產(chǎn)品目錄

規(guī)格	1mg 5mg 10mg 25mg 50mg 100mg
CAS	1959551-26-8
別名	N/A
化學(xué)名	N/A
分子式	C24H23F4N7O3
分子量	533.48
溶解度	DMSO: 50 mg/mL (93.72 mM)
儲存條件	Store at -20°C
General tips	For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition	Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request

產(chǎn)品描述：

FT671 is a potent and selective USP7 inhibitor with an IC50 of 52 nM and binds to the USP7 catalytic domain with a Kd of 65 nM.

FT671 binds to the USP7 catalytic domain (USP7CD; residues 208-560) with apparent dissociation constant (Kd) value of 65nM (s.e.m. range: 45-92). FT671 inhibits USP7 with half-maximal inhibitory concentration (IC50) value of 52 (29-94) nM (USP7CD). Cell lines derived from colorectal carcinoma (HCT116) or bone osteosarcoma (U2OS) respond to USP7 knockdown with p53 stabilization and p21 induction, leading to growth arrest and apoptosis. Similarly, FT671 increases p53 protein levels in these cell lines, leading to induction of p53 target genes including BBC3 (which encodes PUMA), CDKN1A (p21), RPS27L (S27L) and MDM2. The increase in p53 correlates with increased MDM2 degradation, which is initially balanced by p53-induced MDM2 expression, but has an effect on MDM2 protein levels after prolonged compound treatment. FT671 leads to the degradation of N-Myc and upregulation of p53 in the neuroblastoma cell line IMR-32. FT671 also stabilizes p53 in the MM.1S multiple myeloma cell line, which correlates with increased MDM2 ubiquitination and leads to expression of p53 target genes. FT671 blocks the proliferation of MM.1S cells, with an IC50 value of 33 nM[1].

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1. 本產(chǎn)品僅供科研使用。請勿用于醫(yī)藥、臨床診斷或治療，食品及化妝品等用途。請勿存放于普通住宅區(qū)。

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原創(chuàng)作者：上海莼試生物技術(shù)有限公司

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