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BitTorrent is the most popular P2P content delivery application where individual users share various type of content with tens of thousands of other users. The growing popularity of BitTorrent is primarily due to the availability of valuable content without any cost for the consumers. However, apart from required resources, publishing (sharing) valuable (and often copyrighted) content has serio...
متن کاملسنتز 1، 3، 5، 7-تترا استیل-1، 3، 5، 7-تترا آزاسیکلواکتان (TAT) از طریق استیل‌دار کردن 3، 7-دی‌استیل-1، 3، 5، 7-تترا آزا بی‌سیکلو-[3.3.1]-نونان (DAPT)
In this study, a novel method to synthesis of 1,3,5,7-tetraacetyl octahydro-1,3,5,7-tetraazocine or 1,3,5,7-tetraacetyl-1,3,5,7-tetraazacyclooctane (TAT) was used through acetolysis of 3,7-diacetyl-1,3,5,7-tetraazabicyclo-[3.3.1]nonane (DAPT) with acetic anhydride in the presence of sodium acetate as catalyst. Optimized reaction conditions were obtained by changing temperature, time and startin...
متن کاملPotent cephalosporinase inhibitors: 7 beta-[2-(1, 3-dithiolan-2-ylidene) acetamido] cephalosporins and related compounds.
Cephalosporins possessing a 1, 3-dithiolane, 1, 3-dithiane, or 1, 3-dithietane ring on their 7 beta-substituents showed potent inhibitory activity against cephaloridine hydrolysis by cephalosporinases purified from proteus morganii, Proteus rettgeri, and Proteus inconstans, which were not inhibited by clavulanic acid, a well-known beta-lactamase inhibitor. The mode of inhibition was competitive...
متن کاملQSAR Analysis for Some 1, 2-Benzisothiazol-3-one Derivatives as Caspase-3 Inhibitors by Stepwise MLR Method
Caspase-3, one of the dominant effectors caspases, is activated in almost every model of apoptosis with various signaling pathways. Hence, inhibition of caspase-3 has become an attractive target in the treatment of neurodegenerative diseases. Caspase-3 inhibitory activities of some 1,2-benzisothiazol-3-one derivatives were modeled by quantitative structure–activity relationship (QSAR) using ste...
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ژورنال
عنوان ژورنال: Blood
سال: 2017
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood-2016-12-754473