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Table 1 UHPLC–Q-TOF-MS data of identified alkaloids from fruits of M. microcarpa

From: Isolation and identification of alkaloids from Macleaya microcarpa by UHPLC–Q-TOF-MS and their cytotoxic activity in vitro, antiangiogenic activity in vivo

Peak no.

TR (min)

Theoretical mass (m/z)

Molecular formula

Error (ppm)

Observed mass (m/z)

Fragment ions of MS2 (m/z)

Identified compounds

1

2.296

372.1805

C21H25NO5

1.21

372.1801

165 (20), 181 (10), 190 (100), 191 (24), 192 (42), 208 (29), 338 (12), 354 (23), 372 (35)

Demethylatedmuramine

2

4.549

354.1336

C20H19NO5

0.56

354.1334

149 (39), 165 (17), 188 (90), 189 (100), 190 (7), 206 (17), 336 (11)

Protopine

3

5.564

386.1962

C22H27NO5

− 3.64

386.1976

222 (91), 386 (100)

Muramine

4

5.676

370.1649

C21H23NO5

− 3.79

370.1663

149 (10), 165 (15), 188 (34), 189 (44), 190 (9), 204 (100), 222 (37), 352 (22)

Allcryptopine

5

6.691

370.1649

C21H23NO5

− 1.09

370.1653

165 (15), 181 (19), 188 (100), 189 (47), 190 (9), 206 (32), 336 (11), 352 (21)

Cryptopine

6

6.747

332.0923

C20H14NO4

− 0.35

332.0924

274 (24), 304 (30), 317 (27), 332 (100)

Sanguinarine

7

6.916

348.1236

C21H18NO4

2.54

348.1227

290 (20), 304 (53), 318 (42), 332 (100), 333 (39), 348 (31)

Chelerythrine

8

15.932

717.2807

C42H40N2O9

1.34

717.2797

348 (100), 349 (5)

(±)-Macleayin G

9

18.749

364.1185

C21H18NO5+

1.37

364.1180

306 (23), 320 (26), 334 (100), 348 (16), 349 (82), 364 (12)

Dihydrochelirubine

10

3.535

   

386.1587

165 (52), 204 (15), 222 (65), 252 (20), 266 (16), 267(25), 283 (68), 306 (26), 309 (37), 325 (66), 386 (29)

Unknown

11

6.803

   

453.3436

435 (100), 114 (58), 209 (65), 226 (20), 227 (10) 228 (24), 322 (86), 340 (13), 453 (86)

Unknown

12

15.819

   

717.2437

332 (100), 717 (2)

Unknown

13

16.157

   

733.2767

348 (100), 733 (15)

Unknown

14

18.749

   

749.2125

386 (100), 749 (2)

Unknown