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Merck
CN

S6951

Sigma-Aldrich

Surfen水合物

≥98% (HPLC)

别名:

1,3-二(4-氨基-2-甲基-6-喹啉)脲水合物, NSC 12155, N,N′-双(4-氨基-2-甲基-6-喹啉)脲, 二-2-甲基-4-氨基喹啉-6-脲水合物, 双氨甲喹脲, 氨喹脲, 氨基尿苷

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About This Item

经验公式(希尔记法):
C21H20N6O · xH2O
分子量:
372.42 (anhydrous basis)
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear

储存温度

2-8°C

SMILES字符串

O.Cc1cc(N)c2cc(NC(=O)Nc3ccc4nc(C)cc(N)c4c3)ccc2n1

InChI

1S/C21H20N6O.H2O/c1-11-7-17(22)15-9-13(3-5-19(15)24-11)26-21(28)27-14-4-6-20-16(10-14)18(23)8-12(2)25-20;/h3-10H,1-2H3,(H2,22,24)(H2,23,25)(H2,26,27,28);1H2

InChI key

UXYZYUHSZVKWTR-UHFFFAOYSA-N

应用

Surfen水合物可用作肝素的拮抗剂。
Surfen水合物已用于抑制人类胚胎肾细胞中的多个电压门控钙通道。

生化/生理作用

Surfen是一种硫酸乙酰肝素拮抗剂,最初于三十年代后期开发,作为生产长效胰岛素的赋形剂。 硫酸乙酰肝素(HS)在结构上与肝素相关,但每个二糖含有较少的硫酸根基团,并且几乎仅存在于蛋白聚糖的蛋白核心上,蛋白聚糖在质膜上显示或分泌到细胞外基质中。Surfen与糖胺聚糖(GAG)/HS的链结合并阻止酶和蛋白质的结合,从而充当HS拮抗剂。 Surfen比鱼精蛋白(一种临床使用的肝素拮抗剂)更有效。
Surfen是硫酸乙酰肝素拮抗剂。

危险声明

预防措施声明

危险分类

Aquatic Chronic 4

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Secreted chemokines are critical mediators of cellular communication that elicit intracellular signaling by binding membrane-bound receptors. Here we demonstrate the development and use of a sensitive real-time approach to quantify secretion and receptor binding of native chemokines in live cells
Sapthaswaran Veerapathiran et al.
eLife, 9 (2020-11-26)
Wnt3 proteins are lipidated and glycosylated signaling molecules that play an important role in zebrafish neural patterning and brain development. However, the transport mechanism of lipid-modified Wnts through the hydrophilic extracellular environment for long-range action remains unresolved. Here we determine
urfen is a broad-spectrum calcium channel inhibitor with analgesic properties in mouse models of acute and chronic inflammatory pain
Rivas-Ramirez P, et al.
Pflugers Archiv : European Journal of Physiology, 469, 1325-1334 (2017)
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International journal of molecular sciences, 21(24) (2020-12-19)
Orthodontic tooth movement (OTM) creates compressive and tensile strain in the periodontal ligament, causing circulation disorders. Hypoxia-inducible factor 1α (HIF-1α) has been shown to be primarily stabilised by compression, but not hypoxia in periodontal ligament fibroblasts (PDLF) during mechanical strain

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