用户名  找回密码
 To register

QQ登录

只需一步,快速开始

扫一扫,访问微社区

Titlebook: Optimization in Drug Discovery; Zhengyin Yan,Gary W. Caldwell Book 2004 Humana Press 2004

[复制链接]
查看: 7035|回复: 62
发表于 2025-3-21 17:58:08 | 显示全部楼层 |阅读模式
书目名称Optimization in Drug Discovery
编辑Zhengyin Yan,Gary W. Caldwell
视频video
概述Includes supplementary material:
丛书名称Methods in Pharmacology and Toxicology
图书封面Titlebook: Optimization in Drug Discovery;  Zhengyin Yan,Gary W. Caldwell Book 2004 Humana Press 2004
描述Recent analyses of drug attrition rates reveal that a significant number of drug candidates fail in the later stage of clinical development owing to absorption, distribution, metabolism, elimination (ADME), and toxicity issues. Lead optimization in drug discovery, a process attempting to uncover and correct these defects of drug candidates, is highly beneficial in lowering the cost and time to develop therapeutic drugs by reducing drug candidate failures in development. At present, parallel synthesis combining with high-throughput screening has made it easier to generate highly potent compounds (i. e. , hits). However, to be a potential drug, a hit must have drug-like characteristics in addition to potency, which include optimal physicochemical properties, reasonable ph- macokinetic parameters, and good safety profiles. Therefore, research tools must be available in drug discovery to rapidly screen for compounds with favorable drug-like properties, and thus adequate resources can be directed to projects with high potential. Optimization in Drug Discovery: In Vitro Methods is a compilation of detailed experimental protocols necessary for setting up a variety of assays important in c
出版日期Book 2004
版次1
doihttps://doi.org/10.1385/1592598005
isbn_softcover978-1-61737-499-9
isbn_ebook978-1-59259-800-7Series ISSN 1557-2153 Series E-ISSN 1940-6053
issn_series 1557-2153
copyrightHumana Press 2004
The information of publication is updating

书目名称Optimization in Drug Discovery影响因子(影响力)




书目名称Optimization in Drug Discovery影响因子(影响力)学科排名




书目名称Optimization in Drug Discovery网络公开度




书目名称Optimization in Drug Discovery网络公开度学科排名




书目名称Optimization in Drug Discovery被引频次




书目名称Optimization in Drug Discovery被引频次学科排名




书目名称Optimization in Drug Discovery年度引用




书目名称Optimization in Drug Discovery年度引用学科排名




书目名称Optimization in Drug Discovery读者反馈




书目名称Optimization in Drug Discovery读者反馈学科排名




单选投票, 共有 1 人参与投票
 

1票 100.00%

Perfect with Aesthetics

 

0票 0.00%

Better Implies Difficulty

 

0票 0.00%

Good and Satisfactory

 

0票 0.00%

Adverse Performance

 

0票 0.00%

Disdainful Garbage

您所在的用户组没有投票权限
发表于 2025-3-21 23:18:28 | 显示全部楼层
Use of Caco-2 Cell Monolayers to Study Drug Absorption and Metabolism,nd dietary chemicals. The Food and Drug Administration (FDA) recognized the model system as useful in classifying a compound’s absorption characteristics in the Biopharmaceutics Classification System. In addition to its usefulness as an absorption model, the Caco-2 cells are useful for studying the
发表于 2025-3-22 02:24:50 | 显示全部楼层
Absorption Screening Using the PAMPA Approach,earliest absorption, distribution, metabolism, and excretion (ADME) primary screening of research compounds. PAMPA’s popularity in the industry has risen rapidly. This chapter focuses on state-of-the-art PAMPA methods. Evidence will be cited demonstrating that as far as predicting passive permeabili
发表于 2025-3-22 07:44:09 | 显示全部楼层
发表于 2025-3-22 09:36:42 | 显示全部楼层
In Vitro Permeation Study With Bovine Brain Microvessel Endothelial Cells, lines such as Caco-2, MDCK, MDCKII, and LLC-PK have been used to predict in vivo intestinal absorption of drugs. However, there are no well-characterized cell lines available representing the blood-brain barrier. In this chapter, the authors describe the primary culture of bovine brain microvessel
发表于 2025-3-22 13:40:12 | 显示全部楼层
发表于 2025-3-22 20:08:49 | 显示全部楼层
发表于 2025-3-22 22:09:10 | 显示全部楼层
发表于 2025-3-23 01:45:40 | 显示全部楼层
Isothermal Titration Calorimetry Characterization of Drug-Binding Energetics to Blood Proteins,les. In this chapter, the authors describe the use of isothermal titration calorimetry (ITC) to measure the binding energetics of drugs bound to blood proteins (i.e., human serum albumin [HSA] and α-acid glycoprotein [AGP]). The stoichiometry (.), the association-binding constant (..), and the entha
发表于 2025-3-23 06:50:22 | 显示全部楼层
Metabolic Stability Assessed by Liver Microsomes and Hepatocytes,c stability assays, the typical test systems are liver microsomes, liver S9, or hepatocytes (plated or suspended), depending on the goal of the assay. To determine the metabolic stability of a new chemical entity, quantification of the drug candidate from incubate supernatants is required and usuall
 关于派博传思  派博传思旗下网站  友情链接
派博传思介绍 公司地理位置 论文服务流程 影响因子官网 SITEMAP 大讲堂 北京大学 Oxford Uni. Harvard Uni.
发展历史沿革 期刊点评 投稿经验总结 SCIENCEGARD IMPACTFACTOR 派博系数 清华大学 Yale Uni. Stanford Uni.
|Archiver|手机版|小黑屋| 派博传思国际 ( 京公网安备110108008328) GMT+8, 2025-6-8 12:51
Copyright © 2001-2015 派博传思   京公网安备110108008328 版权所有 All rights reserved
快速回复 返回顶部 返回列表