High-Energy-Density Materials: Synthesis and Characterization of N5+[P(N3)6]−, N5+ [B(N3)4]−, N5+ [HF2]−⋅n HF, N5+ [BF4]−, N5+ [PF6]−, and N5+ [SO3F]−

ENANO n5 requeteok.qxd

Embedding of N5 and the contiguous degrees

Downey and Lempp 8] have shown that the contiguous computably enumerable (c.e.) degrees, i.e. the c.e. Turing degrees containing only one c.e. weak truth-table degree, can be characterized by a local distributivity property. Here we extend their result by showing that a c.e. degree a is noncontiguous if and only if there is an embedding of the nonmodular 5-element lattice N5 into the c.e. degre...

Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5

Site-Directed Mutagenesis of Conserved Amino Acids Residues in NCarboxyaminoimidazole Ribonucleotide Mutase & Developing a High-Throughput Screen Assay for the Discovery of NCarboxyaminoimidazole Ribonucleotide Mutase Inhibitors by ZHIWEN SHI July 2014 Advisor: Dr. Steven M. Firestine Major: Pharmaceutical Sciences Degree: Master of Science The de novo purine biosynthesis pathway plays a critic...

Influenza A virus N5 neuraminidase has an extended 150-cavity.

There are 9 serotypes of neuraminidase (NA) from influenza A virus (N1 to N9), which are classified into two groups based on primary sequences (groups 1 and 2). The structural hallmark of the two groups is the presence or absence of an extra 150-cavity (formed by the 150-loop) in the active site. Thus far, structures of NAs from 6 out of the 9 serotypes have been solved. Here, we solved the N5 ...

Synthesis and Antitubercular Activity of N3,N5-Diaryl-4-(5-arylisoxazol-3-yl)-1,4-dihydropyridine-

5-Arylisoxazolyl-3-carboxaldehydes were condensed with N-aryl acetoaceta¬mide and ammonium acetate in methanol to give N3,N5-diaryl-4-(5-arylisoxazol-3-yl)-1,4-dihydropyridine-3,5-dicarboxamides. All compounds were screened for their antitubercular activity against Mycobacterium tuberculosis (H37Rv). The results for new synthesized compounds showed a moderate activity in comparison to rifampicin.