AZD8186

产品编号: DC8380 Featured
AZD8186
结构式
1627494-13-6
此产品仅供科研所需,我们不出售给病人
​我们将匹配市场上最好的价格给您
Email:order@dcbio.cn
免费咨询电话:4008862077
我们的合作伙伴:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
中国地区超过5000个高品质化合物库存
应用领域
AZD8186 是一种 PI3K 抑制剂,抑制 PI3Kβ (IC5050=4 nM),PI3Kδ (IC5050=12 nM),PI3Kα (IC50=35 nM) 和 PI3Kγ (IC50=675 nM)。
Cas No.: 1627494-13-6
名称: (R)-8-(1-(3,5-difluorophenylamino)ethyl)-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide
别名: AZD8186,AZD-8186,AZD 8186
SMILES: O=C(N(C)C)C1=CC([C@@H](C)NC2=CC(F)=CC(F)=C2)=C3C(C(C=C(O3)N4CCOCC4)=O)=C1
分子式: C24H25F2N3O4
分子量: 457.47
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: AZD8186 is and inhibitor of the beta isoform of phosphoinositide-3 kinase (PI3K), with potential antineoplastic activity. Upon administration, PI3Kbeta inhibitor AZD8186 selectively inhibits the activity of PI3Kbeta in the PI3K/Akt/mTOR signaling pathway, which may result in a decrease of tumor cell proliferation. It also induces cell death in PI3K-expressing cancer cells. By specifically targeting class I PI3K beta, this agent may be more efficacious and less toxic than pan PI3K inhibitors. PI3K-mediated signaling is often dysregulated in cancer cells and contributes to increased tumor cell growth, survival, and tumor resistance to a variety of antineoplastic agents. AZD8186 is currently under Phase I clinical trials. For the detailed information of AZD8186, the solubility of AZD8186 in water, the solubility of AZD8186 in DMSO, the solubility of AZD8186 in PBS buffer, the animal experiment (test) of AZD8186, the cell expriment (test) of AZD8186, the in vivo, in vitro and clinical trial test of AZD8186, the EC50, IC50,and affinity,of AZD8186, For the detailed information of AZD8186, the solubility of AZD8186 in water, the solubility of AZD8186 in DMSO, the solubility of AZD8186 in PBS buffer, the animal experiment (test) of AZD8186, the cell expriment (test) of AZD8186, the in vivo, in vitro and clinical trial test of AZD8186, the EC50, IC50,and affinity,of AZD8186, Please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC9311 Serabelisib(TAK-117,INK1117,MLN1117) Serabelisib (MLN1117) 是一种选择性的 p110α 抑制剂, IC50 值为 15 nM。
DC8380 AZD8186 AZD8186 是一种 PI3K 抑制剂,抑制 PI3Kβ (IC5050=4 nM),PI3Kδ (IC5050=12 nM),PI3Kα (IC50=35 nM) 和 PI3Kγ (IC50=675 nM)。
DC5081 Apitolisib(GDC-0980) Apitolisib (GDC-0980; GNE 390; RG 7422) 是一种口服有效的 PI3K 和 mTOR (TORC1/2) 激酶抑制剂,抑制 PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ 的活性,IC50 值为 5 nM/27 nM/7 nM/14 nM。 抑制mTOR,Ki 为 17 nM。
DC1054 GDC0941(Pictilisib) Pictilisib (GDC-0941) 是有效的 PI3Kα/δ 抑制剂,IC50为 3 nM;对110β (11倍) 和 p110γ (25倍) 具有适度的选择性。