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Pyrimidines purines

Note Flavonoids react with the reagent even at room temperature [1] mycotoxins, steroids, purines, pyrimidines, cardiac glycosides and lipids only react on heating [2, 4-6]. Zirconyl sulfate can be used to replace the zirconyl chloride in the reagent this is reported to result in an increase in the sensitivity to certain groups of substances (e.g. cholesteryl esters, triglycerides) [4]. [Pg.439]

Prebiotic chemistry of natural heterocycles, among them purines, pyrimidines, sugars, and riboflavin 97T11493. [Pg.225]

Thin-layer chromatography of antibiotics, drugs, alkaloids, purines, pyrimidines, nucleic acids, toxins, and vitamins 98AC7R. [Pg.242]

PNA targeting of duplex DNA is not limited to homopurine sequences. Under special circumstances (high negative superhelical stress) mixed purine-pyrimidine PNA-peptide conjugates can bind by duplex invasion (Fig. 4.7) [31], but such complexes are of limited stability. However, using a set of pseudo-complementary PNAs containing diaminopurine-thiouracil substitutions, very stable double duplex invasion complexes can be formed (Fig. 4.4) and the only sequence requirement is about 50% AT content. Very recently, it was also demonstrated that reasonably stable helix invasion complexes can be obtained with tail-clamp PNA comprising a short (>six bases) homopyrimidine bis-PNA clamp and a mixed sequence tail extension [32] (Fig. 4.7). [Pg.159]

A few ex vivo and in vivo studies have been published claiming an antigene (and antisense) effect of mixed purine/pyrimidine sequence PNA [48, 49, 78-80]. However, as pointed out by us in recent reviews [81, 82] these studies lack fundamental controls such as the inclusion of relevant internal standards as a control for sequence-specific non-antigene/antisense effects, thus confirmatory studies are warranted. The in vivo antigene studies from Richelsoris group [79, 83] completely lack a rational basis for the claimed effects. First of all there is no evidence that... [Pg.165]

Glutamine as an important source for the synthesis of purines, pyrimidines and amino sugars is essential for most cell lines, too. High concentrations of glutamine may also effect cell growth indirectly as the major end-products are lactate and ammonia [15]. Both known to be toxic metabohtes. [Pg.126]

Several amino acids are also the precursors of other compounds, eg, purines, pyrimidines, hormones such as epinephrine and thyroxine, and neurotransmitters. [Pg.124]

Important products derived from amino acids include heme, purines, pyrimidines, hormones, neurotransmitters, and biologically active peptides. In addition, many proteins contain amino acids that have been modified for a specific function such as binding calcium or as intermediates that serve to stabilize proteins—generally structural proteins—by subsequent covalent cross-hnk-ing. The amino acid residues in those proteins serve as precursors for these modified residues. Small peptides or peptide-like molecules not synthesized on ribosomes fulfill specific functions in cells. Histamine plays a central role in many allergic reactions. Neurotransmitters derived from amino acids include y-aminobutyrate, 5-hydroxytryptamine (serotonin), dopamine, norepinephrine, and epinephrine. Many drugs used to treat neurologic and psychiatric conditions affect the metabolism of these neurotransmitters. [Pg.264]

Under physiologic conditions, the amino and oxo tautomers of purines, pyrimidines, and their derivatives predominate. [Pg.292]

Purine Pyrimidine Nucleotide Biosynthesis Are Coordinately Regulated... [Pg.299]

Purines, pyrimidines and their nucleosides and nucleoside triphosphates are synthesized... [Pg.173]

Treatment of bacterial cells with appropriate concentrations of such substances as eetrimide, chlorhexidine, phenol and hexylresorcinol, causes a leakage of a group of eharacteristic chemical species. The potassium ion, being a small entity, is the fust substance to appear when the cytoplasmic membrane is damaged. Amino acids, purines, pyrimidines and pentoses are examples of other substances which will leak horn treated cells. [Pg.258]

Z-form Few synthetic DNAs of poly purine-pyrimidine sequences 0.36-0.38 12 2... [Pg.158]

Caffeine Xanthine derivatives Purines Purines, pyrimidines Purines Chloraminc-T Iron (111) chloride followed by iodine Silver nitrate followed by sodium dichromate Fluorescein Silver nitrate followed by bromophenol blue... [Pg.31]

Voelter W, Records R, Bunnenberg E, Djerassi C (1968) Magnetic circular dichroism studies, vi. investigation of some purines, pyrimidines, and nucleosides. J Am Chem Soc 90 6163—6170... [Pg.333]

