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Biological compounds

The reaction of the hydrated electron with biological molecules is of considerable importance to the radiobiologist for an understanding of the effect of radiation on living cells. [Pg.448]

Carbohydrates, like alcohols, are generally unreactive [64] (fe 10 1 mole sec ). Amino acids are relatively unreactive unless they contain a functional group which is reactive to eaq [62]. Deamination occurs as a result of electron capture by aliphatic amino acids [65], viz. [Pg.449]

However, amino acids containing the —SH group undergo preferential C—S bond fission. Proteins are complicated molecules having many groups present and their reactivity depends on the nature of such groups. [Pg.449]

In this account we shall restrict attention to the phenomenological aspects of the Mossbauer spectra, and neglect the deeper physiological viewpoint. Many of the earlier references have now been superseded by later data, and are accordingly omitted. [Pg.352]


W.S. Hancock, J.T. Sparrow, HPLC Analysis of Biological Compounds A Laboratory Guide, (Chromatographic Science Series, Vol 26), Marcel Dekker, New York, 1984. ISBN 0824771400. [Pg.48]

Barker, R., 1971. Organic Chemistry of Biological Compounds, Chap. 4. Englewood Cliffs, NJ Prentice-Hall. [Pg.106]

FIGURE 3-27 Three-dimensional chromatogram for oxidizable biological compounds at a multichannel amperometric detection system, consisting of an array of 16 carbon-paste electrodes held at different potentials. AA = ascorbic acid NE = norepinephrine DOPAC = 3,4-dihydroxyphenylacetic acid 5-HIAA = 5-hydroxyindole-3-acetic acid DA = dopamine HVA = homovanillic acid. (Reproduced with permission from reference 68.)... [Pg.94]

Chapter 19 ORGANIC CHEMISTRY II POLYMERS AND BIOLOGICAL COMPOUNDS... [Pg.12]

Comprehensive Organic Chemistry , Pergamon, Elmsford, NY, 1979, is a six-volume treatise on the synthesis and reactions of organic compounds. The first three volumes cover the various functional groups, vol. 4, heterocyclic compounds, and vol. 5, biological compounds such as proteins, carbohydrates, and lipids. Probably the most useful volume is vol. 6, which contains formula, subject, and author indexes, as well as indexes of reactions and... [Pg.1623]

Warner, D.T. (1962). Some possible relationships of carbohydrates and other biological compounds with water structure at 37°. Nature, 196, 1053-8. [Pg.129]

The type of data produced in a f.a.b. experiment is affected by the pH and ionic strength of the matrix. The former may be controlled either by the addition of acids or bases, although, in practice, it is usually preferable to keep the matrix acidic. The ionic strength is partly dictated by the purity of the sample (many biological compounds are still contaminated with salts, even after extensive purification) and partly by exogenous additives. Three additives are especially useful for carbohydrate work. They are as follows. [Pg.27]

HPLC Analysis of Biological Compounds A Laboratory Guide, William S. Hancock and James T Sparrow... [Pg.431]

In order to describe the problems of the nonlinear optical response from biological systems, the question of chirality must be addressed. Linear circular dichroism (CD) has been investigated extensively for biological compounds and a wealth of data are available on... [Pg.143]

Chen, L.A., Carbonell, R.G., and Serad, G.A., Recovery of proteins and other biological compounds using fibrous materials I adsorption by salt addition, /. Chem. Technol. Biotechnol., 74, 733, 1999. [Pg.137]

The Functional Value of the Elements in Organisms Introduction to Biological Compounds... [Pg.137]

Bu Lock JD (1979) Biological Compounds. In Barton DHR, Ollis WD (eds) Comprehensive Organic Chemistry, Pergamon Press, New York vol. 5, p 927... [Pg.118]


See other pages where Biological compounds is mentioned: [Pg.17]    [Pg.164]    [Pg.22]    [Pg.336]    [Pg.171]    [Pg.151]    [Pg.873]    [Pg.874]    [Pg.894]    [Pg.899]    [Pg.160]    [Pg.396]    [Pg.21]    [Pg.192]    [Pg.235]    [Pg.5]    [Pg.417]    [Pg.823]    [Pg.824]    [Pg.7]    [Pg.35]    [Pg.233]    [Pg.61]    [Pg.64]    [Pg.125]    [Pg.210]   
See also in sourсe #XX -- [ Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 , Pg.114 ]




