نتایج جستجو برای: pharmacokinetic properties

تعداد نتایج: 890912  

2015
Daniel H. Ahn Junan Li Lai Wei Austin Doyle John L. Marshall Larry J. Schaaf Mitch A. Phelps Miguel A. Villalona-Calero Tanios Bekaii-Saab

Biliary cancers (BC) are rare, chemoresistant and are associated with a poor prognosis. Targeting the Akt pathway is of significance in BC. We hypothesized that the allosteric inhibitor MK-2206 will be active in BC. This was a multi-institutional phase II study of MK-2206 given to patients with advanced, refractory BC. The primary end point was overall response rate. We also characterized pharm...

Journal: :Cancer prevention research 2016
Abu Syed Md Anisuzzaman Abedul Haque Mohammad Aminur Rahman Dongsheng Wang James R Fuchs Selwyn Hurwitz Yuan Liu Gabriel Sica Fadlo R Khuri Zhuo Georgia Chen Dong M Shin A R M Ruhul Amin

Despite its high promise for cancer prevention and therapy, the potential utility of curcumin in cancer is compromised by its low bioavailability and weak potency. The purpose of the current study was to assess the in vitro and in vivo efficacy and pharmacokinetic parameters of the potent curcumin analogue FLLL12 in SCCHN and identify the mechanisms of its antitumor effect. IC50 values against ...

2014
Frank Kloprogge Vincent Jullien Patrice Piola Mehul Dhorda Sulaiman Muwanga François Nosten Nicholas P. J. Day Nicholas J. White Philippe J. Guerin Joel Tarning

OBJECTIVES Oral quinine is used for the treatment of uncomplicated malaria during pregnancy, but few pharmacokinetic data are available for this population. Previous studies have reported a substantial effect of malaria on the pharmacokinetics of quinine resulting from increased α-1-acid glycoprotein levels and decreased cytochrome P450 3A4 activity. The aim of this study was to investigate the...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Takafumi Akabane Kenji Tabata Keitaro Kadono Shuichi Sakuda Shigeyuki Terashita Toshio Teramura

To verify the availability of pharmacokinetic parameters in cynomolgus monkeys, hepatic availability (Fh) and the fraction absorbed multiplied by intestinal availability (FaFg) were evaluated to determine their contributions to absolute bioavailability (F) after intravenous and oral administrations. These results were compared with those for humans using 13 commercial drugs for which human phar...

2014
Lidija R Jevrić Sanja O Podunavac-Kuzmanović Jaroslava V Švarc-Gajić Strahinja Z Kovačević Bratislav Ž Jovanović

The properties relevant to pharmacokinetics and pharmacodynamics of four series of synthesized s-triazine derivatives have been studied by Quantitative structure-retention relationship (QSRR) approach. The chromatographic behavior of these compounds was investigated by using reversed-phase high performance thin-layer chromatography (RP-HPTLC). Chromatographic retention (R M (0)) was correlated ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید