| Literature DB >> 2788271 |
M A Hussain1, A B Shenvi, S M Rowe, E Shefter.
Abstract
alpha-Aminoboronic acid derivatives, potent and reversible inhibitors of aminopeptidases, were tested nasally in situ in rats for stabilizing externally administered peptides. These inhibitors, at nanomolar concentrations, were found to inhibit greatly the degradation of the model peptide, leucine-enkephalin (Leu-enk) in the nasal perfusate. Enzyme inhibition was greater with boroleucine and borovaline than that observed with boroalanine. Boroleucine was more than 100 times more effective in enzyme inhibition than bestatin and more than 1000 times more effective than puromycin.Entities:
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Year: 1989 PMID: 2788271 DOI: 10.1023/a:1015949013644
Source DB: PubMed Journal: Pharm Res ISSN: 0724-8741 Impact factor: 4.200