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Plant Extracts With Antibiotic Eect
antibacterial compounds isolated from S. officinalis leaves, potentiate the effects of aminoglycosides on
methicillin-resistant S. aureus (Horiuchi et al., 2007, Pavić et al., 2019).
Thymus vulgaris L.
Plant Description
T. vulgaris L. or thyme, also known as “garden thyme,” is an aromatic, perennial plant belonging to
the Lamiaceae family. Thymus vulgaris, presents several chemovarieties: T. vulgaris geranoliferum, T.
vulgaris linaloliferum, T. vulgaris mircenoliferum and T. vulgaris terpenoliferum, chemovarieties rich in
monoterpenic alcohols; T. vulgaris cineoliferum, rich in monoterpenic oxides; T. vulgaris thujanoliferum,
rich in monoterpenic hydrocarbons; T. vulgaris carvacroliferum and T. vulgaris thymoliferum rich in
monoterpenic phenols (carvacrol and thymol). The aerial parts of the plant are traditionally used for
bronchitis, whooping cough, flu, fermentative colitis, biliary colic, intestinal parasitosis, buccopharyngeal
infections, myalgia, for various skin problems such as acne, dermatitis, insect bites.
Biological Activities
The various extracts of T. vulgaris L. (ethanol and water) and essential oils obtained from the plant
were evaluated and reported as having broad-spectrum antibacterial action (chemotypes thymoliferum,
geranioliferum and linanoliferum) and of choice on Chlamydia (T. vulgaris thujanoliferum). In a study,
Hammad et al., (2007) investigated the effect of aqueous extracts of T. vulgaris on the growth and adhesion
of Streptococcus mutans to human oral epithelial cells. The 20% aqueous extract resulted in a significant inhibition of bacterial cell growth (96%), and a greater reduction in bacterial cell adhesion to oral
epithelial cells compared to the effect of chlorhexidine digluconate. The ethanolic extract obtained from
the aerial parts of Thymus vulgaris showed MIC between 3.12-6.25 mg/μL on the bacteria Escherichia
coli, Klebsiella pneumoniae, Staphylococcus aureus, Listeria monocytogenes, Yersinia enterocolitica,
Enterococcus faecalis (Gnat et al.). Another in vivo study in an animal model showed that methanolic
extract of T. vulgaris L. is effective against methicillin-resistant S. aureus (MRSA); MIC was 2.53 and
3.83 CFU / mL, for bacteria isolated from the throat and lungs, respectively (Arshad et al., 2017).
Thyme essential oil develops antimicrobial activity on both Gram-positive and Gram-negative bacteria.
In vitro studies have shown strong antibacterial action of Thymus vulgaris oil on S. pyogenes, S. mutans,
A. actinomycetemcomitans and P. gingivalis. In the case of Salmonella typhirium, the essential oil of T.
vulgaris L. showed a MIC of 25.5 mm (Fadil et al., 2018), and the biofilm of Salmonella enteritidis was
inhibited at MIC/MBC of 0.156/0.315 μL/mL (Čabarkapa et al., 2019). Thyme essential oil has also been
shown to act against methicillin resistant S. aureus (MIC 18.50 μg/mL) (Tohidpour et al., 2010). The most
intense antibacterial activity of this essential oil was observed against blaCTX-M-1-producing E. coli
S22 / 12 and ESBL-producing Klebsiella pneumoniae S34 / 15 with a MIC of 2.87 μg / mL. In addition,
E. coli producing blaCTX-M-1 was more sensitive than E. coli producing blaSHV-12 (Benameur et al.,
2019). Even thyme essential oil vapors are highly effective against respiratory tract pathogens (Inouye
et al., 2006). The antimicrobial properties are mainly attributed to monoterpenic phenols, thymol and
carvacrol, strong anti-infective agents, but also to geraniol, linalool alcohols. Experimental studies have
suggested that a higher content of phenolic terpene compounds results in a higher inhibitory activity
(Fani et al., 2017). In addition to thymol and carvacrol, phenolic acids, polyphenolic carboxylic acids
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Plant Extracts With Antibiotic Eect
(chlorogenic acid, rosmarinic acid) and tannins are also compounds responsible for the antibacterial
potential of thyme. Regarding the antibacterial activity, thyme essential oil develops a higher inhibitory
activity compared to that of aqueous extracts, ethanol and even some antibiotics (Fadil et al., 2018).
