Anti-inflammatory, Anti-oxidative and Anti-bacterial Activities of the Constituents Extracted from Leaves of Talipariti hamabo
TableS1.
1H and 13C NMR data of compound 1 (400 and 100 MHz, CDCl3)
|
Compound 1 |
|
No.
|
δH (int, multi, JHz)
|
δC |
|
1
|
|
178.1
|
|
2
|
2.31 ( 2H, t, 7.6)
|
33.9
|
|
3
|
1.61 ( 2H, m)
|
25.0
|
|
4
|
1.29 (2H, m)
|
29.6
|
|
5
|
1.29 (2H, m)
|
29.5
|
|
6
|
1.29 (2H, m)
|
29.4
|
|
7
|
1.29 (2H, m)
|
29.9
|
|
8
|
2.09-1.98 (2H, m)
|
27.4
|
|
9
|
5.38-5.28 (1H, m)
|
130.0
|
|
10
|
5.38-5.28 (1H, m)
|
130.2
|
|
11
|
2.09-1.98 (2H, m)
|
27.4
|
|
12
|
1.29 (2H, m)
|
30.0
|
|
13
|
1.29 (2H, m)
|
29.7
|
|
14
|
1.29 (2H, m)
|
29.8
|
|
15
|
1.29 (2H, m)
|
29.7
|
|
16
|
1.29 (2H, m)
|
32.1
|
|
17
|
1.29 (2H, m)
|
22.9
|
|
18
|
0.86 (3H , t, 6.9)
|
14.3
|
FigureS1.
1H and 13C NMR spectra of compound 1 in CDCl3.
TableS2.
1H and 13C NMR data of compound 2 (400 and 100 MHz, CD3OD)
|
Compound 2 |
|
No.
|
δH (int, multi, JHz)
|
δC |
|
1
|
|
128.4
|
|
2
|
7.11 (1H, d, 1.8)
|
111.6
|
|
3
|
|
149.4
|
|
4
|
|
149.9
|
|
5
|
6.79 (1H, d, 8.2)
|
116.6
|
|
6
|
7.02 (1H, dd, 8.2, 1.8)
|
123.4
|
|
7
|
7.41 (1H, d, 15.6)
|
142.2
|
|
8
|
6.40 (1H, d, 15.6)
|
118.8
|
|
9
|
|
169.3
|
|
1'
|
|
131.2
|
|
2'
|
7.04 (1H, d, 8.7)
|
130.9
|
|
3'
|
6.71 (1H, d, 8.7)
|
116.4
|
|
4'
|
|
157.1
|
|
5'
|
6.71 (1H, d, 8.7)
|
116.4
|
|
6'
|
7.04 (1H, d, 8.7)
|
130.9
|
|
1"
|
3.46 (2H, t, 7.3)
|
42.7
|
|
2"
|
2.75 (2H, t, 7.6)
|
35.9
|
|
-OCH3 |
3.88 (3H, s)
|
56.5
|
FigureS2.
1H and 13C NMR spectra of compound 2 in CD3OD.
TableS3.
1H and 13C NMR data of compound 3 (400 and 100 MHz, CD3OD)
|
Compound 3 |
|
No.
|
δH (int, multi, JHz)
|
δC |
|
2
|
|
158.7
|
|
3
|
|
135.6
|
|
4
|
|
179.6
|
|
5
|
|
163.2
|
|
6
|
6.21 (1H, d, 1.8)
|
100.0
|
|
7
|
|
166.2
|
|
8
|
6.41 (1H, d, 1.8)
|
65.0
|
|
9
|
|
159.5
|
|
10
|
|
105.8
|
|
1'
|
|
122.9
|
|
2'
|
8.07 (1H, d, 8.7)
|
132.5
|
|
3'
|
6.89 (1H, d, 8.7)
|
116.3
|
|
4'
|
|
161.7
|
|
5'
|
6.89 (1H, d, 8.7)
|
116.3
|
|
6'
|
8.07 (1H, d, 8.7)
|
132.5
|
|
1"
|
5.12（1H. d, 7.8)
|
104.7
|
|
2"
|
3.35-3.63 (1H, sugar H)
|
75.9
|
|
3"
|
3.35-3.63 (1H, sugar H)
|
77.3
|
|
4"
|
3.35-3.63 (1H, sugar H)
|
71.6
|
|
5"
|
3.35-3.63 (1H, sugar H)
|
78.3
|
|
6"
|
3.35-3.63 (1H, sugar H)
|
68.7
|
|
1"'
|
4.52 ( 1H, d, 0.9)
|
102.6
|
|
2"'
|
3.30-3.63 (1H, sugar H)
|
72.2
|
|
3"'
|
3.30-3.63 (1H, sugar H)
|
72.4
|
|
4"'
|
3.30-3.63 (1H, sugar H)
|
74.0
|
|
5"'
|
3.30-3.63 (1H, sugar H)
|
69.9
|
|
6"'
|
1.12 (3H , d, 5.95)
|
17.1
|
FigureS3.
1H and 13C NMR spectra of compound 3 in CD3OD.
