Exploitation of bile acid transport systems in prodrug design.
about
Role of the intestinal bile acid transporters in bile acid and drug dispositionA multiple multicomponent approach to chimeric peptide-peptoid podands.Structural requirements of the human sodium-dependent bile acid transporter (hASBT): role of 3- and 7-OH moieties on binding and translocation of bile acids.Effects of Karela (Bitter Melon; Momordica charantia) on genes of lipids and carbohydrates metabolism in experimental hypercholesterolemia: biochemical, molecular and histopathological studyInhibition requirements of the human apical sodium-dependent bile acid transporter (hASBT) using aminopiperidine conjugates of glutamyl-bile acidsImpact of impurity on kinetic estimates from transport and inhibition studiesStructural requirements of bile acid transporters: C-3 and C-7 modifications of steroidal hydroxyl groups.Decreasing cartilage damage in a rat model of osteoarthritis by intra-articular injection of deoxycholic acidTherapeutic Effect of Chenodeoxycholic Acid in an Experimental Rabbit Model of OsteoarthritisEffects of food on the relative bioavailability of lapatinib in cancer patients.Novel Liver-targeted conjugates of Glycogen Phosphorylase Inhibitor PSN-357 for the Treatment of Diabetes: Design, Synthesis, Pharmacokinetic and Pharmacological Evaluations.Novel liver-specific cholic acid-cytarabine conjugates with potent antitumor activities: Synthesis and biological characterization.Transporters, Trojan horses and therapeutics: suitability of bile acid and peptide transporters for drug delivery.Anticancer steroids: linking natural and semi-synthetic compounds.Bile acids and bile acid derivatives: use in drug delivery systems and as therapeutic agents.The effect of a tertiary bile acid, taurocholic acid, on the morphology and physical characteristics of microencapsulated probucol: potential applications in diabetes: a characterization study.Transport and killing mechanism of a novel camptothecin-deoxycholic acid derivate on hepatocellular carcinoma cells.L-arginine conjugates of bile acids-a possible treatment for non-alcoholic fatty liver disease.Synthesis of cholic-acid-carrying polymer and in-vitro evaluation of hepatoma-targeting nanoparticles decorated with the polymer.Synthesis via RAFT polymerization of thermo- and pH-responsive random copolymers containing cholic acid moieties and their self-assembly in waterSynthesis and in vitro cytotoxicity of deoxyadenosine–bile acid conjugates linked with 1,2,3-triazole
P2860
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P2860
Exploitation of bile acid transport systems in prodrug design.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Exploitation of bile acid transport systems in prodrug design.
@en
type
label
Exploitation of bile acid transport systems in prodrug design.
@en
prefLabel
Exploitation of bile acid transport systems in prodrug design.
@en
P2860
P356
P1433
P1476
Exploitation of bile acid transport systems in prodrug design
@en
P2093
Elina Sievänen
P2860
P304
P356
10.3390/12081859
P407
P577
2007-08-16T00:00:00Z