Rosmarinus officinalis L.
Plant Description
Rosemary belongs to the Lamiaceae family. It is an aromatic shrub, evergreen, native to the Mediterranean
region, naturalized worldwide. It is traditionally used to relieve muscle pain, to support the immune and
circulatory system, to maintain the health of the digestive system due to its choleretic, stomachic, antispasmodic, antioxidant, antibacterial properties. The species has several chemovars, of which the most
used are: R. officinalis camphoriferum, R. officinalis L. cineoliferum, R. officinalis L. verbenoniferum.
R. officinalis camphoriferum has a stronger antibacterial action than the other two.
Biological Activities
Numerous studies have shown the effectiveness of the essential oil obtained from the aerial parts of the
species and its components on pathogens. Recently, Stojiljkovic et al. (2018) investigated the antibacte-
rial action of rosemary volatile oil on Gram-positive and Gram-negative bacteria such as Staphylococcus
aureus, Bacillus cereus, B. subtilis, B. pumilis, Pseudomonas aeruginosa, Salmonella poona, E. coli.
The test results showed a higher antibacterial activity of the essential oil against Gram-positive bacteria
-1
(MIC 0.20-0.48 mg/mL
) than against Gram-negative bacteria (MIC 1.16-1.72 mg / mL-1). In vitro
studies done by the micro-dilution method against S. aureus and S. epidermidis strains showed inhibitory and bactericidal effects of this oil, the minimum inhibitory concentration (MIC) varying between
-1
1.25 and 2.5 μl ml
for S. aureus and between 0.312 and 0.625 μl ml-1 for S. epidermidis. The minimum
bactericidal concentration (MBC) against the two bacteria reached higher values and was of the order
of 5.0 and 2.5 μl/mL, respectively. In addition, the tested oil resulted in an inhibition of S. epidermidis
biofilm of over 57% at a concentration of 25 μL/ mL (Jardak et al., 2017). Experimentally, it has been
shown that R. officinalis essential oil shows improved antibacterial effects in combination with other
oils, such as clove essential oil (Syzygium aromaticum), results observed in testing on pathogens such
as S. epidermidis, S. aureus, B. subtilis, E. coli, P. vulgaris, and P. aeruginosa (Fu et al., 2007). The
antibacterial activity of rosemary volatile oil is mainly imprinted with 1.8 cineole, camphor, limonene,
α-pinene, Z-linalool oxide and borneol, terpene compounds known for their anti-infective profile
(Bozin et al., 2007). According to Manilal et al., (2021), the hydroalcoholic extract of R. officinalis
leaves reduced the growth in different degrees of some clinical isolates of MDR. The best inhibitory
values (MIC) were recorded against S. aureus, Enterococcus sp. and Salmonella sp. and ranged from
4.103 to 32.103 µg/mL. Inhibitory activity on S. pyogenes, Proteus sp. and Campylobacter sp., proved
to be small. In a comparative analysis, Moreno et al. (2006) evaluated the antibacterial efficacy of a
methanolic extract with a content of 30% carnosic acid, 16% carnosol and 5% rosmarinic acid and an
aqueous extract containing only 15% rosmarinic acid. They concluded that the antimicrobial activity of
rosemary extracts is associated with the content of phenolic compounds; rosmarinic acid and carnosic
acid being the main bioactive compounds with antimicrobial action. Furthermore, the study suggested
that the methanolic extract was effective against both Gram-positive bacteria (MIC between 2 and 15
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59

Plant Extracts With Antibiotic Eect
μg/mL) and Gram-negative bacteria (MIC between 2 and 60 μg / mL) as opposed to the aqueous extract
which showed low activity, the study indicating a synergistic action of the compounds in the methanolic
extract. The antibacterial potential of rosemary was also observed in a clinical study, which evaluated
the efficacy of a mouthwash containing hydroalcoholic extracts of Zingiber officinale, R. officinalis and
Calendula officinalis, concluding that the preparation was effective in patients with gingivitis, and the
effectiveness was comparable to chlorhexidine mouthwash. (Mahyari et al., 2016).
