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Acidizing alteration

Reflux 1 g. of the sulphonamide with 2-5 ml. of acetyl chloride for 30 minutes if solution is not complete within 5 minutes, add up to 2-5 ml. of glacial acetic acid. Remove the excess of acetyl chloride by distillation on a water bath, and pour the cold reaction mixture into water. Collect the product, wash with water and dissolve it in warm sodium bicarbonate solution. Acidify the Altered solution with glacial acetic acid Alter oflF the precipitated sulphonacetamide and recrystaUise it from aqueous alcohol. [Pg.555]

Figure 38-4. Examples of three types of missense mutations resulting in abnormal hemoglobin chains. The amino acid alterations and possible alterations in the respective codons are indicated. The hemoglobin Hikari p-chain mutation has apparently normal physiologic properties but is electrophoretically altered. Hemoglobin S has a p-chain mutation and partial function hemoglobin S binds oxygen but precipitates when deoxygenated. Hemoglobin M Boston, an a-chain mutation, permits the oxidation of the heme ferrous iron to the ferric state and so will not bind oxygen at all. Figure 38-4. Examples of three types of missense mutations resulting in abnormal hemoglobin chains. The amino acid alterations and possible alterations in the respective codons are indicated. The hemoglobin Hikari p-chain mutation has apparently normal physiologic properties but is electrophoretically altered. Hemoglobin S has a p-chain mutation and partial function hemoglobin S binds oxygen but precipitates when deoxygenated. Hemoglobin M Boston, an a-chain mutation, permits the oxidation of the heme ferrous iron to the ferric state and so will not bind oxygen at all.
This type of mixing could reasonably explain the occurrence of acidic alteration minerals such as kaolinite and alunite in the low-sulfidation epithermal gold vein district (e.g., Seta in northeast Hokkaido, Hishikari in southern Kyushu) (Yajima et al., 1997)... [Pg.175]

Yoneda, T. and Shirahata, H. (1995) Acid alteration associated with Kuroko-type mineralization and Sr isotope study of hydrothermal alteration at the Minamishiraoi barite deposit, southwestern Hokkaido, Japan. Resource Geology Special Issue, 18, 203-210. [Pg.293]

Gena et al. (2001) reported advanced argillic alteration of basaltic andesite from the Desmos caldera, Manus back-arc basin which was caused by interaction of hot acid hydrothermal fluid originated from a mixing of magmatic gas and seawater. It is noteworthy that the acid alteration is found in back-arc basins (Manus, Kuroko area) but not in midoceanic ridges. [Pg.359]

Another phenolic compound, caffeic acid, altered the mineral content of Argyrodendron trlfoliolatum after 6 months (25). Zn2+,... [Pg.165]

R. (1992). Retinoic acid alters hindbrain Hox code and induces transformation of rhombomeres 2/3 into a 4/5 identity. Nature 360 737-741. [Pg.122]

Dobson CL, Davis SS, Chauhan S, Sparrow RA, Wilding IR. Does the site of intestinal delivery of oleic acid alter the ileal brake response . Int J Pharm 2000 195 63-70. [Pg.121]

Guffy, M. M., North, J. A., and Bums, C. P., 1984, Effect of cellular fatty acid alteration on adriamycin sensitivity in cultured L1210 murine leukemia cells, Cancer Res. 44 1863-1866. [Pg.118]

Single-site amino acid alterations were carried out to show that mutations in the T1 domain loop region disrupt p subunit binding to the a subunit and abolish inactivation. Similar mutations on the p subunit surface that contacts the T1 domain also affected inactivation. The conclusion is that both subunits are necessary for inactivation peptides to carry out their function. [Pg.213]

An entirely different property of subtilisin was affected by substituting leucine at the 222 location. Native BPN is extremely sensitive to the presence of oxidation agents, showing rapid inactivation when incubated in the presence of 0.3% H2O2 (Figure 4). The Leu-222 variant, in contrast, was found to be totally stable under the same oxidation conditions. The data clearly show that single amino acid alterations can have dramatic effects upon the activity of the enzyme. Similarly, other changes have been shown to affect catalytic properties, substrate specificities and thermostability (7,2,9). [Pg.87]

