Skip to main content
. 2018 Dec 5;56(1):559–566. doi: 10.1080/13880209.2018.1492000

Table 1.

Characterization of compounds of ALR by UHPLC-Q-TOF-MS.

No. tR (min) Identification Formula MW calculated Quasi-molecular Error (ppm)
B1 11.325 6,7-Dihydroxy-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromoe C17H18O4 286.1205 287.1278 (M + H)+ –3.50
B2 15.452 5,6,7,8-Tetrahydroxy-2-(3-hydroxy-4-methoxyphenethyl)-5,6,7,8-tetrahydro-4H-chromen-4-one C18H20O8 364.1158 387.1050 (M + Na)+ –6.85
B3 17.971 (5S*,6R*,7S*)-5,6,7-Trihydroxy-2-(3-hydroxy-4-methoxyphenethyl)-5,6,7,8-tetrahydro-4H-chromen-4-one C18H21O7 349.1209 372.1179 (M + Na)+ –6.42
C1 18.700 Aquilarinoside A1 C28H32O15 608.1741 609.1834 (M + H)+ –3.95
B4 19.031 5,6,7,8-Tetrahydro-5β,6β,7α,8β-tetrahydroxy-2-(2-phenylethyl)chromone C17H19O6 319.1103 342.1074 (M + Na)+ –3.92
C2 21.932 7,4′-Dimethylapigenin-5-O-xylosylglucoside C28H32O14 592.1792 593.1865 (M + H)+ –4.97
C3 23.871 7,4′-Dimethyl-5-O-glucosideflavonoide C23H24O10 460.1369 461.1442 (M + H)+ –4.37
B5 24.500 5-Hydroxy-6-methoxy-2-[2-(3-hydroxy-4-methoxyphenyl)ethyl]chromone C19H18O6 342.11.3 343.1176 (M + H)+ –3.95
A1 25.395 cis-1,10-Epoxyguaia-11-en-2-ol C15H24O2 236.1776 237.1749 (M + H)+ –4.42
A2 25.895 Agarofuran-4-hydroxylbaimuxinol C15H26O3 254.1882 259.1669 (M + Na)+ [–H2O] 0.93
B6 27.102 6,7-Dimethoxy-2-[2-(3-methoxyphenyl)ethyl]chromone; 5,8-Dihydroxy-2-[2-(4-methoxyphenyl)ethyl]-chromone C18H16O5 312.0998 313.1071 (M + H)+ –4.62
D1 28.362 Dodecanoic acid C12H24O2 200.1776 223.1669 (M + Na)+ –2.20
A3 28.941 Epoxybulnesene C15H24O 220.1827 203.1794 (M + H)+ [–H2O] –3.96
A4 29.273 Baimuxinic acid C15H24O3 252.1725 275.1618 (M + H)+ –2.28
A5 30.751 Hinesol C15H26O 222.1984 205.1951 (M + H)+ [H2O] 0.66
B7 31.046 7-Hydroxy-2-(2-phenylethyl)chromone; 6-Hydroxy-2-(2-phenylethyl)chromone C17H15O3 267.0943 290.0613 (M + Na)+ 3.21
B8 32.256 6,7-Dimethoxy-2-[2-(4′-methoxyphenyl)ethyl]chromone C20H20O5 340.1311 363.1203 (M + Na)+ –5.00
A6 32.919 Nootkanone C15H22O 218.1671 209.1743 (M + H)+ –1.78
A7 34.808 β-Vatirenene C15H22 202.1722 203.1794 (M + H)+ –2.06
B9 34.924 2-(2-Phenyleyhyl)chromone C17H14O2 250.1994 251.1067 (M + H)+ –4.54
A8 36.382 (–)-Guaia-1(10),11-dien-15,2-olide C15H20O2 232.1463 255.1356 (M + Na)+ –5.12
A9 37.626 7b-H-9(10)-ene-11,12-Epoxy-8-oxoeremophilane; 7a-H-9(10)-ene-11,12-epoxy-8-oxoeremophilane C15H22O2 234.1620 235.1693 (M + H)+ –3.36
D2 39.150 n-Hexadecanoic acid C16H32O2 256.2402 279.2295 (M + Na)+ –4.58

t R: retention time; A: sesquiterpenes; B: phenylethyl chromone; C: flavonoids; D: fatty acid.