Melaleuca alternifolia (Maiden & Betche) Cheel
Plant Description
Tea tree is a shrub or tree from Myrtaceae family, native to Australia. It has been used by Australians
in traditional medicine as antiseptic and anti-inflammatory to treat various infections for almost 100
years. Tea tree essential oil contains terpinene-4-ol, α-terpinene, γ-terpinene, α-terpineol, 1,8-cineole,
ρ-cymene, terpinolene, and limonene, as major constituents and exerts a strong antioxidant and antibacterial activity, as confirmed by many in vitro tests.
Biological Activities
Zhang et al. (2018) noticed that the essential oil of M. alternifolia displayed significant antimicrobial
activity on Gram-positive and Gram-negative bacteria as Staphylococcus aureus, Pseudomonas aerugi-
nosa, P. italicum, P. digitatum and Escherichia coli strains, with a MIC raging between 2 and 24 mg/mL.
According to these authors, ” the hydrophobic terpenes from the essential oil interact with the membrane
lipids of the pathogenic microorganisms, which affect the permeability of the membrane, leading to a
deficit in the production of cellular energy caused by the decrease in ATP generation, and cellular lyses
due to leakage or coagulation of the cytoplasm” (Zhang et al., 2018). Ferrini et al. (2006) found that
from terpien-4-ol, from the tea tree essential oil has an efficient antibacterial activity on Staphylococ-
cus aureus, even for the antibiotic resistant strains. Another in vitro study performed by Kokina et al.
(2019) showed the inhibition of tea tree essential oil on the bacterial growth of Staphylococcus aureus
and Salmonella Typhimurium with a MIC of 10, respectively > 10 μg/mL.
Allium sativum L.
Plant Description
Garlic is an alimentary plant belonging to Amaryllidaceae family. Garlic has been used in traditional
medicine since ancient times. It contains phenolic, polysaccharides and thiosulfinates as major components. Garlic also contains flavonoids, saponins, aminoacids, enzymes, vitamins A, B and C, and
minerals (Parham et al., 2020). The alliinase enzyme transforms alliin to allicin which is one of the main
components of garlic (Figure 17.4). Allicin is the thiosulfinate responsible for the antimicrobial activity
of this medicinal plant, having both bacteriostatic and bactericidal effects.
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Plant Extracts With Antibiotic Eect
Figure 4. The conversion of Alliin to Allicin in Garlic
Biological Activities
Many in vitro studies demonstrated the antibacterial effect of garlic extracts against Gram positive and
Gram-negative bacteria, including those resistant to antibiotics, such as Staphylococcus aureus, Pseu-
domonas, Klebsiella, Salmonella typhi, Enterococcus faecalis, Proteus, and Escherichia coli (Bakri &
Douglas, 2005; Yadav et al., 2015; Rawat, 2015; Petropoulos et al., 2018; Ismail et al., 2020; Parham
et al., 2020; Pancu et al., 2021). The antibacterial effect of Allium sativum was proved using different
extracts: crude extracts, powder, various solvents extracts, and also the biocompounds isolated from this
plant. The aqueous and alcoholic extract of garlic contain organosulfur compounds as S-allyl cysteine,
S-methyl cysteine, and S-allylmercapto-
that garlic distilled oil with diallyl disulfide and diallyl trisulfide is effective on different Gram-positive
and negative bacteria cultures (S. aureus, B. subtilis, P. aeruginosa and E. coli). The mechanism of action
consists in binding to the thiol groups of enzymes in bacteria, which leads to the microbial inactivation.
l-cysteine (Bhatwalkar et al., 2021). Avato et al. (2000) revealed
Arctostaphylos uva-ursi L.
