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Table 1 1 H and 13 C NMR assignments* of Trichothecinol-A

From: Isolation, purification and characterization of Trichothecinol-A produced by endophytic fungus Trichotheciumsp. and its antifungal, anticancer and antimetastatic activities

Position

δ 1H (JHH) Hz

δ 13C

2

3.80(4.95)

79.31

3

4.27(4.95,3.00)

78.93

OH– 3.48,br

 

4

4.93(3.00)

83.38

5

 

48.87

6

 

44.71

7a

2.33(15.18, 1.54)

42.06

7b

2.96, (15.18,1.10)

 

8

 

198.52

9

 

137.52

10

6.60(5.80,1.54)

137.27

11

4.40(5.80)

71.02

12

 

64.54

13a

2.81,(3.90)

46.63

13b

3.08,(3.90)

 

14(CH3)

0.76, s

6.00

15 (CH3)

1.03, s

18.46

16 (CH3)

1.83, s

15.43

17

 

168.05

18

5.89(11.50,1.80)

119.90

19

6.48(11.50,7.30)

147.26

20 (CH3)

2.17(1.80,7.30)

15.65

  1. * Numbering of various atoms are given in Figure 2.