نتایج جستجو برای: 0.73

تعداد نتایج: 600  

2006
Nobuyuki Fukazawa Tsuneji Suzuki Wakao Sato Keisuke Yusa Takashi Tsuruo

Newly synthesized quinoline derivatives were investigated for their efficacy to reverse multidrug resistance (MDR). In this study, one of the most effective quinoline derivatives, MS-073, was compared with verapamil with regard to its ability to overcome MDR in vitro and in vivo. MS-073 at 0.1 MMalmost completely reversed in vitro resistance to vincristine (VCR) in VCR-resistant P388 cells. The...

2006
Wakao Sato Nobuyuki Fukazawa Tsuneji Suzuki Keisuke Yusa Takashi Tsuruo

Newly synthesized quinoline derivatives were investigated for their efficacy to reverse multidrug resistance (MDR). In this study, one of the most effective quinoline derivatives, MS-073, was compared with verapamil with regard to its ability to overcome MDR in vitro and in vivo. MS-073 at 0.1 MMalmost completely reversed in vitro resistance to vincristine (VCR) in VCR-resistant P388 cells. The...

Journal: :Cancer research 1991
W Sato N Fukazawa T Suzuki K Yusa T Tsuruo

Newly synthesized quinoline derivatives were investigated for their efficacy to reverse multidrug resistance (MDR). In this study, one of the most effective quinoline derivatives, MS-073, was compared with verapamil with regard to its ability to overcome MDR in vitro and in vivo. MS-073 at 0.1 microM almost completely reversed in vitro resistance to vincristine (VCR) in VCR-resistant P388 cells...

Journal: :Antimicrobial agents and chemotherapy 2009
M Steven Oberste Deborah Moore Barbara Anderson Mark A Pallansch Daniel C Pevear Marc S Collett

V-073, an enterovirus capsid inhibitor, was evaluated for its spectrum of antipoliovirus activity. V-073 inhibited all 45 polioviruses tested in a virus-induced cytopathic effect protection assay, with 50% effective concentration (EC50) values ranging from 0.003 to 0.126 microM. Ninety percent of the polioviruses tested were inhibited at EC(50)s of < or = 0.076 microM (MIC90 = 32 ng/ml). V-073 ...

2009
Jing Zhou Ryan Dupont Jeanette M. Norton Darwin L. Sorensen Joan E. McLean

Various molecular tools including real-time PCR, clone library, and automated ribosomal intergenic spacer analysis were used in this column study to analyze the change of microbial composition in response to the addition of various carbon donors and microbial inocula. Whey, emulsified oil and emulsified oil plus surfactant were used as carbon donors. According to the competitive electron accept...

2016
Shimpei Watanabe Unnikrishnan Kuzhiumparambil Zophia Winiarski Shanlin Fu

Synthetic cannabinoids JWH-018, JWH-073 and AM2201 were metabolised by the fungus Cunninghamella elegans. In this article, data on individual metabolites of their retention times, mass accuracies, major product ions and structures indicated by product ions are presented. The data in this article is related to "Biotransformation of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunningham...

2016
Moytrey Chatterjee Swagata Ganguly Pabitra Saha Dilip K. Bera Nandita Basu Ardhendu K. Maji A. P. C. Roy

1 Protozoology Unit, Department of Microbiology, Calcutta School of Tropical Medicine, 108, C. R. Avenue, Kolkata 700 073, India 2 Department of Microbiology, NRS Medical College, 138 AJC Bose Road, Kolkata 700 014, India 3 Department of Zoology, A. P. C. Roy Govt. College, Himachal Bihar, Matigara, Siliguri734 010, West Bengal, India 4 Director, Calcutta School of Tropical Medicine, 108, C. R....

2011
Brett C. Ginsburg David R. Schulze Lenka Hruba Lance R. McMahon

Products containing naphthalen-1-yl-(1-pentylindol-3-yl) methanone (JWH-018) and naphthalen-1-yl-(1-butylindol-3-yl) methanone (JWH-073) are emerging drugs of abuse. Here, the behavioral effects of JWH-018 and JWH-073 were examined in one behavioral assay selective for cannabinoid agonism, rhesus monkeys (n 4) discriminating -tetrahydrocannabinol ( -THC; 0.1 mg/kg i.v.), and another assay sensi...

Journal: :Theriogenology 2013
Malgorzata A Pozor Margo L Macpherson Sue M McDonnell Maggie Nollin Janet F Roser Charles Love Scott Runyon Brian F Thomas Mats H Troedsson

The objective of this study was to determine whether an indenopyridine derivative RTI-4587-073(l) was a good candidate for male contraception in horses. We hypothesized that a single administration of RTI-4587-073(l) causes significant suppression of testicular function in stallions without affecting sexual behavior. Three Miniature horse stallions received a single dose of 12.5 mg/kg RTI-4587-...

Journal: :Journal of analytical toxicology 2012
Kevin G Shanks Tim Dahn Andrea R Terrell

Synthetic cannabinoids have been detected in various herbal blends sold legally in convenience stores, smoke shops, and on the Internet. Many of these compounds have extreme forensic significance. We developed and validated a rapid ultra-performance liquid chromatography-tandem mass spectrometry method for the determination of trace concentrations of two of these compounds, JWH-018 and JWH-073,...

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