The initial report within this area described the regiospecific alkylation of pyrroles using imidazolidinone 12 (20 mol%) as the catalyst [82]. A mixture of THF and water provided optimal reaction conditions, but low temperatures (-60 °C to -30 °C) were required to ensure the chemospecificity of the reaction. The functional group tolerance at the P-position of the substrate and A-substitution on the pyrrole nucleophile was explored (Scheme 15). It was noticed that subtle changes in the nature of the co-acid altered selectivities and this had to be modified depending on the substrates adopted. [Pg.296]

Li, Y. and Watkins, B.A. 1998. Conjugated linoleic acids alter bone fatty acid composition and reduce ex vivo prostaglandin E2 biosynthesis in rats fed n-6orn-3 fatty acids. Lipids 33 417-425. [Pg.451]

Kelley, D.S., Nelson, G.J., Love, J.E., Branch, L.B., Taylor, P.C., Schmidt, P.C., Mackey, B.E., and Iacono, J.M. 1993. Dietary alpha-linolenic acid alters tissue fatty acid composition, but not blood lipids, lipoproteins or coagulation status in humans. Lipids 28, 533-537. [Pg.84]

Cowles, R.L., Lee, J.-Y., Gallaher, D.D., Stuefer-Powell, C.L., and Carr, T.P. 2002. Dietary stearic acid alters gallbladder bile acid composition in hamsters fed cereal-based diets. J. Nutr. 132, 3119-3122. [Pg.195]

Allison, S. D. (2006b). Soil minerals and humic acids alter enzyme stability Implications for ecosystem processes. Biogeochemistry. 81, 361-373. [Pg.96]

Peptide mapping is a method that enables the determination of protein identity when compared to a standard. When compared to previous lots of the same product, it serves to determine the stability of the protein s primary sequence, which in turn reflects the genetic stability of the producer cells. This method is capable of detecting small differences between proteins in one or more amino acids. The detection will be dependent upon an amino acid alteration affecting the observed peptide profile (Figure 13.1 see color section). [Pg.337]

Chouinard, P.Y., Corneau, L., Barbano, D.M., Metzger, L.E., Bauman, D.E. 1999a. Conjugated linoleic acids alter milk fatty acid composition and inhibit milk fat secretion in dairy cows. /. Nutr. 129, 1579-1584. [Pg.127]

Lock, A.L., Horne C.A.M., Bauman D.E., Salter A.M. 2005b. Butter naturally enriched in conjugated linoleic acid and vaccenic acid alters tissue fatty acids and improves the plasma lipoprotein profile in cholesterol-fed hamsters. J. Nutr. 135, 1934—1939. [Pg.131]

Observed that iron in cone, nitric acid altered in its properties Suggested the state of iron in cone. HNO3 as passivity... [Pg.5]

CYP2C9 Amino acid Altered Km Warfarin Excessive bleeding... [Pg.208]


See other pages where Acidizing alteration is mentioned: [Pg.315]    [Pg.143]    [Pg.350]    [Pg.113]    [Pg.195]    [Pg.200]    [Pg.181]    [Pg.156]    [Pg.29]    [Pg.187]    [Pg.615]    [Pg.231]    [Pg.162]    [Pg.238]    [Pg.345]    [Pg.137]    [Pg.170]    [Pg.152]    [Pg.136]    [Pg.224]    [Pg.529]    [Pg.23]    [Pg.259]    [Pg.58]    [Pg.250]    [Pg.251]    [Pg.251]   
See also in sourсe #XX -- [ Pg.39 ]

See also in sourсe #XX -- [ Pg.39 ]




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Alteration of fatty acid profile

Altering Lewis acidic site

Amino-acid sequence alteration

Fatty acid chain length, alteration

Hyaluronic acid altered

White solid acidity, alterations

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