- 英
- reversible inhibitor
- 関
- 可逆的阻害薬
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- 1. 慢性非癌性疼痛治療の概要overview of the treatment of chronic non cancer pain [show details]
… against gastroduodenal toxicity can be achieved with a proton pump inhibitor. Nephrotoxicity associated with NSAID includes reversible renal insufficiency due to renal vasoconstriction, acute interstitial …
- 2. 哺乳類ラパマイシン標的タンパク質(mTOR)阻害薬の薬理学pharmacology of mammalian mechanistic target of rapamycin mtor inhibitors [show details]
… hematological effects have been reported with everolimus . Anemia associated with mTOR inhibitors is generally mild and reversible. If a patient has anemia posttransplant, bleeding, iron deficiency, and malignancy …
- 3. シクロスポリンおよびタクロリムスの腎毒性cyclosporine and tacrolimus nephrotoxicity [show details]
…calcineurin inhibitors (CNIs) cyclosporine and tacrolimus are at high risk of developing kidney injury . CNI nephrotoxicity is manifested either as acute kidney injury (AKI), which is largely reversible after …
- 4. 成人におけるうつ病治療としてのモノアミン酸化酵素阻害剤(MAOI)monoamine oxidase inhibitors maois for treating depressed adults [show details]
… called into question. Several compounds with selective MAOa and MAOb inhibiting properties have been developed, as well as reversible MAOIs. Properties of the MAOIs most commonly prescribed in the United …
- 5. 急性リン酸腎症acute phosphate nephropathy [show details]
…angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) appear to be at increased risk for acute phosphate nephropathy . ACE inhibitors and ARBs worsen the… oral sodium phosphate (OSP): an acute form that is reversible and may not represent acute phosphate nephropathy,…
Japanese Journal
- メタロ-β-ラクタマーゼ(IMP-1)の非可逆的阻害剤の開発
- 山口 佳宏,黒崎 博雅
- 日本結晶学会誌 48(4), 259-264, 2006-08-30
- Pathogenic bacteria that produce metallo-β-lactamases (MBLs) are emerging as a new threat to the medical community. These enzymes catalyze the hydrolysis of almost β-lactam antibiotics. Moreover, seri …
- NAID 10019293571
- β-ラクタム剤耐性菌が産生するメタロ-β-ラクタマーゼの三次元構造に立脚した非可逆的阻害剤の開発
- 山口 佳宏
- The Japanese journal of antibiotics 59(1), 51-56, 2006-02-25
- NAID 10017296202
- Metabolism-dependent inhibition of CYP3A4 and CYP2D6 by extracts from 26 herbal medicines
- Iwata Hiroshi,手塚 康弘,KADOTA Shigetoshi,HIRATSUKA Akira,Watabe Tadashi
- 和漢医薬学雑誌 21(6), 281-286, 2004-12-20
- … これら7種生薬によるCYP3A4活性低下作用は, CYP3A4に対する不可逆的阻害剤であるtroleandomycinによる残存率(49.4%)に匹敵した。 …
- NAID 110001867610
Related Links
- 酵素阻害剤の作用には、酵素の基質が活性中心に入って反応が始まるのを阻止する もの、あるいは酵素による反応の触媒作用を阻害するものがある。また酵素に可逆的に 結合するもの(濃度が下がれは解離する)と、酵素分子の特定部分と共有結合を形成し て ...
Related Pictures
★リンクテーブル★
[★]
- 英
- reversible inhibitor
- 関
- 可逆的阻害剤
[★]
[★]
- 英
- drug、agent
- 関
- 薬、作用薬、ドラッグ、媒介物、病原体、麻薬、薬剤、薬物、代理人、薬品
[★]
- 英
- blocking(精神医学), inhibition(生化学)
- 同
- 遮断 blockade、途絶
[★]
- 英
- reversible、reversibly
- 関
- 可逆、可逆性
[★]
- 英
- inhibitor
- 同
- 阻害薬?
- 関
- 酵素阻害物質
[★]
- 英
- reversible
- 関
- 可逆性、可逆的