Metabolism and in vitro antiretroviral activities of bis(pivaloyloxymethyl) prodrugs of acyclic nucleoside phosphonates
about
Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogsSynthesis of nucleoside phosphate and phosphonate prodrugsSusceptibilities of zidovudine-resistant variants of human immunodeficiency virus type 1 to inhibition by acyclic nucleoside phosphonatesAntiretroviral activity and pharmacokinetics in mice of oral bis(pivaloyloxymethyl)-9-(2-phosphonylmethoxyethyl)adenine, the bis(pivaloyloxymethyl) ester prodrug of 9-(2-phosphonylmethoxyethyl)adenineAnti-human immunodeficiency virus activity and cellular metabolism of a potential prodrug of the acyclic nucleoside phosphonate 9-R-(2-phosphonomethoxypropyl)adenine (PMPA), Bis(isopropyloxymethylcarbonyl)PMPAAntiviral activities of 9-R-2-phosphonomethoxypropyl adenine (PMPA) and bis(isopropyloxymethylcarbonyl)PMPA against various drug-resistant human immunodeficiency virus strainsA novel compound from the mushroom Cryptoporus volvatus inhibits porcine reproductive and respiratory syndrome virus (PRRSV) in vitroInhibition of duck hepatitis B virus replication by 9-(2-phosphonylmethoxyethyl)adenine, an acyclic phosphonate nucleoside analogueHuman immunodeficiency virus protease inhibitors serve as substrates for multidrug transporter proteins MDR1 and MRP1 but retain antiviral efficacy in cell lines expressing these transportersAccumulation and oriented transport of ampicillin in Caco-2 cells from its pivaloyloxymethylester prodrug, pivampicillin.Oral, subcutaneous, and intramuscular bioavailabilities of the antiviral nucleotide analog 9-(2-phosphonylmethoxyethyl) adenine in cynomolgus monkeysSelective intracellular activation of a novel prodrug of the human immunodeficiency virus reverse transcriptase inhibitor tenofovir leads to preferential distribution and accumulation in lymphatic tissue.Single-dose pharmacokinetics and safety of the oral antiviral compound adefovir dipivoxil in children infected with human immunodeficiency virus type 1. The Pediatrics AIDS Clinical Trials GroupExpression of multidrug resistance associated protein 5 (MRP5) on cornea and its role in drug efflux.Prodrug and antedrug: two diametrical approaches in designing safer drugs.Considerations and development of topical microbicides to inhibit the sexual transmission of HIV.Clinical pharmacokinetics of adefovir in human immunodeficiency virus type 1-infected patients.Antiviral therapy for human immunodeficiency virus infections4'-modified nucleoside analogs: potent inhibitors active against entecavir-resistant hepatitis B virus.The human multidrug resistance protein 4 (MRP4, ABCC4): functional analysis of a highly polymorphic gene.Bisamidate Prodrugs of 2-Substituted 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA, adefovir) as Selective Inhibitors of Adenylate Cyclase Toxin from Bordetella pertussis.Amidate prodrugs of 9-[2-(phosphonomethoxy)ethyl]adenine as inhibitors of adenylate cyclase toxin from Bordetella pertussis.Use of helper-free replication-defective simian immunodeficiency virus-based vectors to study macrophage and T tropism: evidence for distinct levels of restriction in primary macrophages and a T-cell line.Design and synthesis of dually branched 5'-norcarbocyclic adenosine phosphonodiester analogue as a new anti-HIV prodrug.Antiretrovirus activity of a novel class of acyclic pyrimidine nucleoside phosphonatesAntiviral activities of MCC-478, a novel and specific inhibitor of hepatitis B virus.Antimalarial and toxic effects of the acyclic nucleoside phosphonate (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)adenine in Plasmodium berghei-infected mice.Human multidrug resistance associated protein 4 confers resistance to camptothecins.Review: Present and future directions in the treatment of chronic hepatitis B infection.Acyclic nucleosides as antiviral compounds.Synthesis and anti-HIV evaluation of new acyclic phosphonate nucleotide analogues and their bis(SATE) derivatives.Determination of adefovir in human plasma by liquid chromatography/tandem mass spectrometry: application to a pharmacokinetic study.Drug-drug and drug-food interactions between tenofovir disoproxil fumarate and didanosine.
P2860
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P2860
Metabolism and in vitro antiretroviral activities of bis(pivaloyloxymethyl) prodrugs of acyclic nucleoside phosphonates
description
1993 nî lūn-bûn
@nan
1993 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@ast
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@en
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@nl
type
label
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@ast
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@en
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@nl
prefLabel
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@ast
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@en
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@nl
P2093
P2860
P356
P1476
Metabolism and in vitro antire ...... cyclic nucleoside phosphonates
@en
P2093
A Fridland
B L Robbins
M C Connelly
N Bischofberger
R V Srinivas
P2860
P304
P356
10.1128/AAC.37.10.2247
P407
P577
1993-10-01T00:00:00Z