Ro 32-0432 hydrochloride

产品编号:Bellancom-108601A| CAS NO:1781828-85-0| 分子式:C28H29ClN4O2| 分子量:489.01

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Bellancom-108601A
8500.00 杭州 北京(现货)

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Ro 32-0432 hydrochloride

产品介绍 Ro 32-0432 hydrochloride 是一种有效的,选择性的,ATP 竞争性和具有口服活性的 PKC 抑制剂,对 PKCαPKCβIPKCβIIPKCγPKCεIC50 值分别为 9.3 nM,28 nM,30 nM,36.5 nM 和 108.3 nM。Ro 32-0432 hydrochloride 也是一种选择性 GRK5 的抑制剂。Ro 32-0432 hydrochloride 可防止 T 细胞活化,并可用于慢性炎症和自身免疫性疾病的研究。
生物活性

Ro 32-0432 hydrochloride is a potent, selective, ATP-competitive and orally active PKC inhibitor. The IC50 values of Ro 32-0432 hydrochloride for PKCα, PKCβI, PKCβII, PKCγ and PKCε are 9.3 nM, 28 nM, 30 nM, 36.5 nM and 108.3 nM, respectively. Ro 32-0432 hydrochloride is also a selective G protein-coupled receptor kinase 5 (GRK5) inhibitor. Ro 32-0432 hydrochloride prevents T-cell activation and has the potential for chronic inflammatory and autoimmune diseases research.

体外研究

Ro 32-0432 inhibits interleukin-2 (IL-2) secretion, IL-2 receptor expression in, and proliferation of, peripheral human T-cells stimulated with phorbol ester together with phytohemagglutin or anti-CD3, but does not inhibit IL-2 induced proliferation in cells already stimulated to express IL-2 receptors. Proliferation of the influenza peptide antigen HA 307-319-specific human T-cell clone (HA27) after exposure to antigen-pulsed autologous presenting cells is also inhibited by Ro 32-0432. Ro 32-0432 inhibits HA27 proliferation with an IC50 of 0.15 μM.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

Ro 32-0432 (10-50 mg/kg; oral administration; once; female AHH/R rats) treatment inhibits subsequent phorbol ester-induced edema in rats demonstrating the systemic efficacy of the compound to inhibit PKC-driven responses. Induction of more physiologically T-cell driven responses such as host vs. graft responses and the secondary paw swelling in adjuvant-induced arthritis are also inhibited by Ro 32-0432.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female AHH/R rats (200-250 g) induced with phorbol ester
Dosage: 10 mg/kg, 30 mg/kg, 50 mg/kg
Administration: Oral administration; once
Result: Inhibited subsequent phorbol ester-induced edema in rats.
体内研究

Ro 32-0432 (10-50 mg/kg; oral administration; once; female AHH/R rats) treatment inhibits subsequent phorbol ester-induced edema in rats demonstrating the systemic efficacy of the compound to inhibit PKC-driven responses. Induction of more physiologically T-cell driven responses such as host vs. graft responses and the secondary paw swelling in adjuvant-induced arthritis are also inhibited by Ro 32-0432.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female AHH/R rats (200-250 g) induced with phorbol ester
Dosage: 10 mg/kg, 30 mg/kg, 50 mg/kg
Administration: Oral administration; once
Result: Inhibited subsequent phorbol ester-induced edema in rats.
性状
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献

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