Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Side chains significance

Unlike penicillins and cephalosporins, which have a side aminoacyl group joined to the beta-lactam ring, imipenem has a a-hydroxyethyl side chain. Significant resistance to hydrolysis by beta-lactamases is observed in this compound, evidently thanks to the fran -configuration of the side chain, while the side chain of penicillins and cephalosporins have a cis-configuration. [Pg.464]

We can see that there is a breadth of substitution that offers good activity against aphids in this primary screen. Furthermore, if one chooses an amide side chain, significant non-aphicidal activity comes into the spectrum. Choosing among these compounds required more advanced tests. [Pg.329]

The free acids cannot be analyzed by GC-MS in the case of trace analysis. They are determined using the methyl ester (Figures 3.110-3.112). If the aromatic character predominates, intense molecular ions occur in the upper mass range. Increasing the length of the side chains significantly reduces the intensity of the molecular... [Pg.446]

A significant fraction of the body s cholesterol is used to form bile acids Oxidation m the liver removes a portion of the CsHi7 side chain and additional hydroxyl groups are intro duced at various positions on the steroid nucleus Cholic acid is the most abundant of the bile acids In the form of certain amide derivatives called bile salts, of which sodium tau rocholate is one example bile acids act as emulsifying agents to aid the digestion of fats... [Pg.1097]

Tocotrienols differ from tocopherols by the presence of three isolated double bonds in the branched alkyl side chain. Oxidation of tocopherol leads to ring opening and the formation of tocoquinones that show an intense red color. This species is a significant contributor to color quaUty problems in oils that have been abused. Tocopherols function as natural antioxidants (qv). An important factor in their activity is their slow reaction rate with oxygen relative to combination with other free radicals (11). [Pg.124]

Uses. Vinyhdene fluoride is used for the manufacture of PVDF and for copolymerization with many fluorinated monomers. One commercially significant use is the manufacture of high performance fluoroelastomers that include copolymers of VDF with hexafluoropropylene (HFP) (62) or chlorotrifluoroethylene (CTFE) (63) and terpolymers with HEP and tetrafluoroethylene (TEE) (64) (see Elastomers, synthetic-fluorocarbon elastomers). There is intense commercial interest in thermoplastic copolymers of VDE with HEP (65,66), CTEE (67), or TEE (68). Less common are copolymers with trifluoroethene (69), 3,3,3-trifluoro-2-trifluoromethylpropene (70), or hexafluoroacetone (71). Thermoplastic terpolymers of VDE, HEP, and TEE are also of interest as coatings and film. A thermoplastic elastomer that has an elastomeric VDE copolymer chain as backbone and a grafted PVDE side chain has been developed (72). [Pg.386]

Deriva.tives, The most important derivatives of 1,2,3,4-benzenetetrol are the ubiquiaones, eg, coenzyme Q, which are dimethoxytoluquiaones with polyisoprenoid side chains (61). They occur ia plants and animals. Mice with hereditary muscular dystrophy have a deficiency of coenzyme Q ia their heart and hind leg muscles. Therapeutic adrninistration of coenzyme Q /7339-63-5] produces physical improvement and a significantly prolonged lifespan (212). Coenzyme Q also has been used to treat deafness when adrninistered either orally or parenteraHy (213). [Pg.387]

The importance of quinones with unsaturated side chains in respiratory, photosynthetic, blood-clotting, and oxidative phosphorylation processes has stimulated much research in synthetic methods. The important alkyl- or polyisoprenyltin reagents, eg, (71) or (72), illustrate significant conversions of 2,3-dimethoxy-5-methyl-l,4-ben2oquinone [605-94-7] (73) to 75% (74) [727-81-1] and 94% (75) [4370-61-0] (71—73). [Pg.412]

Benzotrichloride is produced from total side-chain chlorination of toluene or of residual products from benzyl chloride production. In Western Europe, Bayer has the largest capacity (14,000 t/yr), and there are only two significant producers in the United States Occidental Chemical in Niagara EaUs, New York (20,000 t/yr), and Velsicol Chemical (11,000 t/yr). Total capacity in the western world is 68,000 t/yr and production of benzotrichloride in 1988 was estimated at 31,500 t. [Pg.60]

The acylation of 6-APA (Scheme 59) has been a very versatile way in which to generate new penicillin derivatives which differ from fermentation-produced penicillins in the 6-side chain. As will be discussed in Section 5.11.5.1, this approach has led to significant improvements in the therapeutic properties of penicillins, and, in fact, of the penicillins in medical use today, only benzylpenicillin and phenoxymethylpenicillin are produced directly by fermentation. [Pg.330]

A second example is that of an Ala-to-Cys mutation, which causes the fonnation of a rare SH S hydrogen bond between the cysteine and a redox site sulfur and a 50 mV decrease in redox potential (and vice versa) in the bacterial ferredoxins [73]. Here, the side chain contribution of the cysteine is significant however, a backbone shift can also contribute depending on whether the nearby residues allow it to happen. Site-specific mutants have confirmed the redox potential shift [76,77] and the side chain conformation of cysteine but not the backbone shift in the case with crystal structures of both the native and mutant species [78] the latter can be attributed to the specific sequence of the ferre-doxin studied [73]. [Pg.407]


See other pages where Side chains significance is mentioned: [Pg.127]    [Pg.265]    [Pg.405]    [Pg.91]    [Pg.42]    [Pg.35]    [Pg.325]    [Pg.1067]    [Pg.1422]    [Pg.127]    [Pg.265]    [Pg.405]    [Pg.91]    [Pg.42]    [Pg.35]    [Pg.325]    [Pg.1067]    [Pg.1422]    [Pg.530]    [Pg.559]    [Pg.99]    [Pg.237]    [Pg.275]    [Pg.166]    [Pg.42]    [Pg.154]    [Pg.202]    [Pg.29]    [Pg.28]    [Pg.66]    [Pg.68]    [Pg.488]    [Pg.43]    [Pg.4]    [Pg.52]    [Pg.301]    [Pg.15]    [Pg.74]    [Pg.287]    [Pg.288]    [Pg.288]    [Pg.294]    [Pg.314]    [Pg.372]    [Pg.399]    [Pg.402]    [Pg.446]    [Pg.16]    [Pg.90]   
See also in sourсe #XX -- [ Pg.69 , Pg.70 , Pg.71 , Pg.72 , Pg.73 , Pg.74 , Pg.75 ]




SEARCH



© 2024 chempedia.info