您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > Bromosporine
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Bromosporine
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Bromosporine图片
CAS NO:1619994-69-2
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
50mg电议
100mg电议
200mg电议

产品介绍
Bromosporine 是一种有效的BET抑制剂,对 PCAF 的IC50为 2.1 μM。Bromosporine 能阻滞癌细胞的细胞周期,诱导细胞凋亡 (apoptosis)。Bromosporine 与 5-FU (HY-90006) 联合使用时,在移植瘤小鼠模型中表现出良好的抗肿瘤活性。在HIV-1潜伏期模型中,Bromosporine 可增加CDK9T-loop 磷酸化,从而保护 HIV-1 复制免受潜伏期的影响。Bromosporine 可用于大肠癌、急性髓系白血病 (AML) 和艾滋病 (AIDS) 的研究。
生物活性

Bromosporine is a potentBETinhibitor with anIC50value of 2.1 μM for PCAF. Bromosporine can arrest cell cycle and induceapoptosisincancercells. Bromosporine exhibits excellent antitumor activity in xenograft mice model when combined with5-FU(HY-90006). Bromosporine can increaseCDK9T-loop phosphorylation inHIV-1latency models, resulting the protection of reactivateHIV-1replication from latency. Bromosporine can be used to research colorectalcancer, acute myeloid leukemia (AML) and AIDS[1][2][3][4].

IC50& Target

IC50: 2.1 μM (PCAF)[2]
Apoptosis, BET, CDK9, HIV-1[1][3][4]

体外研究
(In Vitro)

Bromosporine (0-1000 nM; 72 h) synergistically inhibits cell growth in CRC cells with5-FU(HY-90006)[1].
Bromosporine (various concentration; 48 h) causes a distinct increase in the cells arrested at G1 phase when combined with5-FU[1].
Bromosporine (various concentration; 48 h) decreases the expressions of PARP, caspase 3, and 9[1].
Bromosporine (0.1, 0.5 and 1 μM; 6-10 days) inhibits AML cells in a dose-dependent manner[3].
Bromosporine (2.5 μM; 72 h) activates HIV-1 replication in vitro in latent HIV-1 J-Lat clone C11 cells[4].
Bromosporine (1-50 μM; 48 h) does not induce marked toxicity in primary CD4+ T cells[4].

Cell Proliferation Assay[1]

Cell Line:HCT116 and HT29
Concentration:0, 30, 60, 120, 240, 480 and 1000 nM
Incubation Time:72 h
Result:Synergistically inhibited cell growth in CRC cells with5-FU(HY-90006) (0-16 μg/mL) and exhibited a dose-dependent manner.

Cell Cycle Analysis[1]

Cell Line:HCT116 and HT29
Concentration:Various concentration
Incubation Time:48 h
Result:Caused a distinct increase in the cells arrested at G1 phase when combined with5-FU(HY-90006).

Western Blot Analysis[1]

Cell Line:HCT116 and HT29
Concentration:Various concentration
Incubation Time:48 h
Result:Elevated the level of apoptosis in both cell lines through cleavage of PARP, caspase 3, and 9.

Cell Proliferation Assay[3]

Cell Line:MV4;11, KASUMI-1, OCI-AML3 and K562
Concentration:0.1, 0.5 and 1 μM
Incubation Time:6-10 days
Result:Inhibited these AML cells in a dose-dependent manner.

Cell Cytotoxicity Assay[4]

Cell Line:PBMCs
Concentration:1 μM, 2.5 μM, 5 μM, 10 μM, 25 μM and 50 μM
Incubation Time:48 h
Result:Did not induce marked toxicity in primary CD4+ T cells with CC50over 10 μM.
体内研究
(In Vivo)

Bromosporine (100 mg/kg; i.p.; daily for 10 days) shows better antitumor activity than individual when co-treated with5-FU(HY-90006)[1].

Animal Model:Female BALB/c nude mice (5-6 weeks; injected with 1 × 106 cells/100 μL of HT116 cells)[1]
Dosage:100 mg/kg
Administration:i.p.; daily for 10 days
Result:Exhibited better antitumor activity than individual Bromosporine or5-FU(HY-90006) when co-treated with the two agent.
分子量

404.44

性状

Solid

Formula

C17H20N6O4S

CAS 号

1619994-69-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 51.7 mg/mL(127.83 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.4726 mL12.3628 mL24.7255 mL
5 mM0.4945 mL2.4726 mL4.9451 mL
10 mM0.2473 mL1.2363 mL2.4726 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 2.5 mg/mL (6.18 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (6.18 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在本网站选购。