The synthesis and biological evaluation of a new class of selective irreversible cysteine protease inhibitors is described. A set of amino acid based chloromethyl sulfoxides was prepared and they were found to inhibit irreversibly the cysteine protease papain. They were selective for cysteine proteases since no inhibition was found for the serine protease chymotrypsin
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN1159 / BLDSC - British Library Do...
SummaryThe papain-family cathepsins are cysteine proteases that are emerging as promising therapeuti...
The development of a new class of cysteine protease inhibitors utilising the thiosulfonate moiety as...
The synthesis and biological evaluation of a new class of selective irreversible cysteine protease i...
AbstractA series of new inhibitors for cysteine proteinases with the general structure Z-Phe-Gly-NHO...
We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic ...
We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic ...
The development of new protease inhibitors is always expanding for active therapies against diseases...
The natural product dephostatin and its unsubstituted analog N-methyl-N-nitroso-aniline were identif...
a-Amino-a´-halomethylketones are interesting scaffolds bearing (at least) two sequential electrophil...
Analogues of the irreversible protease inhibitors TPCK and TLCK have been synthesized and tested as ...
a-Amino-a´-halomethylketones are interesting scaffolds bearing (at least) two sequential electrophil...
Cysteine proteases are crucial regulatory enzymes in human physiology and disease. Inhibitors are us...
Full text of this article is not available in SOAR.The existence of subtle differences in the Sn' su...
AbstractThe three-membered ring of aziridine-2-carboxylic acid, which is susceptible to opening by n...
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN1159 / BLDSC - British Library Do...
SummaryThe papain-family cathepsins are cysteine proteases that are emerging as promising therapeuti...
The development of a new class of cysteine protease inhibitors utilising the thiosulfonate moiety as...
The synthesis and biological evaluation of a new class of selective irreversible cysteine protease i...
AbstractA series of new inhibitors for cysteine proteinases with the general structure Z-Phe-Gly-NHO...
We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic ...
We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic ...
The development of new protease inhibitors is always expanding for active therapies against diseases...
The natural product dephostatin and its unsubstituted analog N-methyl-N-nitroso-aniline were identif...
a-Amino-a´-halomethylketones are interesting scaffolds bearing (at least) two sequential electrophil...
Analogues of the irreversible protease inhibitors TPCK and TLCK have been synthesized and tested as ...
a-Amino-a´-halomethylketones are interesting scaffolds bearing (at least) two sequential electrophil...
Cysteine proteases are crucial regulatory enzymes in human physiology and disease. Inhibitors are us...
Full text of this article is not available in SOAR.The existence of subtle differences in the Sn' su...
AbstractThe three-membered ring of aziridine-2-carboxylic acid, which is susceptible to opening by n...
SIGLEAvailable from British Library Document Supply Centre- DSC:DXN1159 / BLDSC - British Library Do...
SummaryThe papain-family cathepsins are cysteine proteases that are emerging as promising therapeuti...
The development of a new class of cysteine protease inhibitors utilising the thiosulfonate moiety as...