lantana camara linn: a review
DESCRIPTION
In recent years, focus on plant research has increased all over the world and large body of evidence has collected to show immense potential of medicinal plants used in various traditional systems. In the traditional systems of medicine, most of the remedies were taken from plants and they were proved to be useful. Lantana camara L, belong to the family Verbenaceae, is such a herb used traditionally to treat various ailments like tetanus, rheumatism, malaria, cough, fevers, cold, rheumatisms, asthma to mention a few. Many phytochemical investigations have been done on this plant. The plant was reported to contain various compounds like triterpenoids, proteins, carbohydrates, lactones, furfural, flavonoids, amino acids, alkaloids, saponins, glycosides, tannins, steroids. Many of the traditional uses have been scientifically proved. The ethnopharmacology, phytochemistry and pharmacology of Lantana camara L. are discussed in this review.TRANSCRIPT
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 66 ~
e - ISSN - 2249-7722
Print ISSN - 2249-7730
International Journal of Phytotherapy
www.phytotherapyjournal.com
Lantana camara Linn: A REVIEW
Jyothi M Joy1*
, Vamsi S1, Satish C
1, Nagaveni K
1
*,1Department of Pharmacognosy, Sree Vidyanikethan College of Pharmacy, Tirupathi, Andhra Pradesh, India.
INTRODUCTION
The genus Lantana (Verbenaceae) as described
by Linnaeus in 1753 contained seven species, six from
South America and one from Ethiopia. Lantana is
mostly native to subtropical and tropical America, but a
few taxa are indigenous to tropical Asia and Africa. It
now occurs in approximately 50 countries where several
species are cultivated under hundreds of cultivar names
[1]. The genus is a difficult one to classify taxonomically
since species are not stable and hybridisation is
widespread, shape of inflorescence changes with age, and
flower colours vary with age and maturity [2]. Lantana
camara L. (Verbanaceae), commonly known as wild or
red sage is the most widespread species of this genus and
regarded both as a notorious weed and a popular
ornamental garden plant [3]. Lantana camara grows
luxuriantly at elevations up to 2000 m in tropical, sub-
tropical and temperate regions [4]. It is a woody
straggling plant with various flower colours, red, pink,
white, yellow and violet. The stems and branches are
sometimes armed with prickles or spines [1].
The plant is native to tropical and subtropical
America. Dutch explorers introduced it into the
Netherlands from Brazil in the late 1600s and later
explorers from other countries brought seeds to Europe,
Great Britain and North America. Following its
introduction into Hawaii as a garden flower, it soon
spread to the islands of the Pacific, Australia and
southern Asia. In the 18th and 19th century, nurserymen
commercialised and popularised many colourful forms
and it is now cultivated world-wide as an ornamental
plant. Of the 650 cultivar names in the genus, the
majority are associated with the L. camara complex. The
plant is an aggressive, obligate out breeder weed that has
invaded vast expanses of pastures, orchards and forest
areas in many tropical and subtropical regions [1]. It has
been regarded as one of the 10 most noxious weeds in the
world [4].
Corresponding Author:- Jyothi M Joy Email: [email protected]
ABSTRACT
In recent years, focus on plant research has increased all over the world and large body of evidence has
collected to show immense potential of medicinal plants used in various traditional systems. In the traditional
systems of medicine, most of the remedies were taken from plants and they were proved to be useful. Lantana
camara L, belong to the family Verbenaceae, is such a herb used traditionally to treat various ailments like tetanus,
rheumatism, malaria, cough, fevers, cold, rheumatisms, asthma to mention a few. Many phytochemical investigations
have been done on this plant. The plant was reported to contain various compounds like triterpenoids, proteins,
carbohydrates, lactones, furfural, flavonoids, amino acids, alkaloids, saponins, glycosides, tannins, steroids. Many of
the traditional uses have been scientifically proved. The ethnopharmacology, phytochemistry and pharmacology of Lantana camara L. are discussed in this review.
Key words: Lantana camara L, Phytochemistry, Phytoconstituents.
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 67 ~
Apart from its popularity as a garden plant, L.
camara is said to form a useful hedge and to provide a
good preparation for crops, covering the ground with fine
leaf mulch [2]. It improves the fertility of rocky, grave, or
hard laterite soils, enriches the soil, serves to retain humus
in deforested areas and checks soil erosion. Lantana
leaves and twigs are often used in India as green mulch.
The ash is rich in potassium and manganese which is
useful in manuring coconut trees [1]. In tropical countries,
the ripe blue black berries are eaten, but ingestion of the
green berry has led to human fatalities. L. camara is
poisonous to stocks and humans [5, 6]. L. camara is
poisonous to stocks and humans. Ingestion of leaves from
L. camara, by grazing animals produces photodermatitis,
jaundice, liver damage and death [7].
