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PD 173212
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。
PD 173212图片
CAS NO:217171-01-2
包装:10mg
市场价:2132元

产品介绍
PD 173212 是一种选择性 N 型电压敏感钙通道 (VSCC) 阻滞剂,在 IMR-32 测定中的 IC50 为 36 nM。
Cas No.217171-01-2
别名N-[[4-叔丁基苯基]甲基]-N-甲基-L-亮氨酰-N-叔丁基-O-苄基-L-酪氨酰胺
化学名(S)-N-((S)-3-(4-(benzyloxy)phenyl)-1-(tert-butylamino)-1-oxopropan-2-yl)-2-((4-(tert-butyl)benzyl)(methyl)amino)-4-methylpentanamide
Canonical SMILESO=C([C@H](CC(C)C)N(C)CC(C=C1)=CC=C1C(C)(C)C)N[C@H](C(NC(C)(C)C)=O)CC(C=C2)=CC=C2OCC3=CC=CC=C3
分子式C38H53N3O3
分子量599.85
溶解度DMSO: 100 mM,Ethanol: 100 mM
储存条件Store at -20℃
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

PD173212 is a selective N-type voltage sensitive calcium channel (VSCC) blocker, with an IC50 of 36 nM in IMR-32 assays.

PD173212 (PD 173212, 300 nM) potently blocks recombinant B-class (N-type) calcium channel currents 78±7.8%, with an IC50 of 74 nM, by whole-cell voltage-clamp techniques. PD 173212 possesses selectivity for non L-type Ca2+ channels versus neuronal Na+, K+, and L-type Ca2+ channels[1].

PD173212 (30 mg/kg, i.v.) shows moderate efficacy in preventing tonic seizures in the audiogenic seizure model[1].

References:
[1]. Hu LY, et al. Structure-activity relationship of N-methyl-N-aralkyl-peptidylamines as novel N-type calcium channel blockers. Bioorg Med Chem Lett. 1999 Aug 2;9(15):2151-6.