Inhibitors of BMP ‐1/tolloid‐like proteinases: efficacy, selectivity and cellular toxicity
نویسندگان
چکیده
منابع مشابه
HIV protease inhibitors: a review of molecular selectivity and toxicity
Highly active antiretroviral therapy (HAART) is recognized as the most effective treatment method for AIDS, and protease inhibitors play a very important role in HAART. However, poor bioavailability and unbearable toxicity are their common disadvantages. Thus, the development of safer and potentially promising protease inhibitors is eagerly needed. In this review, we introduced the chemical cha...
متن کاملAspartic proteinases and their inhibitors.
Proteolytic enzymes are classified on the basis of their catalytic mechanism as belonging to one of four groups: the serine, cysteine, metallo and aspartic proteinases (Kay, 1982). In contrast to the detailed sequence information and three-dimensional structures that have been produced for many enzymes belonging to the first three groups, relatively little is known about the aspartic proteinase...
متن کاملEndogenous inhibitors of lysosomal proteinases.
Specific inhibitors of three lysosomal proteinases are present in the cytosolic and lysosomal compartments of rabbit liver. The cytosolic inhibitors, purified by chromatography on DEAE-Trisacryl and Sephadex G-75, show specificities toward cathepsin M, cathepsins B and L, and fructose 1,6-bisphosphatase converting enzyme (CE), respectively, and are designated IM, IB/L, and ICE. Inhibitors with ...
متن کاملa comparison of teachers and supervisors, with respect to teacher efficacy and reflection
supervisors play an undeniable role in training teachers, before starting their professional experience by preparing them, at the initial years of their teaching by checking their work within the proper framework, and later on during their teaching by assessing their progress. but surprisingly, exploring their attributes, professional demands, and qualifications has remained a neglected theme i...
15 صفحه اولThe synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinases.
A synthesis of peptidylfluoromethanes is described that utilizes the conversion of phthaloyl amino acids into their fluoromethane derivatives. These can be deblocked and elongated. The inactivation of chymotrypsin by Cbz-Phe-CH2F (benzyloxycarbonylphenylalanylfluoromethane) was found to be considerably slower than that of the analogous chloromethane. The fluoromethane analogue inactivates chymo...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: FEBS Open Bio
سال: 2018
ISSN: 2211-5463,2211-5463
DOI: 10.1002/2211-5463.12540