Orange powder, yield: 90%; mp: 286–288 °C; IR (KBr, cm−1): 3320 (N–H), 2990 (Ar–CH), 1690 (C O), 1580 (C N), 1560 (N N); 1H NMR (300 MHz, DMSO-d6) δ (ppm): 2.48 (s, 6H, N(CH3)2), 2.94–2.95 (d, 6H, CH3), 6.69–6.76 (m, 4H, ArH), 7.33–7.96 (m, 6H, ArH), 10.65 (s, 1H, pyrrolic NH), 10.82 (S, 1H, CONH); 13C NMR (75 MHz, DMSO-d6) δ (ppm): 8.5, 10.1, 114.8, Fasudil cost 1217, 123.3, 125.5, 126.4, 128.8, 129.3, 129.9, 148.5, 152.7, 157.1; MS (ESI) m/z: 389.22 [M + H]+. Pale yellow powder, yield: 86%; mp: 298–300 °C; IR (KBr, cm−1): 3400 (CONH), 3310 (N–H), 2950 (Ar–CH), 1680 (C O), 1590 (C N), 1520 (N N); 1H NMR (300 MHz, DMSO-d6) δ (ppm): 2.41–2.44
(d, 6H,
CH3), 6.54 (s, 1H, ArH), 6.85 (s, 1H, Pyrrolic ArH), 7.34–7.58 (m, 4H, ArH), 7.85–7.86 (m, 3H, ArH), 10.92 (s, 1H, Pyrrolic NH), 11.48 (s, 1H, CONH); 13C NMR (75 MHz, DMSO-d6) δ (ppm): 8.4, 10.1, 109.8, 121.6, 126.7, 127.5, 129.3, 131.3, 142.3, 152.6, 158.9; MS (ESI) m/z: 336.15 [M + H]+ Yellow powder, yield: 83%; mp: 284–286 °C; IR (KBr, cm−1): 3320 (N–H), 2980 (Ar–CH), 1700 (C O), 1630 (C N), 1490 (N N); 1H NMR (300 MHz, DMSO-d6) δ (ppm): 2.29–2.33 (d, 6H, CH3), 7.07 (s, 2H, CH2 CH2–Ar), 7.30–7.63 (m, 8H, ArH), 7.82–7.84 (d, 2H, ArH), 8.09 (s, 1H, Pyrrolic ArH), 11.55 (s, 1H, Pyrrolic NH), 11.59 (s, 1H, CONH); 13C NMR (75 MHz, DMSO-d6) δ (ppm): 8.2, 10.6, 112.2, 121.6, 125.2, 122.0, 128.9, 129.6, 140.1, 152.9, 158.0; MS (ESI) m/z: 372.19 [M + H]+ Pale yellow powder, yield: 86%; mp: 290–292 °C; IR (KBr, cm−1): 3500 (OH), 3370 (CONH), 3100 (N–H), 3000 Obeticholic Acid ic50 (Ar–CH), 1690 (C O), 1560 (C N), 1470 (N N); 1H NMR (300 MHz, DMSO-d6) δ (ppm): 2.28–2.47 (d, 6H, CH3), 6.85 (s, 2H, ArH), 7.55–8.18 (m, 8H, ArH), 9.94 (s, br, 1H, OH), 11.50 (d, 2H, Pyrrolic NH), 11.62 (CONH); 13C NMR (75 MHz, DMSO-d6) δ (ppm): 8.6, 10.3, 108.4, 121.6, 123.2, 126.2, 128.6, 129.3, 129.9, 142.3, 152.7, Vasopressin Receptor 157.0; MS (ESI) m/z: 406.20 [M + H]+. Pale yellow powder, yield: 90%; mp: 290–292 °C; IR (KBr, cm−1): 3500 (OH), 3330 (CONH), 3100 (N–H), 2990 (Ar–CH), 1690 (C O), 1550 (C N), 1470 (N N); 1H NMR (300 MHz, DMSO-d6) δ (ppm): 2.30–2.33 (d, 6H, CH3), 6.91–6.93 (d, 2H, ArH), 7.25–7.54 (m, 5H, ArH), 7.80–7.83 (d, 2H, ArH), 8.48 (s, 1H, Pyrrolic ArH), 11.12 (s, 1H, OH), 11.54 (s, 1H, Pyrrolic NH), 11.86 (s, 1H, CONH); 13C NMR (75 MHz, DMSO-d6) δ (ppm): 8.4, 9.7, 110.3, 116.3, 121.7, 122.7, 126.8, 129.9, 130.8, 131.3, 142.5, 152.7, 156.9, 157.3; MS (ESI) m/z: 362.