This review features the plant biography,
ethnopharmacology, phytochemistry and pharmacology
of Lantana camara L. are considered. This information
provides a basis for the evaluation of Lantana camara as
a useful source of renewable material.
PLANT BIOGRAPHY
Botanical name:
Lantana camara L. Family: Verbenaceae
Synonyms
Camara vulgaris and Lantana scabrida
Common names
It is commonly called as sleeper weed, lantana, and wild
sage. The plant is distributed all over the world and
occurs widely in the Asia-Pacific region, Australia, New
Zealand, Central and South America, West Indies and
Africa. Linguistic variations lead in various names to the
plant.
Some of them are given below.
English: Common Lantana
Hindi : Raimuniya
Tamil : Unni chedi
Malayalam: Arippoo
Telugu: Pulikampa
Marathi: Tantani
HABIT
Lantana camara is a low, erect or subscandent,
vigorous shrub which can grow to 2 - 4 meters in height.
The leaf is ovate or ovate oblong, 2 - 10 cm long and 2 - 6
cm wide, arranged in opposite pairs. Leaves are bright
green, rough, finely hairy, with serrate margins and emit a
pungent odour when crushed. The stem in cultivated
varieties is often non- thorny and in weedy varieties with
recurved prickles. It is woody, square in cross section,
hairy when young, cylindrical and up to 15 cm thick as it
grows older. Lantana is able to climb to 15 m with the
support of other vegetation. Flower heads contain 20 - 40
flowers, usually 2.5 cm across; the colour varies from
white, cream or yellow to orange pink, purple and red.
Flowering occurs between August and March, or all year
round if adequate moisture and light are available.
Pollinators include lepidopteran species and thrips. The
fruit is a greenish blue-black colour, 5 - 7 mm in
diameter, drupaceous, shining, with two nutlets; seed
setting takes place between September to May with 1 - 20
seeds on each flower head. Mature plants produce up to
12,000 seeds annually. Seed germination occurs when
sufficient moisture is present; germination is reduced by
low light conditions. The root system is very strong with a
main taproot and a mat of many shallow side roots [8].
ETHNOPHARMACOLOGY
The plant has been used in many parts of the
world to treat a wide variety of disorders [1]. The leaves
of the plant are boiled like tea and the decoction is a
remedy against cough [9]. A decoction of the plant is
given as treatment for tetanus, rheumatism, malaria and
ataxy of abdominal viscera. Pounded leaves are applied to
cuts, ulcers and swellings; a decoction of the leaves is
used as a lotion for wound [10]. Lantana camara found
use in folk remedies for cancers and tumours. A tea
prepared from the leaves and flowers was taken against
fever, influenza and
stomach-ache. In Central and South America, the
leaves were made into a poultice to treat sores, chicken
pox and measles. Fevers, cold, rheumatisms, asthma and
high blood pressure were treated with preparations from
the plant. In Ghana, infusion of the whole plant was used
for bronchitis and the powdered root in milk was given to
children for stomach-ache [1, 11]. It has been claimed that
a steroid, lancamarone, from the leaves exhibited
cardiotonic properties [12]. Traditionally it is also used as
a tonic, in abdominal pains, as anthelmintic and
Insecticide [13]. In Asian countries, leaves were used to
treat cuts, rheumatisms and ulcers [14].
PHYTOCHEMISTRY
All the plant parts were investigated for the
chemical constituents. The plant was reported to contain
various compounds like Triterpenoids [14, 15], proteins
[16], carbohydrates [17], lactones [18], furfural [19],
flavonoids [14, 20] amino acids [13], alkaloids, saponins,
glycosides, tannins and steroids [14].
GC and GC/MS analyses of the hydro distilled
essential oil from the leaves of Lantana camara showed
large amount of sesquiterpene, mainly -caryophyllene (35.70%) and caryophyllene oxide (10.04%). The tested
essential oil showed good fumigant activity. The essential
oil of L. camara showed a wide spectrum of antibacterial,
antimicrobial and antifungal activities [21]. For L.
camara, the maximum yield obtained by hydrodistillation
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 68 ~
from the leaves reached 0.2% and, from the flowers, up to
0.6% [22, 23]. A sample obtained from L. camara trees
grown in Brazil had a terpene-like, leathery, fatty, and
sweaty odour. The constituents were found to be mainly
bisabolene derivatives (65%) with only traces of
monoterpenes. The sesquiterpenes present were -curcumene (1.5%), E-nuciferal and Z-nuciferol (3.9%), (-
)-ar-curcumen-15-al (5.6%), -curcumene (8%), ar-curcumene (9.7%), (-)--b-bisabolol (10%), (-)- -curcumen-15-al (14.9%) [1]. Bicyclogermacrene (26.1%),
caryophyllene (24.4%), germacrene D (19.2%) and
valecene (12.0%) also have been isolated from the
essential oil [24].
