A new class of inhibitors of human leucocyte elastase.

Abstract:

:Studies of the inhibition of elastases at a molecular level have resulted in the identification of protected dipeptides which are reversible and highly specific inhibitors of human leucocyte elastase (HLE). These have been further developed by increasing their hydrophilicity and potency to give a new family of elastase inhibitors, typically N alpha-(1-adamantanesulphonyl)-N epsilon-(4-carboxybenzoyl)-L-lysyl-L-alanyl-L-valinal. These compounds are active in pharmacological models designed to detect compounds of potential therapeutic value in the treatment of emphysema.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Hassall CH,Johnson WH,Kennedy AJ,Roberts NA

doi

10.1016/0014-5793(85)80776-6

subject

Has Abstract

pub_date

1985-04-22 00:00:00

pages

201-5

issue

2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(85)80776-6

journal_volume

183

pub_type

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