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CAS: 88191-84-8
分子式: C22H26N2O4
分子量: 382.45
英文名称: 
mdl 28170
calpain inhibitor iii
用途: MDL-28170 (Calpain Inhibitor III) 是一种有效的、选择性的、具有膜渗透性的半胱氨酸蛋白酶 (calpain)抑制剂,可在全身给药后迅速穿过血脑屏障。MDL-28170 还能阻断γ-secretase。
推荐供应商
货号品牌产品名称规格包装、参考价格
M876800MACKLINMDL-28170≥99%270元/5mg;   515元/10mg;   咨询
储存:2-8℃
M6690Sigma-AldrichMDL 28170≥90% (TLC)3056.06元/25 MG;   咨询

产品说明

Amino Acid Sequence

Z-Val-Phe-al

应用

MDL 28170已被用作钙蛋白酶抑制剂:

  • 在大鼠心脏骤停模型中研究对神经炎症和坏死的影响
  • 分析对牛肉半膜肌神经元一氧化氮合酶(nNOS)降解的影响
  • 研究对大鼠脑损伤的保护作用及骨髓间充质干细胞在大鼠脑内的存活率

生化/生理作用

MDL 28170 是一种有效的细胞渗透性钙蛋白酶 I 和 II 抑制剂;减少培养的背根神经节神经元中辣椒素介导的细胞死亡。减少 H2O2 和 A23187 处理的 PC12 细胞凋亡的发生。γ-分泌酶抑制剂。
MDL 28170对大鼠脊髓损伤、局灶性脑缺血和新生儿缺氧缺血均有神经保护作用。它还有抗炎和抗神经退化特性。MDL 28170可穿过血脑屏障,并轻松穿透细胞膜。

基本信息

经验(实验)分子式C22H26N2O4
分子量382.45
MDL编号MFCD00798796
PubChem化学物质编号24278565
NACRESNA.77

产品性质

质量水平200
测定≥90% (TLC)
组成Peptide Content, >90%
溶解性DMSO: 26 mg/mL
H2O: insoluble
methanol: soluble
运输wet ice
储存温度2-8℃
SMILES string[H]C(=O)C(Cc1ccccc1)NC(=O)[C@@H](NC(=O)OCc2ccccc2)C(C)C
InChI1S/C22H26N2O4/c1-16(2)20(24-22(27)28-15-18-11-7-4-8-12-18)21(26)23-19(14-25)13-17-9-5-3-6-10-17/h3-12,14,16,19-20H,13,15H2,1-2H3,(H,23,26)(H,24,27)/t19?,20-/m0/s1
InChI keyNGBKFLTYGSREKK-ANYOKISRSA-N
Gene Informationhuman ... CAPN1(823), CAPN2(824)

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
个人防护装备Eyeshields, Gloves, type N95 (US)
208722Sigma-AldrichCalpain Inhibitor III-CAS 88191-84-8-CalbiochemThe Calpain Inhibitor III, also referenced under CAS 88191-84-8, controls the biological activity of Calpain. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.2741.8元/25 MG;   咨询

产品说明

一般描述

A potent, cell-permeable inhibitor of calpain I and II (Ki = 8 nM) that also reduces capsaicin-mediated cell death in cultured dorsal root ganglion. Reported to block A23187-induced suppression of neurite outgrowth in isolated hippocampal pyramidal neurons. Exhibits neuroprotective effects against glutamate-induced toxicity.
A potent, cell-permeable inhibitor of calpain I and II (Ki = 8 nM). Reduces capsaicin-mediated cell death in cultured dorsal root ganglion. Reported to block A23187-induced suppression of neurite outgrowth in isolated hippocampal pyramidal neurons. Exhibits neuroprotective effect in glutamate-induced toxicity.

包装

25 mg in Plastic ampoule

生化/生理作用

Cell permeable: yes
Primary Target
calpain 1, calpain 2
Product does not compete with ATP.
Reversible: no

警告

Toxicity: Standard Handling (A)

序列

Z-Val-Phe-CHO

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.

其他说明

Chatterjee, S., et al. 1998. J. Med. Chem.41, 2663.
Rami, A., et al. 1997. Neurosci. Res. 27, 93.
Yamazaki, T., et al. 1997. Biochemistry36, 8377.
Klafki, H., et al. 1996. J. Biol. Chem.271, 28655.
Chard, P.S., et al. 1995. Neuroscience 65, 1099.
Song, D.K., et al. 1994. J. Neurosci. Res. 39, 474.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C22H26N2O4
分子量382.45
MDL编号MFCD00798796
NACRESNA.77

产品性质

质量水平100
测定≥95% (HPLC)
形式lyophilized solid
效能8 nM IC50
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
颜色 white
溶解性DMSO: 20 mg/mL (Use only anhydrous DMSO.)
运输ambient
储存温度2-8℃
InChI1S/C22H26N2O4/c1-16(2)20(24-22(27)28-15-18-11-7-4-8-12-18)21(26)23-19(14-25)13-17-9-5-3-6-10-17/h3-12,14,16,19-20H,13,15H2,1-2H3,(H,23,26)(H,24,27)/t19-,20-/m0/s1
InChI keyNGBKFLTYGSREKK-PMACEKPBSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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