Skip to main content

Table 1 13 C-NMR Chemical shift data of compounds 1–9, δ in ppm

From: Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone

Compounds

C

1

2

3

4

5

6

7

8

9

1

38.7

38.3a

32.9

37.5

155.3

37.4

158.6

155.1

155.0

2

38.2

32.1

30.6

34.2

127.7

34.1

125.1

127.8

127.8

3

211.8

71.8

67.2

200.3

186.3

199.9

186.7

186.2

186.2

4

44.5

38.9

36.7

124.6

124.2

124.8

124.8

124.3

124.2

5

46.8

46.3

40.4

170.9

168.3

170.1

167.4

167.9

167.9

6

28.9

29.9

29.6

33.6

32.5

33.3

32.8

32.5

32.4

7

31.3

32.9

33.5

31.1

32.3

30.3

32.1

33.4

31.9

8

35.6

36.9

36.9

35.3

35.1

34.6

33.9

34.4

35.0

9

53.8

56.0

56.1

59.2

52.2

59.2

60.4

52.1

51.9

10

35.8

36.7

37.2

39.9

43.4

40.0

43.9

43.4

43.3

11

21.0

21.9

21.5

68.9

22.1

68.7

67.7

36.1

21.7

12

36.8

38.1a

38.1

48.5

31.1

42.9

42.3

86.0

30.9

13

43.1

44.1

44.1

43.7

47.7

47.9

47.8

42.7

38.7

14

50.9

52.4

52.5

49.8

50.4

50.0

49.6

44.1

47.3

15

23.5

24.3

24.3

23.3

21.9

21.7

21.8

22.2

30.6

16

30.6

30.6

29.7

30.6

35.6

35.7

35.8

35.5

71.1

17

81.9

82.5

82.6

81.0

220.1

218.4

218.3

216.2

218.3

18

11.1

11.7

11.7

12.3

13.8

14.6

14.6

11.5

14.1

19

11.5

12.8

11.6

18.4

18.7

18.3

18.7

18.7

18.7

  1. Note:
  2. a interchangeable δ values.
  3. CDCl3 at 125 MHz (1, 6).
  4. CDCl3 at 150 MHz (4, 5, 7, 8, 9).
  5. CD3OD at 150 MHz (2).
  6. CD3OD at 100 MHz (3).