Published September 30, 2019
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Table 1 1 H in Amaryllidaceae alkaloids from Narcissus pseudonarcissus L. cv. Dutch Master as potential drugs in treatment of Alzheimer's disease
Authors/Creators
- 1. ∗ & ADINACO Research Group, Department of Pharmaceutical Botany, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05, Hradec Králové, Czech & Department of Pharmacognosy, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05, Hradec Králové, Czech Republic
Description
Table 1 1 H-NMR and 13 C-NMR data of new alkaloid 6 (diastereomeric ratio 1:1.1) isolated from Narcissus pseudonarcissus cv. Duch Master.
| POSITION | NARCIMATULINE | |||
|---|---|---|---|---|
| δC of | δH of isomer A | δC of | δH of isomer B | |
| isomer A | isomer B | |||
| 1 | 29.7 | 2.39–2.26 m | 29.6 | 2.39–2.26 m |
| 1.84–1.64 m | 1.84–1.64 m | |||
| 2 | 35.7 | 2.39–2.26 m | 35.6 | 2.39–2.26 m |
| 2.13–1.98 m | 2.13–1.98 m | |||
| 3 | 209.2 | 209.2 | ||
| 4 | 40.0 | 2.60 dd, overlapped | 40.0 | 2.56 dd, overlapped |
| (18.4, 2.9) | (18.0, 2.9) | |||
| 4a | 88.3 | 4.68 t (2.9) | 88.2 | 4.55 t (2.9) |
| 5a | 146.7 | 146.7 | ||
| 6 | 143.6 | 143.6 | ||
| 7 | 110.9 | 6.65 d, overlapped | 111.0 | 6.62 d, overlapped |
| (8.0) | (8.0) | |||
| 8 | 122.23 | 6.44 d (8.0) | 122.20 | 6.56 d (8.0) |
| 8a | 129.9 | 129.9 | ||
| 8b | 132.0 | 132.0 | ||
| 9 | 57.6 | 3.88 d, overlapped | 57.9 | 3.98 d (15.0) |
| (15.0) | 3.66 d (15.0) | |||
| 3.51 d (15.0) | ||||
| 11 | 52.3 | 3.05–2.88 m | 51.1 | 3.05–2.88 m |
| 2.86–2.74 m | ||||
| 12 | 37.4 | 2.13–1.98 m | 36.4 | 1.84–1.64 m |
| 1.56–1.50 m | 1.38–1.31 m | |||
| 13 | 47.5 | 47.4 | ||
| 1′ | 54.9 | 3.45 d (14.2) | 53.7 | 3.35 bs |
| 3.33–3.24 m | ||||
| 2′ | 122.8 | 122.8 | ||
| 3′ | 108.7 | 7.01 s | 108.4 | 7.07 s |
| 3a′ | 146.9 | 146.9 | ||
| 5′ | 101.0 | 6.00–5.98 m | 100.9 | 6.00–5.98 m |
| 6a′ | 146.0 | 145.8 | ||
| 7ֹ’ | 110.5 | 6.74 s | 110.3 | 6.77 s |
| 8′ | 133.6 | 133.4 | ||
| 9′ | 131.7 | 131.4 | ||
| 10′ | 130.4 | 6.83 d (7.4) | 130.2 | 6.71 d, overlapped |
| (7.4) | ||||
| 11′ | 117.9 | 6.68 t, overlapped | 117.9 | 6.62 t, overlapped |
| (7.4) | (7.4) | |||
| 12′ | 123.22 | 7.03 d, overlapped | 123.24 | 7.03 d, overlapped |
| (7.4) | (7.4) | |||
| 12a′ | 131.0 | 131.0 | ||
| 13′ | 28.6 | 3.05–2.88 m | 28.5 | 3.05–2.88 m |
| 2.86–2.74 m | 2.86–2.74 m | |||
| 14′ | 57.1 | 3.33–3.24 m | 56.9 | 3.33–3.24 m |
| 3.18 dd (17.5, 8.8) | 3.09 dd (18.4, 9.2) | |||
| 15a′ | 150.5 | 150.4 | ||
| N15′-CH3 | 38.8 | 2.25 s | 38.7 | 2.20 s |
| C6-OCH3 | 55.96 | 3.86–3.83 m | 55.95 | 3.86–3.83 m |
Spectra were acquired in chloroform-d at 500 MHz (1 H) and 125.7 MHz (13 C);
1 J values are in parentheses and reported in Hz; chemical shifts are given in ppm.
Notes
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