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Table 1 1H-NMR (δH, J) and 13C-NMR (δC) spectral data obtained in this study for lycorine (1) in comparison to those of a previous report (δHa, Ja, δCa)

From: Standardization of the ethanolic extract of Crinum latifolium leaves by two bioactive markers with antiproliferative activity against TGF-β-promoted prostate stromal cells (WPMY-1)

Position

δH, mult. (J)

δHa, mult. (Ja)

δC

δCa

1

4.27 brs

4.25 m

70.2

70.3

2

3.97 brs

3.96 m

71.7

71.8

3

5.37 brs

5.35 brs

118.5

118.6

4

-

-

141.7

141.9

4a

2.60 brd (10.3)

2.59 d (10.4)

60.8

60.8

3.32 d (14.2)

3.31 d (14.0)

85.7

85.6

4.01 d (14.2)

4.00 d (14.0)

  

6a

-

-

129.8

129.9

7

6.68 s

6.66 s

107.0

107.2

8

-

-

145.2

145.4

9

-

-

145.7

145.8

10

6.80 s

6.79 s

105.1

105.2

10a

-

-

129.6

129.7

10b

2.41 m

2.42 m

40.2

40.2

11

2.45–2.54 m

2.45–2.53 m

28.1

28.2

12α

2.20 q (8.7)

2.19 m

53.3

53.4

12β

3.33 ddd (13.0, 10.1, 4.4)

3.31 ddd (13.0, 10.5, 4.5)

  

-OCH2O-

5.94–5.95 m

5.90–5.96 m

100.6

100.7

1-OH

4.77 d (4.1)

4.79 m

  

2-OH

4.87 d (6.2)

4.91 m

  
  1. The chemical shift (δ) is represented in ppm
  2. The coupling constant (J) is represented in Hz
  3. δHa, δCa and Ja were obtained from [30]