4SC-202 tosylate
CAS No. 1186222-89-8
4SC-202 tosylate ( 4SC-202 )
产品货号. M17177 CAS No. 1186222-89-8
4SC-202 是 HDAC1/2/3 的 I 类 HDAC 选择性抑制剂(IC50:1.20/1.12/0.57 μM)。它还对赖氨酸特异性脱甲基酶 1 (LSD1) 具有抑制活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥478 | 有现货 |
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| 5MG | ¥786 | 有现货 |
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| 10MG | ¥1191 | 有现货 |
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| 25MG | ¥2163 | 有现货 |
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| 50MG | ¥3588 | 有现货 |
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| 100MG | ¥5289 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称4SC-202 tosylate
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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
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产品简述4SC-202 是 HDAC1/2/3 的 I 类 HDAC 选择性抑制剂(IC50:1.20/1.12/0.57 μM)。它还对赖氨酸特异性脱甲基酶 1 (LSD1) 具有抑制活性。
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产品描述4SC-202 is a selective inhibitor of class I HDAC for HDAC1/2/3 (IC50: 1.20/1.12/0.57 μM). It also displays inhibitory activity against Lysine-specific demethylase 1 (LSD1).
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体外实验Domatinostat tosylate significantly reduces proliferation of all epithelial and mesenchymal UC cell lines (IC50 0.15-0.51 μM), inhibits clonogenic growth and induces caspase activity. Domatinostat tosylate provokes apoptosis activation in CRC cells, while caspase inhibitors (z-VAD-CHO and z-DVED-CHO) significantly alleviate Domatinostat tosylate-exerted cytotoxicity in CRC cells. Meanwhile, Domatinostat tosylate induces dramatic G2-M arrest in CRC cells. Further studies show that AKT activation might be an important resistance factor of Domatinostat tosylate. Domatinostat tosylate-induced cytotoxicity is dramatically potentiated with serum starvation, AKT inhibition (by perifosine or MK-2206), or AKT1-shRNA knockdown in CRC cells. On the other hand, exogenous expression of constitutively active AKT1 (CA-AKT1) decreases the sensitivity by Domatinostat tosylate in HT-29 cells. Notably, Domatinostat tosylate, at a low concentration, enhances oxaliplatin-induced in vitro anti-CRC activity. Domatinostat tosylate treatment induces potent cytotoxic and proliferation-inhibitory activities against established HCC cell lines (HepG2, HepB3, SMMC-7721) and patient-derived primary HCC cells. Domatinostat tosylate induces apoptosis signal-regulating kinase 1 (ASK1) activation, causing it translocation to mitochondria and physical association with Cyp-D.
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体内实验Oral gavage of Domatinostat tosylate inhibits HT-29 xenograft growth in nude mice, and when combined with oxaliplatin, its activity is further strengthened.
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同义词4SC-202
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通路Metabolic Enzyme/Protease
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靶点Phosphatase
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受体HDAC1|HDAC2|HDAC3|HDAC5|HDAC9|HDAC10|HDAC11|
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研究领域Cancer
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适应症——
化学信息
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CAS Number1186222-89-8
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分子量619.71
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分子式C30H29N5O6S2
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 51 mg/mL. 82.30 mM
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SMILESCC1=CC=C(C=C1)S(=O)(=O)O.CN1C=C(C=N1)C2=CC=C(C=C2)S(=O)(=O)N3C=CC(=C3)/C=C/C(=O)NC4=CC=CC=C4N
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Pinkerneil M, Hoffmann M J, Kohlhof H, et al. Targeted Oncology, 2016, 11(6):783-798.
产品手册
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