Six phenolic compounds such as salicylic acid,
gentisic acid, -resorcylic acid, coumarin, ferulic acid, and 6-Me coumarin were identified in L. camara extract
by HPLC [25]. Three new pentacyclic triterpenoids,
lantacin, camarin, and camarinin, were isolated from the
aerial parts of L.camara. The structures were elucidated
by chemical transformation, HR-EI mass spectrometry,
and NMR spectroscopy, including 1D (1Hand 13C-NMR)
and 2D (1H, 1H-COSY, NOESY, H, 1HTOCSY, J-
resolved, HMQC, and HMBC) experiments [26].
The active fractions of the leaves, twigs, stems,
and roots of L. camara yielded known oleanonic acid,
lantadene A, and oleanolic acid, which were very toxic to
brine shrimp larvae [27]. Lantanilic acid, camaric acid
and oleanolic acid,were isolated from the methanol
extract of the aerial parts of L. camara through bioassay
guided fractionation, all of which possess nematocidal
activity. [28, 29]. Two triterpenoids named lantadene A
and lantadene B were isolated from the chloroform extract
fraction of leaves of L. camara [30,31,32,33,34].
Two novel triterpenoids such as 3, 19-dihydroxyursan-28-oic acid and 21, 22 -epoxy-3-hydroxyolean-12-en-28-oic acid have been isolated from
the roots of L. camara [35]. Two new compounds,
lantanoside and lantanone, and the known compounds
linaroside and camarinic acid were isolated from the
aerial parts of L. camara. Camarolide and lancamaric
acid, two new constituents also have been isolated from
the aerial parts of L. camara [36]. The triterpenoid lantic
acid was isolated from L. camara plants cultivated in
Egypt, which possess strong antibacterial activity aganist
Gram-positive and Gram-negative bacteria [37, 38, 39,
40]. Three new pentacyclic triterpenoids were isolated
from the aerial parts of L. camara namely camaryolic
acid, methylcamaralate and camangeloyl acid [41]. A new
ursane derivative was isolated from the leaves of L.
camara and its structure elucidated as 3, 24- dioxo-urs-
12-en-28-oic acid by spectral analysis [42]. Three new
pentacyclic triterpenes, ursoxy acid, methyl ursoxylate
and ursangilic acid along with oleanolic acid acetate were
also isolated from the aerial parts of L. camara [43].
Ursethoxy acid, a new pentacyclic triterpene, was isolated
from the aerial parts of L. camara. Its structure has been
elucidated as 3, 25-epoxy-3-ethoxy-urs-12-en-28-oic acid through extensive NMR studies [43].
The triterpenoids betulonic acid, icterogenin and
betulinic acid the known flavonoid, -sitosterol 3-O--D-glucoside and a mixture of campesterol, stigmasterol and
-sitosterol were isolated from the stems of pink-flowering L. camara [44].
The methanol extract of L. camara revealed trace
quantities (0.00004-0.0002%) of euphane triterpene
lactones. Five active compounds were isolated and the
structure of these compounds was determined by means
of spectroscopic methods. All compounds were potent
inhibitors of human thrombin [45]. A well known
phenylethanoid, verbascoside has been isolated from L.
camara [46]. The Z-isomer of verbascoside, lantanaside
has also been found to co-occur with verbascoside in L.
camara [47]. Isoverbascoside which often co-occurs with
verbascoside, martynoside, isonuomioside A,
derhamnosylverbascoside and calceolarioside E has been
isolated from L. camara [48].
Two triterpenes, 25-hydroxy-3-oxoolean-12-en-
28-oic acid and hederagenin have been isolated from L.
camara [49]. 12-oleanane triterpenoid and 12-ursane type triterpenoid, camarilic acid and camaracinic acid
have been reported from the aerial parts of L. camara
collected in Pakistan [50]. A number of triterpenoids were
isolated from the roots of L. camara and they were
identified as lantanolic acid, 22-hydroxy-oleanonic acid and lantaiursolic acid [51].
A mixture of -amyrin, -amyrin and pomolic acid were isolated from the stems of L. camara [52].
Three quercetin derivatives named contained 3-methoxy-,
3, 7-dimethoxy- and 3, 7, 4-trimethoxyquercetin were also separated from L. camara [53]. A novel triterpene,
22-acetoxylantic acid and the known triterpenes lantic acid and lantanolic acid were also isolated from L.
camara [54].
Geniposide, the biosynthetic precursor of
theveside, has been isolated from the roots of L. camara,
together with 8-epiloganin, shanzhside methyl ester and
lamiridoside. Six oligosaccharides, ajugose, stachyose,
verbascotetraose, verbascose, lantanose A and B and
flavone named camaroside were isolated from the roots of
L. camara [55].
Lantadene C has been isolated from the leaves of
the hepatotoxic plant L. camara was identical with
dihydrolantadene A. The molecular structure of lantadene
C has been deduced from single crystal X ray diffraction
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 69 ~
analysis. It resembles lantadene A in the pentacyclic
portion of the molecule but differs in the side chain
region. Atom C-34 is cis to C-35 in lantadene C but is
trans in lantadene A [56]. Another pentacyclic triterpene
named lantabetulic acid was isolated from L. camara [57].
PHARMACOLOGICAL ACTIVITIES
Antibacterial activity
Deepak Ganjewala etal carried out the
antibacterial activities of leaves and flowers extracts
obtained with ethyl acetate. The test organisms used in
this study were Escherichia coli (MTCC901),
Pseudomonas aeruginosa (MTCC429), Bacillus subtillis
(1429) and Staphylococcus aureus (MTCC96). Leaf and
flower ethyl acetate extracts exhibited considerable
antibacterial activities against the bacteria used where the
value of zone of inhibition ranged from 10-21 and 9-15
mm, respectively. For flower and leaf ethyl acetate
extracts, the zone of inhibition (mm) measured ranged
from 10-21 and 9-15 mm, respectively. Antibacterial
activities vary from one L. camara to the other. The
effectiveness of the extracts varies with its concentration
and the kind of bacteria used in the study [3]. Mary Kensa
V has also performed the antibacterial activity of various
extracts of L. camara. Methanol, Petroleum ether, water
and Chloroform extracts of leaf, stem and root were tested
against various pathogenic bacterial species of E.coli,
Pseudomonas aeruginosa, Staphylococcus aureus and
staphylococcus saprophiticus by disc diffusion method.
Leaves were showed strong inhibition compared to stem
and root extracts on all tested bacterial strains [58].
Antihelmintic activity
Successive extracts from the leaves of Lantana
camara Linn were investigated for their anthelmintic
activity against Pheretima posthuma and three
concentrations (10, 50 and 100 mg/ml) of each extracts
were used in the study. The parameters used to determine
the activity were determination of time of paralysis and
time of death of the worm. Ethanolic extract exhibited
significant anthelmintic activity at highest concentration
of 100 mg/ml. Piperazine citrate in 10 mg/ml
concentration was included as standard reference and 1%
Gum acacia in normal saline as control. The anthelmintic
activity of ethanol extract was significant followed by
hydroalcoholic extract of Lantana camara [59].
Antiulcer activity
Methanolic extract of Lantana camara was
evaluated for antiulcerogenic effect in aspirin induced
gastric ulcerogenesis in pyloric ligated rats, ethanol
induced gastric ulcer, and cysteamine induced duodenal
ulcer models. The extract was administered orally at two
different doses of 250 mg/kg and 500 mg/kg. The lipid
peroxidation, reduced glutathione levels of ethanol
induced gastric ulcer model and inhibition zone in
diameter against Helicobacter pylori also determined. The
L. camara extract significantly (P < 0.01) reduced ulcer
index, total acidity and significantly (P < 0.01) increased
the gastric pH of aspirin + pylorus-ligation induced
ulcerogenesis and ethanol induced gastric ulcer models.
The extract also significantly (P < 0.01) reduced the ulcer
index of cysteamine induced duodenal ulcer. The L.
camara showed significant (P < 0.01) reduction in lipid
peroxidation and increase in reduced glutathione levels.
The methanolic extract of Lantana camara leaves shown
healing of gastric ulcers and also prevents development of
duodenal ulcers in rats [14].
Termiticidal activity
Extracts of Lantana camara var. aculeata leaves
were studied for their termiticidal effects against adult
termite workers. The 5% chloroform extract was found to
be significantly effective against termite workers [20].
Wound healing activity
Burn wound healing activity of the ethanol leaf
extract of L.camara was carried out in Sprague dawley
rats. Healing was assessed by the rate of wound
contraction and period of epithelialization. Extract treated
wounds were healed in about 21 days which is not distinct
from the controls. The data suggested that L. camara has
no wound healing promoting activity on burn wound [60].
