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Subject acid production effects

None of the TCAs seem to have an effect on dopaminergic neurotransmission in the central nervous system (CNS). This has been supported by the lack of alterations in dopamine receptor sensitivity in chronically treated patients who have shown response to treatment (Sugrue, 1983). More recent investigations have also shown that administration of DMI to depressed subjects had no effect on levels of homovanillic acid, the principal metabolite of dopamine, in a measure of brain neurotransmitter production. In this investigation, DMI administration did increase norepinephrine production and overall cerebral metabolism (Lambert, 2000). [Pg.285]

Subsequent to this breakthrough, the subject was extensively investigated and was subsequently reviewed [390]. The acids most effective are BTCA, tricarballylic acid, and citric acid. Owing to the low cost and wide availability of citric acid, it is undergoing widespread commercial development for esterification cross-linking of cotton and paper products, often with minor amounts of BTCA as an activator, together with suitable catalysts. [Pg.94]

In four children with nephropathic cystinosis receiving mercaptamine 14.35 mg/kg qds serum gastrin concentrations up to 90 minutes later rose as did gastric acid output (10). Two of the four subjects had visual and histological evidence of gastric inflammation. The clinical effect of this acid production is unknown. [Pg.2258]

Plants in the UK, USSR and France are now reprocessing irradiated UO2/PUO2 fuels and LMFBR fuel reprocessing has been the subject of international conferences. " The plant at Cap la Hague, France, employs a 30% TBP solution and no U/Pu separation is undertaken, so that a mixed U/Pu product is obtained. Fluoride is added to the process feed to complex zirconium and suppress its extraction." The Dounreay plant in the UK employs a 20% TBP/OK solution and uses sulfuric acid to effect the U/Pu separation. TBP poorly extracts Pu or U from sulfuric acid solutions, but in mixed HNO3/H2SO4 the equilibria shown in equations (206) and (207) must be considered. The equilibrium constants for these reactions, Kj, and K i, are given... [Pg.954]

Mr A.P. Sy ( Jour. Amer. Chem. Soc., 1903) describes a new stability test for nitro-cellulose which he terms "The Elastic Limit of Powder Resistance to Heat." The test consists in heating the powder on a watch glass in an oven to a temperature of 115° C., after eight hours the watch glass and powder are weighed and the process repeated daily for six days or less. He claims that the powder is tested in its natural state, all the products of decomposition are taken into account, whilst in the old tests only the acid products are shown, and in the Will test only nitrogen, that it affords an indication of the effect of small quantities of added substances or foreign matters on the stability and that it is simple, and not subject to the variations of the old tests. [Pg.119]

Daily cholic acid production appeared to bear some relationship to body weight in a study in which the effect of butter and corn oil on the cholesterol metabolism was investigated. Thus the correlation coefficient between the average cholic acid production rate of each control subject and the average weight is 0.75 (73). [Pg.208]

Diastereoselective complexation of a chiral [antagonist] ketone with a racemic aluminium Lewis acid catalyst effectively removes one enantiomer of the latter, leaving the uncomplexed antipode free to function as a chiral Lewis acid. E Asym. heterodiene synthesis. 0.1 eq. D-3-bromocamphor, 1.05 eqs. startg. siloxydiene, and benzaldehyde added sequentially to 0.1 eq. of the racemic aluminium complex in degassed methylene chloride at —78°, stirred for 3 h, then subjected to acidic work-up (2S,3S)-product. Y 78% (e.e. 82%, upgraded to > 98% by one recrystallization with ca. 60% recovery). F.e.s. K. Maruoka, H. Yamamoto, J. Am. Chem. Soc. Ill, 789-90 (1989). [Pg.180]

Many aryhydrazones provide two or more isomers when subjected to the conditions of the Fischer indole cyclization. The product ratio and the direction of indolization can also be affected by different reaction conditions (i.e. catalysts and solvents), which is attributed, at least in part, to the relative stabilities of the two possible tautomeric ene-hydrazine intermediates. Generally, strongly acidic conditions favor formation of the least substituted ene-hydrazine, while cyclization carried out in weak acids favors the most substituted ene-hydrazine. Eaton s acid (10% P2O5 in MeSOsH) has been demonstrated to be an effective catalyst for the preparation of 3-unsubstituted indoles from methyl ketones under strongly acidic conditions. Many comprehensive reviews on this topic have appeared. ... [Pg.119]

Pyrimidinopyrazines related to folic acid have been investigated in some detail for their antimeta-bolic and antineoplastic activities. A related compound, which lacks one nitrogen atom, has been described as an antiproliferative agent, indicating it too has an effect on cell replication. Aldol condensation of the benzaldehyde 99 with ethyl acetoacetate gives the cinnamate 100. This is then reduced catalytically to the acetoacetate 101. Reaction of that keto ester with 2,4,6- triami-nopyrimidine gives the product 102 which is subsequently chlorinated (103) and subjected to hydrogenolysls. There is thus formed piritrexim (104) [17]. [Pg.169]


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See also in sourсe #XX -- [ Pg.141 ]




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Product effect

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Subjective effects

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