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: Optimizing the "Drug-Like" Properties of Leads in Drug Discovery; Ronald T. Borchardt,Edward H. Kerns,James L. Steve Book 2006 Springer-Ve

[复制链接]
查看: 46231|回复: 56
发表于 2025-3-21 19:43:27 | 显示全部楼层 |阅读模式
书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery
编辑Ronald T. Borchardt,Edward H. Kerns,James L. Steve
视频video
概述Outlines strategies and methodologies designed to guide pharmaceutical and biotechnology companies through the drug discovery and development process.Emphasis on advancing higher quality drug candidat
丛书名称Biotechnology: Pharmaceutical Aspects
图书封面Titlebook: Optimizing the
描述Drug discovery and development is a very complex, costly, and ti- consuming process. Because of the uncertainties associated with predicting the pharmacological effects and the toxicity characteristics of new chemical entities in man, their clinical development is quite prone to failure. In recent years, phar- ceutical companies have come under increasing pressure to introduce new blockbuster drugs into the marketplace more rapidly. Companies have responded to these pressures by introducing new technologies and new strategies to expedite drug discovery and development. Drug discovery and development have traditionally been divided into three separate processes (i. e. , discovery research, preclinical development, and clinical development) that ideally should be integrated both organizationally and functionally. Instead, separate and distinct discovery research, preclinical development, and clinical development divisions were created within many companies during the 1980s and 1990s, Because of their isolation, scientists in the discovery research divisions often were advancing drug candidates into preclinical development that had marginal drug-like properties. For the purpose of thi
出版日期Book 2006
关键词Borchardt; Discovery; Drug; Leads; Like; Optimizing; Properties; lead
版次1
doihttps://doi.org/10.1007/978-0-387-44961-6
isbn_softcover978-1-4939-5047-8
isbn_ebook978-0-387-44961-6
copyrightSpringer-Verlag New York 2006
The information of publication is updating

书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery影响因子(影响力)




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery影响因子(影响力)学科排名




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery网络公开度




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery网络公开度学科排名




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery被引频次




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery被引频次学科排名




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery年度引用




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery年度引用学科排名




书目名称Optimizing the "Drug-Like" Properties of Leads in Drug Discovery读者反馈




书目名称Optimizing the "Drug-Like" Properties of Leads 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 21:32:50 | 显示全部楼层
Metabolic Activation-Role in Toxicity and Idiosyncratic Reactions,ole of chemically reactive metabolites has been well recognized (.). Type B reactions, also referred to as idiosyncratic or hypersensitivity reactions, have been the subject of extensive reviews in recent years (., .). These are generally believed to be immune mediated, and are not predictable from
发表于 2025-3-22 02:08:49 | 显示全部楼层
,Case History — Use of ADME Studies for Optimization of Drug Candidates, Vd) in the body, and cleared from the body through metabolism and excretion. The area under the drug plasma concentration versus time curve (AUC) provides an indirect assessment of the exposure level and duration of action of the therapeutic agent at the site of action (e.g. synovial fluid, tumor,
发表于 2025-3-22 06:58:38 | 显示全部楼层
Computational Models Supporting Lead Optimization in Drug Discovery,, it can increase metabolic clearance, thus making difficult sustaining the pharmacologically relevant systemic exposure. In contrast, permeability, in many cases, increases with increasing lipophilicity, favoring absorption (.; .). The actual result will be determined by the relative contributions
发表于 2025-3-22 11:21:45 | 显示全部楼层
发表于 2025-3-22 14:33:55 | 显示全部楼层
发表于 2025-3-22 19:24:35 | 显示全部楼层
发表于 2025-3-22 21:13:29 | 显示全部楼层
发表于 2025-3-23 02:02:19 | 显示全部楼层
发表于 2025-3-23 06:06:22 | 显示全部楼层
Book 2006nd clinical development divisions were created within many companies during the 1980s and 1990s, Because of their isolation, scientists in the discovery research divisions often were advancing drug candidates into preclinical development that had marginal drug-like properties. For the purpose of thi
 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 04:54
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