Nayak etal.,has performed the wound healing activity of
the aqueous extract of L. camara and the extract showed
significant activity in excision wound model. Wound
healing time, wound contraction and synthesis of collagen
were considered as the major parameters to evaluate the
wound healing activity. [61]
Anticancer activity
Pet ether, chloroform, ethanol and aqueous
extracts of Lantana camara were screened for preliminary
anticancer activity by using antimitotic activity. Ethanol
extract exhibited better antimitotic activity as reduction in
mitotic index was observed from 90.2 % to 61.4 % and
from 97.6 % to 49.4 % after 1 and 3 hour treatment of
extract having concentration of 10 mg/ ml. Mitotic index
of all the extracts treated roots were significantly lower
than the mitotic index of control. Mitotic index of
methotrexate was found to be 57.0 % and 55.8 % after 1
and 3 hour treatment respectively [62].
Effect on red blood cells
The effects of an aqueous extract of Lantana
camara on the osmotic fragility and on the morphology of
RBC were carried out. In the presence of the extract, the
data obtained indicated a significant (p < 0.05) increase of
hemolysis and modifications on the morphology of RBC.
These effects of the Lantana camara may be associated
with some pharmacological properties of the chemical
compounds of aqueous extract [63].
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 70 ~
Antimotility activity
Evaluation of antimotility activity was done in
intestine of mice treated with Lantana camara leaf
powder, Lantana camara methanol extract (LCME),
lantadene A, neostigmine and neostigmine + LCME.
Neostigmine was used as a promotility agent. Intestinal
motility was assessed by charcoal meal test and
gastrointestinal transit rate was expressed as the
percentage of the distance traversed by the charcoal
divided by the total length of the small intestine. The
intestinal transit with LCME at a dose of 500 mg/kg was
26.46% whereas the higher dose (1g/kg) completely
inhibited the transit of charcoal in normal mice. The %
intestinal transit in the neostigmine pretreated groups was
24 and 11 at the same doses respectively. When the plant
extracts at 125 and 250 mg/kg doses were administered
intraperitonealy, there was significant reduction in fecal
output compared with castor oil treated mice. At higher
doses (500 and 1000 mg/kg), the fecal output was almost
completely stopped [64].
Cytotoxicity and antitubercular activity
The Antitubercular activity of Lantana camara
on multiple-drug-resistant Mycobacterium was
investigated among Nigerian HIV-infected-persons.
Minimal inhibitory concentration (MIC) was estimated by
the well-in-agar-diffusion method and potency of extracts
compared with standard drugs. Cytotoxicity was
determined using brine shrimps. MIC of drugs was
0.33mg/ml, 0.25mg/ml and 0.20mg/ml for streptomycin,
isoniazide and rifampicin. L. camara had MIC of
0.63mg/ml for M. tuberculosis and unidentified M. avium
complex and 0.89mg/ml for M. avium complex. LC50 of
L. camara had 32.6ppm for M. tuberculosis, 55.9ppm for
M. avium complex and 51.3ppm for unidentified species.
The observed activity of the extracts is consistent with
their use in traditional medicine for the treatment of
Mycobacterium species [65].
Anti hyperglycemic Activity:
Methanol extract of Lantana camara Linn fruits
were orally tested at the dose of 100 and 200 mg/kg for
hypoglycemic activity for normal and streptozotocin
induced diabetic rats. Methanol extract of Lantana
camara Linn fruit 200 mg/kg produced a significant
reduction in fasting blood glucose level in the normal and
streptozotocin induced diabetic rats [66].
Effect on general reproductive performance and
teratology
Effects of hydroalcoholic extract from Lantana
camara var. aculeata leaves on fertility, general
reproductive performance and teratology in the rat were
reported. The data showed that the extract interfered in
the frequency of fetal skeleton anomalies from dams
treated with the extract and induced embryotoxicity as
indicated by post-implantation loss, without any signs of
maternal toxicity [7].
Lanata camara Linn.
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 71 ~
Prickles on Lantana stem
CONCLUSION
Demand to herbal drugs is increasing day by
day. Plants contain number of chemical moieties with
varied pharmacological activities. Many potent and
efficous medicinal principles used for treating dreadful
diseases have been isolated from plant kingdom. So it is
very clear that the study of the medicinal plants is
important to meet the requirements in effective therapy.
