Evidence-Based Complementary and Alternative Medicine / 2014 / Article / Tab 1 / Research Article
Mikania glomerata : Phytochemical, Pharmacological, and Neurochemical StudyTable 1 Fatty acids methyl esters and other constituents identified by GC/MS, after hydrolysis and methylation of the standardized ethanol extract of leaves of M. glomerata Sprengel.
Compound number Compound name R.T. Area (%) Main fragments (%) M+ /base peak 1 Methyl cinnamate 8.39 2.60 131 (100); 162 (53); 103 (52); 77 (37); 51 (30)162/131 2 2H-1-Benzopyran-2-one 9.49 20.47 118 (100); 146 (70); 90 (41); 89 (40); 63 (28)146/118 3 (2-Hydroxyphenyl)methyl propionate 10.65 2.66 120 (100); 148 (90); 91 (70); 44 (44); 180 (10)180/120 4 (Z)-Methyl-hexadec-7-enoate 17.49 2.64 43 (100); 55 (80); 41 (72); 74 (60); 268 (>10)268/43 5 Methyl hexadecanoate 17.77 36.00 74 (100); 87 (65); 43 (30); 55 (22); 270 (>10)270/74 6 Hexadecanoic acid 18.12 5.77 73 (100); 43 (96); 60 (73); 57 (65); 256 (>10)256/73 7 (Z)-Methyl-octadec-9-enoate 19.44 15.90 55 (100); 41 (76); 69 (75); 74 (100); 296 (<10)296/55 8 Octadecanoic acid 19.63 7.40 74 (100); 87 (61); 43 (38); 55 (24); 298 298/74 9 Squalene 26.96 3.89 69 (100); 81 (69); 41 (28); 95 (20)ā/69
R.T.: retention time; M+ : ion molecule.