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. 2016 Dec 1;10(6):382–388. doi: 10.1049/iet-nbt.2015.0101

Table 2.

Chemical composition of methanol leaf extracts of E. agallocha

S.No RT Area Area, % Compound name Activity
1 15.549 58,725,120.0 21.400 myo‐Inositol,4‐c‐methyl‐ no known activity
2 17.815 7,829,957.0 2.853 N‐hexadecanoic acid insecticidal property
3 19.150 3,293,158.5 1.200 Phytol antimicrobial activity
4 19.465 10,038,550.0 3.658 methyl 8,11,14‐heptadecatrienoate no known activity
5 24.677 8,243,940.0 3.004 2,6,10,14,18,22‐tetracosahexane,2,6,10,15,19,23‐hexa,ethyl‐, (all‐e)‐ pesticide, antioxidant activity
6 25.053 3,742,039.2 1.364 3,3′‐dimenthol antibacterial activity
7 26.308 4,112,334.2 1.499 gamma‐tocopherol antioxidant, antimicrobial
8 26.888 47,870,352.0 17.444 alpha‐tocopherol antioxidant, antimicrobial
9 28.629 14,447,939.0 5.265 gamma‐sitosterol antidiabetic, antimicrobial
10 28.749 18,494,970.0 6.740 betulin antimalarial, anticancer, antibacterial activity
11 28.909 12,068,890.0 4.398 betulin antimalarial, anticancer, antibacterial activity
12 29.104 12,519,889.0 4.562 4,4,6B,8A,11,11,14B‐octamethyl‐1,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12, 12A,14,14A,14B‐Octadecahhydro‐2 antimalarial, antibacterial activity
13 29.284 3,208,045.2 1.169 2R‐acetoxymethyl‐1,3,3‐trimethyl‐4t‐(3‐methyl‐2‐buten‐1‐yl)‐1t‐cyclohexanol anti‐inflammatory activity
14 29.389 25,794,414.0 9.400 lupeol antiprotozoal activity
15 29.489 5,251,148.5 1.914 2R‐acetoxymethyl‐1,3,3‐trimethyl‐4t‐(3‐methyl‐2‐buten‐1‐yl)‐1t‐cyclohexanol anti‐inflammatory activity
16 29.614 25,281,340.0 9.213 2R‐acetoxymethyl‐1,3,3‐trimethyl‐4t‐(3‐methyl‐2‐buten‐1‐yl)‐1t‐cyclohexanol anti‐inflammatory activity
17 30.040 3,493,336.5 1.273 4,4,6A,6B,8A,11,11,14B‐octamethyl‐1,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12, 12A,14,14A,14B‐Octadecahhydro‐2 antimalarial, antibacterial activity
18 30.290 10,006,224.0 3.646 9,19‐cyclolanost‐25‐en‐3‐ol,24‐methyl‐,(3.beta.,24s)‐ no known activity