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OP-5244 sodium
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。
OP-5244 sodium图片
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
OP-5244 sodium 是一种有效和具有口服活性的CD73抑制剂,IC50值为 0.25 nM。OP-5244 sodium 通过阻断腺苷的产生来逆转免疫抑制作用,具有进行癌症研究的潜力。
生物活性

OP-5244 sodium is a potent and orally active inhibitor ofCD73, with anIC50of 0.25 nM. OP-5244 sodium reverses immunosuppression through blocking of adenosine production, and has the potential for thecancerresearch[1].

IC50& Target

IC50: 0.25 nM (CD73)[1]

体外研究
(In Vitro)

OP-5244 inhibits the production of adenosine (ADO), with an EC50of 0.79±0.38 nM in H1568 (NSCLC) cells[1].
OP-5244 inhibits AMP hydrolysis to ADO in peripheral blood derived CD8+T cells with an EC50of 0.22 nM[1].
OP-5244 (4.1-1000 nM; 96 h) rescues AMP-suppressed CD8+T cells proliferation and cytokine production[1].
OP-5244 (0.01 nM-10 μM) inhibits ADO production completely in human and murine cancer cell lines (H1568 and EMT6, respectively)[1].

体内研究
(In Vivo)

OP-5244 (15 mg/kg/day; s.c. for 13 d) exhibits anti-tumor effects as a single agent as shown by the tumor growth inhibition in mice[1].
OP-5244 (150 mg/kg; p.o. twice daily for 16 d) increases CD8+T cells infiltration and reverses immunosuppression in mice[1].
OP-5244 (0.2 mg/kg; i.v.) exhibits terminal elimination half-lives (rat 8.5, dog 0.82, cyno 4.6 h) due to moderate plasma clearance (rat 0.18, dog 1.22, cyno 0.05 L/kg/h) and low steady-state volume of distribution (rat 0.22, dog 0.29, cyno 0.10 L/kg/h)[1].
OP-5244 (10 mg/kg; p.o.) exhibits Cmax(rat 0.82, dog 1.25, cyno 1.72 μM) and AUC (rat 1.96, dog 1.75, cyno 14.2 μMoh)[1].

Animal Model:BALB/c mice with breast cancer[1]
Dosage:15 mg/kg/day
Administration:S.c. for 13 days
Result:Inhibited tumor growth.
Showed a 95% lower ADO/AMP ratio compared to that of the vehicle group.
分子量

559.87

性状

Solid

Formula

C19H28ClN5NaO9P

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

溶解性数据
In Vitro: 

DMSO : 33.33 mg/mL(59.53 mM;ultrasonic and warming and heat to 60℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.7861 mL8.9306 mL17.8613 mL
5 mM0.3572 mL1.7861 mL3.5723 mL
10 mM0.1786 mL0.8931 mL1.7861 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 (sealed storage, away from moisture and light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。