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Table 1 13C-NMR spectroscopic data of compounds 1–5 (δ in ppm)

From: Anti-bacterial effect of phytoconstituents isolated from Alimatis rhizoma

 

1

2

3

4

5

C-1

30.9

30.8

31.0

55.0

50.6

C-2

36.7

33.6

33.8

24.8

22.5

C-3

220.1

219.4

220.1

40.2

40.4

C-4

47.0

47.0

47.0

80.7

80.2

C-5

48.4

48.7

48.5

47.3

50.3

C-6

20.1

20.0

20.1

121.3

121.3

C-7

34.2

34.8

34.3

149.8

149.7

C-8

40.7

40.0

40.6

30.0

25.1

C-9

49.9

49.8

49.6

37.1

42.5

C-10

36.9

36.9

36.9

153.9

75.3

C-11

70.1

69.8

69.8

37.4

37.3

C-12

34.4

35.5

34.3

21.3

21.2

C-13

138.2

177.2

138.1

21.5

21.4

C-14

57.0

49.8

57.0

24.1

21.5

C-15

30.6

45.7

30.6

106.5

21.3

C-16

29.1

208.1

29.1

  

C-17

134.1

134.4

134.8

  

C-18

23.2

23.1

23.3

  

C-19

25.7

25.5

25.5

  

C-20

27.8

26.7

27.7

  

C-21

20.1

20.1

20.2

  

C-22

33.7

35.0

38.8

  

C-23

71.5

71.9

69.1

  

C-24

65.1

64.9

67.8

  

C-25

58.5

58.7

59.2

  

C-26

19.4

19.7

19.2

  

C-27

24.7

24.7

24.9

  

C-28

29.6

29.6

29.6

  

C-29

20.0

19.3

20.1

  

C-30

23.8

23.1

24.0

  

–O–COCH3

170.1

170.2

   

–O–COCH3

21.2

21.2

   
  1. 15 in CDCl3, 75 MHz