Adenosine-5 -monophosphoric acid

Adenosine-5 -monophosphoric acid Papaverine monophosadenine Adipic acid dichloride lodipamide Adrenalin... 

The reaction of monosodium salt of adenosine-5 -monophosphoric acid (19E) (AMP) with cadmium nitrate in the presence of nitric acid formed a binuclear... 

Adenosine-5 -monophosphoric acid monohydrate [5 -adenylic acid, 5 -AMP] [18422-05-4]... 

SYNS ADENOSINE-S -MONOPHOSPHATE ADENOSINE-5-MONOPHOSPHORIC ACID ADENOSINE-5 -MONOPHOSPHORIC ACID ... 

ADENOSINE-5 -MONOPHOSPHATE see AOA125 ADENOSINE-5-MONOPHOSPHORIC ACID see AOA12S... 

AMP, Adenosine-3 -monophosphoric acid 5 -AMP, Adenosine-5 -monophosphoric acid Anhydrone Anion exchange resin... 

To 3.65 g (0X)1 moi) of monohydrated adenosine-5 -monophosphoric acid, brought into suspension in a mixture of 45 ml of water and 5 mi of ethanol, are added 3.39 g (0.01 mol) of papaverine base (meiting point, The mixture is gently heated until a final tempera-... 

Adeninimine. See Adenine Adenosine monophosphate Adenosine-5 -monophosphate Adenosine-5 -monophosphoric acid. See Adenosine phosphate... 

Experiments in vitro, in which much simpler conditions prevail than in vivo, were used for a calculation of the rate of renewal of the labile phosphorus in ATP. In determining the rate of interchange between free phosphate and pyrophosphate, Meyerhof and associates (125,127) studied the reaction 2 triosephosphoric acid -f- 2 pyruvic acid -h 1 adenosine-monophosphoric acid + 2 phosphoric acid 2 phosphoglyceric acid -p 2 lactic acid -p 1 adenosinetriphosphoric acid. 

Adenosine-3 -monophosphoric acid hydrate [3 -adenylic acid, 3 -AMP] [84-21-9] M 347.3, m 197°(dec, as 2H2O), 210°(dec), m 210°(dec), [a]s46 -50° (c 0.5, 0.5M Na2HP04), pK 3.65, pKz 6.05. It crystallises from large volumes of H2O in needles as the monohydrate, but is not very soluble in boiling H2O. Under acidic conditions it forms an equilibrium mixture of 2 and 3 adenylic acids via the 2, 3 -cyclic phosphate. When heated with 20% HCl it gives a quantitative yield of furfural after 3hours, unlike 5 -adenylic acid which only gives traces of furfural. The yellow monoacridine salt has m 175°(dec) and... 

Figure 4. Separation of ribonucleoside monophosphofic acids. Conditions 250-cm anion exchange column gradient, 0.01M KHgPO containing HsPOi, (pH 2.6) to 0.15M KHiFO in 30 min column tempera-ture, 70 C detector, UV at 254 nm. 1, cyti-dine-S -monophosphoric acid 2, uridine-5 -monophosphoric acid 3, adenosine-5 -mon-ophosphofic acid 4, inosine-5 -monophosphoric acid 5, 3, 5 -cyclic adenosine mono-phosphoric add 6, guanosine-5 -monophosphoric acid (36).

To 3.65 g (0.01 mol) of monohydrated adenosine-S -monophosphoric acid, brought into suspension in a mixture of 45 ml of water and 5 ml of ethanol, are added 339 g (0.01 mol) of papaverine base (melting point, 147°C). The mixture is gently heated until a final temperature of 40°C is reached. The solution obtained is then filtered and the filtrate is concentrated under vacuum. The remaining product quickly crystallizes. After drying to 50°C to constant weight, there are obtained 6.68 g of desired product, in the monohydrated state, as a white crystalline powder, which melts at 140°C and is very soluble in water. 

Budzikiewicz addressed the problems encountered by chemists working on FD-MS of nucleotides. The assignment of ions originating from, e.g., adenosine 3 -monophosphoric acid (or its 5 -isomer) (Fig. 13) has been confirmed. Numerous problems related to desorption temperature, heating rate, and anode deterioration are inherent to the technique. 

Adenosine-3 -monophosphoric acid hydrate [3 -adenylic acid, 3 -AMP] [84-21-9] M 347.3,... 

Adenylic Acid. Muscle adenylic acid ergaden -ylic acid t -adenylic acid adenosine S -monophosphate adenosine phosphate adenosine-5 -phosphoric add edeno-sine-5. monophosphoric acid A5MP AMP NSC-20264 Addiyl Cardiomone (Na salt) Lycedan My -B-Den My-oston Phosaden. C,0HhNjO7P mol wt 347.23, C 34.59%, H 4.06%, N 20.17%, O 32,25%, P 8,92%. Nucleotide widely distributed in nature. Prepn from tissues Embden, Zimmerman, Z. Physrot Chem. 167, 137 (1927) Embden, Schmidt, ibid. 181, 130 (1929) cf. Kalckar, J. B.ol Chem. 167, 445 (1947). Prepn by hydrolysis of ATP with barium hydroxide Kerr, 3. Biot Chem. 139, 13l (1941). Synthesis Baddiley, Todd. 3. Chem. Soc. 1947, 648. Commercial prepn by enzymatic phosphorylation of adenosine. Monograph on synthesis of nucleotides G. R. Pettit. Synthetic Nucleotides vol, 1 (Van Nostrand-Reinhold. New York, 1972) 252 pp. Crystal structure Kraut, lensen, Acta Cryst 16, 79 (1963). Reviews see Adenosine Nucleic Acids. 

CAS 61-19-8. C10H14N5O7P. The monophosphoric ester of adenosine, i.e., the nucleotide containing adenine, d-ribose, and phosphoric acid. Adenylic acid is a constituent of many important coenzymes. Cyclic adenosine-3, 5 -monophosphate is designated by biochemists as cAMP. 

A nucleotide is a nucleoside in which a molecule of phosphoric acid is esterified with a free hydroxyl of the monosaccharide, most commonly either the 3 -hydroxyl or the 5 -hydroxyl. A nucleotide is named by giving the name of the parent nucleoside followed by the word monophosphate. The position of the phosphoric ester is specified by the number of the carbon to which it is bonded. Figure 28.3 shows a structural formula of adenosine 5 -monophosphate, AMP. Monophosphoric esters are diprotic acids with values of approximately 1 and 6. Therefore, at pH 7, the two hydrogens of a phosphoric monoester are fully ionized, giving a nucleotide a charge of -2. 

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