• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

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
5MG ¥818 有现货
10MG ¥1215 有现货
25MG ¥2325 有现货
50MG ¥3572 有现货
100MG ¥5257 有现货
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

  • 产品名称
    4SC-202 free base
  • 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
    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。
  • 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.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    4SC202 | 4SC-202 | 4SC 202 | domatinostat
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    HDAC
  • 受体
    HDAC3| HDAC2| HDAC1
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    910462-43-0
  • 分子量
    447.51
  • 分子式
    C??H??N?O?S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:82 mg/mL (183.2 mM);Ethanol:<1 mg/mL;Water:<1 mg/mL
  • SMILES
    O=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
  • 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

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 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
关联产品
  • 4SC-202 free base

    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。

  • HDAC8-IN-20a

    HDAC8-IN-20a 是一种有效的选择性 HDAC8 抑制剂,IC50 为 27 nM。

  • Patamostat mesylate

    Patamostat (E-3123) mesylate 是一种有效的蛋白酶 (protease) 抑制剂。Patamostat mesylate 有效抑制胰蛋白酶,纤溶酶和凝血酶,IC50 值分别为 39 nM,950 nM 和 1.9 μM。Patamostat mesylate 有潜力用于急性胰腺炎的研究。