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. 2012 Apr 10;17(4):4326–4342. doi: 10.3390/molecules17044326

Table 1.

Compounds identified in C. papaya leaf extract.

No tR (min) [M−H]/[M−H]+ (m/z) MS2 (m/z) Assignment
1 0.26 nd/381.0846 LOW INTENSITY Unidentified
2a 0.29 133.016/nd 133, 115, 89, 87, 73 Malic acid
2b 0.30 191.0214/nd 191, 173, 149, 129, 111, 87, 85 Quinic acid
3 2.93 nd/256.1935 256, 238, 220, 218, 122, 108 Unidentified
4 3.04 LOW INTENSITY nd Unidentified
5 3.22 447.1533/nd LOW INTENSITY Unidentified
6 3.32 295.0484/nd 295, 277, 195, 179, 146, 135, 133, 115, 89 Caffeoyl malate
7 3.37 LOW INTENSITY nd Unidentified
8 3.86 755.2078/757.2274 755, 301, 300, 271, 255, 179, 151 Quercetin-3-O-(2'',6''-di- O-rhamnopyranosyl)glucopyranoside (manghaslin)
9 3.94 279.0531/nd 279, 163, 133, 119, 115, 93 p-Coumaroyl malate (Isomer 1)
10 4.06 279.0535/nd 279, 163, 133, 119, 115, 93 p-Coumaroyl malate (Isomer 2)
11 4.16 739.2128/741.2327 739, 284, 285, 255, 227, 151, 133 Kaempferol-3- O-(2'',6''-di-O-rhamnopyranosyl)glucopyranoside (clitorin)
12 4.24 609.1479/611.1684 609, 301, 300, 271, 255, 179, 151 Quercetin-3- O-rutinoside (rutin)
13 4.28 309.0630/nd 309, 291, 247, 197, 193, 149, 134, 133, 115 Feruloyl malate (Isomer 1)
14 4.37 309.0637/nd 309, 291, 247, 197, 193, 149, 134, 133, 115 Feruloyl malate (Isomer 2)
15 4.64 593.1533/nd 593, 284, 285, 255, 227, 151, 133 Kaempferol-3- O-rutinoside (nicotiflorin)
16 5.25 nd/386.2125 a LOW INTENSITY Unidentified
17 5.51 nd/479.3898 479, 240, 222 Carpaine

All MS2 were in negative ion mode except for peak no 3, 16 and 17; a [M+H]2+; nd: not detected.