Lantana camara is considered as weed used in folk
medicine in many parts of the world. Phytochemical
studies showed that the plant is free from diterpenoids and
rich in essential oils. Monoterpenes, triterpenes, flavones
coumarin, steroids, iridoid glycosides, are reported from
Lantana camara. Triterpenes and flavones are the more
common secondary metabolites in Lantana camara. Most
of the pharmacological studies were preliminary, carried
out in animals and are not sufficient for the development
of a pharmaceutical product. Still, intensive preclinical
and clinical studies are required to evaluate the efficacy
and toxicity of these plant products.
REFERENCE
1. Ghisalberti EL. Review Lantana camara L. (Verbenaceae). Fitoterapia, 71, 2000, 467- 486. 2. Munir AA. J Adelaide Bot Gard, 17, 1996, 1. 3. Deepak Ganjewala, Silviya Sam, Kishwar Hayat Khan. Biochemical compositions and antibacterial activities of
Lantana camara plants with yellow, lavender, red and white flowers. Eur Asia J Bio Sci, 3, 2009, 69-77.
4. Sharma OP, Makar HPS, Dawra RK. Toxicon, 26, 1988, 975. 5. Ross IA. Medicinal plants of the world. Chemical constituents, traditional and modern medical uses. New Jersey:
Humana Press, 1999.
6. Morton JF. Econ Bot, 48, 1994, 259. 7. Fernanda B Mello, Daniela Jacobus, Kelly Carvalho, Joao RB Mello. Effects of Lantana camara (Verbenaceae) on
general reproductive performance and teratology in rats. Toxicon, 45, 2005, 459466. 8. Anonymous. The Asia-Pacific Forest Invasive Species Network. Asia-Pacific Forestry Commission (APFC) - a statutory
body of the Food and Agricultural Organization of the United Nations (FAO).
9. Watt JM, Breyer-Brandwijk MG. The medicinal and poisonous plants of southern and eastern Africa. E & S Livington Ltd, 1962, 1947.
10. Anonymous. The Wealth of India. New Delhi: Publication and Information Directorate, 6, 1962, 34. 11. E.L. GhisalbertiU and Irvine FR. Woody plants of Ghana. London: Oxford University Press, 1961. 12. Sharma VS, Kaul KN. Indian 59418. Chem Abstr, 53, 1959, 652. 13. Yadav SB, Vyasji Tripathi. A new triterpenoid from Lantana camara. Fitoterapia, 74, 2003, 320321. 14. Sathish R, Bhushan Vyawahare, Natarajan K. Antiulcerogenic activity of Lantana camara leaves on gastric and duodenal
ulcers in experimental rats. Journal of Ethnopharmacology, 134, 2011, 195197. 15. Barre JT, Bowden BF, Coll JC, De-Jesus J, De-La-Fuente VE, Janairo JC, et al. Phytochemistry, 45, 1997, 321.
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 72 ~
16. Sundararamaiah T, Bai VV. J Indian Chem Soc, 50, 1973,620. 17. Ahmed ZF, El-Moghazy Shoaib AM, Wassel GM, El-Sayyad SM. Planta Med, 21, 1972,282. 18. Ahmed ZF, El-Moghazy-Shoaib AM, Wassel GM, El-Sayyad SM. Planta Med, 22, 1972,34. 19. Al-Showiman SS. J Sci Ind Res, 57, 1998,907. 20. Rajesh K Verma, Suman K Verma. Phytochemical and termiticidal study of Lantana
camara var. aculeata leaves. Fitoterapia, 77, 2006, 466468. 21. Safia Zoubiri, Aoumeur Baaliouamer.GC and GC/MS analyses of the Algerian Lantana camara leaf essential oil: Effect
against Sitophilus granarius adults. Journal of Saudi Chemical Society, 2011, 1-7.
22. Ahmed ZF, El-Moghazi Shoaib AM, Wassel GM, El-Sayyad SM. Planta Med, 21, 1972, 282. 23. Gildermeister E, Hoffmann Fr. Die Aetherischen Ole. Berlin: Akademie-Verlag, Vol. VI, 1961. 24. Erlnio O. Sousa1, Thiago S. Almeida, Irwin R. A Menezes, Fabola FG. Rodrigues, Adriana R. Campos, Sidney G.
Lima and Jos GM. Da Costa. Chemical Composition of Essential Oil of Lantana camara L.(Verbenaceae) and
Synergistic Effect of the Aminoglycosides Gentamicin and Amikacin. Rec. Nat. Prod, 6(2), 2012, 144-150.
25. Yi Z, M. Zhang, B. Ling, D. Xu and J. Ye. Inhibitory effects of Lantana camara and phenolic compounds from it on growth of Eichhornia crassipes. Yingyong Shengtai Xuebao, 17, 2006, 1637-1640.
