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Glycine sodium salt

Figure 2 Stability of /3-poly(L-malate) measured by its activity to inhibit purified DNA polymerase a of P. polyceph-alum. The relative degree of inhibition is shown (100 rel. units refer to complete inhibition). The DNA polymerase assay was carried out in the presence of 5 /tg/ml /S-poly(L-malate) as described [4]. The polymer was preincubated for 7 days at 4°C in the following buffer solutions (50 mM) KCl/HCl (—A—). Citrate (—V—). 2-(A/-Morpholino)-ethanesulfonic acid, sodium salt (—O—). Sodium phosphate (— —). N-(2-Hydroxyethyl)piperazine-N -(2-ethanesul-fonic acid), sodium salt (— — ). N,N-b s (2-Hydroxyethyl)-glycine, sodium salt (—T—). Tris/HCl (— —). 3-(Cyclo-hexylamino)-l-propanesulfonic acid, sodium salt (— —). Figure 2 Stability of /3-poly(L-malate) measured by its activity to inhibit purified DNA polymerase a of P. polyceph-alum. The relative degree of inhibition is shown (100 rel. units refer to complete inhibition). The DNA polymerase assay was carried out in the presence of 5 /tg/ml /S-poly(L-malate) as described [4]. The polymer was preincubated for 7 days at 4°C in the following buffer solutions (50 mM) KCl/HCl (—A—). Citrate (—V—). 2-(A/-Morpholino)-ethanesulfonic acid, sodium salt (—O—). Sodium phosphate (— —). N-(2-Hydroxyethyl)piperazine-N -(2-ethanesul-fonic acid), sodium salt (— — ). N,N-b s (2-Hydroxyethyl)-glycine, sodium salt (—T—). Tris/HCl (— —). 3-(Cyclo-hexylamino)-l-propanesulfonic acid, sodium salt (— —).
D(-)-4-hydr6xy N-(2-methoxycorbonyf-1 -methylethenyl)phenyl-glycine sodium salt... [Pg.387]

SYNS N,N-BIS(CARBOXYMETHYL)GLYCINE SODIUM SALT GLYCINE, N,N-BIS(CARBOXYMETHYL)-, SOD-... [Pg.1241]

N-Methyl-N-(l-oxododecyl) glycine, sodium salt. See Sodium lauroyl sarcosinate 2-[Methyl (1-oxohexadecyl) amino] ethanesulfonic acid, sodium salt. See Sodium methyl palmitoyl taurate 2-[Methyl (1-oxo-9-octadecenyl) amino] ethanesulfonic acid, sodium salt. See Sodium methyl oleoyl taurate... [Pg.2666]

Sodium 4-[2,4-dihydroxy-3-(2,4-dimethylphenylazo) phenylazo] benzenesulfonate. See Acid orange 24 Sodium dihydroxyethylglycinate CAS 139-41-3 EINECS/ELINCS 205-360-4 Synonyms Bicine N,N-Bis (2-hydroxyethyl) glycine, monosodium salt N,N-Bis (2-hydroxyethyl) glycine, sodium salt DHEG DHEGNa... [Pg.4015]

N-Methyl N>(1 OXododecyl) glycine, sodium salt See Sodium lauroyl sarcosinate... [Pg.2215]

Synonyms Glycine,N-methyl-N-(1-oxotetradecyl)-, sodium sail (9Ci) N-Melhyi-N-(1-oxotetradecyl) glycine, sodium salt Sodium N-melhyi-N-(1-oxoletrade(yi) ami-noacetate... [Pg.2447]

Mammalian bile contains sodium salts of conjugated bile acids, e.g. glycocholic acid and taurocholic acid, in which cholic acid is combined (amide linkage) with glycine and taurine respectively. [Pg.96]

Bouchonnet, S., and Y. Hoppiliard. 1992. Proton and Sodium Ion Affinities of Glycine and Its Sodium Salt in the Gas Phase. Ab Initio Calculations. Qrg. Mass Spectrometry 27, 71-76. [Pg.143]

Flavour Enhancer 640 Glycine and its sodium salt Ace 25th p 16 Not evaluated... [Pg.276]

Excessive activity of the enzyme aldose reductase sometimes accompanies diabetes. The net result is often accumulation of reduced sugars such as galactose in the lens of the eye and ensuing cataract formation. A1 restatin (43), an aldose reductase inhibitor, is one of the first agents found that holds promise of preventing diabetes-induced cataracts. The compound, actually used as its sodium salt, is prepared in straightforward manner by imide formation between 1,8-naphthalic anhydride (41) and glycine. ... [Pg.1121]

The second way differs from the first in that the methylation of nitrogen is accomphshed before the cyclocondensation reaction. In order to do this, the initial 2-amino-5-chlorobenzo-phenone is first tosylated by p-toluenesulfonylchloride and the obtained tosylate (5.1.3) transformed into the N-sodium salt, which is then alkylated by dimethylsulfate. The resulting 2-A -tosyl-A -methyl-5-chlorobenzophenone (5.1.4) is hydrolyzed in an acidic medium, giving 2-methylamino-5-chlorobenzophenone (5.1.5), which undergoes cyclocondensation by reaction with ethyl ester of glycine hydrochloride, forming the desired diazepam (5.1.2) [1-5]. [Pg.71]

