Phosphate ester prodrug

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August undefined, 2024

Webtriphenylethylene phosphate prodrug, TAT-59, were also conducted in the rat intestinal perfusion model. Finally, the utility of a phosphate ester prodrug strategy for entacapone to increase that drugs systemic levels was evaluated in rats. MATERIALS AND METHODS Materials TAT-59 and its parent drug, DP-TAT-59, were gifts of WebJun 28, 2008 · A series of amino acid monoester prodrugs of floxuridine was synthesized and evaluated for the improvement of oral bioavailability and the feasibility of target drug delivery via oligopeptide transporters. All floxuridine 5′-amino acid monoester prodrugs exhibited PEPT1 affinity, with inhibition coefficients of Gly-Sar uptake (IC50) ranging from …

Phosphonate prodrugs: an overview and recent advances

Web3. Phosphate Esters as Prodrugs of Hydroxyl or Amine Functionalities Phosphate ester prodrugs are typically designed for hydroxyl and amine functionalities of poorly water-soluble drugs with an aim to enhance their aqueous solubility to allow a more favorable oral or parenteral administration (see examples in Table 2). WebMar 1, 2003 · This approach is particularly valuable in the case of biologically active phosphates because of the high intrinsic hydrophilicity and the multitude of biological … cycloplegics and mydriatics

Prodrug Metabolites: Implications for Therapeutic Drug …

WebMar 3, 2024 · Cycloalkyl esters of 3',5'-cyclic phosphate nucleotide prodrugs demonstrated the ability to produce high levels of active triphosphate in clone-A cells and primary human hepatocytes. WebFosphenytoin is a phosphate ester prodrug developed as an alternative to intravenous phenytoin for acute treatment of seizures. Advantages include more convenient and rapid intravenous administration, availability for intramuscular injection, and low potential for adverse local reactions at injectio … WebBy the design of phosphate ester prodrugs, the poor aqueous solubility of various drugs such as estramustine and prednisolone could be addressed. When given orally these prodrugs rapidly dissolve in gastrointestinal (GI) fluids, yet being efficiently absorbed from the intestinal mucosa. Their high membrane permeability is ascribed to the ... cyclopithecus

Phosphate ester definition of Phosphate ester by Medical …

Alkaline Phosphatase: A Reliable Endogenous ... - Wiley Online …

WebPhosphate prodrugs of amines are made to increase solubility, owing to the presence of the highly ionized species in the GI tract. ... Prodrugs are ester derivatives synthesized using the alcoholic functional group at the C-2 or the C-7 position of paclitaxel [70,71]. Such prodrugs have produced cytotoxic activity comparable to paclitaxel ... WebApr 12, 2024 · Organophosphorus compounds have found widespread applications in pharmaceuticals, agrochemicals, and materials science. Phosphonates, in particular, can be regarded as isosteres of the corresponding phosphate esters and serve as phosphate mimics in biochemical investigations. 1 The introduction of a phosphonic acid of suitable … cyclopinclopanWebThe usual strategy for phosphate prodrugs is to modify the acidic oxygen atoms with metabolically labile protecting groups to produce a charge … cycloplegic eye refraction

"WebMay 20, 2024 · To overcome this problem, various prodrug strategies have been used to mask the carboxylates and/or phosphonate functionalities of 2-PMPA with POM, POC, … " - Phosphate ester prodrug

Phosphate ester prodrug

Webprodrug activation processes. Ester prodrugs to enhance oral absorption Oral absorption is a key component of oral bioavailability. Kevin Beaumont (Pfizer Ltd, UK) discussed issues … Weborganophosphate. [ or″gah-no-fos´fāt] an organic ester of a phosphate such as phosphoric acid with an organic compound such as glucose or sorbitol; see also organophosphorus. …

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WebPhosphate ester prodrugs substantially enhance the aqueous solubility of some poorly soluble parent drugs due to ionization of the phosphate group at physiological pH. While phosphate prodrugs have proven successful in parenteral formulations, few oral phosphate prodrugs have been marketed to date as they have generally failed to improve parent ... WebProdrugs of phosphonates and phosphates: crossing the membrane barrier A substantial portion of metabolism involves transformation of phosphate esters, including pathways …

WebMar 20, 2003 · This approach is particularly valuable in the case of biologically active phosphates because of the high intrinsic hydrophilicity and the multitude of biological … WebJul 31, 2007 · An increasing number of phosphate esters of pharmaceutical interest (mainly antiviral agents and signaling regulators) has encouraged the advancement of the …

WebPhosphate ester prodrugs of propofol (fospropofol, HX0969W) were designed to avoid the unsatisfactory water solubility of the parent drug. However, in previous clinical trials, there … WebMar 1, 2003 · Phosphate esters play a dominant role in the physiology of cells and hence are essential to any organism. Most prominent is the participation of phosphate esters as …

WebJul 23, 2024 · The ester family of prodrugs is comprised of molecules where the prodrug has phosphor (mono)ester or phosphodiester bonds connecting the pro-moiety to the rest of the molecule (Fig. 1 ). In this section, we chose to examine PK data for Adefovir, Tenofovir, and Cidofovir (CDV) (Table 1 ).

WebOnce the prodrug gets into the systemic circulation or target tissues, the ester prodrug moiety may be cleaved through an enzymatic and/or chemical process to release the corresponding free acid of phosphinate, phosphonate, or phosphate to achieve the desirable biological effect. cycloplegic mechanism of actionWebThe result indicated that 1,3‐cyclic propanyl phosphate esters of 18 β‐glycyrrhetic acid have sustained‐release properties to avoid the quick metabolism of 18β‐ glycyRRhetic acid. A new class of potential prodrugs, 1,3‐cyclic propanyl phosphate esters of 18β‐glycyrrhetic acid, was designed and synthesized through the key reaction of 18β‐glycyrrhetic acid with … cyclophyllidean tapewormsWebAug 28, 2008 · Preformulation studies were performed on a hemiglutarate ester prodrug of Δ 9-tetrahydrocannabinol (THC-HG), to facilitate the development of stable formulations by hot-melt methods.The various studies performed included solid-state thermal characterization, pKa, logP, aqueous and pH dependent solubility, pH stability and effect … cycloplegic refraction slideshareWebNov 13, 2014 · An early focus was pivaloyloxymethyl (POM) modified phosphonates, a prodrug format which was first advanced for use with phosphate monoesters [ 50, 51 ]. However, this approach was readily adapted to phosphonates such as foscarnet esters ( 20) [ 52] and a phosphonate inhibitor of insulin receptor tyrosine kinase [ 53 ]. cyclophyllum coprosmoidesWebAug 30, 2024 · Phosphonates, often used as isosteric replacements for phosphates, can provide important interactions with an enzyme. Due to their high charge at physiological … cyclopiteWebApr 27, 2024 · Fospropofol (Lusedra) is a phosphonooxymethyl prodrug of the sedative or hypnotic drug propofol in which the phosphate promoiety is linked to the sterically … cyclop junctionsWebFeb 8, 2024 · The presence of phosphate mono ester breaking alkaline phosphatase (ALP) enzyme throughout the whole human body, is the main consideration behind the development of phosphate prodrug strategy. cycloplegic mydriatics