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Table 1 1H and 13C NMR data of compound 1 measured in methanol-d4

From: In vivo anti-malarial activity of the hydroalcoholic extract of rhizomes of Kniphofia foliosa and its constituents

Present data

Reference data [33]

Position

δC (ppm)

δH (ppm)

δC (ppm)

δH (ppm)

1

151.49

–

150.2

–

2

124.73

–

125.2

–

3

133.30

–

132.8

–

4

119.58

7.12 (1H, s)

119.4

7.21 (1H, s)

5

122.58

7.40 (1H, dd, J = 1.3, 8.2 Hz)

122.3

7.47 (1H, dd, J = 1.0, 8.0 Hz)

6

127.20

7.36 (1H, d, J = 8.2 Hz)

127.3

7.40 (1H, dd, J = 8.0, 8.0 Hz)

7

110.51

7.28 (1H, dd, J = 1.3, 7.3, Hz)

110.7

7.30 (1H, dd, J = 1.0, 8.0 Hz)

8

154.71

–

154.2

–

9

113.54

–

113.2

–

10

136.74

–

135.7

–

1′

102.84

5.05 (1H, d, J = 7.9 Hz)

102.6

5.04 (1H, d, J = 7.5 Hz)

2′

73.57

3.46 (1H, t, J = 8.8 Hz)

73.3

3.39 (1H, m)

3′

76.82

3.37 (1H, m)

76.2

3.36 (1H, m)

4′

70.13

2.91 (1H, m)

70.1

3.18 (1H, m)

5′

76.10

3.68 (1H, m)

76.0

3.59 (1H, m)

6′

66.59

4.05 ( 1H, d, J = 8.9 Hz); 3.63 (1H, m)

66.6

3.93 (1H, dd, J = 1.5, 11.0 Hz); 3.50 (2H, m)

1′′

100.86

4.71 (1H, d, J = 1.4 Hz)

100.7

4.62 (1H, d, J = 1.5 Hz)

2′′

70.84

3.84 (1H, dd, J = 1.6, 3.4 Hz)

70.4

3.68 (1H, m)

3′′

71.03

3.63 (1H, m)

70.7

3.50 (2H, m)

4′′

72.59

3.31 (1H, m)

71.9

3.20 (1H, m)

5′′

68.55

3.52 (1H, m)

68.4

3.49 (1H, m)

6′′

16.55

1.17 (3H, d, J = 6.2 Hz)

17.7

1.12 (3H, d, J = 6.0 Hz)

ArCH3

18.49

2.25 (3H, s)

19.0

2.25 (3H, s)

COCH3

41.3

2.97 (3H, s)

31.9

2.52 (3H, s)

COCH3

207.07

–

204.4

–

  1. s, singlet, d, doublet, dd, doublet of doublets, m, multiplet, br, broad, t, triplet