Plant Description
Arctostaphylos uva-ursi L., from the Ericaceae family, is an evergreen shrub that grows in the northern
hemisphere, abounds in the Arctic regions, and only at high altitudes in the temperate and Mediterranean
area. For a long time, the leaves of this plant have been used in traditional medicine to combat and treat
urinary tract diseases, like infections such as cystitis or urethritis, as a diuretic and anti-inflammatory
agent for various diseases of the urogenital tract.
Biological Activities
Many studies have shown the effectiveness of bearberry leaf extracts in urinary tract infections through
antibacterial activity and the ability to reduce recurrences in people at risk of contracting these infections. Moskalenko (1986) showed that the ethanolic extract of Uvae ursi folium has strong bacteriostatic
activity on Bacillus subtilis, Escherichia coli, Shigella sonnei and Shigella flexneri. In another study,
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61

Plant Extracts With Antibiotic Eect
Anukk et al., (1999) reported that aqueous bearberry leaf extracts show remarkable bacteriostatic activ-
ity on H. pylori strains. This activity could be related to the ability of the aqueous extract to modulate
the hydrophobicity of the cell surface and to increase the aggregation of cells, an effect determined by
the high content of tannins. Various extracts (aqueous, ethanolic and ethyl acetate) from A. uva - ursi
leaves were tested on strains of Enterococcus faecalis and strains of Escherichia coli, etiological agents
of urinary tract infections. In vitro results concluded that the aqueous extract has a stronger antibacterial effect on E. coli (MIC 0.625-5 mg/mL) compared to ethanolic and ethyl acetate extracts (MIC 10
mg/mL), while the effect on Enterococcus faecalis was similar for the three types of extracts. It should
be noted that the extracts showed stronger antibacterial activity against Gram-positive strains (Vučić et
al., 2013). Arbutin metabolites (hydroquinone, hydroquinone glucuronide, hydroquinone sulfate) are
considered to be the compounds responsible for the urinary antiseptic activity of the plant. They exert
antimicrobial action on a wide range of pathogens involved in the infectious pathology of the urinary
tract, E. coli, Proteus vulgaris, Acinetobacter baumanii, Ataphylococcus aures, Bacillus subtilis, Entero-
coccus faecalis, Neisseria gonorrhoeae (Ștefănescu et al., 2019). Although it was initially thought that
hydroquinone could be released from arbutin only by alkalizing urine, more recent research challenges
this hypothesis. Hydroquinone deconjugation is now thought to be catalyzed by intracellular enzymes
present in the bacterial cytoplasm. Alkalization of urine does not appear to be a prerequisite for the release
of hydroquinone from arbutin (Quintus et al., 2005). The pharmacology of the whole plant has also been
shown to be different from that of arbutin alone. Crude plant extracts are more medically effective than
isolated arbutin (Asensio et al., 2020). In addition, A. uva - ursi extracts have been shown to be helpful
in increasing the susceptibility of antibiotic-resistant bacteria such as beta-lactams. A group of Japanese
researchers studied the effect of corilagin, a polyphenolic compound isolated from A. uva - ursi, against
methicillin-resistant Staphylococcus aureus. Corilagin reduced the minimum inhibitory concentration
of oxacillin and other beta-lactam antibiotics by 100 to 2000 times, the effect of corilagin and oxacillin
being synergistic (Shimizu et al., 2001).
Glycyrrhiza glabra L.
