Antibacterial Activity of Coumarins and Carbazole Alkaloid from Roots of Clausena anisata

Table 5

¹H NMR (CDCl₃, 400 MHz), ¹³C NMR, and DEPT-135 (100 MHz) spectral data of compound 4.

Position	^1H NMR	^13C NMR	DEPT-135	[13]
				^1H NMR	^13C NMR
2	—	162.3	—	—	162.3
3	—	130.8	—	—	130.9
4	7.48 (1H, s, H-4)	138.1	138.1	7.48, 1H, s	138.1
5	7.17 (1H, s, H-5)	123.3	123.25	7.20, 1H, s	123.3
6	—	124.6	—	—	124.6
7	—	160.3	—	—	160.2
8	6.68 (1H, s, H-8)	97.1	97.1	6.71, 1H, s	97.1
9	—	154.6	—	—	154.6
10	—	113.1	—	—	113.1
2′	4.73 (1H, dd, J = 10, 6 Hz)	90.9	90.9	4.72 (1H, t, J = 12, 6 Hz)	90.9
3′	3.19 (2H, dd, J = 18, 8 Hz)	29.7	29.7	3.21 (2H, dd)	29.6
4′	—	71.7	—	—	71.7
5′	1.37 (3H, s)	26.0	26.02	1.37 (3H, s)	26.0
6′	1.27 (3H, s)	24.21	24.21	1.27 (3H, s)	24.2
1″	—	40.3	—	—	40.3
2″	6.17 (1H, dd, J = 10.8, 6.4 Hz)	145.6	145.6	6.17, 1H, dd, J = 18, 12 Hz)	145.6
3″	5.10 (2H, m, H-3″)	112.1	112.1	5.09 (2H, dd)	112.1
4″, 5″	1.47 (6H, s, H-4″, 5″)	26.2	26.2	1.47 (6H, s)	26.11