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S-22153
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。
S-22153图片
CAS NO:180304-07-8
包装与价格：
包装价格(元)
5mg电议
10mg电议

产品介绍
S-22153 是一种有效的褪黑素受体 (melatonin receptor) 拮抗剂，对 hMT1 和 hMT2 的 EC50 值分别为 19 nM 和 4.6 nM。S-22153 对 hMT1 的 Ki 值为 8.6 nM (CHO 细胞) 和 16.3 nM (HEK 细胞)，hMT2 的 Ki 值为 6.0 nM (CHO 细胞) 和 8.2 nM (HEK 细胞)。S-22153 是 MT1 和 MT2 褪黑素受体亚型的特异性配体。
Cas No.180304-07-8
分子式C14H17NOS
分子量247.36
储存条件Store at -20°C
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

S-22153 is a potent melatonin receptor antagonist with EC50 values of 19 nM, 4.6 nM for hMT1 and hMT2 melatonin receptor, respectively. S-22153 has Ki values of 8.6 nM (CHO cells) and 16.3 nM (HEK cells) for hMT1, and 6.0 nM (CHO cells) and 8.2 nM (HEK cells) for hMT2. S-22153 is a specific ligand of MT1 and MT2 melatonin receptors subtypes[1][2].

S-22153 sets the temperature and activity periods to approximately 24 hr and increase the circadian amplitude of both rhythms in mice, which exposed to continuous light[1] .

[1]. Li XM, et al. Circadian rhythm entrainment with melatonin, melatonin receptor antagonist S22153 or their combination in mice exposed to constant light. J Pineal Res. 2004;37(3):176-184. [2]. Audinot V, et al. New selective ligands of human cloned melatonin MT1 and MT2 receptors. Naunyn Schmiedebergs Arch Pharmacol. 2003;367(6):553-561.