In Z-DNA, guanine residues are syn, whereas cytosine and thymine residues are anti. Eukaryotic DNA contains several alternating purine-pyrimidine sequences consistent with die Z-DNA conformation however, the biologic significance of Z-DNA is still unclear. [Pg.222]

AO is also effective in metabolizing a wide range of nitrogen-containing heterocycles such as purines, pyrimidines, pteridines, quinolines, and diazanaphthalenes (95). For example, phthalazine is rapidly converted to 1-phthalazinone by AO and the prodrug, 5-ethynyl-2-(l//)-pyrimidone, is oxidized to the dihydropyrimidine dehydrogenase mechanism-based inhibitor, 5-ethynyluracil, by AO (Fig. 4.40) (96). [Pg.66]

Proteins, Solid, Adsorption of Water on (Eley Leslie). Proteins and Nucleic Acids, Electronic Structure Proteins and Nucleic Acids, Influence of Physical Agents on Purine-Pyrimidine Pairs, Steroids, and Polycyclic Aromatic Carcinogens (Pullman). ... [Pg.403]


See other pages where Pyrimidines purines is mentioned: [Pg.1166]    [Pg.250]    [Pg.118]    [Pg.325]    [Pg.22]    [Pg.447]    [Pg.121]    [Pg.438]    [Pg.1166]    [Pg.328]    [Pg.214]    [Pg.578]    [Pg.166]    [Pg.228]    [Pg.14]    [Pg.286]    [Pg.290]    [Pg.293]    [Pg.293]    [Pg.297]    [Pg.299]    [Pg.301]    [Pg.164]    [Pg.144]    [Pg.946]    [Pg.1411]    [Pg.823]    [Pg.164]    [Pg.225]    [Pg.349]   
See also in sourсe #XX -- [ Pg.128 , Pg.129 , Pg.130 , Pg.131 , Pg.132 , Pg.140 , Pg.145 , Pg.148 , Pg.163 , Pg.164 ]




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Acid dissociation constant purine and pyrimidine bases

Annelated Pyrimidines (Except Purines, Pteridines, and Flavins)

Ascaris spp purine and pyrimidine metabolism

Aza analogs, of pyrimidine and purine

Aza analogs, of pyrimidine and purine bases

Base Pairing in the Purine and Pyrimidine Crystal Structures

Base-Pair Configurations with Purine and Pyrimidine Homo-Association

Bases purine and pyrimidine

Coordination of Purine and Pyrimidine Nucleotide Biosynthesis

Deoxyribonucleic acid purine and pyrimidine bases

Electron Affinities of Purines and Pyrimidines

Fused Pyrimidines Purines and Pteridines

Gut, J., Aza Analogs of Pyrimidine and Purine

Halogenated Pyrimidines and Purines

Heterocyclic compounds Purine Pyridine Pyrimidine

Leishmania spp purine and pyrimidine metabolism

Nucleic acids purines and pyrimidines

Nucleotides Purine Pyrimidines

Properties of Purine and Pyrimidine Bases

Purine and Pyrimidine Structures

Purine and pyrimidine biosynthesis

Purine and pyrimidine metabolism

Purine and pyrimidine nucleotide

Purine and pyrimidine nucleotide biosynthesis

Purine and pyrimidine synthesis

Purine and pyrimidine transport

Purine pyrimidine and

Purine-Pyrimidine Metabolism

Purine-pyrimidine base pairing

Purine-pyrimidine base pairs

Purine-pyrimidine base pairs mismatch

Purine-pyrimidine complexes

Purine-pyrimidine hairpin

Purine-pyrimidine pairs, steroids

Purine-pyrimidine transversions

Purine/pyrimidine ratio

Purine:pyrimidine, Watson-Crick

Purines pyrimido pyrimidines

Purines tetrazolo pyrimidine

Purines, Pyrimidines and Nucleosides

Purines, Pyrimidines, and Other Basic N-Compounds

Pyrimidine Nucleoside Bases, Purines, Nucleotides, Nucleosides, and Nucleic Acids

Pyrimidine and Purine Derivatives

Pyrimidine and Related Compounds Excluding Purines

Pyrimidine and purine radiation products problematic cases

Pyrimidine nucleoside bases and purines

Pyrimidine, Purine, and Related Alkaloids

Pyrimidine-purine dinucleosides

Ribonucleic acid purine and pyrimidine bases

Solubility purine and pyrimidine bases

Substituted purines and pyrimidines

Trypanosoma spp purine and pyrimidine metabolism

Van der Waals contact surfaces of purines and pyrimidines

Watson-Crick purine-pyrimidine base

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