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Table 1 Positive ionization HR-ESI-MS data and common neutral losses of diterpenoids 1–6

From: Electrospray tandem mass spectrometric analysis of a dimeric conjugate, salvialeriafone and related compounds

S.No.

[M+H]+

Exact Mass

Observed mass

Error

(ppm)

[M+H-H2O]+

[M+H-CO]+

[M+H-C3H6]+

[M+H-2H2O]+

[M+H- C3H7]+.

[M+H-C3H6- H2O]+

[M+H- H2O-CO]+

[M+H-C3H6- H2O-CO]+

Base Peak

1

C39H49O7+

629.3472

629.3444

−4.58

611

-

569

-

568 [M+H- H2O-C3H7]+.

569

-

-

569 [M+H-C3H6- H2O]+

2

C20H27O3+

315.1965

315.1983

5.49

297

-

273

-

272

255

269

227

245 [M+H-C3H6-C2H4]+

3

C20H27O5+

347.1863

347.1871

2.02

329

319

-

311

-

-

301

255

283 [M+H-2H2O-CO]+

4

C21H31O4+

347.2227

347.2226

−0.53

315 [M+H- CH3OH]+

-

-

-

-

297 [M+H- CH3OH-H2O]+

255 [M+H- CH3OH-H2O-C3H6]+

269 [M+H- CH3OH-H2O-CO]+

269 [M+H- CH3OH-H2O-CO]+

5

C20H27O5+

347.1863

347.1862

−0.57

329

-

 

311

-

-

301

259

281 [M+H-2H2O-CH2O]+

6

C19H23O3+

299.1641

299.1674

10.79

281

-

-

-

256

239

253

211

256 [M+H- C3H7]+.