Ten histone deacetylase inhibitor IEM 1754 Practices Explained

While in the MS2 spectra of three monomer standards, such as small molecules such as CO2, CO and H2O had been developed while in the fragmentation pathways, which indicated the presence of carboxyl, carbonyl or hydroxyl groups. Danshensu showed a ion at m/z 197, and developed m/z 179 and m/z 135.

Other two fragment ions, ion at m/z 321 and ion at m/z 339 corresponding to the loss on the second danshensu plus the rst caffeic acid. These data are constant with these while in the literature. Thus, peak 10 was tentatively identied as salvianolic acid B. Similarly, histone deacetylase inhibitor peaks 9, 14 were identied as rosmarinic acid and salvianolic acid A separately. Rhizoma Coptids alkaloids, which were the most abundant constituents in the alcohol extra of FTZ, exhibited a special fragmentation pathway in the positive ion mode. It is well known that loss the neutral species such as CO, CH3, CH4 and CH2O were observed in the MS2 spectra of Rhizoma Coptids alkaloids.

In addition to Rhizoma Coptids alkaloids in positive ion IEM 1754 mode, three diterpenoids also exhibited ions in positive ion mode. It is well known that hydrogen at C 1 and oxygen at C 11 of tanshinones were the source of the dissociated H2O and the neutral species such as CO, H2O, C2H5 and C3H6 were also observed in the MS2 spectra. Peak 45 showed a molecular ion at m/z 297 in MS spectra, and exhibited an ion at m/z 279 in MS2 spectra, which corresponded to three fragment ions at m/z 268 , m/z 227 and m/z 251 , showing the neutral loss of CO, H2O, C2H5 and C3H6 in the fragmentation pathway. According to these data, peak 45 was tentatively identied as cryptotanshinone.

By comparison with literature data, this component was ascertained as coniferin. IEM 1754 By comparison with the mass chromatography of FTZ and the rat serum samples from control group, the MS spectra for rat serum samples from FTZ treated group exhibited 27 peaks in common, which demonstrated that the 27 components from FTZ were absorbed into the rat blood after oral administration.