货号	规格	价格	上海	北京	珠海	重庆	武汉
S87865-5mg买3赠1	≥98%	￥190.00 S87865-5mg ￥190.00 现货（买3赠1）	100 >10	-	-	-	-
S87865-10mg买3赠1	≥98%	￥300.00 S87865-10mg ￥300.00 现货（买3赠1）	50 >10	-	-	-	-
S87865-25mg买3赠1	≥98%	￥650.00 S87865-25mg ￥650.00 现货（买3赠1）	20 >10	-	-	-	-
S87865-50mg买3赠1	≥98%	￥1100.00 S87865-50mg ￥1100.00 现货（买3赠1）	10 10	-	-	-	-
S87865-100mg买3赠1	≥98%	￥1900.00 S87865-100mg ￥1900.00 现货（买3赠1）	5 5	-	-	-	-

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产品描述：

Y06036, a potent and selective BET inhibitor, can bind to the BRD4(1) bromodomain (Kd: 82 nM)

靶点：

Epigenetic Reader Domain;EpigeneticReaderDomain

体外研究：

Y06036 bounds to the BRD4(1) bromodomain with Kd values of 82 nM. Y06036 potently inhibited cell growth, colony formation, and the expression of AR, AR-regulated genes, and MYC in prostate cancer cell lines.

体内研究：

The mice were randomized and intraperitoneally (i.p.) treated with either vehicle or BET inhibitor Y06036 (50 mg/kg, 5 times per week) when the tumor volume reached approximately 100 mm3. Y06036 exhibited strong antitumor activities during the 25-day treatment period, with a tumor growth inhibition (TGI) of 70%

细胞实验：

LNCaP, C4-2B, 22Rv1, and VCaP prostate cancer cells were cultured in RPMI 1640 with 10% FBS at 37 °C and an atmosphere of 5% CO2. For cell viability, cells were seeded in 384-well plates at 500?1000 cells per well (optimum density for growth) in a total volume of 20 μL of media. After 12 h, 10 μL of chemical compounds with 2-fold or 3-fold serial dilution was added to each well with final concentration from 5 nM to 100 μM. The measurement was conducted 96 h after seeded for LNCaP, C4-2B, and 22Rv1 and 144 h after seeded for VCaP. Then, 25 μL of CellTiter-GLO reagents was added, and luminescence was measured on GLOMAX microplate luminometer, according to the manufacturer's instructions. The estimated in vitro half-maximal inhibitory concentration (IC50) values were calculated using Prism 6 software.

动物实验：

Four-week-old male mice (strain: C.B-17/IcrHsd-Prkdcscid for C4-2B) were used for tumor inoculation. Each mouse was inoculated subcutaneously at the dorsal flank on both sides of the mice with C4-2B tumor cells (2 × 10^6 cells) in a mixture of 100 μL PBS and Matrigel (1:1). When the tumor volume reached approximately 100 mm3, the mice were randomized into groups (n = 5?7 per group) and then treated intraperitoneally (ip) with 100 μL of either vehicle or Y06036 and 7m (in a formulation of 15% Cremophor EL, Calbiochem, 82.5% PBS, and 2.5% DMSO) five times per week. The length (L) and width (W) of the tumor mass were monitored by calipers, and volume was expressed in mm3 calculated with the equation V = (π/6)(L × W2). Tumor growth inhibition (TGI) was calculated using the equation TGI = [1 ? (T ? T0)/(C ? C0)] × 100, wherein T and T0 are the mean tumor volumes on a specific experimental day and on the first day of treatment, respectively, for the test groups; and likewise C and C0 are the mean tumor volumes for

参考文献：

1. Zhang M, et al. Structure-Based Discovery and Optimization of Benzo[ d]isoxazole Derivatives as Potent and Selective BET Inhibitors for Potential Treatment of Castration-Resistant Prostate Cancer (CRPC). J Med Chem. 2018 Apr 12;61(7):3037-3058.

溶解性：

Soluble in DMSO

保存条件：

-20℃

配置溶液浓度参考：

	1mg	5mg	10mg
1 mM	2.34 ml	11.702 ml	23.404 ml
5 mM	0.468 ml	2.34 ml	4.681 ml
10 mM	0.234 ml	1.17 ml	2.34 ml
50 mM	0.047 ml	0.234 ml	0.468 ml

注意：

部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

参考文献

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