FT-671
CAS No. 1959551-26-8
FT-671 ( FT671;FT 671 )
产品货号. M13072 CAS No. 1959551-26-8
FT-671 is a novel potent, specific, non-covalent USP7 inhibitor with Kd of 65 nM (USP7 catalytic domain).
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥11097 | 有现货 |
|
50MG | ¥22518 | 有现货 |
|
100MG | ¥29970 | 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FT-671
-
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FT-671 is a novel potent, specific, non-covalent USP7 inhibitor with Kd of 65 nM (USP7 catalytic domain).
-
产品描述FT-671 is a novel potent, specific, non-covalent USP7 inhibitor with Kd of 65 nM (USP7 catalytic domain); inhibits USP7 with IC50 values of 52 nM (USP7 CD) and 69 nM (USP7C-term), display good USP7 selectivity in a panel of 38 deubiquitinases (DUBs); destabilizes USP7 substrates including MDM2, increases levels of p53, and results in the transcription of p53 target genes and induces tumour suppressor p21; blocks the proliferation of MM.1S cells (IC50=33 nM), suppresses tumour growth in mice; orally available.
-
同义词FT671;FT 671
-
通路Proteasome/Ubiquitin
-
靶点DUB
-
受体DUB
-
研究领域Cancer
-
适应症——
化学信息
-
CAS Number1959551-26-8
-
分子量533.49
-
分子式C24H23F4N7O3
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESO=C1C2=C(N=CN1CC3(CCN(CC3)C(C[C@@H](C(F)F)N4N=C(C=C4)F)=O)O)N(N=C2)C5=CC=C(C=C5)F
-
化学全称(S)-5-((1-(4,4-difluoro-3-(3-fluoro-1H-pyrazol-1-yl)butanoyl)-4-hydroxypiperidin-4-yl)methyl)-1-(4-fluorophenyl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one
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. Turnbull AP, et al. Nature. 2017 Oct 26;550(7677):481-486.
产品手册
关联产品
-
MK8745
MK-8745 is a potent and selective Aurora A inhibitor.
-
USP30 inhibitor 18
USP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.
-
USP7-IN-8
USP7-IN-8 is a selective ubiquitin-specific protease 7 (USP7) inhibitor with an IC50 of 1.4 μM. USP7-IN-8 has anticancer effects.