نتایج جستجو برای: benzyl thio

تعداد نتایج: 12199  

Journal: :The Journal of biological chemistry 1993
J P Shaw M Rekik F Schwager S Harayama

The nucleotide sequence of the structural gene for benzyl alcohol dehydrogenase encoded by TOL plasmid pWWO of Pseudomonas putida has been determined. Benzyl alcohol dehydrogenase is a member of the long-chain zinc alcohol dehydrogenase family and, like other alcohol dehydrogenases of this family, contains two zinc atoms per subunit. Benzyl alcohol dehydrogenase, while sharing 31% identical res...

Journal: :Antiviral chemistry & chemotherapy 2011
Yohei Isono Norikazu Sakakibara Paula Ordonez Takayuki Hamasaki Masanori Baba Masahiro Ikejiri Tokumi Maruyama

BACKGROUND Nine novel uracil analogues were synthesized and evaluated as inhibitors of HIV-1. METHODS Key structural modifications included replacement of the 6-chloro group of 1-benzyl-6-chloro-3-(3,5-dimethylbenzyl)uracil by other functional groups or N(1)-alkylation of 3-(3,5-dimethylbenzyl)-5-fluorouracil. RESULTS These compounds showed only micromolar potency against HIV-1 in MT-4, tho...

Journal: :Genes, brain, and behavior 2009
Y Wang A Ghezzi J C P Yin N S Atkinson

Pharmacodynamic tolerance is believed to involve homeostatic mechanisms initiated to restore normal neural function. Drosophila exposed to a sedating dose of an organic solvent, such as benzyl alcohol or ethanol, acquire tolerance to subsequent sedation by that solvent. The slo gene encodes BK-type Ca(2+)-activated K(+) channels and has been linked to alcohol- and organic solvent-induced behavi...

2002
W. Kudelska

Treatment of O-benzyl protected S-glucosyl phosphorothioates with 1,3,5-trimethoxybenzene in the presence of iodine or boron trifluoride etherate led to appropriate aryl C-Dglucosides. The reaction of O-benzyl and O-acetyl-protected phosphorothioates of monosaccharides with allyltrimethylsilane, using boron trifluoride etherate as activator, gave mainly or exclusively, the corresponding 3-(α-Dg...

Journal: :Chemical & pharmaceutical bulletin 2000
A Miyadera K Satoh A Imura

Two efficient and practical methods of synthesis of the C-10 substituent of DV-7751 (1), a novel quinolone carboxylic acid, were established. The first method utilizes an optical resolution of racemic 8-amino-6-benzyl-6-azaspiro[3.4]octane (13), while the second employs an enantioselective microbial reduction of 6-benzyl-5,8-dioxo-6-azaspiro[3.4]octane (8b). The enantiomeric excess of (S)-8-ami...

2012
Tao Yu Yimin Hu

The crystal structure of the title compound, C(26)H(21)NO(3)·0.25H(2)O, reveals one stereogenic centre in the mol-ecule. Nevertheless, due to the observed centrosymmetric space group, both enanti-omers are present in the crystal packing. The water molecule of crystallisation is located on a crystallographic inversion center. The mol-ecule contains one five-membered ring (A) and three six-member...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 1987
W C Cole S J DeNardo C F Meares M J McCall G L DeNardo A L Epstein H A O'Brien M K Moi

Serum incubation of monoclonal antibodies chelate labeled by DTPA, benzyl-EDTA and benzyl-TETA with 111In, 57Co, and 67Cu demonstrated marked differences in their stability. In serum, 111In-benzyl-EDTA-antibody was more stable than 111In-DTPA-antibody. Cobalt-57 or 67Cu chelated antibody were less stable than either 111In chelated antibody; 67Cu was only firmly attached to the antibody as 67Cu-...

Journal: :Nanoscale 2015
Mengmeng Wang Cuiping Fu Xingang Liu Zhipeng Lin Ning Yang Shaoning Yu

Protein-nanoparticle interactions are important in biomedical applications of nanoparticles and for growing biosafety concerns about nanomaterials. In this study, the interactions of four plasma proteins, human serum albumin (HSA), myoglobin (MB), hemoglobin (HB), and trypsin (TRP), with Au and Ag nanoparticles were investigated by FT-IR spectroscopy. The secondary structure of thio-proteins ch...

Journal: :The Biochemical journal 2000
A Verri F Focher R J Duncombe I Basnak R T Walker P L Coe E de Clercq G Andrei R Snoeck J Balzarini S Spadari

The antiviral activity of several nucleoside analogues is often limited by their rapid degradation by pyrimidine nucleoside phosphorylases. In an attempt to avoid this degradation, several modified nucleosides have been synthesized. A series of 4'-thio-2'-deoxyuridines exhibits an anti-[herpes simplex virus (HSV)] activity significantly higher (20-600 times) than that shown by the corresponding...

Journal: :Sen-iso Kogyo 1935

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