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Phosphate ester prodrug

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 ... 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.

Design, Synthesis, and Sustained‐Release Property of 1,3‐Cyclic ...

WebApr 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 … WebIn this study, a phosphate group was added to position C-4 of 1, leading to the more water-soluble prodrug 2 and its ammonium salt 3, which possesses increased stability compared to 2. Herein are reported the synthesis, characterization, solubility, and stability of phosphate prodrug 3 in biological medium in comparison to 1 , as well as new ... piselinten https://pickfordassociates.net

Preformulation Studies of a Prodrug of Δ9-Tetrahydrocannabinol

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. … WebGW433908 is the water-soluble, phosphate ester prodrug of the human immunodeficiency virus type 1 protease inhibitor amprenavir (APV). A high-yield synthesis of GW433908 is achieved by phosphorylation of the penultimate precursor of APV with phosphorous oxychloride (POCl(3)) in pyridine. WebMay 1, 2001 · Fosphenytoin is a phosphate ester prodrug of phenytoin with an improved solubility and better tolerance after intramuscular or intravenous administration. It is rapidly hydrolyzed in vivo to phenytoin with a half-life of 5–15 min. The prodrug is not pharmacologically active, but it has been shown to cross-react in various immunoassays … atlantik landkarte

Prodrug - an overview ScienceDirect Topics

Category:An Improved Design of Water-Soluble Propofol Prodrugs Charac ...

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Phosphate ester prodrug

Prodrugs of phosphonates and phosphates: crossing the …

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 … 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 …

Phosphate ester prodrug

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WebMay 23, 2016 · Phosphate Esters In drug design, forming phosphate esters is a common strategy making the drug more soluble in water. In addition to good water solubility, the phosphate ester can also be a site of the substrate for alkaline phosphatases, this property enables the paclitaxel prodrug to have a fast release of the parent 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.

WebEster and phosphate hydrolysis are widely used in prodrug design because of their simplicity, but such approaches are relatively ineffective for targeting drugs to specific sites. The activation of prodrugs by the cytochrome P450 system provides a highly versatile approach to prodrug design that is particularly adaptable for targeting drug ... WebOseltamivir phosphate is an ethyl ester prodrug requiring ester hydrolysis for conversion to the active form, oseltamivir carboxylate. ... In 2-year carcinogenicity studies in mice and rats given daily oral doses of the prodrug oseltamivir phosphate up to 400 mg/kg and 500 mg/kg, respectively, the prodrug and the active form oseltamivir ...

WebNov 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 ]. WebApr 12, 2024 · The phosphate prodrug of dexamethasone has a very short half-life of just over 5 min, and it could not be detected in the plasma of healthy volunteers after 30 min [ …

WebPhosphate 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 …

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). piselli attilioWebNov 11, 2024 · Main protease (M pro) is a superior target for anti-SARS-COV-2 drugs. PF-07304814 is a phosphate ester prodrug of PF-00835231 that is rapidly metabolized into the active metabolite PF-00835231 by alkaline phosphatase (ALP) and then suppresses SARS-CoV-2 replication by inhibiting M pro. atlantik sedlčanyWebJul 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 ). pisek kosickyWebNov 15, 2024 · These eight prodrugs are aripiprazole lauroxil, isavuconazonium sulfate, ixazomib citrate, sacubitril, selexipag, tenofovir alafenamide sulfate, uridine triacetate, and telotristat etiprate with their respective metabolites aripiprazole, isavuconazole, ixazomib, LBQ657, ACT-333679, tenofovir, uridine, and telotristat being pharmacologically … piselli 7 mesiWebSep 1, 2024 · Phenytoin is a low aqueous solubility antiepileptic drug, but its phosphate ester prodrug fosphenytoin is soluble, although less permeable. In a previous study, the intranasal administration of aqueous-based formulations of fosphenytoin led to high but delayed phenytoin bioavailability compared to the intravenous route. atlantik road camping webcamWebtriphenylethylene 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 atlantik restaurant berlinWebPhosphonates, phosphinates, and phosphates are prominently represented as pharmacophores in various classes of biological agents. These include antiviral and anticancer nucleotides, inhibitors of biosynthesis of cholesterol, angiotensin-converting enzyme inhibitors, and bisphosphonates for the treatment of osteoporosis. atlantik radweg portugal