Results 11 to 20 of about 33,100 (295)

Dendrimer Prodrugs [PDF]

open access: yesMolecules, 2016
The main objective of this review is to describe the importance of dendrimer prodrugs in the design of new drugs, presenting numerous applications of these nanocomposites in the pharmaceutical field.
Soraya da Silva Santos   +2 more
doaj   +4 more sources

Flurbiprofen–antioxidant mutual prodrugs as safer nonsteroidal anti-inflammatory drugs: synthesis, pharmacological investigation, and computational molecular modeling

open access: yesDrug Design, Development and Therapy, 2016
Zaman Ashraf,1,2 Alamgeer,3 Munazza Kanwal,1 Mubashir Hassan,2 Sahar Abdullah,3 Mamuna Waheed,3 Haseeb Ahsan,3 Song Ja Kim2 1Department of Chemistry, Allama Iqbal Open University, Islamabad, Pakistan; 2Department of Biological Sciences, College of ...
Ashraf Z   +7 more
doaj   +1 more source

Aryloxy Pivaloyloxymethyl Prodrugs as Nucleoside Monophosphate Prodrugs [PDF]

open access: yesJournal of Medicinal Chemistry, 2021
Intracellular phosphorylation of therapeutic nucleoside analogues into their active triphosphate metabolites is a prerequisite for their pharmacological activity. However, the initial phosphorylation of these unnatural nucleosides into their monophosphate derivatives can be a rate-limiting step in their activation. To address this, we herein report the
Ashwag S. Alanazi   +2 more
openaire   +2 more sources

smProdrugs: A repository of small molecule prodrugs [PDF]

open access: yes, 2022
In modern drug discovery and development, the prodrug approach has become a crucial strategy for enhancing the pharmacokinetic profiles of drugs. A prodrug is a chemical compound, which gets metabolized into a pharmacologically active form (drug) inside ...
Vivek, Kumar   +3 more
core   +2 more sources

Morphine is not a prodrug [PDF]

open access: yesBritish Journal of Anaesthesia, 2015
Editor–A prodrug is defined as a medication that is administered in an inactive or less than fully active form and is then converted to its active form through a normal metabolic process (http://en. wikipedia.org/wiki/Prodrug). The title of a recent publication in the British Journal of Analgesia, ‘Morphine-6-glucuronide is responsible for the ...
A, Dahan, J, Lötsch
openaire   +2 more sources

Aryl phosphoramidates of 5-phospho erythronohydroxamic acid, a new class of potent Trypanocidal compounds [PDF]

open access: yes, 2010
RNAi and enzymatic studies have shown the importance of 6-phosphogluconate dehydrogenase (6-PGDH) in Trypanosoma brucei for the parasite survival and make it an attractive drug target for the development of new treatments against human African ...
Ruda, Gian Filippo   +20 more
core   +1 more source

Investigating the crucial roles of aliphatic tails in disulfide bond-linked docetaxel prodrug nanoassemblies

open access: yesAsian Journal of Pharmaceutical Sciences, 2021
Disulfide bond-bridging strategy has been extensively utilized to construct tumor specificity-responsive aliphatic prodrug nanoparticles (PNPs) for precise cancer therapy.
Yuequan Wang   +10 more
doaj   +1 more source

Increased/Targeted Brain (Pro)Drug Delivery via Utilization of Solute Carriers (SLCs)

open access: yesPharmaceutics, 2022
Membrane transporters have a crucial role in compounds’ brain drug delivery. They allow not only the penetration of a wide variety of different compounds to cross the endothelial cells of the blood–brain barrier (BBB), but also the accumulation of them ...
Johanna Huttunen   +3 more
doaj   +1 more source

Dopamine and Levodopa Prodrugs for the Treatment of Parkinson’s Disease

open access: yesMolecules, 2017
Background: Parkinson’s disease is an aggressive and progressive neurodegenerative disorder that depletes dopamine (DA) in the central nervous system.
Fatma Haddad   +4 more
doaj   +1 more source

Anticancer Drugs: Recent Strategies to Improve Stability Profile, Pharmacokinetic and Pharmacodynamic Properties

open access: yesMolecules, 2022
In past decades, anticancer research has led to remarkable results despite many of the approved drugs still being characterized by high systemic toxicity mainly due to the lack of tumor selectivity and present pharmacokinetic drawbacks, including low ...
Giuseppina Ioele   +6 more
doaj   +1 more source

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