Fumonisin B1
CAS No. 116355-83-0
Fumonisin B1 ( ——— )
产品货号. M38015 CAS No. 116355-83-0
Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Fumonisin B1
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.
-
产品描述Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.
-
体外实验———
-
体内实验Fumonisin B1 改变猴肾细胞的基因表达和信号转导通路。 Fumonisin B1 增加鞘脂代谢的初始破坏和鞘氨醇在 LLC-PK1 肾细胞中的积累,引起大鼠星形胶质细胞凋亡型 DNA 损伤。
-
同义词———
-
通路Others
-
靶点Other Targets
-
受体Sphingosine N-acyltransferase
-
研究领域———
-
适应症———
化学信息
-
CAS Number116355-83-0
-
分子量721.83
-
分子式C34H59NO15
-
纯度>98% (HPLC)
-
溶解度H2O : 16.67 mg/mL (23.09 mM)
-
SMILESO.CCCC[C@@H](C)[C@@H](OC(=O)C[C@@H](CC(O)=O)C(O)=O)C(C[C@@H](C)C[C@H](O)CCCC[C@@H](O)C[C@H](O)[C@H](C)N)OC(=O)C[C@@H](CC(O)=O)C(O)=O
-
化学全称O.CCCC[C@@H](C)[C@@H](OC(=O)C[C@@H](CC(O)=O)C(O)=O)C(C[C@@H](C)C[C@H](O)CCCC[C@@H](O)C[C@H](O)[C@H](C)N)OC(=O)C[C@@H](CC(O)=O)C(O)=O
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Henry MH, et al. The toxicity of fumonisin B1, B2, and B3, individually and in combination, in chicken embryos. Poult Sci. 2001 Apr;80(4):401-7.?
产品手册
关联产品
-
Neuropeptide W-23(hu...
Neuropeptide W-23 (human) (NPW-23) 是 Neuropeptide W 的主要活性形式,为 NPBW1 (GPR7) 和 NPBW2 (GPR8) 的内源性激动剂。
-
NDMC101
NDMC101 是人类 T 细胞中二肽基肽酶 IV 活性的抑制剂,具有免疫调节作用。它还可作为 NFATc1 和 NF-κB 活性的新型抑制剂。NDMC101 显着抑制 RANKL 诱导的 RAW264.7 和骨髓巨噬细胞 (BMM) 中 TRAP+ 多核细胞的形成。
-
2-Aminopurine-9-beta...
2-Aminopurine-9-beta-D-(2’-deoxy)riboside, a derivative of 2-Aminopurine, is a modified nucleoside composed of a purine base linked to a (2’-deoxy)ribose sugar moiety.
021-51111890
购物车()
sales@molnova.cn

