The expanding role of prodrugs in contemporary drug design and development
J Rautio, NA Meanwell, L Di… - Nature reviews drug …, 2018 - nature.com
Prodrugs are molecules with little or no pharmacological activity that are converted to the
active parent drug in vivo by enzymatic or chemical reactions or by a combination of the two …
active parent drug in vivo by enzymatic or chemical reactions or by a combination of the two …
The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold
KL Seley-Radtke, MK Yates - Antiviral research, 2018 - Elsevier
This is the first of two invited articles reviewing the development of nucleoside-analogue
antiviral drugs, written for a target audience of virologists and other non-chemists, as well as …
antiviral drugs, written for a target audience of virologists and other non-chemists, as well as …
Approved antiviral drugs over the past 50 years
E De Clercq, G Li - Clinical microbiology reviews, 2016 - Am Soc Microbiol
Since the first antiviral drug, idoxuridine, was approved in 1963, 90 antiviral drugs
categorized into 13 functional groups have been formally approved for the treatment of the …
categorized into 13 functional groups have been formally approved for the treatment of the …
The ProTide Prodrug Technology: From the Concept to the Clinic: Miniperspective
Y Mehellou, HS Rattan, J Balzarini - Journal of medicinal …, 2017 - ACS Publications
The ProTide technology is a prodrug approach developed for the efficient intracellular
delivery of nucleoside analogue monophosphates and monophosphonates. In this …
delivery of nucleoside analogue monophosphates and monophosphonates. In this …
[HTML][HTML] Drug-induced nephrotoxicity
GTM Sales, RD Foresto - Revista da Associação Médica Brasileira, 2020 - SciELO Brasil
Acute kidney injury is a very common diagnosis, present in up to 60% of critical patients, and
its third main cause is drug toxicity. Nephrotoxicity can be defined as any renal injury caused …
its third main cause is drug toxicity. Nephrotoxicity can be defined as any renal injury caused …
Current trends and limitations in dengue antiviral research
JO Obi, H Gutiérrez-Barbosa, JV Chua… - Tropical Medicine and …, 2021 - mdpi.com
Dengue is the most prevalent arthropod-borne viral disease worldwide and affects
approximately 2.5 billion people living in over 100 countries. Increasing geographic …
approximately 2.5 billion people living in over 100 countries. Increasing geographic …
A review and clinical understanding of tenofovir: tenofovir disoproxil fumarate versus tenofovir alafenamide
C Wassner, N Bradley, Y Lee - Journal of the International …, 2020 - journals.sagepub.com
HIV is a serious chronic medical condition. Significant improvements in antiretroviral therapy
have led to a transformation in its management. No curative treatment is available for HIV …
have led to a transformation in its management. No curative treatment is available for HIV …
Phosphine Oxides from a Medicinal Chemist's Perspective: Physicochemical and in Vitro Parameters Relevant for Drug Discovery
P Finkbeiner, JP Hehn, C Gnamm - Journal of Medicinal …, 2020 - ACS Publications
Phosphine oxides and related phosphorus-containing functional groups such as
phosphonates and phosphinates are established structural motifs that are still …
phosphonates and phosphinates are established structural motifs that are still …
Nucleoside analogs as a rich source of antiviral agents active against arthropod-borne flaviviruses
L Eyer, R Nencka, E de Clercq… - Antiviral Chemistry …, 2018 - journals.sagepub.com
Nucleoside analogs represent the largest class of small molecule-based antivirals, which
currently form the backbone of chemotherapy of chronic infections caused by HIV, hepatitis …
currently form the backbone of chemotherapy of chronic infections caused by HIV, hepatitis …