4SC-202 free base
CAS No. 910462-43-0
4SC-202 free base ( 4SC202 | 4SC-202 | 4SC 202 | domatinostat )
产品货号. M16538 CAS No. 910462-43-0
4SC-202 是一种选择性 I 类 HDAC 抑制剂,对 HDAC1、HDAC2 和 HDAC3 的 IC50 值分别为 1.20 μM、1.12 μM 和 0.57 μM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥510 | 有现货 |
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| 5MG | ¥818 | 有现货 |
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| 10MG | ¥1215 | 有现货 |
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| 25MG | ¥2325 | 有现货 |
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| 50MG | ¥3572 | 有现货 |
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| 100MG | ¥5257 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称4SC-202 free base
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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 是一种选择性 I 类 HDAC 抑制剂,对 HDAC1、HDAC2 和 HDAC3 的 IC50 值分别为 1.20 μM、1.12 μM 和 0.57 μM。
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产品描述4SC-202 is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. Also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). Phase 1.(In Vitro):Domatinostat (4SC-202 free base) 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 (4SC-202 free base) tosylate provokes apoptosis activation in CRC cells, while caspase inhibitors (z-VAD-CHO and z-DVED-CHO) significantly alleviate Domatinostat (4SC-202 free base) tosylate-exerted cytotoxicity in CRC cells. Meanwhile, Domatinostat (4SC-202 free base) 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 (4SC-202 free base) 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 (4SC-202 free base) tosylate, at a low concentration, enhances oxaliplatin-induced in vitro anti-CRC activity. Domatinostat (4SC-202 free base) 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 (4SC-202 free base) tosylate induces apoptosis signal-regulating kinase 1 (ASK1) activation, causing it translocation to mitochondria and physical association with Cyp-D.(In Vivo):Oral gavage of Domatinostat (4SC-202 free base) inhibits HT-29 xenograft growth in nude mice, and when combined with oxaliplatin, its activity is further strengthened.
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体外实验——
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体内实验——
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同义词4SC202 | 4SC-202 | 4SC 202 | domatinostat
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通路Cell Cycle/DNA Damage
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靶点HDAC
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受体HDAC3| HDAC2| HDAC1
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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 Number910462-43-0
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分子量447.51
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分子式C??H??N?O?S
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纯度>98% (HPLC)
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溶解度DMSO:82 mg/mL (183.2 mM);Ethanol:<1 mg/mL;Water:<1 mg/mL
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SMILESO=C(NC1=CC=CC=C1N)/C=C/C2=CN(S(=O)(C3=CC=C(C4=CN(C)N=C4)C=C3)=O)C=C2.O=S(C5=CC=C(C)C=C5)(O)=O
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化学全称(E)-N-(2-aminophenyl)-3-(1-((4-(1-methyl-1H-pyrazol-4-yl)phenyl)sulfonyl)-1H-pyrrol-3-yl)acrylamide.
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.Henning SW, et al. 22nd EORTC-NCI-AACR symposium. 2010. Abstract # 178.
产品手册
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