26. Begum S, Zehra Q, Syeda A. Wahab and BS. Siddiqui .Triterpenoidal secondary metabolites from Lantana camara Linn. Helv. Chim. Acta, 89, 2006, 1932-1941.
27. Fatope MO, L. Salihu, SK. Asante and Y. Takeda..Larvicidal activity of extracts and triterpenoids from Lantana camara. Pharm. Biol., 40, 2002, 564-567.
28. Barua AK, P. Chakrabarti, MK. Chowdhury, A. Basak and K. Basu. The structure and stereochemistry of lantanilic acid, the ,-dimethylacryloyl ester of lantaninilic acid, isolated from Lantana camara. Phytochemistry, 15, 1976, 987-989.
29. Qamar F, S. Begum, SM. Raza, A. Wahab and BS. Siddiqui. Nematicidal natural products from the aerial parts of Lantana camara Linn. Nat. Prod. Res., 19, 2005, 609-613.
30. Hart NK, JA. Lamberton, AA. Sioumis and H. Suares. New triterpenes of Lantana camara. A comparative study of the constituents of several taxa. Aust. J. Chem., 29, 1976a, 655-671.
31. Sharma P, RK. Dawra and HPS. Makkar. Isolation and partial purification of lantana (Lantana camara L.) toxins. Toxicology Letters, 37, 1987, 165-172.
32. Pattabhi V, N Sukumar and OP Sharma. Structure of lantadene A, the major triterpenoid of Lantana camara, red variety. Acta Cryst. C, C47, 1991, 810-812.
33. Misra LN, AK Dixit and RP Sharma. High concentration of hepatoprotective oleanolic acid and its derivatives in Lantana camara roots. Planta Med., 63, 1997, 582.
34. Ma W, D Xiao and S Deng. Terpenoid constituents of the leaves of Lantana camara. Guangzhou Huaxue, 29, 2004, 14-19.
35. Misra L and H. Laatsch. Triterpenoids, essential oil and photo-oxidative lactonization of olanolic acid from Lantana camara. Phytochemistry, 54, 2000b, 969-974.
36. Siddiqui BS, A Wahab and S Begum. Two new pentacyclic triterpenoids from the aerial parts of Lantana camara Linn. Heterocycles, 53, 2000, 681-687.
37. Barua AK, P Chakrabarti, PK Sanyal and B Das. Triterpenoids XXXII. Structure of lantic acid: a new triterpene from Lantana camara. J. Indian Chem. Soc., 46, 1969, 100-101.
38. Barua AK, P Chakrabarti, PK Sanyal K Basu and K Nag. Triterpenoids XL. Structure of lantic acid, a new triterpene from Lantana camara. J. Indian Chem. Soc., 49, 1972, 1063-1064.
39. Siddiqui BS, WM Raza, S Begum, S Siddiqui and S. Firdous. Pentacyclic triterpenoids from Lantana camara. Phytochemistry, 38, 1995, 681-685.
40. Saleh M, A Kamel, X Li and J. Swaray. Antibacterial triterpenoids isolated from Lantana camara. Pharm. Biol., 37, 1999, 63-65.
41. Begum S, A Wahab and BS Siddiqui. Pentacyclic triterpenoids from the aerial parts of Lantana camara.hem. Pharm. Bull., 51, 2003a, 134-137.
42. Yadav SB and V Tripathi. A new triterpenoid from Lantana camara. Fitoterapia, 74, 2003, 320-321. 43. Begum S, A Wahab and BS Siddiqui. Ursethoxy acid,a new triterpene from Lantana camara. Nat. Prod. Lett, 16,
2002,235-238.
44. Lai JS, YF Chan and KF Huang. Constituents from the stems of Lantana camara. Chin. Pharm. J., 50, 1998, 385-392. 45. ONeill MJ, JA Lewis, HM Noble, S Holland, C Mansat, JE Farthing, G Foster, D Noble, SJ Lane, PJ Sidebottom, SM
Lynn, MV Hayes and CJ Dix. Isolation of translactone-containing triterpenes with thrombin inhibitory activities from
the leaves of Lantana camara. J. Nat. Prod., 61, 1998, 1328-1331.
46. Herbert JM, JP Maffrand K Taoubi, JM Augereau, I Fouraste and J Gleye. Verbascoside isolated from Lantana camara, an inhibitor of protein kinase C. J. Nat. Prod., 54, 1991, 1595-600.
-
Inter. J. of Phytotherapy / Vol 2 / Issue 2 / 2012 / 66-73.
~ 73 ~
47. Mahato SB, NP Sahu, SK Roy and OP Sharma. Potential antitumor agents from Lantana camara: structures of flavonoid and phenylpropanoid glycosides. Tetrahedron, 50, 1994, 9439-9446.