Plant Description
Liquorice is an herbaceous perennial plant from Fabaceae family, native to Southern Europe, Western
Asia, and North Africa. This specie has an important therapeutical value, being used since centuries for
a wide range of pharmacological properties, including anti‐inflammatory, antibacterial, antiviral, antiulcer, and antidiabetic activities. Many biological compounds have been found in this medicinal plant:
simple glucides, polysaccharides, pectins, gums, resins, coumarins, tannins, oestrogens, phytosterols,
amino acids, proteins, minerals, vitamins (B
, B2, B3, B5, C and E), Triterpenoid saponins (glycyrrhizin,
1
responsible for the sweet taste), and flavonoids (liquiritigenin and isoliquiritigenin) are the most important constituents (Pastorino et al., 2018).
Biological Activities
Gupta et al., 2008 and Wang et al., 2015 showed the antimicrobial action of G. glabra extract on Gram‐
positive and Gram‐negative bacteria cultures, as Staphylococcus aureus, Pseudomonas aeruginosa,
Escherichia coli, and Bacillus subtilis (Gupta et al., 2008; Wang et al., 2015). Responsible for the
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Plant Extracts With Antibiotic Eect
antibacterial effect are the secondary metabolites from plant: flavonoids, saponins, and alkaloids, (hispaglabridin A, hispaglabridin B, glabridin, glabrol glabrene, 40‐methylglabridin, and 3‐hydroxyglabrol).
Authors noticed that “the mechanism behind this could be the decrease of bacterial gene expression, the
inhibition of bacterial growth, and the reduction of bacterial toxin production” (Gupta et al., 2008; Wang
et al., 2015). Liquorice may inactivate methicillin resistant Staphylococcus aureus (MRSA) through a
mechanism that involves lowering the expression of the key virulence genes of MRSA and can also have
an inhibitory action on Streptococcus pyogenes, as Fukai et al. (2002) has shown. Gupta et al. (2008)
also demonstrated the antibacterial action of G. glabra against Mycobacterium tuberculosis, glabridin
beeing the responsible compound for this activity. Asha et al. (2013) noticed that the flavonoid glabridin
from liquorice exherts activity against H. pylori, by inhibition of the protein synthesis, DNA gyrase, and
dihydrofolate reductase. Another in vitro study showed that the liquorice polysaccharides also present
activity against Porphyromonas gingivalis adhesion (Chinsembu, 2016).
Hypericum perforatum L.
Plant Description
Hypericum perforatum L. (Hypericaceae) is a perennial plant native to Asia and Europe, known as St.
John’s wort. In traditional medicine it is used as a remedy against skin lesions, sunburn, for diseases of
the gallbladder, depression, dysentery, and diarrhea. More recent studies have focused on the antidepressant effects and antimicrobial activity of St. John’s wort extracts and their components.
Biological Activities
Avato et al., 2004 tested the microbiological activity of various extracts against Gram-positive bacteria
(Bacillus subtilis, B. cereus, Staphylococcus aureus, Enterococcus) as well as Gram-negative (Pseudo-
monas aeruginosa, Acinetobacter calcoaceticus, A. baumanii). It turned out that the pharmacological
activity depends on the type of extract and the solvent used to obtain it. The most active were chloroform
and ethanolic extracts against B. subtilis and B. cereus with a MIC value of 12.5 μg / mL. In addition, the
ethanolic extract significantly inhibited all other Gram-positive bacteria tested, showing a MIC of 12.5
μg/mL, except for E. faecalis (MIC = 50 μg/ mL). The active compounds responsible for the antibacte-
rial activity have been shown to be hypericin, hyperforin and its stable ammonium dicyclohexyl salt. In
a study on the antibacterial activity of an extract in petroleum ether from aerial parts of H. perforatum,
Reichling et al. (2001) reported that hyperforin is the major active compound against Gram-positive
bacteria, including methicillin-resistant Staphylococcus aureus strains, with a MIC of 1 μg / mL. Various extracts and isolated fractions of aerial parts of Hypericum perforatum have been tested for antiHelicobacter activity. In such a study, the butanolic fraction showed anti-Helicobacter pylori activity at
MIC values between 15.6 and 31.2 μg/mL (Saddiqe et al., 2010).
