Search Results
identified as aliphatic, aromatic, and monoterpene compounds were located in the region marked (a)–(c), respectively. Similarly, some components identified as C13-norisoprenoids were located in region (d). The peaks were distributed over the entire
1 Lacosamide 3.85 251.1382 251.1390 −3.18 C 13 H 19 N 2 O 3 219.1119 209.1273 177.1008 144.0651 116.0704 108.0808 91.0546 74
) 1 Lacosamide C 13 H 19 N 2 O 3 251.1385 251.1390 −1.99 219.1144, 177.1035, 144.0663, 116.0726, 108.0796, 91
-19), 4.63 (1H, s, H b -12), 4.65 (1H, s, H a -12), 5.24 (1H, d, J = 15.2 Hz, H-15), 5.75 (1H, d, J = 11.2 Hz, H-17), 6.21 (1H, dd, J = 11.2, 15.2 Hz, H-16). 13 C-NMR (DMSO- d 6 , 100 MHz) δ : 13.1 (C-14), 21.8 (C-20), 24.3 (C-13), 26.4 (C-8
.0268 370.0274 −0.6 C 12 H 12 N 5 O 5 S 2 + 9.5 352.0555 352.0533 2.2 C 13 H 14 N 5 O 3 S 2
, 62 , 505 – 507 . 10.1248/cpb.c13-00988 13. Zhang , Q. ; Wu , H. ; Wen , C. ; Sun , F. ; Yang
.0823 -0.1 C 13 H 16 O 7 283.0710, 107.0572 p-Cresol glucuronide 8 8.85 291.0146 291
0 kGy 27.0 ± 0.2 b 32.1 ± 0.5 c 13.1 ± 0.2 b 42.0 ± 0.4 e 40.1 ± 1.0 d 52.8 ± 0.2 c 45.9 ± 0.3 a
. 12. Tabero , P , Filipek , E 2004 Synthesis and properties of a solid solution formed in the CrVMoO 7 -AlVMoO 7 system . J Therm Anal Calorim 77 : 183 – 191 10.1023/B:JTAN.0000033202.46419.2c