伏马菌素 B1-13C34 溶液结构式
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常用名 | 伏马菌素 B1-13C34 溶液 | 英文名 | Fumonisin B1-13C34 |
|---|---|---|---|---|
| CAS号 | 1217458-62-2 | 分子量 | N/A | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | 13C34H59NO15 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 2 °C | |
| 符号 |
GHS02, GHS07 |
信号词 | Danger |
伏马菌素 B1-13C34 溶液用途伏马菌素B1-13C34是13C-标记的伏马菌蛋白B1(HY-N6719)[1]。伏马菌素B1是由串珠镰刀菌产生的真菌毒素。伏马菌素B1是鞘氨醇N-酰基转移酶(神经酰胺合成酶)的有效抑制剂,并破坏鞘脂的从头生物合成。伏马菌素B1是含量最高、毒性最强的伏马菌菌素[2][3]。 |
| 中文名 | 伏马菌素 B1-13C34 溶液 |
|---|---|
| 英文名 | Fumonisin B1-13C34 solution |
| 英文别名 | 更多 |
| 描述 | 伏马菌素B1-13C34是13C-标记的伏马菌蛋白B1(HY-N6719)[1]。伏马菌素B1是由串珠镰刀菌产生的真菌毒素。伏马菌素B1是鞘氨醇N-酰基转移酶(神经酰胺合成酶)的有效抑制剂,并破坏鞘脂的从头生物合成。伏马菌素B1是含量最高、毒性最强的伏马菌菌素[2][3]。 |
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| 相关类别 | |
| 靶点实验 |
Sphingosine N-acyltransferase[2] |
| 体外研究 | 氢、碳和其他元素的稳定重同位素已被纳入药物分子中,主要作为药物开发过程中定量的示踪剂。氘化引起了人们的关注,因为它可能影响药物的药代动力学和代谢谱[1] 伏马菌素B1改变猴肾细胞基因表达和信号转导通路[2] 伏马菌素B1增加鞘脂代谢的初始破坏和鞘氨醇在 LLC-PK1型肾细胞中的积累,导致大鼠星形胶质细胞凋亡型 脱氧核糖核酸损伤[2] |
| 参考文献 |
| 分子式 | 13C34H59NO15 |
|---|---|
| 闪点 | 2 °C |
| InChIKey | UVBUBMSSQKOIBE-HTPIOKJKSA-N |
| SMILES | CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCC(O)CC(O)C(C)N)OC(=O)CC(CC(=O)O)C(=O)O |
| 储存条件 | −20°C |
| 符号 |
GHS02, GHS07 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H225-H302 + H312 + H332-H319 |
| 警示性声明 | P210-P280-P305 + P351 + P338 |
| 危害码 (欧洲) | F,Xn |
| 风险声明 (欧洲) | 11-20/21/22-36 |
| 安全声明 (欧洲) | 26-36/37-16 |
| 危险品运输编码 | UN 1648 3/PG 2 |
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