48. Taoubi K, MT Fauvel, J Gleye, C Moulis and I Fouraste. Phenylpropanoid glycosides from Lantana camara and Lippia multiflora. Planta Med., 63, 1997, 192-193.
49. Singh SK, A Singh VJ. Tripathi and PV Finzi. Minor constituents of Lantana camara. J. Indian Chem. Soc., 73, 1996, 547-548.
50. Begum S, SM Raza, BS Siddiqui and S Siddiqui. Triterpenoids from the aerial parts of Lantana camara. J.Nat. Prod., 58, 1995, 1570-1574.
51. Pan WD, YJ Li, LT Mai, K Ohtani, R Kasai, O Tanaka and DW Yu. Triterpenoid constituents of the roots of Lantana camara. Yaoxue Xuebao, 28, 1993a, 40-44.
52. Lai JS, JY Huang and KF Huang. Constituents from the stems of Lantana camara. Chin. Pharm. J., 48, 1996, 451-458. 53. Wollenweber E, M Dorr, R Muniappan and K Siems. Flavonoid aglycons and triterpenoids from the leaf exudates of
Lantana camara and Lantana montevidensis. Biochem. Syst. Ecol., 25, 1997, 269-270.
54. Barre JT, BF Bowden, JC Coll, J De Jesus, VE De La Fuente, G Janairo and CY Ragasa. A bioactive triterpene from Lantana camara. Phytochemistry, 45, 1997, 321-324.
55. Pan WD, YJ Li, LT Mai, K Ohtani, R Kasai and O Tanaka. Chemical constituents of the roots of Lantana camara. Yaoxue Xuebao, 27, 1992, 515-521.
56. Sharma OP, J Vaid, V Pattabhi and KK Bhutani. Biological action of lantadene C, a new hepatotoxicant from Lantana camara var. aculeata. J. Biochem. Toxicol, 7, 1992, 73-79.
57. Hart NK, JA Lamberton, AA Sioumis, H Suares and AA Seawright. Triterpenes of toxic and non-toxic taxa of Lantana camara. Experientia, 32, 1976b, 412-413.
58. Mary Kensa V. Studies on phytochemical screening and antibacterial activities of Lantana camara Linn. Plant Sciences Feed, 1 (5), 2011, 74-79.
59. Jitendra Patel, Kumar GS, Deviprasad SP, Deepika S, Samim Qureshi MD. Phytochemical and anthelmintic evaluation of Lantana camara (L.) Var. aculeate leaves against Pheretima posthuma. Journal of Global Trends in Pharmaceutical
Sciences, 2(1), 2011, 11-20.
60. Nayak BS, Raju SS, Ramsubhag A. Investigation of wound healing activity of Lantana camara L. in Sprague Dawley rats using a burn wound model. International Journal of Applied Research in Natural Products, 1(1), 2008, 15-19.
61. Nayak BS, Raju SS, Eversley M, Rramsubhaq A. Phytotherapy research, 23(2), 2009, 241-5. 62. Derle RV, Tare HL, Gore MS, Deore SR, Dama GY, Khandagale ST, Kandekar AE. Preliminary anticancer activity of
Lantana camara by using Allium cepa root tips model. International of pharmacy review and research, 1(1), 2011, 21-
24.
63. Adalgisa I. Maiworm, Giuseppe A. Presta, Sebastio D. Santos-Filho, Severo de Paoli, Tnia S. Giani, Adenilson S. Fonseca, Mario Bernardo-Filho. Osmotic and morphological effects on red blood cell membrane:action of an aqueous
extract of Lantana camara. Brazilian Journal of Pharmacognosy, 18(1), 2008, 42-46.
64. Lenika Sagar, Rajesh Sehgal and Sudarshan Ojha. Evaluation of antimotility effect of Lantana camara L. var. acuelata constituents on neostigmine induced gastrointestinal transit in mice. BMC Complementary and Alternative Medicine, 5,
2005, 18.
65. Dibua UE, Odo GE, Udengwu S, Esimone C. Cytotoxicity and antitubercular activity of Allium sativum and Lantana camara against mycobacterial isolates from people living with HIV/AIDS. The Internet Journal of Infectious Diseases,
2010, 8(1).
66. Venkatachalam T, Kishor Kumar V, Kalai Selvi P, Avinash O. Maske, Anbarasan V, Siva Kumar P. Antidiabetic activity of Lantana camara Linn fruits in normal and streptozotocin-induced diabetic rats. Journal of pharmacy and
research, 4(5), 2011, 1550-1552.