. 2021 Mar 5;84(3):676–682. doi: 10.1021/acs.jnatprod.0c01093

Table 2. ¹³C NMR Data of Compounds 1–5 in DMSO-d₆ at 200 MHz.

	1	2	3	4	5
position	δ_C, type	δ_C, type	δ_C, type	δ_C, type	δ_C, type
1	155.2, C	155.7, C	156.0, C	155.6, C	161.2, C
3	136.2, CH	136.8, CH	136.4, CH	136.5, CH	132.4, CH
4	122.1, CH	122.7, CH	122.3, CH	122.4, CH	104.9, CH
4a	135.6, C	136.2, C	136.2, C	136.1, C	132.9, C
5	106.4, CH	106.9, CH	106.6, CH	106.8, CH	107.0, CH
6	156.7, C	157.2, C	157.6, C	157.3, C	153.3, C
7	152.6, C	153.2, C	153.2, C	153.1, C	149.2, C
8	106.0, CH	106.4, CH	106.6, CH	106.4, CH	107.2, CH
8a	123.7, C	124.2, C	124.1, C	124.3, C	119.5, C
α	33.0, CH₂	33.5, CH₂	33.1, CH₂	33.5, CH₂
9	127.8, C	128.2, C	126.7, C	128.5, C
10	122.0, CH	122.3, CH	122.8, CH	123.0, CH
11	143.3, C	144.0, C	142.6, C	142.7, C
12	150.4, C	151.0, C	149.0, C	150.9, C
13	114.0, CH	114.5, CH	118.1, CH	114.6, CH
14	125.4, CH	125.8, CH	125.7, CH	126.7, CH
1′	155.4, C	64.3, CH	156.0, C
3′	136.3, CH	44.7, CH₂	136.4, CH
4′	122.2, CH	21.3, CH₂	122.3, CH
4a′	135.7, C	122.3, C	136.2, C
5′	106.4, CH	112.1, CH	106.6, CH
6′	156.8, C	148.9, C	157.6, C
7′	152.7, C	146.9, C	153.2, C
8′	105.9, CH	111.6, CH	106.3, CH
8a′	123.8, C	121.3, C	124.1, C
α′	33.2, CH₂	40.2, CH₂	33.8, CH₂	191.6, CH
9′	128.6, C	130.1, C	129.2, C	131.3, C
10′/14′	129.6, CH	131.7, CH	129.8, CH	132.1, CH
11′/13′	116.4, CH	116.3, CH	116.8, CH	116.2, CH
12′	156.7, C	157.2, C	157.4, C	163.2, C
CH₃N-2	45.8, CH₃	46.4, CH₃	46.1, CH₃	46.3, CH₃	46.3, CH₃
CH₃O-6	56.7, CH₃	57.2, CH₃	57.2, CH₃	57.2, CH₃	57.2, CH₃
CH₃O-7	56.8, CH₃	57.0, CH₃	56.9, CH₃	56.9, CH₃	56.9, CH₃
CH₃O-12	55.7, CH₃	56.3, CH₃		56.2, CH₃
CH₃N-2′	45.9, CH₃	39.9, CH₃	46.1, CH₃
CH₃O-6′	56.8, CH₃	55.9, CH₃	57.2, CH₃
CH₃O-7′	56.6, CH₃	55.1, CH₃	56.9, CH₃

Table 2. 13C NMR Data of Compounds 1–5 in DMSO-d6 at 200 MHz.

Table 2. ¹³C NMR Data of Compounds 1–5 in DMSO-d₆ at 200 MHz.