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Adenosine deaminase (ADA, EC 3.5.4.4) catalyses the irreversible deamination of adenosine and 2'-deoxyadenosine to inosine and 2'-deoxyinosine, respectively. In this study the inhibition of ADA from bovine spleen by several molecules with structure related to that of the substrate or product has been quantified. The inhibitors adenine, purine, inosine, 2-aminopurine, 4-aminopyrimidine, 4-aminopyridine, 4-hydroxypyridine and phenylhydrazine are shown to be competitive inhibitors with KI (mM) values of 0.17, 1.1, 0.35, 0.33, 1.3, 1.8, 1.4 and 0.25, respectively. Synergistic inhibition by various combinations of molecules that imitate the structure of the substrate has never been observed. Some general conclusions are: i) the enzyme ADA from bovine spleen we have used is appropriate for kinetic studies of inhibition and mechanistic studies; it can be a reference catalytic system for the homogeneous comparison of various inhibitors; ii) this enzyme presents very rigid requirements for binding the substrate: variations in the structure of adenosine imply the loss of important interactions. [ABSTRACT FROM AUTHOR]

Abstract: Zirconium phosphates methyl and/or phenyl phosphonates-supported l-proline have been prepared as amorphous solids by precipitation of (4R)-4-(phosphonooxy)-l-proline, methyl and/or phenyl phosphonic acid with ZrOCl2. The supported l-proline catalysts were tested on the direct asymmetric aldol addition of cyclohexanone to p-nitrobenzaldehyde in DMF/H2O (9:1) and in sole water. The hydrophobic groups on solid surface favor reagents’ diffusion toward proline chiral moiety increasing the catalytic activity of supported l-proline. High diastereoselectivity (anti/syn up to 94:6) and high enantiomeric excess up to 97% have been obtained. [Copyright &y& Elsevier]

Abstract: New zirconium hydrogen phosphate alkyl and/or aryl phosphonates of general formula Zr(PO3OH)2−( x + y )(PO3R) x (PO3R1) y have been prepared as amorphous solids. The presence of hydrophobic groups such as Me, Ph and Pr and their percentage have an important role in the definition of the corresponding solid structure. All the prepared solids are micro- and mesoporous and show an extraordinary surface area (200–380m2/g). The Brønsted acid catalytic activity of the solids was tested on the direct aza-Diels–Alder reaction of 2-cyclohexen-1-one with N-PMP-pCl-benzaldimine in aqueous medium. The hydrophobic groups on the solid catalyst surface favor reagents’ diffusion toward the acidic sites, aiding proton transfer to reagents, increasing the catalytic activity of the prepared solids compared with the layered α-zirconium hydrogen phosphate (α-ZrP). [ABSTRACT FROM AUTHOR]

Abstract: The aza-Diels–Alder reaction between benzaldimines 1 and Danishefsky''s diene in solvent-free conditions is reported for the first time. The reaction occurs rapidly at 30°C and is catalyzed by porous α-zirconium hydrogen phosphate (p-αZrP) in the presence of sodium dodecyl sulfate (SDS). The yields were excellent. The recycling of the catalyst has also been investigated. [Copyright &y& Elsevier]