CONCLUSION
As most of the studies that proved the antibacterial effect of plant extracts have been performed on in
vitro cultures of bacteria, in vivo studies and clinical trials are required to be realized in future. The
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63

Table 1. Antibacterial Activity of Some Plant Extracts
Plant Extracts With Antibiotic Eect
Plant Extract Tested bacteria /MIC
• Staphylococcus aureus, Streptococcus pneumoniae, E. coli,
P. aeruginosa, Salmonella typhi and Klebsiella pneumoniae /
0.5–8 μg/mL
• Salmonella enterica/4.12μg/mL
• S. aureus, P. aeruginosa, E. coli, and K. pneumoniae
• Salmonella typhius, B. subtilis, S. aureus,, Staphylococcus
epidermititis, P.aeruginosa, and Klebsiella pneumonia
• Helicobacter pylori /25–100 μg/mL
• Asaia bogorensis, and A. lannensis
• Aeromonashydrophila, Aero monassobria, E. coli, Klebsiella
oxytoca, Pseudomonas morgani, Salmonella anatum,
Klebsiella pneumonia, Salmonella enteritidis, Salmonella typhi
and Shigella sonaan/
12.5-225 μg / mL
• Strptococcus puogenes and Staphylococcus aures/ 62.5 and
300 μg / mL
• S pyogenes, S mutans, P. gingivalis
and A actinomycetemcomitans
• Salmonella enteritidis/ 0.156 μl / ml
• S. aureus (MRSA)/ 2.53 and 3.83 CFU (log10) / ml
• Escherichia coli, Klebsiella pneumoniae, Yersinia
enterocolitica, Staphylococcus aureus, Listeria monocytogenes,
Enterococcus faecalis / 3.12-6.25 mg / μL
• Staphylococcus aureus, Bacillus cereus, Bacillus pumilis
Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa,
Salmonella poona,
• Staphylococcus aureus (ATCC 9144)/ 1.25 to 2.5 μl ml
• Staphylococcus epidermidis/ 0.312 to 0.625 μl ml
• S. aureus, Salmonella sp and Enterococcus sp / 4.103 to
32.103 µg / mL.
• Staphylococcus saprophyticus, S. epidermidis, P. aeruginosa,
and Enterococcus faecalis /70–350 μg / mL
• E. coli, S. aureus,, P. italicum Wehmer, P. aeruginosa and P.
digitatum Sacc. / 2 - 24 mg/mL
• Staphylococcus aureus and Salmonella Typhimurium/ 10,
and > 10 μg/mL
• Neisseria gonorrhoeae, S. aureus, and Enterococcus faecalis
• M. tuberculosis, S. aureus, S. mutans, and P. aeruginosa
• S. aureus, Bacillus subtilis, E. col,i and P. aeruginosa
• Bacillus subtilis, Escherichia coli, Helicobacter pylori,
Shigella sonnei and Shigella flexner
• E.coli /MIC 0.625-5 mg / mL)
• Staphylococcus aureus, Escherichia coli, Pseudomonas
aeruginosa, and Bacillus subtilis
• S. aureus (MRSA)
• Helicobacter pylori
• Mycobacterium tuberculosis
• B. subtilis and B. cereus / 12.5 μg / ml
• Bacillus subtilis, B. cereus, Staphylococcus aureus, 25923,
Enterococcus faecalis / 12.5 - 50 μg / ml μg / ml
•Helicobacter pylori / 15.6 - 31.2 μg / ml
Mentha x
piperita
Salvia
officinalis
Thymus
vulgaris
Rosmarinus
officinalis
Melaleuca
alternifolia
Allium sativum
Arctostaphylos
uva-ursi
Glycyrrhiza
glabra
Hypericum
perforatum
• essential oil
• methanolic
extract
• ethanolic extract
• essential oil
• ethanolic
extracts
• essential oil
• methanolic
extract
• ethanolic extract
