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I.INTRODUCTION
RT
COMPOUND NAME
MOLECULAR
FORMULA
MOLECULAR
WEIGHT
PEAK
AREA%
1
2
4.99
6.51
Styrene
Triethoxysilanola
C8H8
C6H16O4Si
104
180
1.09
1.00
9.22
4-Hydroxy-5,6dimethylpyridin-2(1H)one (Deferiprone)
C7H9NO2
139
1.59
10.45
C14H16O3
232
1.34
5
6
7
8
11.09
12.84
13.50
14.23
4'-Methylpent-3'-enyl
Phenylglyoxylate
Acetic acid, pentyl ester
1-Hexadecanol
Behenic alcohol
2,2-Dideuterooctadecanal
C7H14O2
C16H34O
C22H46O
C18H34D2O
130
242
326
268
3.68
8.91
0.97
1.11
20.85
C7H6O3S
170
1.30
10
22.24
C18H36
252
11.91
11
23.97 2,2-Dimethyl-2,3dihydrocyclopentano[b]i
ndanone-1,4(4H)-dione
C14H12O2
212
1.36
12
24.97 1,3-diformyl-2-chloro-5isopropylbenzene
C11H11O2
210
2.55
13
25.90
(2S,4R,5S)-2-Ethyl-5methoxycarbonyl-4methyl-5-hexanolide
C9H14O4
186
2.18
14
28.77
C18H36O2
284
1.35
15
30.14
C13H17ClO3
256
1.65
16
31.81
2-Ally-4-chloro-1,3dimethoxy-5(methoxymethyl)benzen
e
Phytol isomer
C20H40O
296
8.22
17
34.28
2,6,10,14,18,22etracosahexaene,
2,6,10,15,19,23hexamethyl(Squalen)
C30H50
410
3.44
18
35.49
3-Pyrrolidin-2-ylpropionic acid
C7H13NO2
143
2.61
19
36.79
Isochiapin B
C19H26O6
350
1.53
20
37.14
504
1.45
46
1.78
392
1.01
347
1.75
41.50 Cholesta-8,14-dien-3-ol,
4,4-dimethyl-, (3,5)Acetate
412
2.41
21
22
23
24
3,4Ethylenedioxythiophene
-2-carboxaldehyde
1-Octadecene
C29H48O
Table-1
Figure 1
The ethanolic extract of Caralluma truncato-coronata was
subjected to GC-MS analysis and the original full Mass
Spectrogram, Library Search Results and the Library Search
Graphics Table were presented in Figure1,with the Compound
Test Organism
Figure 3
Control
Sample 1
(mm)
8.0
9.0
7.0
14.0
9.0
Klebsiella oxytoca
6.0
Candida albicans
6.0
Candida krusei
6.0
Candida tropicalis
6.0
Staphylococcus
6.0
aureus
Escherichia coli
6.0
7.0
Enterococcus faecalis
6.0
11.0
Zone of Inhibition Report (mm)
The ethanolic extracts of C.truncato-coronata were tested
for their antibacterial and antifungal efficacies against both
Gram-positive and Gram-negative bacteria, including some
clinically-important Risk group 2 human pathogens, possessed
a broad spectrum antibacterial and antifungal activity against a
variety of both Gram-negative and Gram-positive human
pathogenic organisms with a zone of inhibition from 7 to
14mm. Ethanolic extract exhibited the most pronounced
antibacterial effectiveness comparable to standard reference
streptomycin, with more potency against Gram-positive than
Gram-negative bacteria. These results revealed the potential of
ethanolic extract as a suitable antibacterial lead compound that
might be used for further development of other derivatives to
increase the antimicrobial efficacy.
VII.DISCUSSION
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