SR-1277

• 常用名: SR-1277
• 英文名: SR-1277
• CAS号: 1446715-47-4
• 分子量: 477.50
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₁H₁₉N₉O₃S
• 熔点: N/A
• 闪点: N/A

SR-1277用途

SR-1277是一种有效、选择性和ATP竞争性CK1δ/ε抑制剂,IC50分别为49 nM和260 nM。SR-1277还抑制FLT3、CDK4/细胞周期蛋白D1、CDK6/细胞周期蛋白D3和CDK9/细胞周期蛋白K,IC50分别为305nm、1340nm、311nm和109nm。SR-1277可用于癌症研究[1]。

SR-1277名称

• 英文名: SR-1277

SR-1277生物活性

• 描述: SR-1277是一种有效、选择性和ATP竞争性CK1δ/ε抑制剂,IC50分别为49 nM和260 nM。SR-1277还抑制FLT3、CDK4/细胞周期蛋白D1、CDK6/细胞周期蛋白D3和CDK9/细胞周期蛋白K,IC50分别为305nm、1340nm、311nm和109nm。SR-1277可用于癌症研究[1]。
• 相关类别:
  研究领域 >> 癌症
  信号通路 >> 细胞周期/DNA损伤 >> 酪蛋白激酶
  信号通路 >> 干细胞及 Wnt 通路 >> 酪蛋白激酶
• 靶点实验:

  CKIδ:49 nM (IC50)

  CKIϵ:260 nM (IC50)

• 体外研究: SR-1277对A375细胞具有抗增殖作用,EC50为22 nM[1]。
• 体内研究: SR-1277(1 mg/kg；静脉注射)在小鼠体内表现出Cmax(1.2μM)、Cl(2.8 ml/min/kg)、AUC(1.26μM•h)、T1/2(1.42 h)和脑渗透(24%)[1]。
• 参考文献:

  [1]. Bibian M, et, al. Development of highly selective casein kinase 1δ/1ε (CK1δ/ε) inhibitors with potent antiproliferative properties. Bioorg Med Chem Lett. 2013 Aug 1;23(15):4374-80.

SR-1277物理化学性质

• 分子式: C₂₁H₁₉N₉O₃S
• 分子量: 477.50
• InChIKey: FLKHSCQMBSUMSH-UHFFFAOYSA-N
• SMILES: O=[N+]([O-])c1cccc2[nH]c(CNc3nc(N4CCOCC4)nc4c3ncn4-c3ccsc3)nc12

SR-1277靶点实验

查看更多实验

实验名称：Fluorescence-based biochemical high throughput primary assay to identify inhibitors o... 来源：The Scripps Research Institute Molecular Screening Center 靶标：Trypanosoma brucei RNA editing ligase 1 External Id：TBREL1_INH_FRET_1536_1X%INH PRUN

实验名称：Primary qHTS assay for small molecule inhibitors of Inositol hexaphosphate kinase 1 (... 来源：NCGC External Id：IP6K1-p1

实验名称：QFRET-based biochemical primary high throughput screening assay to identify exosite i... 来源：The Scripps Research Institute Molecular Screening Center 靶标：disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens] External Id：ADAM17_INH_QFRET_1536_1X%INH PRUN

实验名称：Luminescence-based cell-based primary high throughput screening assay to identify act... 来源：The Scripps Research Institute Molecular Screening Center 靶标：TTR [Homo sapiens] External Id：TTR_ACT_LUMI_1536_1X%ACT PRUN

实验名称：Cytochrome P450 family 3 subfamily A member 4 (CYP3A4) small molecule antagonists: lu... 来源：NCGC External Id：CYP3A4437

实验名称：Cytochrome P450 family 2 subfamily D member 6 (CYP2D6) small molecule antagonists: lu... 来源：NCGC External Id：CYP2D6395

实验名称：Fluorescence-based biochemical high throughput primary assay to identify inhibitors o... 来源：The Scripps Research Institute Molecular Screening Center 靶标：Phospholipase C, beta 3 (phosphatidylinositol-specific) [Homo sapiens] External Id：PLCB3_INH_QFRET_1536_1X%INH PRUN

实验名称：Cytochrome P450 family 2 subfamily C member 9 (CYP2C9) small molecule antagonists: lu... 来源：NCGC External Id：CYP2C9536

实验名称：QFRET-based biochemical primary high throughput screening assay to identify exosite i... 来源：The Scripps Research Institute Molecular Screening Center 靶标：ADAM10 [Homo sapiens] External Id：ADAM10_INH_QFRET_1536_1X%INH PRUN

实验名称：Cytochrome P450 family 3 subfamily A member 7 (CYP3A7) small molecule antagonists: lu... 来源：NCGC External Id：CYP3A7681

共43条，当前第1页，共5页

1

2

3

4

5