GlyH-101
目录号: PL04799 纯度: ≥98%
CAS No. :328541-79-3
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中文名称
GlyH-101
中文别名
GlyH-101 抑制剂;N-2-萘-甘氨酸 2-[(3,5-二溴-2,4-二羟基苯基)亚甲基]肼;阿扎那韦双硫酸盐
英文名称
GlyH-101
英文别名
Glycine, N-2-naphthalenyl-, [(3,5-dibromo-2,4-dihydroxyphenyl)methylene]hydrazide;N-2-Naphthalenyl-glycine 2-[(3,5-Dibromo-2,4-dihydroxyphenyl)methylene]hydrazide;CFTR Inhibitor II;CFTR Inhibitor II, GlyH-101;GLYH 101;GlyH-101;N'-[(3,5-dibromo-4-hydroxy-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]-2-(naphthalen-2-ylamino)acetohydrazide;N-2-Naphthalenyl-gly;N-2-Naphthalenylglycine [(3,5-dibromo-2,4-dihydroxyphenyl)methylene]hydrazide
Cas No.
328541-79-3
分子式
C19H15N3O3Br2
分子量
493.15
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
GlyH-101 是一种有效的 CFTR 抑制剂。GlyH-101 也是一种有效且可逆的 VSORC 电导的抑制剂。GlyH-101 显示出抗增殖活性。GlyH-101 抑制 CFTR 样电流和 VSORC 电流。
生物活性
GlyH-101 is a potent CFTR inhibitor. GlyH-101 also is a potent and reversible inhibitor of the VSORC conductance. GlyH-101 shows antiproliferative activity. GlyH-101 inhibits CFTR-like current and VSORC current.
性状
Solid
体外研究(In Vitro)
GlyH-101 (0-50 μM) shows antiproliferative activity in PCT and PS120 cells.
GlyH-101 (0.5, 1, 5, 10 μM) inhibits CFTR-like current in a concentration-dependent manner in PCT cells.
GlyH-101 (0.5, 1, 5, 10 μM) inhibits the VSORC current with IC50s of 5.38, 6.26 μM for PS120, PCT cells, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.Cell Viability Assay
体内研究(In Vivo)
GlyH-101 (2.5 μg) reduces by about 80% cholera toxin-induced intestinal fluid secretion in mouse. 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
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Muanprasat C, et al. Discovery of glycine hydrazide pore-occluding CFTR inhibitors: mechanism, structure-activity analysis, and in vivo efficacy. J Gen Physiol. 2004 Aug;124(2):125-37.
[2]. Kelly M, et al. Cystic fibrosis transmembrane regulator inhibitors CFTR(inh)-172 and GlyH-101 target mitochondrial functions, independently of chloride channel inhibition. J Pharmacol Exp Ther. 2010 Apr;333(1):60-9.
溶解度数据
In Vitro: DMSO : ≥ 58 mg/mL (117.61 mM)配制储备液
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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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