021-51111890
购物车（）
sales@molnova.cn
KA2507
CAS No. 1636894-46-6
KA2507 ( —— )
产品货号. M23733 CAS No. 1636894-46-6
KA2507 is a potent and selective HDAC6 inibitor with an IC50 of 2.5nM.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ￥1596 | 有现货 |
|
| 10MG | ￥2568 | 有现货 |
|
| 25MG | ￥4334 | 有现货 |
|
| 50MG | ￥6253 | 有现货 |
|
| 100MG | ￥8748 | 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KA2507
-
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KA2507 is a potent and selective HDAC6 inibitor with an IC50 of 2.5nM.
-
产品描述KA2507 is a potent and selective HDAC6 inibitor with an IC50 of 2.5nM.
-
同义词——
-
通路Cell Cycle/DNA Damage
-
靶点HDAC
-
受体HDAC6; HDAC8
-
研究领域——
-
适应症——
化学信息
-
CAS Number1636894-46-6
-
分子量322.3
-
分子式C16H14N6O2
-
纯度>98% (HPLC)
-
溶解度DMSO : 60 mg/mL (186.15 mM; Need ultrasonic)
-
SMILESO=C(NO)C1=CC=C(CN(C2=NC=CN=C2)C3=NC=CN=C3)C=C1
-
化学全称——
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.Apostolia M Tsimberidou, et al. Preclinical Development and First-in-Human Study of KA2507, a Selective and Potent Inhibitor of Histone Deacetylase 6, for Patients with Refractory Solid Tumors. Clin Cancer Res. 2021 May 4.
产品手册
关联产品
-
Valproic acid sodium...
A HDAC inhibitor that selectively inhibits the catalytic activity of class I HDACs, and induces proteasomal degradation of HDAC2.
-
BRD 8184
BRD 8184 is a potent, selective HDAC6 inhibitor with IC50 of 8 nM.
-
SW-100
SW-100 (SW100) is a potent, selective, brain penetrable HDAC6 inhibitor with IC50 of 2.3 nM.
