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Luotonin E结构式
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常用名 | Luotonin E | 英文名 | Luotonin E |
|---|---|---|---|---|
| CAS号 | 244616-84-0 | 分子量 | 315.3 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H13N3O2 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | N/A | |
| 符号 |
GHS07 |
信号词 | Warning |
| 英文名 | Luotonin E |
|---|
| 分子式 | C19H13N3O2 |
|---|---|
| 分子量 | 315.3 |
| Smiles | COC1c2cc3ccccc3nc2-c2nc3ccccc3c(=O)n21 |
| 符号 |
GHS07 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H315-H319-H335 |
| 警示性声明 | P261-P305 + P351 + P338 |
| 危险品运输编码 | NONH for all modes of transport |
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Recent advances in the studies on luotonins.
Molecules 16 , 4861-83, (2011) Luotonins are alkaloids from the aerial parts of Peganum nigellastrum Bunge. that display three major skeleton types. Luotonins A, B, and E are pyrroloquinazolino-quinoline alkaloids, luotonins C and ... |
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Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities.
Bioorg. Med. Chem. Lett. 14 , 1193-1196, (2004) Two new synthetic analogues of luotonins A and F, 7-acetylaminoluotonin A (6) and 3-[3H(quinazolino-4-one)]quinoline (7) were synthesized. The new analogues, along with four natural quinazoline-quinol... |
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Two New Quinazoline-Quinoline Alkaloids from Peganum nigellastrum Ma, Z.-Z., et al.
Heterocycles 51 , 1883-1889, (1999)
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