Structure–activity relationships for dipeptide prodrugs of acyclovir: Implications for prodrug design

Cledir Santos; Rita Capela; Cláudia S. G. P. Pereira; Emília Valente; Luís F. Gouveia; Christophe Pannecouque; De Clercq Erik; Rui Moreira; Paula Gomes

doi:10.1016/j.ejmech.2008.08.009

Back

Discussion(0)

No comments yet. Be the first to comment.

Related publications

Article2001

Antiviral Activity of Cyclosaligenyl Prodrugs of Acyclovir, Carbovir and Abacavir

Jan Balzarini, Friederike Haller-Meier, De Clercq Erik, Chris Meier

Article2005

Synthesis and antimicrobial activity of dipeptide esters of the anti-rectroviral drug acyclovir

Cláudia S. G. P. Pereira, Cledir Santos, João C.M. Barreira, Rui Moreira, Isabel Cristina Fernandes Rodrigues Ferreira, Letı́cia M. Estevinho, Paula Gomes

Article2005

Antiviral prodrugs – the development of successful prodrug strategies for antiviral chemotherapy

De Clercq Erik, Hugh J. Field

Article2025

Design, synthesis and structure-activity relationships of novel HIV capsid inhibitors with potent antiviral activities

Dazhou Shi, Shujing Xu, Lin Sun, Prem P. Sharma, Brijesh Rathi, Mei Wang, Linan Wu, Xiangyi Jiang, De Clercq Erik, Christophe Pannecouque, Xinyong Liu, Alexej Dick, Shujing Xu

Preprint2025

Design, Synthesis and Structure-Activity Relationships of Novel HIV Capsid Inhibitors with Potent Antiviral Activities

Dazhou Shi, Shujing Xu, Lin Sun, Prem P. Sharma, Brijesh Rathi, Mei Wang, Linan Wu, Xiangyi Jiang, De Clercq Erik, Christophe Pannecouque, Xinyong Liu, Alexej Dick, Peng Zhan