YM-01(YM-1) structure
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Common Name | YM-01(YM-1) | ||
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CAS Number | 409086-68-6 | Molecular Weight | 417.975 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C20H20ClN3OS2 | Melting Point | N/A | |
MSDS | USA | Flash Point | N/A |
Use of YM-01(YM-1)YM-1 is a stable and soluble MKT-077 (HY-15096) analog and an orally active Hsp70 inhibitor. YM-1 induces cell death of HeLa cells and up-regulates the level of p53 and p21 proteins[1][2]. |
Name | PyridiniuM, 2-[[3-ethyl-5-(3-Methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]Methyl]-1-Methyl-, chloride (1:1) |
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Synonym | More Synonyms |
Description | YM-1 is a stable and soluble MKT-077 (HY-15096) analog and an orally active Hsp70 inhibitor. YM-1 induces cell death of HeLa cells and up-regulates the level of p53 and p21 proteins[1][2]. |
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Related Catalog | |
In Vitro | YM-1 促进 Nnos 成熟过程中依赖 Hsp70 的步骤,阻断部分与 ATP 的结合[1]。 YM-1 (0-200 μM) 激活 Hsp70 与未折叠底物的结合[1]。 YM-1 (0.001-1000 μM) 将 Hsp70 转化为紧密亲和构象,与 Hsp70 结合的 IC50 值为 8.2 μM[1]。 YM-1 (0,0.1,0.5 和 1 μM;24 小时) 促进 nNOS 泛素化[1]。 YM-1 (5 和 10 μM;24 和 48 小时) 诱导 HeLa 细胞死亡和 hTERT-RPE1 细胞生长停滞[2] YM-1 (10 μM;48 小时) 上调 p53 和 p21,下调 FoxM1 和 survivin 的蛋白水平[2]。 Western Blot Analysis[2] Cell Line: HeLa and hTERT-RPE1 cell lines Concentration: 10 μM Incubation Time: 48 hoursI Result: Increased the level of p53 and p21 and decreased the level of FoxM1 and survivin. |
In Vivo | YM-1 (1 mM;口服,持续 7 天) 通过激活 Hsp70 挽救果蝇中的 polyQ 毒性[1]。 Animal Model: UAS-hAR52Q flies with polyQ AR-induced dihydrotestosterone (DHT) phenotype[1] Dosage: 1 mM Administration: Oral administration; 1 mM, for 7 days Result: Weakened the DHT-dependent eye degeneration phenotype and rescued DHT-dependent pupal toxicity of the polyQ AR. |
References |
Molecular Formula | C20H20ClN3OS2 |
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Molecular Weight | 417.975 |
Exact Mass | 417.073639 |
Storage condition | 2-8°C |
RIDADR | NONH for all modes of transport |
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2-{(Z)-[(5E)-3-Ethyl-5-(3-methyl-1,3-benzothiazol-2(3H)-ylidene)-4-oxo-1,3-thiazolidin-2-ylidene]methyl}-1-methylpyridinium chloride |
Pyridinium, 2-[(Z)-[(5E)-3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]-1-methyl-, chloride (1:1) |
YM-1 |