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The Design And Synthesis Of New Oxazole Ring Functional Groups Of Carboxypeptidase A Inhibitor

Posted on:2006-09-05Degree:MasterType:Thesis
Country:ChinaCandidate:C H JinFull Text:PDF
GTID:2191360155476071Subject:Organic Chemistry
Abstract/Summary:PDF Full Text Request
On the basis of the active site topology and enzymic catalytic mechanism of carboxypeptidase-A(CPA),2-benzyl-3-(2-oxo-2,3-dihydrooxazol-5-yl)propanoic acid and 2-benzyl-4-oxo-5-(pyridine-1-yl)pentanoate was designed as a novel type of inactivator. In the designing, the unique property of the oxazolone heterocycle was exploited as a latent inactivating species, the inhibitor were synthesized from succinic anhydride.The reduction of Δ7-6-keto-ergostane with Na2S2O4 in the presence of a phase transfer catalyst & Li in the presence liquid NH3 & Pd/C is performed and the effect of experimental conditions is discussed.
Keywords/Search Tags:Carboxypeptidase-A, oxazol, reduction
PDF Full Text Request
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