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76824-35-6NC(N)=Nc1nc(CSCC/C(N)=N/S(N)(=O)=O)cs1XUFQPHANEAPEMJ-UHFFFAOYSA-N76824-35-6CHEMBL902化学的特性White Powder
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
解説ファモチジン,C8H15N7O2S3(337.45).白色~帯黄白色の結晶.融点約164 ℃(分解).氷酢酸に易溶,エタノール,水に難溶,エーテルに不溶.ヒスタミン H2-受容体遮断作用による抗胃潰瘍,十二指腸潰瘍薬として用いられる.LD50 244.4 mg/kg(マウス,静注).
用途ヒスタミンH2 受容体遮断剤 です。胃粘膜のヒスタミンH2受容体を遮断し、 胃酸分泌を抑制作用を示します。
用途ヒスタミンH2 受容体遮断剤 です。胃粘膜のヒスタミンH2 受容体を遮断し、 胃酸分泌抑制作用を示します。
説明Famotidine is a competitive histamine H2-receptor antagonist, and the main pharmacodynamic effect of famotidine is to cause the inhibition of gastric secretion. Famotidine on decomposition releases toxic products such as carbon oxides (CO, CO2), nitrogen oxides (NO, NO2), and sulphur oxides (SO2, SO3). Famotidine is a medication that is available both in prescription and over-the-counter forms. It is used to treat conditions related to the oesophagus, stomach, and intestines. Some specific famotidine is used for the treatment of duodenal ulcers, gastric ulcers (stomach ulcers), gastroesophageal reflux disease (GERD), and pathological hypersecretory conditions that occur when stomach acid is secreted/ produced in very large quantities, an abnormal health condition called ‘Zollinger-Ellison syndrome’.
使用Contact dermatitis from famotidine, a H2 -receptor agonist, was described in a nurse. In industry, three cases were reported due to intermediates of synthesis, 2- diamino-ethylene-amino-thiazolyl-methylenethiourea-dichloride and 4-chloromethyl-2-guanidinothiazolenitrochloride.
一般的な説明Famotidine is a histamine H2-receptor antagonist, which promotes the healing of erosive esophagitis, gastric and duodenal ulcers since it inhibits the gastric acid secretion in humans.Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
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