For quantitative estimation, a sealed reusable capillary tube, with a known quantity of sodium salt of trimethylsilyl propionic acid (TSP) dissolved in 35 pi of D20, is inserted into the NMR tube while obtaining NMR spectra. The internal standard TSP is used as a chemical shift reference as well as a quantitative standard for the estimation of metabolites, and D20 is used as the field-frequency-lock . Spectra are acquired at room temperature. Typical spectra acquired at room temperature of human bile and standard glycine- and taurine-conjugated BAs are shown in Fig. 5.4.16. [Pg.653]

Ames and Ribeira (75JCS(Pl)1390) described a method for the preparation of thieno[2,3-c]pyridin-7-ones (Scheme 68). The sodium salt of 3-bromothiophene-2-carboxylic acid reacts with carbanions in the presence of copper or copper(II) acetate to give condensation products (274) by displacement of bromide ion, often with simultaneous deacetylation. Cyclization of (274) provides a convenient route to thieno[2,3-c]pyridin-7-ones. Thieno[2,3-c]pyridin-4-ones and thieno[3,2-c]pyridin-7-ones have been prepared by Friedel-Crafts cyclization of AT-(2-thenyl)- and A-(3-thenyl)-glycine derivatives (81H(l6)127l). [Pg.1007]

Vanilloylglycine, feruloylglycine and /w-coumaric acid glucuronide are identified after oral administration of caffeic acid to humans [15], Intraperitoneal injection of the sodium salt of caffeic acid to rats also produces these conjugates. Thus, conjugation with glycine or glucuronic acid in body tissues is demonstrated. [Pg.923]

The bile acids are usually conjugated to the amino acids, glycine or taurine, as shown for the formation of glycocholate in figure 20.21. It is in this form that the bile acids are secreted via the gallbladder into the intestine where they are critically important for the solubilization of dietary lipids. At pH 7, these acids exist as the sodium salts and are often referred to as bile salts. Of course in the acidic environment of the small intestine, they occur largely in their acidic form. [Pg.475]

Parenthetically, DNA is a fibrous sodium salt of double-stranded ribose-poly-phosphate covalently bonded to precise sequences of the four nucleotides adenine (A), thymine (T), glycine (G), and cytosine (C), with intemu-cleotide hydrogen bonds connecting the two strands, and which, in trios, form one bit of the genetic code. [Pg.252]

SYNS N,N-BIS(CARBOXYMETHYL)GLYCINE TRISODIUM SALT MONOHYDRATE NCI-C01445 NITRILOACETIC ACID TRISODIUM SALT MONOHYDRATE NTA SODIUM HYDRATE TRISODIUM NITRILOTRIACETATE MONOHYDRATE... [Pg.1003]

N-(Phenyl - p - arsinic acid)- glycine - 4 - acetylaminobenzyl-amide,AsO(OH)a.C8H4.NH.CHa.CO.NH.CH2.C8H4.NH.CO.CHs, occurs in flat, microscopic needles, which remain unmelted at 280° C. From 50 per cent, alcohol it deposits diamond-shaped plates. It forms a sodium salt, crystallising in microscopic needles, containing 4j molecules of water of crystallisation. [Pg.235]

N -(Phenyl -p -arsinic acid) - glycine-3 -methyl -4 -acetylamino -benzylamide, AsO(OH)2.CeH4.NH.CH2.CO.NH.CHa.C6H3(CH3)(NH. CO.CH3), is deposited in flat minute needles from 50 per cent, sdcohol. When rapidly heated it decomposes at 278° C. The sodium salt yields mioroscopie needles from 85 per cent, alcohol. [Pg.236]

N-(Phenyl-p-arsinic acid) - glycine - a - aminopropionamide, AsO(OH)2.C 4.NH.CH(CHs).CO.NHa, is obtained by employing a-bromopropionamide in the condensation. From water or hot 50 per cent, alcohol, thin hexagonal plates are deposited, darkening at 255° C. and decomposing at 262° to 263-6° C. The sodium salt forms flat, microscopic needles, containing about 2 - molecules of water. [Pg.236]


See other pages where Glycine sodium salt is mentioned: [Pg.70]    [Pg.175]    [Pg.1540]    [Pg.83]    [Pg.1932]    [Pg.4029]    [Pg.4053]    [Pg.4073]    [Pg.150]    [Pg.6]    [Pg.70]    [Pg.175]    [Pg.1540]    [Pg.83]    [Pg.1932]    [Pg.4029]    [Pg.4053]    [Pg.4073]    [Pg.150]    [Pg.6]    [Pg.196]    [Pg.40]    [Pg.260]    [Pg.270]    [Pg.534]    [Pg.39]    [Pg.289]    [Pg.112]    [Pg.68]    [Pg.57]    [Pg.430]    [Pg.433]    [Pg.433]    [Pg.205]    [Pg.235]   
See also in sourсe #XX -- [ Pg.149 ]




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