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---|---|---|---|---|---|---|---|
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产品名称 | eNOS ↓ ↑ | iNOS ↓ ↑ | nNOS ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1400W 2HCl |
+
eNOS, Ki: 50 μM |
++++
iNOS, Kd: <7 nM |
++
nNOS, Ki: 2 μM |
99%+ | |||||||||||||||
L-NAME HCl |
+++
eNOS, Ki: 39 nM |
++
iNOS, Ki: 4.4 μM |
+++
nNOS, Ki: 15 nM |
98% | |||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | YM-1, a stable, soluble analog of MKT-077, functions as an orally active inhibitor of Hsp70. It triggers cell death in HeLa cells and significantly increases the levels of p53 and p21 proteins, indicating its potential in modulating cell cycle and apoptosis pathways[1][2]. |
Animal study | In vivo, oral administration of YM-1 at 1 mM for 7 days demonstrated therapeutic effects in Drosophila models of polyglutamine (polyQ) toxicity, attributed to the activation of Hsp70. This outcome highlights YM-1's potential for treating neurodegenerative diseases by enhancing the protective functions of molecular chaperones[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.39mL 0.48mL 0.24mL |
11.96mL 2.39mL 1.20mL |
23.92mL 4.78mL 2.39mL |
CAS号 | 409086-68-6 |
分子式 | C20H20ClN3OS2 |
分子量 | 417.98 |
SMILES Code | C[N+]1=CC=CC=C1C=C(N(CC)C2=O)SC2=C3SC4=CC=CC=C4N3C.[Cl-] |
MDL No. | MFCD28009511 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Inert atmosphere, 2-8°C |