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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).