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Addition reactions biologically active compounds

Antioxidant Efficiency of Hyaluronan and other Biologically Active Compounds as Potential Products for Aesthetic Medicine

Antioxidants Compounds that prevent biologically active

Aromatic compound biological hydroxylation

Asymmetric reactions biologically active compounds involving

Biological Activity of Organic Compounds

Biological Effects of Reduced Oxygen Compounds

Biological Properties of Compounds

Biological Systems Metalloproteins and Related Model Compounds

Biological Transformation of Nitrogen Compounds

Biological active compounds

Biological active compounds asymmetric synthesis

Biological active compounds stereoselectivity

Biological active compounds steric effects

Biological activity, of organotin compounds

Biological chemistry lead compounds

Biological compounds carbohydrates

Biological compounds, fluorescence

Biological compounds, fluorescence analysis

Biological interphases compounds

Biological model compounds

Biological systems organic compounds

Biological systems, phosphorus compounds

Biologically active compounds

Biologically active compounds analogue generator

Biologically active compounds databases

Biologically active compounds through

Biologically active compounds through bioreduction

Biologically active compounds, configuration

Biologically active compounds, design

Biologically active compounds, nuclei

Biologically active compounds, nuclei location

Biologically active quinoline compounds

Biologically available organic compounds

Biologically important compounds

Biologically important compounds alcohols

Biologically important compounds indoles

Biologically important compounds nucleotides

Biologically important compounds phenols

Biologically important compounds purines

Biology coordination compounds

Biology of the Compounds

Carbonyl compounds biological

Compounds Showing Various Biological Activities

Compounds for Iron in Biological Systems

Compounds with Biological Activity

Compounds, biological data

Coordination compounds biologic

Coordination compounds biological importance

Coordination compounds biological systems

Decay rates biological compounds

Growth inhibiting compounds biological activity

Heck reaction biologically active compounds applying

Henry biologically active compounds

Iron compounds biological activities

Isomerism biological compounds

Lead compounds biological activity

Lead compounds biological information

Lead compounds molecular biology

Magnolia biologically active compounds

Mercury compounds biological effects

Micelles interactions with biological compounds

Monofunctional Epoxides as Chiral Building Blocks for the Synthesis of Biologically Active Compounds

Natural Products and Biologically Active Compounds

Natural product synthesis large biologically active compounds

Nitrogen compounds biological transformations

ORGANIC CHEMISTRY II POLYMERS AND BIOLOGICAL COMPOUNDS

Oligomeric compound biological activity

Organic compounds biological macromolecules (

Organogermanium compounds biological activity

Organolead compounds biological activity

Organometallic Compounds in Biological Chemistry

Organometallic compounds interactions with biological

Organotin compounds biological activity

Organotin compounds interactions with biological

Other Iron Compounds of Biological Interest

Other Strategies to Construct Biologically Active Compounds

Oxidation-reduction potential, biological compounds

Palladium compounds biological applications

Reduced oxygen compounds, biological

Reduced oxygen compounds, biological effects

Schmidt Rearrangements of Hydroxyalkyl Azides toward Biologically Relevant Compounds

Section 3 Biological Compounds

Selenium compounds, biological methylation

Silver compounds biology

Sources of Compounds for Biological Screening

Stereoselectivity in biologically active compounds

Study 6.26 Biology photoactivatable compounds

Submitting Compounds for Biological Testing

Sulfur compounds biological oxidation

Supramolecular Host Recognition Processes with Biological Compounds, Organometallic Pharmaceuticals, and Alkali-metal Ions as Guests

Syntheses of Heterocycles, Natural Products, and Other Biologically Active Compounds Applying Heck Reactions

Syntheses of natural products and biologically active compounds

Synthesis of Biologically Active Compounds via Allylic Substitution

The Influence of Vanadium Compounds on Biological Systems

Vanadium Compounds on Biological Systems Cellular Growth, Oxidation-Reduction Pathways, and Enzymes

Volatile compounds, biological

Volatile compounds, biological treatment

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