1) PK-PD model
药动-药效同步模型
2) pharmacokinetics
药动学
1.
In Vivo Tissues Distribution and Pharmacokinetics:Survey of2Kinds of Monostearin Solid Lipid Nanoparticle Preparations;
2种单硬脂酸甘油酯固体脂质纳米粒制剂的体内组织分布及药动学研究
2.
Study on the preparation of sustained-release suppository of progesterone and its pharmacokinetics in rabbits;
黄体酮缓释栓的制备及药动学
3.
Preparation of melatonin controlled-release bilayer tablets and its pharmacokinetics in Beagle dogs;
褪黑素双层控释片制备及其在Beagle犬体内的药动学
3) pharmacokinetic
药动学
1.
Comparison of Pharmacokinetics of Clidamycin Between Clindamycin Phosphate Vaginal Gel and Clidamycin Hydrochloride Tablets;
克林霉素局部给药与口服给药药动学比较研究
2.
Advances in studies on pharmacokinetics of aristolochic acid I;
马兜铃酸I药动学研究进展
3.
Pharmacokinetic comparison of levofloxacin aspartate and other levofloxacin salts;
门冬氨酸左氧氟沙星与其他左氧氟沙星盐的药动学比较
4) Pharmacodynamics
药动学
1.
Pharmacokinetics and pharmacodynamics of famotidine in children with upper gastrointesinal bleeding;
上消化道出血儿童法莫替丁的药动学和药效学考察
2.
Study on Pharmacokinetics and Pharmacodynamics of Total Alcaloids Extracted from Sophora Flavescens;
苦参总碱贴片的药动学与药效学研究
3.
The pharmacology,pharmacodynamics,clinical efficacy,safety and tolerability of the zolmitriptan formulations(common tablets,orally disintegrating tablets,nasal spray) were reviewed.
现就佐米曲普坦普通片剂、口腔崩解片和鼻喷剂的药动学、临床疗效及安全性和耐受性等进行综述。
5) bioavailability
药动学
1.
Relative bioavailability and phamacokinetics of tamsulosin hydrochloride controlled-release capsules in human volunteers;
盐酸坦洛新缓释胶囊在人体内的药动学和生物等效性
2.
Objective: To study the pharmacokinetics and bioavailability of danshensu in rat.
目的:研究丹参素在大鼠体内药动学和口服生物利用度。
3.
Objective: To study the relative bioavailability of paracetamol and amantadine hydro-chloride compound (PAHC) capsules.
血药浓度-时间数据经DAS软件处理后得药动学数据,并进行等效性检验。
6) Phamacokinetics
药动学
参考词条
补充资料：同步变构模型
分子式：
CAS号：
性质：多数受体是亚基的多聚结构，同步变构模型认为当药物与受体相互作用时，其中的亚基是同步变构。同步变构适用于同种亚基或等效亚基，主要是正合作效应。
CAS号：
性质：多数受体是亚基的多聚结构，同步变构模型认为当药物与受体相互作用时，其中的亚基是同步变构。同步变构适用于同种亚基或等效亚基，主要是正合作效应。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。