Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Thymine 6-amino

Cellular Protein Biosynthesis. The process of cellular protein biosynthesis is virtually the same in all organisms. The information which defines the amino acid sequence of a protein is encoded by its corresponding sequence of DNA (the gene). The DNA is composed of two strands of polynucleotides, each comprising some arrangement (sequence) of the four nucleotide building blocks of the nucleic acids adenine (A), thymine (T),... [Pg.196]

Pyrimidine and imidazole rings are particularly important in biological chemistry. Pyrimidine, for instance, is the parent ring system in cytosine, thymine, and uracil, three of the five heterocyclic amine bases found in nucleic acids An aromatic imidazole ring is present in histidine, one of the twenty amino acids found in proteins. [Pg.529]

Treatment of the allylic sulfoxide 1227 a with diisopropylethylamine (DIPEA) or of 1227 b with N-trimethylsilyldiethylamine 146 and TMSOTf 20 leads in ca. 90% yield to the quaternary amino derivatives 1228 and 1229 and HMDSO 7 [36] (Scheme 8.15). Tetramethylene sulfoxide 1230 reacts with silylated thymine 1231 in the presence of three equivalents of TMSOTf 20 to give the 4 -thio-nucleoside analogue 1232 and HMDSO 7 [37]. Other silylated pyrimidine, pyridine, and purine bases react analogously with cyclic sulfoxides to give 4 -thio-nucleoside analogues [37, 37a, 38]. [Pg.195]

Thus, thymine-tyrosine, thymine-aliphatic amino acid and cytosine-tyrosine links have been identified in isolated calf thymus chromatin subjected to 7-irradiation, or treated with metal ions and H2O2 (Dizdaroglu, 1991 Nackerdien et al., 1991). [Pg.205]

Other reactions characterized for pyrimidine residues include mercuration at C-5 of cytosine or uracil (Hopman et al., 1986), cycloaddition to the 5,6-double bond of thymine and uracil (Cimino et al., 1985), and thiolation at the C-4 amino group of cytosine (Malcom and Nicolas, 1984). [Pg.57]

Table XIX contains stability constants for complexes of Ca2+ and of several other M2+ ions with a selection of phosphonate and nucleotide ligands (681,687-695). There is considerably more published information, especially on ATP (and, to a lesser extent, ADP and AMP) complexes at various pHs, ionic strengths, and temperatures (229,696,697), and on phosphonates (688) and bisphosphonates (688,698). The metal-ion binding properties of cytidine have been considered in detail in relation to stability constant determinations for its Ca2+ complex and complexes of seven other M2+ cations (232), and for ternary M21 -cytidine-amino acid and -oxalate complexes (699). Stability constant data for Ca2+ complexes of the nucleosides cytidine and uridine, the nucleoside bases adenine, cytosine, uracil, and thymine, and the 5 -monophosphates of adenosine, cytidine, thymidine, and uridine, have been listed along with values for analogous complexes of a wide range of other metal ions (700). Unfortunately comparisons are sometimes precluded by significant differences in experimental conditions. Table XIX contains stability constants for complexes of Ca2+ and of several other M2+ ions with a selection of phosphonate and nucleotide ligands (681,687-695). There is considerably more published information, especially on ATP (and, to a lesser extent, ADP and AMP) complexes at various pHs, ionic strengths, and temperatures (229,696,697), and on phosphonates (688) and bisphosphonates (688,698). The metal-ion binding properties of cytidine have been considered in detail in relation to stability constant determinations for its Ca2+ complex and complexes of seven other M2+ cations (232), and for ternary M21 -cytidine-amino acid and -oxalate complexes (699). Stability constant data for Ca2+ complexes of the nucleosides cytidine and uridine, the nucleoside bases adenine, cytosine, uracil, and thymine, and the 5 -monophosphates of adenosine, cytidine, thymidine, and uridine, have been listed along with values for analogous complexes of a wide range of other metal ions (700). Unfortunately comparisons are sometimes precluded by significant differences in experimental conditions.
The genetic code is composed of four letters —two pyrimidine nitrogenous bases, thymine and cytosine, and two purine bases, guanine and adenine—which can be regarded functionally as arranged in codons (or triplets). Each codon consists of a combination of three letters therefore, 43 (64) different codons are possible. Sixty-one codons code for specific amino acids (three produce stop signals), and as only 20 different amino acids are used to make proteins, one amino acid can be specified by more than one codon. [Pg.177]

PES has been applied to study biologically active molecules with amino groups and their constituents like nucleic bases and related compounds (e.g. adenine, guanine, thymine, cytosine, hypoxanthine and their methyl derivatives)113-120 and amino acids92,121,122 or their methyl esters123. [Pg.188]

Enzymes dependent on folic acid as coenzyme include participants in the synthesis of thymine, an essential component of DNA, and methionine, a common amino acid in proteins, among other important metabolites. A deficiency of folic acid results in the disease megaloblastic anemia. [Pg.203]


See other pages where Thymine 6-amino is mentioned: [Pg.154]    [Pg.263]    [Pg.24]    [Pg.127]    [Pg.26]    [Pg.157]    [Pg.1164]    [Pg.330]    [Pg.59]    [Pg.64]    [Pg.67]    [Pg.401]    [Pg.42]    [Pg.244]    [Pg.540]    [Pg.4]    [Pg.204]    [Pg.76]    [Pg.29]    [Pg.302]    [Pg.300]    [Pg.86]    [Pg.36]    [Pg.97]    [Pg.537]    [Pg.147]    [Pg.166]    [Pg.119]    [Pg.39]    [Pg.46]    [Pg.51]    [Pg.224]    [Pg.206]    [Pg.69]    [Pg.447]    [Pg.10]    [Pg.365]    [Pg.158]    [Pg.154]    [Pg.47]    [Pg.54]   
See also in sourсe #XX -- [ Pg.344 ]




SEARCH



Thymine

© 2024 chempedia.info