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Sufotidine

Sufotidine

产品编号 T68146   CAS 80343-63-1
别名: AH 25352X, AH25352X, AH-25352X

Sufotidine (AH 25352X) 是一种具有高度选择性的竞争性 H2 受体拮抗剂。

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Sufotidine Chemical Structure
Sufotidine, CAS 80343-63-1
规格 价格/CNY 货期 数量
1 mg ¥ 1,750 现货
5 mg ¥ 4,360 现货
10 mg ¥ 6,220 现货
25 mg ¥ 9,390 现货
50 mg ¥ 12,600 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: Sufotidine (T68146)
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纯度: 100%
纯度: 99.28%
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生物活性
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存储 & 溶解度
参考文献
产品描述 Sufotidine (AH 25352X) is a highly selective competitive H2 receptor antagonist.
体外活性 The acid inhibitory effect of sufotidine, a potent, long-lasting, competitive H2-receptor antagonist, was studied in 12 healthy males in a double-blind, randomized, three-way cross-over study of the effect of placebo, sufotidine 600 mg nocte and sufotidine 600 mg b.d. given over 15 days. On days 1 and 15 of dosing with each regimen, each subject's 24-hour ambulatory intragastric acidity was measured by radiotelemetry, and 24-hour plasma gastrin profiles were derived from hourly venous blood samples. Acid suppression was calculated as the decrease in the area under the curve of hydrogen ion activity vs time from that observed on placebo, and 24-h plasma gastrin was calculated as the area under the curve of plasma gastrin concentration vs time. 24h intragastric acidity during the fifteenth day of dosing with sufotidine 600 mg nocte and sufotidine 600 mg b.d. did not differ significantly, but on the first and fifteenth day of dosing nocturnal acidity was decreased to a greater extent by sufotidine 600 mg nocte than sufotidine 600 mg b.d. (P less than 0.005). After 15 days, the acid suppression afforded by sufotidine 600 mg b.d. was significantly attenuated (P less than 0.0005); this was associated with a rise in 24-h plasma gastrin (P less than 0.001). Thus, tolerance to the acid-inhibitory effect of H2-receptor antagonists exists and is of rapid onset.[1]
别名 AH 25352X, AH25352X, AH-25352X
分子量 421.56
分子式 C20H31N5O3S
CAS No. 80343-63-1

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 55 mg/mL (130.47 mM)

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.3721 mL 11.8607 mL 23.7214 mL 59.3035 mL
5 mM 0.4744 mL 2.3721 mL 4.7443 mL 11.8607 mL
10 mM 0.2372 mL 1.1861 mL 2.3721 mL 5.9304 mL
20 mM 0.1186 mL 0.593 mL 1.1861 mL 2.9652 mL
50 mM 0.0474 mL 0.2372 mL 0.4744 mL 1.1861 mL
100 mM 0.0237 mL 0.1186 mL 0.2372 mL 0.593 mL

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TargetMol Library Books参考文献

1. Rogers MJ, et al. The effects of 15 days of dosing with placebo, sufotidine 600 mg nocte or sufotidine 600 mg twice daily upon 24-hour intragastric acidity and 24-hour plasma gastrin. Aliment Pharmacol Ther. 1990;4 Suppl 1:65-74. 2. Johnston DA, et al. Inhibition of gastric secretion following single morning or twice daily oral administration of sufotidine to volunteers. Br J Clin Pharmacol. 1989 Oct;28(4):403-7.
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相关化合物库

该产品包含在如下化合物库中:
膜蛋白靶向化合物库 GPCR靶点分子库 经典已知活性库 已知活性化合物库

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体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

Sufotidine 80343-63-1 GPCR/G Protein Immunology/Inflammation Neuroscience Histamine Receptor AH 25352X AH25352X AH-25352X Inhibitor inhibitor inhibit

 

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