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1)  D4G prodrug
D4G前药
1.
Aim To develop a simple and specific high performance liquid chromatographic (HPLC) method, suitable for the pharmacokinetic studies in vivo , to determine the concentrations of 2 amino 6 cyclopropylamino 9 (2,3 dideoxy β D glyceropent 2 enofuranosyl)purine (Cyclo D4G, D4G prodrug) in rat plasma, urine and liver homogenates.
目的 建立高效液相法测定大鼠血浆、尿和肝匀浆中 2′,3′ 二脱氢 2′,3′ 二脱氧核糖 2 氨基 6 环丙胺基嘌呤核苷 (Cyclo D4G ,D4G前药 )的简单而特异、适合于研究其体内药物代谢动力学的方法。
2)  prodrug [英]['prəʊ,drʌg]  [美]['pro,drʌɡ]
前药
1.
Design, Synthesis, and Primary Evaluation on Curcumin Derivative as Prodrugs of Antitumor;
抗肿瘤前药-姜黄素衍生物的设计合成及初步活性测试
2.
Synthesis and Characterization of Scutellarin PEG Prodrugs;
灯盏乙素聚乙二醇前药的合成与表征
3.
Ester prodrug of scutellarin: synthesis,physicochemical property and degradation;
灯盏乙素酯类前药的合成、理化性质及降解研究
3)  Prodrugs
前药
1.
Study on prodrugs of naproxen and their dermal permeability;
萘普生前药及其经皮渗透特征
2.
CONCLUSION:Many natural products may be metabolized in vivo and are called prodrugs.
结论 :许多天然药物以前药形式存在 ,肠道细菌在其代谢中发挥着至关重要的作
4)  prodrug [英]['prəʊ,drʌg]  [美]['pro,drʌɡ]
前体药物
1.
Design,synthesis and antitumor activity of ATRA and butyric acid or valproic acid prodrugs;
全反式维甲酸-正丁酸(丙戊酸)前体药物的设计、合成及抗肿瘤活性研究
2.
Preparation of curcumin prodrugs and their anti-tumor activities in vitro;
姜黄素前体药物的合成及其体外抗肿瘤活性研究
3.
Studies on the Stereoselectivity in Transdermal Permeation and Metabolism of Ketoprofen Prodrugs;
酮洛芬前体药物皮肤渗透代谢的立体选择性研究
5)  prodrug structural modification
前药改造
1.
Aim To search for compounds for the treatment of cardiovascular diseases through prodrug structural modifications of cyclovirobuxine D, a single efficient composition distilled from Box plant in China, which was used to treat angina and myocardial infarction.
目的通过对植物活性单体———环维黄杨星D的前药改造,以寻求疗效更好、治疗安全范围更宽的心血管药物。
6)  premedication
术前药
1.
Objective: To investigate the effectiveness of administration of Penehyclidine Hydrochloride which is selective antagonist on receptor-M as Premedication in abdominal surgery.
方法:选取腹部外科择期手术69例,随机分为3组(每组23例):对照组(Ⅰ组),不应用术前药;阿托品组(Ⅱ组)和长托宁组(Ⅲ组),分别于麻醉诱导前30min肌肉注射阿托品或长托宁0。
补充资料:前药
分子式:
CAS号:

性质:即前体药物。指用化学方法合成原有药物的衍生物,这种衍生物在机体内能转化成原来药物而发挥作用。因此,前体药物又可称为生物可逆性衍生物。前药应具备以下三个条件:(1)根据具有生物活性的药物分子性质,按治疗需要进行化学改造;(2)进入机体后,不论是否需要酶的作用,要保证恢复原来的药物分子;(3)本身不显示生物活性。

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