Adenine acids

Coemymes effecting transfer of hydrogen. These include the pyridine nucleotides, nicotinamide-adenine dinucleolide and nicotinamide-adenine dinucleolide phosphate the flavin nucleotides such as flavin-adenine dinucleotide and lipoic acid. 

Volkov, S.N. Conformational transitions and the mechanism of transmission of long-range effects in DNA. Preprint ITP-88-12E, Kiev (1988) 22 Krumhansl, J.A., Alexander, D.M. Nonlinear dynamics and conformational exitations in biomolecular materials. In Structure and dynamics nucleic acids and proteins. (Clementi, E., Sarma, R.H., eds) Adenine Press, New York (1983) 61-80... 

Ammonia reacts with the ketone carbonyl group to give an mine (C=NH) which is then reduced to the amine function of the a ammo acid Both mine formation and reduc tion are enzyme catalyzed The reduced form of nicotinamide adenine diphosphonu cleotide (NADPH) is a coenzyme and acts as a reducing agent The step m which the mine is reduced is the one m which the chirality center is introduced and gives only L glutamic acid... 

Adenine is a weak base Which one of the three nitrogens designated by arrows in the struc tural formula shown is protonated in acidic solution" A resonance evaluation of the three protonated forms will tell you which one is the most stable... 

Any one nucleotide, the basic building block of a nucleic acid, is derived from a molecule of phosphoric acid, a molecule of a sugar (either deoxyribose or ribose), and a molecule of one of five nitrogen compounds (bases) cytosine (C), thymine (T), adenine (A), guanine (G), uracil (U). 

Benzylamine Purine. The purine 6-benzylaminopurine [1214-39-7] (13) is an analogue of the natural product adenine, a component of both deoxyribonucleic acid and ribonucleic acid. It is not employed alone, but rather in combination with the natural products GA and GA to improve the size, weight, and thereby, yield per hm of Red DeHcious apples (10,24,25). Compounds with cytokinin activity were reported in 1913 (26) and asymmetric growth in apples was pubHshed in 1968 (27). 

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),... 

Fig. 9. Glucuionic acid pathway. NAD = nicotinamide-adenine dinucleotide NADH = reduced nicotinamide—adenine dinucleotide ...

The biological importance of these compounds stems from their use as cofactors. Both nicotinamide and nicotinic acid ate building blocks for coen2yme I (Co I), nicotinarnide—adenine dinucleotide (NAE)) (3) and coen2yme II (Co II), nicotinarnide—adenine dinucleotide phosphate (NAE)P) (4) (2). 

The result of this biosynthesis is that the product is nicotinic acid mononucleotide rather than free nicotinic acid. Ingested nicotinic acid is converted to nicotinic acid mononucleotide which, in turn, is converted to nicotinic acid adenine dinucleotide. Nicotinic acid adenine dinucleotide is then converted to nicotinamide adenine dinucleotide. If excess nicotinic acid is ingested, it is metabolized into a series of detoxification products (Fig. 4). Physiological metabohtes include /V-methylnicotinamide (19) and A/-methyl-6-pyridone-2-carboxamide (24) (1). 

Riboflavin-5 -Adenosine Diphosphate. Riboflavin-5 -adenosine diphosphate [146-14-5] (flavin—adenine dinucleotide, FAD), C27H33N9O15P2 (2), mol wt 785.56, was first isolated in 1938 from the D-amino acid oxidase as its prosthetic group (95), where it was postulated to be... 

Thraustomycin. Thraustomycin and P-thraustomycin are isolated from S. exfoliatus (4). Although their stmctures have not been totally elucidated, hydrolysis of thraustomycin shows that it contains equimolar quantities of adenine, L-leucine, and a tetrahydroxymonocarboxyhc acid. Thraustomycin is a potent inhibitor of the fungus, Af. hiemallis (+), but does not inhibit bacteria. 

Octosyl Acids. Three octosyl uronic acid nucleosides, produced by S. cacaoi sub sp. asoensis are shown in Figure 3. The biosynthesis of (172) and (173) has been reported (1). The replacement of the pyrimidine chromophore of (171) with adenine results in a nucleoside analogue that is a competitive inhibitor of cAMP. 

The sugars are typically ribose (ribonucleic acids, RNA), or 2-deoxyribose (deoxyribonucleic acids, DNA). There are five common bases in nucleic acids adenine (A) thymine (T) uracil (U) cytosine (C) and guanine (G). DNA polymers incorporate the four bases. A, T, C, and G, and RNA, the set A, U, C, and G. 

The pixyl ether is prepared from the xanthenyl chloride in 68-87% yield. This group has been used extensively in the protection of the 5 -OH of nucleosides it is readily cleaved by acidic hydrolysis (80% AcOH, 20°, 8-15 min, 100% yield, or 3% trichloroacetic acid). It can be cleaved under neutral conditions with ZnBrj, thus reducing the extent of the often troublesome depurination of A -6-benzyloxy-adenine residues during deprotection. Conditions which remove the pixyl group also partially cleave the THP group (t,/2 for THP at 2 -OH of ribonucleoside = 560 s in 3% Cl2CHC02H/CH2Cl2). ... 

Many protective groups have been developed for the amino group, including carbamates (>NCO,R), used for the protection of ammo acids in peptide and protein syntheses, and amides (>NCOR). used more widely in syntheses of alkaloids and for the protection of the nitrogen bases adenine, cytosine, and guanine in nucleo-... 

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