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Table 4 13C (200 MHz) and 1H-NMR (800 MHz) data for compound 12 (CDCl3)

From: Screening for cytotoxic chemical constituents from Justicia procumbens by HPLC–DAD–ESI–MS and NMR

Position

δC

δH (J in Hz)

Position

δC

δH (J in Hz)

1

136.11

 

1′

132.40

 

2

105.70

6.29 or 6.30 (d, 1.7)

2′

111.90

6.63 (m)

3

153.10

 

3′

147.33

 

4

153.10

 

4′

148.84

 

5

153.10

 

5′

111.04

6.76 (m)

6

105.70

6.29 or 6.30 (d, 1.7)

6′

120.91

6.66 (m)

7a

7b

35.83

2.61 (m)

7′a

34.99

2.65 (m)

2.75 (m)

7′b

2.70 (m)

8

42.97

1.95 (m)

8′

39.59

2.21 (m)

9

62.59

3.67 (2H, dtt)

9′a

64.69

4.06 (ddd)

9′b

4.24 (ddd)

3-OCH3

60.89

3.80 (3H, s)

10′

171.05

 

4-OCH3

60.89

3.80 (3H, s)

11′

21.11

2.07 (3H, s)

5-OCH3

60.89

3.80 (3H, s)

3′-OCH3

55.83

3.86 (3H, s)

   

4′-OCH3

56.03

3.83 (3H, s)

  1. Atom numbering as indicated in Fig. 7
  2. All assignments are based on 1H-1H COSY, HSQC, and HMBC data