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Table 1 NMR data of compound 1 (C 5 D 5 N, 400 MHZ)

From: Cytotoxic Benzophenanthridine and Furoquinoline Alkaloids from Zanthoxylum buesgenii(Rutaceae)

Position

δH(multi,J = Hz)

C

1

7.31, s

105.3 (CH)

2

-

148.8 (C)

3

-

148.2 (C)

4

7.89, s

101.7 (CH)

4a

-

128.2 (C)

4b

-

140.1 (C)

5

-

-

6

6.54, s

80.0 (CH)

6a

-

124.3 (C)

7

-

146.9 (C)

8

-

150.6 (C)

9

7.41, d (8.4)

118.3 (CH)

10

7.82, d (8.4)

120.4 (CH)

10a

-

129.1 (C)

10b

-

124.3 (C)

11

8.02, d (8.5)

121.0 (CH)

12

7.62, d (8.5)

124.2 (CH)

12a

-

131.7 (C)

OCH2O

6.04, d (1.2)

102.0 (CH2)

6.08, d (1.2)

NCH3

2.77, s

40.6 (CH3)

OCH3

4.24, s

62.2 (CH3)

  1. δH, and δC are chemical shifts of protons and carbons, respectively in ppm.