• essential oil
•hydroalcoholic
extract
• ethanol extracts
• essential oil
• aqueous extract
• ethanolic extract
• distilled oil
• ethanolic extract
• aqueous extract
• ethanolic extract
• chloroform
extract •ethanolic
extracts
• butanol extract
in
Responsible antibacterial
compounds
• mentol, menthone
• carvone, menthol, and
menthone
• menthol, menthone, camphane,
menthofuran
• carvone, carveol, menthone,
menthol
• phenolic compounds
• gallic, chlorogenic,
neochlorogenic, p-coumaric,
ferulic, rosmarinic acids,
epicatechin, quercetin-3rutinoside and quercetin
• thujone, 1,8-cineole and
camphor
• rosmarinic acid, quercetin,
ellagic acid, chlorogenic acid
• thymol, carvacrol, p-cymene
• thymol, carvacrol, p-cymene
• phenolic and
polyphenolcarboxylic acids
• phenolic and
polyphenolcarboxylic acids
• Limonene, camphor,
eucalyptol, α-pinene, Z-linalool
-1
-1
oxide and borneol
• carnosic acid, carnosol,
rosmarinic acid
• carnosic acid, carnosol,
rosmarinic acid
• terpinene-4-ol, γ-terpinene,
and α-terpinene
• valencene, trans-cadina-1(6),4diene, aromadendrene
• S-allyl cysteine,
S-allylmercapto-
S-methyl cysteine
• allicin
• diallyl and allyl methyl sulfides
• arbutin metabolites
(hydroquinone, hydroquinone
glucuronide, hydroquinone
sulfate)
• glycyrrhizin,
18β-glycyrrhetinic acid,
liquiritigenin, licochalcone A,
licochalcone E, and glabridin
• flavonoids
• vestitol, licoricone,
1-methoxyphaseollidin and
gancaonol
glycyrrhizin, 18β-glycyrrhetinic
acid, liquiritigenin, licochalcone
A, licochalcone E, and glabridin
• glabardin
• hypericin, hyperforin,
ammonium dicyclohexyl salt
l-cysteine, and
Authors
• Abolfazl et al., 2014
• Valková et al., 2021
• Osanloo et al., 2020
• Saba & Anwar, 2018
• Mahady et al., 2005
• Antolak et al., 2018
• Ghorbani et al., 2017;
Santos et al.; 2017;
Sonboli, et al., 2006
• Wijesundara and
Rupasinghe, 2019
• Fani et al., 2017
• Čabarkapa et al., 2019
• Arshad et al., 2017
• Gnat et al., 2017
• Stojiljkovic et
al.,2018; Bozin et al.
2007
• Jardak et al., 2017
• Manilal et al., 2021
• Petrolini et al., 2013
• Zhang et al., 2018
• Kokina et al., 2019
• Bhatwalkar et al.,
2021
• Bhatwalkar et al.,
2021
• Avato et al., 2011
• Moskalenko,
1986
• Vučić et al., 2013
• Wang et al., 2015
• Fukai et al., 2002
• Fukai et al., 2002
• Gupta et al., 2008
• Avato et al., 2004
• Reichling et al., 2001
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Plant Extracts With Antibiotic Eect
mechanisms of antimicrobial action of biological compounds from plants must be completely elucidated,
and additionally, their toxicity on humans should be evaluated.
This chapter summarizes the significance of the antibacterial activity of some plant extracts due to
their constituents, as demonstrated by the scientific studies. Biological compounds from plants can be
used as an alternative to chemical, synthetic antibiotics, or used complementary, synergistic for better
therapeutically results.
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