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MnTBAP Chloride
本半岛bd体育手机客户端 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。
MnTBAP Chloride图片
CAS NO: 55266-18-7
规格: 98%
分子量: 879.15
包装与价格:
包装 价格(元)
10mg 电议
50mg 电议

半岛bd体育手机客户端 介绍
Cell-permeable superoxide dismutase mimetic
CAS:55266-18-7
分子式:C48H28ClMnN4O8
分子量:879.15
纯度:98%
存储:Store at -20°C

Background:

Superoxide (O(2)(·-)) is the proximal mitochondrial reactive oxygen species underlying pathology and redox signaling. This central role prioritizes development of a mitochondria-targeted reagent selective for controlling O(2)(·-). MnTBAP is a novel, stable and cell-permeable superoxide dismutase mimetic.


In vitro: Due to its superoxide dismutase mimetic property, 50 microM MnTBAP was found to attenuate the injury produced dose-dependently by exposure to various concentrations of paraquat for 4 h. MnTBAP also protected endothelial cells in a dose-dependent manner against paraquat. The protective effect of MnTBAP appears to be caused by its intracellular superoxide-scavenging activity because neither the zinc form nor CuZnSOD protected the cells against paraquat-induced injury [1].


In vivo: Local administration of MnTBAP significantly and reduced carrageenan-induced paw oedema dose-dependently at all time points, which was related to its superoxide dismutase mimetic property. MnTBAP also caused a significant dose-dependent reduction in paw myeloperoxidase activity, as well as preventing histological injury. Immunohistochemical analyses for nitrotyrosine showed a positive staining in paw from carrageenan-treated rats [2].


Clinical trial: Up to now, MnTBAP is still in the preclinical development stage.


参考文献:
[1] Day BJ, Shawen S, Liochev SI, Crapo JD.? A metalloporphyrin superoxide dismutase mimetic protects against paraquat-induced endothelial cell injury, in vitro. J Pharmacol Exp Ther. 1995 Dec;275(3):1227-32.
[2] Cuzzocrea S, Costantino G, Mazzon E, Zingarelli B, De Sarro A, Caputi AP.? Protective effects of Mn(III)tetrakis (4-benzoic acid) porphyrin (MnTBAP), a superoxide dismutase mimetic, in paw oedema induced by carrageenan in the rat. Biochem Pharmacol. 1999 Jul 1;58(1):171-6.
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