フロセミド 化學(xué)特性,用途語(yǔ),生産方法
解説
4-chloro-N-furfuryl-5-sulfamoylanthranilic acid．C12H11ClN2O5S(330.74)．2,4-ジクロロ安息香酸にアミノスルホニル基を?qū)毪罚?-アミノメチルフランと縮合させると得られる．白色の結(jié)晶．分解點(diǎn)205 ℃．フロセミドは，水に不溶，メタノール，アセトンに可溶，DMFに易溶．高血圧癥，うっ血性心不全治療薬として使用される．また，降圧利尿剤として尿路結(jié)石排出促進(jìn)に用いられる．LD50 3000 mg/kg(ラット，経口)．森北出版「化學(xué)辭典（第2版）
用途
フロセミド (Furosemide)は、心不全、肝硬変、腎疾患（英語(yǔ)版）による浮腫の治療に用いられるループ利尿薬の一つである。降圧を目的とした処方も行われる。
用途
利尿剤。フロセミドは，腎臓のヘンレ係蹄でのナトリウム再吸収を抑制する，すなわち尿の濃縮，希釈機(jī)構(gòu)を抑制することにより，血漿とほぼ同じ浸透圧の尿を生成する。また，遠(yuǎn)位尿細(xì)管にナトリウムが流入するため，カリウムの排泄が促進(jìn)される。ネフローゼ癥候群，慢性腎不全に用いられる。副作用としては低カリウム血癥，代謝性アルカロージス，聴力障害，高尿酸血癥などを起すおそれがある。
効能
利尿薬, Na-K-Cl共輸送體阻害薬
商品名
オイテンシン (サノフィ); ラシックス (サノフィ); ラシックス (サノフィ); ラシックス (サノフィ)
説明
Furosemide (Item No. 26298) is an analytical reference standard categorized as a diuretic. Formulations containing diuretics, including furosemide, have been misused in sports for weight reduction and as masking agents in humans and to prevent exercise-induced pulmonary hemorrhage in racehorses. This product is intended for use in analytical forensic applications. This product is also available as a general research tool .
化學(xué)的特性
white to light yellow crystal powde
使用
Furosemide inhibits ion co-transport in the kidney. Furosemide is used as a diuretic.
定義
A benzoic-sulfonamide-furan. It is a diuretic with
fast onset and short duration and anti-hypertensive
agent.
一般的な説明
Odorless white to slightly yellow crystalline powder. A diuretic drug. Almost tasteless.
空気と水の反応
Light sensitive. Air sensitive. Slightly soluble in water.
反応プロフィール
Furosemide may undergo hydrolysis at sufficiently low pH. The pH of aqueous solutions should be maintained in the basic range to prevent hydrolysis. Alcohol has been shown to improve the stability of Furosemide. Incompatible with strong oxidizing agents .
危険性
Poison; moderately toxic; teratogen; questionable carcinogen; mutagen.
火災(zāi)危険
Flash point data for Furosemide are not available; however, Furosemide is probably combustible.
生物活性
Loop diuretic that inhibits the Na + /2Cl - /K + (NKCC) cotransporter. Also acts as a non-competitive antagonist at GABA A receptors with ~ 100-fold greater selectivity for α 6-containing receptors than α 1-containing receptors.
作用機(jī)序
Furosemide is a highly effective and quick-acting diuretic whose action, like all of the
examined loop diuretics, is associated with blocking reabsorption of ions in the ascending
bend of Henle’s loop. It is used for edema syndrome of various origins, edema of the lungs
and brain, chronic renal insufficiency, some forms of hypertonic crises, and poisoning by
barbiturates and other compounds excreted mainly with urine.
臨床応用
Furosemide has a saluretic effect 8- to 10-fold that of the thiazide diuretics; however, it has a shorter duration of action (~6–8 hours). Furosemide causes a marked
excretion of sodium, chloride, potassium, calcium, magnesium, and bicarbonate ions, with as much as 25% of the filtered load of sodium excreted in response to initial
treatment. It is effective for the treatment of edemas connected with cardiac, hepatic, and renal sites. Because it lowers the blood pressure similar to the thiazide
derivatives, one of its uses is in the treatment of hypertension.
副作用
Clinical toxicity of furosemide and other loop diuretics primarily involves abnormalities of fluid and electrolyte balance. As with the thiazide diuretics, hypokalemia is an
important adverse effect that can be prevented or treated with potassium supplements or coadministration of potassium-sparing diuretics. Increased calcium ion excretion
can be a problem for postmenopausal osteopenic women, and furosemide generally should not be used in these individuals. Hyperuricemia, glucose intolerance,
increased serum lipid levels, ototoxicity, and gastrointestinal side effects might be observed as well. Hypersensitivity reactions also are possible with furosemide (a
sulfonamide-based drug), and cross-reactivity with other sulfonamide containing drugs is possible.
安全性プロファイル
Poison by intravenous
route. Moderately toxic by ingestion and
intraperitoneal routes. Human systemic
effects by intravenous route: change in the
sensitivity of the ear to sound, tinnitus,
unspecified effects on the heart, constriction
of the arteries, a decrease in urine volume,
interstitial nephritis, metabolic alkalosis,
pulse rate decrease, fall in blood pressure.
Ingestion can damage the liver.
Experimental teratogenic and reproductive
effects. Questionable carcinogen with
experimental carcinogenic effects. Human
mutation data reported. When heated to
decomposition it emits very toxic fumes of
Cl-, NOx, and SOx.
フロセミド 上流と下流の製品情報(bào)
原材料
準(zhǔn)備製品