2006
DOI: 10.1002/0471141755.ph0909s35
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Overview of Drug Discovery and Development

Abstract: This overview unit describes the core activities involved in the drug discovery and development process, from target identification - including preclinical biology, medicinal and process chemistry - to pharmacokinetics and metabolism (ADME), and also activities related to the to the drug approval process. The latter include the activities related to the filing of an IND (Investigational New Drug) application and also Phases I - III of clinical trials that form the basis of an NDA (New Drug Application) submiss… Show more

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Cited by 11 publications
(7 citation statements)
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“…However, it should be noted that in the ex vivo experiment, chrysin was added to the medium in which lenses were incubated, thus the lenses were exposed directly to this flavonoid action. In the in vivo experiments, when substances are given orally or by intragastric tube, they may be metabolized or bound to plasma proteins and, in consequence, they do not interact directly with the organ [81,82]. Therefore, the discrepancies between our investigation and the ex vivo study are a result of experimental design and the complexity of the living organism.…”
Section: Discussionmentioning
confidence: 93%
“…However, it should be noted that in the ex vivo experiment, chrysin was added to the medium in which lenses were incubated, thus the lenses were exposed directly to this flavonoid action. In the in vivo experiments, when substances are given orally or by intragastric tube, they may be metabolized or bound to plasma proteins and, in consequence, they do not interact directly with the organ [81,82]. Therefore, the discrepancies between our investigation and the ex vivo study are a result of experimental design and the complexity of the living organism.…”
Section: Discussionmentioning
confidence: 93%
“…This final output from a laboratory notebook can then be included in a patent application or scientific manuscript. In industry, (e.g., pharmaceutical companies), interim internal reports also exist to support federal regulatory requirements for IND (Investigational New Drug; see Current Protocols article Ator, Mallamo, & Williams, 2006) filing. In performing quality control on such data or researching them for a patent application, it is unfortunately not always obvious from where cited IC 50 values are derived.…”
Section: Hard Copy Paper Notebooksmentioning
confidence: 99%
“…This final output from a laboratory notebook can then be included in a patent application or scientific manuscript. In industry, (e.g., pharmaceutical companies) interim internal reports also exist to support federal regulatory requirements for IND (Investigational New Drug; Ator, 2006) filing. In performing quality control on such data or researching them for a patent application, it is unfortunately not always obvious from where cited IC 50 values are derived.…”
Section: Data Replicationmentioning
confidence: 99%
“…Interest in ELNs has increased significantly in the past few years, with many commercial products being available from scientific software, instrumentation, and database-management companies. Major vendors include Waters, CambridgeSoft, Elsevier MDL, and Symyx Technologies (see Ator et al, 2006). Each company approached the ELN from a unique perspective, in the case of Waters, interfacing with their HPLC and Laboratory Informatics Systems; and CambridgeSoft, their ChemDraw software platform.…”
Section: A2mentioning
confidence: 99%