 2012; 111(1):497-501.
  66. Kopelman P. G. (2000). Obesity as a medical problem. Nature 404, 635–643.
  67. Fontaine K. R., Redden D. T., Wang C., Westfall A. J., Allison D. B. (2003). Years of life lost due to obesity. JAMA298, 187–193.
  68. Haslam D. W., James W. P. T. (2005). Obesity. Lancet 366, 1197–1209.
  69. Rupesh Kanhere, Kandula Ravindra Reddy, Korlakanti Narasimha Jayaveera,SadhuNelson Kumar and Cuddapa Rajaram.. Evaluation of Anti-Obesity Potential of Erythroxylon Monogynum Against High Fat Diet Induced Obesity In Wistar Rats.American Journal of Pharmacy and Health Research 2014;2(1):23-35.
  70. Maton A, Jean H, McLaughlin CW,Warner MQ,Lattart D, Wright JD (1993). Human Biology and health. Eaglewood Cliffs, New Jersy, Prentice Hall, USA.
  71. Gupta, R; Sharma, A.K; Dobhal, M.PI Sharma, M.C, Gupta, R.S (2013). Antidiabetic and Antioxidant potential of β-sitosterol in streptozotocin-induced experimental hyperglycemia. J.Diabetes 3, 29-37.
  72. Kainsa S, Kumar P, Rani P. Medicinal Plantsof Asian Origin Having Anticancer Potential:Short Review.Asian J Biomed and PharmaSci. 2012; 2:1-7
  73. Ma X, Yu H. Global Burden of Cancer. Yale JBiol Med. 2006; 79: 85-94.
  74. Koshland D, Kent JC, Hartwell LH. Geneticanalysis of the mitotic transmission of minichromosomes. Cell. 1985; 40: 393-402.
  75. Privitera G, Napoli E, Luca T, Ruberto G,Castorina S. In vitro Anti-Proliferative Effect of Salvia officinalis Essential Oil and itsThree Main Components on Human LungCancer Cells. AJPCT. 2014; 2: 1159-1168.
  76. Ramesh KS. A Review: BiomedicalCompounds and Anticancer drugs from Marine and Tropical Herbal medicine.International Journal of Chemistry and Pharmaceutical Sciences. 2014; 2: 997-1006.
  77. Tulsi Naik K S, Kiragandur Manjunath , Siddamadappa Chandrashekaran andAppanna V Koppad. Cytotoxic and antitumour activity of methanolic extracts of medicinally important plants. International Journal of Pharma and Bio Sciences2014:5(3):344-353.
  78. Larson R. A. (1988) Phytochemistry, 4: 969-978.
  79. Manach C., Morand C., Crespy V., Demigne C., Texier O., Regerat F. and Remesy C.(1998) FEBS Lett., 426: 331-336.
  80. Rupesh S Kanhere, Ravindra Reddy K and Jayveera K N. In vitro antioxidant activityof various extracts and/or fractions of Erythroxylon monogynum. Int J Pharma Sci 2014; 4(5):750-760.
  81. Vijay Kumar R, Venkatraji Reddy G, Prabhakar B, Rama V, Krishna Reddy M andNarsimha Reddy Y. Ameliorative activity of Erythroxylum monogynum in chromiuminduced testicular toxic rats. International Journal of Institutional Pharmacy and LifeSciences 2015; 5(3):148-166.
  82. Xu QY, Liu yH, Zhang Q, Ma B, Yang ZD, Liu L, et.al. Metabolomic Analysis of Simvastatin and Fenofibrate Intervention in High-Lipid Diet-Induced Hyperlipidemia Rats. Acta Pharmacol Sin. 2014; 35: 1265-1273.
  83. Jacobson MS. Heart healthy diets for all children: no longer controversial. The journal of pediatrics. 1998; 133: 1-2.
  84. Mehnoor Farheen and Chakrapani Ramesh. Phytochemical Evaluation and Pharmacological Screening of Ethanolic Leaf Extracts of Erythroxylum monogynumand Pupalia lappacea for Hepatoprotective, Nephroprotective, Antihyperlipidemicand Antihyperglycemic Activity in Alloxan- Induced Diabetic Albino Wistar Rats.IOSR Journal of Pharmacy and Biological Sciences 2015;10(6):83-107.
(Visited 1,047 times, 1 visits today)

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.