Sulazepam

(Synonyms: 硫西泮)
目录号: PL08136
Sulazepam 是一种苯二氮卓类药物,是一种选择性卵巢癌 G 蛋白偶联受体 (OGR1) 激动剂。Sulazepam 具有抗惊厥作用,也有用于气道高反应性 (AHR) 研究的潜力。
CAS No. :2898-13-7
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PL08136-5mg 5mg ¥1607.00 请登录
PL08136-10mg 10mg ¥2732.00 请登录
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中文名称
Sulazepam
中文别名
硫西泮
英文名称
Sulazepam
英文别名
2H-1,4-Benzodiazepine-2-thione,7-chloro-1,3-dihydro-1-methyl-5-phenyl-;7-chloro-1-methyl-5-phenyl-3H-1,4-benzodiazepine-2-thione;1-Methyl-7-chlor-5-phenyl-1H-1,4-benzodiazepin-2(3H)-thion;2H-1,4-BENZODIAZEPINE-2-THIONE,7-CHLORO-1,3-DIHYDRO-1-METHYL-5-PHENYL;7-Chlor-1-methyl-5-phenyl-1.3-dihydro-2H-1.4-benzodiazepin-thion-(2);7-Chlor-1-methyl-5-phenyl-3H-1,4-benzodiazepin-2(1H)-thion;7-Chloro-1-;7-Chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepine-2-thione;7-chloro-1-methyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepine-2-thione;Sulazepamum [INN-Latin];W 3676
Cas No.
2898-13-7
分子式
C16H13N2Scl
分子量
300.81
包装储存
Please store the product under the recommended conditions in the Certificate of Analysis.
详情描述
Sulazepam 是一种苯二氮卓类药物,是一种选择性卵巢癌 G 蛋白偶联受体 (OGR1) 激动剂。Sulazepam 具有抗惊厥作用,也有用于气道高反应性 (AHR) 研究的潜力。
产品详情
Sulazepam 是一种苯二氮卓类药物,是一种选择性卵巢癌 G 蛋白偶联受体 (OGR1) 激动剂。Sulazepam 具有抗惊厥作用,也有用于气道高反应性 (AHR) 研究的潜力。
生物活性
Sulazepam, a benzodiazepine, is a selective ovarian cancer G protein-coupled receptor (OGR1) agonist. Sulazepam has anticonvulsive action and has the potential for airway hyperresponsiveness (AHR) research.
体内研究(In Vivo)
Sulazepam (3.2 mg/kg in 25 μL via intranasal route ~30 min before HDM challenge; 5 days a week for three consecutive weeks) inhibits the development of airway hyperresponsiveness (AHR) in Male and female wild-type C57BL/6 mice (8-10 wk old), but not in age-matched OGR1KO mice (C57BL/6 background) with house dust mite (HDM) allergen (25 μg; intranasally). has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Ajay P Nayak, et al. OGR1-dependent regulation of the allergen-induced asthma phenotype. Am J Physiol Lung Cell Mol Physiol. 2021 Dec 1;321(6):L1044-L1054.
[2]. Tonio Pera, et al. Biased signaling of the proton-sensing receptor OGR1 by benzodiazepines. FASEB J. 2018 Feb;32(2):862-874.
溶解度数据
In Vitro: DMSO : 50 mg/mL (166.22 mM; ultrasonic and warming and heat to 60°C)配制储备液
搜索质检报告(COA)
[1]. Ajay P Nayak, et al. OGR1-dependent regulation of the allergen-induced asthma phenotype. Am J Physiol Lung Cell Mol Physiol. 2021 Dec 1;321(6):L1044-L1054.
[2]. Tonio Pera, et al. Biased signaling of the proton-sensing receptor OGR1 by benzodiazepines. FASEB J. 2018 Feb;32(2):862-874.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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