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Ruboxistaurin-d6 hydrochloride

更新时间:2025-10-17 11:28:49

Ruboxistaurin-d6 hydrochloride结构式
Ruboxistaurin-d6 hydrochloride结构式
品牌特惠专场
常用名 Ruboxistaurin-d6 hydrochloride 英文名 Ruboxistaurin-d6 hydrochloride
CAS号 1794767-04-6 分子量 511.04
密度 N/A 沸点 N/A
分子式 C28H23D6ClN4O3 熔点 N/A
MSDS N/A 闪点 N/A

 Ruboxistaurin-d6 hydrochloride用途


Ruboxistaurin-d6(LY333531-d6)盐酸盐是氘标记的Ruboxistaurin盐酸盐。盐酸Ruboxistaurin(LY333531)是一种口服活性、选择性PKCβ抑制剂(Ki=2 nM)。盐酸Ruboxistaurin对PKCβI具有ATP依赖性竞争性抑制作用,IC50为4.7nM。盐酸Ruboxistaurin抑制PKCβII的IC50为5.9 nM[1][2]。

 Ruboxistaurin-d6 hydrochloride名称

中文名 鲁伯斯塔盐酸盐 d6 (盐酸盐)
英文名 Ruboxistaurin-d6 hydrochloride

 Ruboxistaurin-d6 hydrochloride生物活性

描述 Ruboxistaurin-d6(LY333531-d6)盐酸盐是氘标记的Ruboxistaurin盐酸盐。盐酸Ruboxistaurin(LY333531)是一种口服活性、选择性PKCβ抑制剂(Ki=2 nM)。盐酸Ruboxistaurin对PKCβI具有ATP依赖性竞争性抑制作用,IC50为4.7nM。盐酸Ruboxistaurin抑制PKCβII的IC50为5.9 nM[1][2]。
相关类别
体外研究 氢、碳和其他元素的稳定重同位素已被纳入药物分子,主要作为药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注[1]。
参考文献

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

[2]. Jirousek MR, et al. (S)-13-[(dimethylamino)methyl]-10,11,14,15-tetrahydro-4,9:16, 21-dimetheno-1H, 13H-dibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecene-1,3(2H)-d ione (LY333531) and related analogues: isozyme selective inhibitors of protein kinase C beta. J Med Chem. 1996;39(14):2664-2671.

[3]. Ruboxistaurin: LY 333531. Drugs R D. 2007;8(3):193-199.

[4]. Kunt T, et al. The beta-specific protein kinase C inhibitor ruboxistaurin (LY333531) suppresses glucose-induced adhesion of human monocytes to endothelial cells in vitro. J Diabetes Sci Technol. 2007 Nov;1(6):929-35.

[5]. Nonaka A, et al. PKC-beta inhibitor (LY333531) attenuates leukocyte entrapment in retinal microcirculation of diabetic rats. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2702-6.

 Ruboxistaurin-d6 hydrochloride物理化学性质

分子式 C28H23D6ClN4O3
分子量 511.04
InChIKey NYQIEYDJYFVLPO-DOVGNSRXSA-N
SMILES CN(C)CC1CCn2cc(c3ccccc32)C2=C(C(=O)NC2=O)c2cn(c3ccccc23)CCO1.Cl
储存条件 2-8°C,密封,干燥
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