Prodrugs—from Serendipity to Rational Design-Reference-Cited by-同舟云学术

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Prodrugs—from Serendipity to Rational Design

Published:2011-07-07 Issue:3 Volume:63 Page:750-771
ISSN:0031-6997
Container-title:Pharmacological Reviews
language:en
Short-container-title:Pharmacol Rev

Author:

Huttunen Kristiina M.,Raunio Hannu,Rautio Jarkko

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference134 articles.

1. Chemical Aspects of Selective Toxicity

2. Activation of 3-Amino-1,2,4-benzotriazine 1,4-Dioxide Antitumor Agents to Oxidizing Species Following Their One-Electron Reduction

3. Bai JPF Pacanowski M Rahman A Lesko LL (2010) The impact of pharmacogenetics on the clinical outcomes of prodrugs, in Prodrugs and Targeted Delivery: Towards Better ADME Properties ( Rautio J ed) pp 453–481, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

4. Direct Evidence for Peptide Transporter (PepT1)-Mediated Uptake of a Nonpeptide Prodrug, Valacyclovir

5. Design of Ester Prodrugs to Enhance Oral Absorption of Poorly Permeable Compounds: Challenges to the Discovery Scientist

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