68-94-0O=c1nc[nH]c2nc[nH]c12FDGQSTZJBFJUBT-UHFFFAOYSA-NHypoxanthine is a purine and a reaction intermediate in the metabolism of adenosine and in the formation of nucleic acids by the salvage pathway.
68-94-0DTXSID8045983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。
Chronic Exposure: Kidney dialysis is usually needed to relieve the symptoms of xanthine toxicity until normal kidney function can be restored. Acute Exposure: EYES: irrigate opened eyes for several minutes under running water. INGESTION: do not induce vomiting. Rinse mouth with water (never give anything by mouth to an unconscious person). Seek immediate medical advice.
As a uremic toxin, this compound can cause uremic syndrome. Uremic syndrome may affect any part of the body and can cause nausea, vomiting, loss of appetite, and weight loss. It can also cause changes in mental status, such as confusion, reduced awareness, agitation, psychosis, seizures, and coma. Abnormal bleeding, such as bleeding spontaneously or profusely from a very minor injury can also occur. Heart problems, such as an irregular heartbeat, inflammation in the sac that surrounds the heart (pericarditis), and increased pressure on the heart can be seen in patients with uremic syndrome. Shortness of breath from fluid buildup in the space between the lungs and the chest wall (pleural effusion) can also be present. Chronically high concentrations of hpyoxanthine can lead to health problems such as renal failure and xanthine kidney stones, one of the rarest types of kidney stones. Chronically high levels of hypoxanthine are associated with at least 4 inborn errors of metabolism including: Xanthinuria type I, Xanthuria type II, Molybdenium Cofactor Deficiency, and Xanthinuria.
Under normal circumstances hypoxanthine is readily converted to uric acid. The enzyme xanthine oxidase makes uric acid from xanthine and hypoxanthine, which in turn are produced from other purines. In humans and higher primates, uric acid is the final oxidation (breakdown) product of purine metabolism and is excreted in urine.
解説ヒポキサンチン,遊離の形で動物,植物界に広く存在する.ヌクレオシド(イノシン)として筋肉や多くのtRNA中にも存在する.針状晶.分解点150 ℃.pKb 8.7.λmax 249.5(ε 10.7×103,pH 6).両性物質で温水に微溶,酸やアルカリの水溶液に可溶.化学的には,シアノ酢酸エチルとチオ尿素から出発し,6-アミノ-4-ヒドロキシ-2-メルカプトピリミジンを経て合成され,種々のプリン誘導体やそれらのヌクレオシド類の合成に用いられる.生体内ではアデニンの脱アミノやイノシンの加リン酸分解によって生成され,キサンチンオキシダーゼの作用を受け,キサンチンを経て尿酸にまで酸化される.
用途同調培養用試薬。
説明Hypoxanthine is a naturally occurring purine derivative and intermediate in the synthesis of uric acid. It is elevated in the spinal fluid of patients with Lesch-Nyhan syndrome, a metabolic disorder whose symptoms include cerebral palsy, cognitive deficits, motor dysfunction, self-mutilation, and hyperuricemia. Injection of hypoxanthine (10 μM) increases succinate dehydrogenase and complex II activities and decreases cytochrome c oxidase activity, resulting in neuroenergetic impairment, ATP depletion, and cellular apoptosis in rat striatum. It is also used to induce hyperuricemia in mice for use in the development of hypouricemic agents.
使用A naturally occurring purine derivative. Pharmaceuticals, Intermediates & Fine Chemicals
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読み込み中…
化学的特性White to off-white powder
一般的な説明Hypoxanthine (6-hydroxypurine), a purine derivative is a naturally occurring compound. It is the deaminated form of adenine and a breakdown product of adenosine monophosphate (AMP).
使用用途ヒポキサンチンは、主に研究用途に用いられます。また、DNAやRNAの構造や機能の研究、細胞・組織培養にも有用です。 特定の細胞株の成長を促進するために、培地にヒポキサンチンを添加することがあります。例として、マラリア原虫の培養が挙げられ、核酸合成とエネルギー代謝のためにヒポキサンチンのを添加します。 そのほか、医薬品の研究や開発において、標的となる酵素や受容体との相互作用の研究に使用されることがあります。 抗ガン剤の研究にも用いられており、細胞の増殖を阻害する薬物の開発に役立ちます。
純化方法Crystallise it from hot water and dry it at 105o. [Beilstein 26 II 252, 26 III/IV 2081.]
定義ChEBI: A purine nucleobase that consists of purine bearing an oxo substituent at position 6.