021-51111890
购物车（0）
sales@molnova.cn
Protonstatin-1
CAS No. 521972-99-6
Protonstatin-1 ( —— )
产品货号. M36384 CAS No. 521972-99-6
Protonstatin-1 is used as a hypoglycemic agent and as a compound for the treatment of Alzheimer's disease, inhibits IGFIR kinase activity and can be used in cancer research.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ￥2519 | 有现货 |
|
| 5MG | ￥3553 | 有现货 |
|
| 10MG | ￥5233 | 有现货 |
|
| 25MG | ￥7718 | 有现货 |
|
| 50MG | ￥10870 | 有现货 |
|
| 100MG | ￥14306 | 有现货 |
|
| 500MG | ￥28535 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Protonstatin-1
-
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Protonstatin-1 is used as a hypoglycemic agent and as a compound for the treatment of Alzheimer's disease, inhibits IGFIR kinase activity and can be used in cancer research.
-
产品描述Protonstatin-1 is used as a hypoglycemic agent and as a compound for the treatment of Alzheimer's disease, inhibits IGFIR kinase activity and can be used in cancer research.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Angiogenesis
-
靶点IGF-1R
-
受体IGF-1R
-
研究领域——
-
适应症——
化学信息
-
CAS Number521972-99-6
-
分子量211.26
-
分子式C8H5NO2S2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESO=C1NC(=S)S\C1=C/C1=CC=CO1
-
化学全称——
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
-
LMPTP INHIBITOR 1 hy...
LMPTP INHIBITOR 1 是低分子量蛋白酪氨酸磷酸酶 (LMPTP) 的选择性抑制剂，IC50 为 0.8 μM LMPTP-A。
-
GIP (3-42), human
GIP (3-42), human 充当葡萄糖依赖性促胰岛素多肽 (GIP) 受体拮抗剂，在体内调节胰岛素分泌和 GIP 的代谢作用。
-
KW-2450 free base
KW-2450 free base is an orally bioavailable inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (IR) tyrosine kinases with potential antineoplastic activity. IGF-1R/IR inhibitor KW-2450 free base selectively binds to and inhibits the activities of IGF-1R and IR, which may result in the inhibition of tumor cell proliferation and the induction of tumor cell apoptosis. IGF-R1 and IR tyrosine kinases, overexpressed in a variety of human cancers, play significant roles in the stimulation of cellular proliferation, oncogenic transformation, and suppression of apoptosis.
