104126-76-3Relevant academic research and scientific papers
Non-nucleoside inhibitors of human adenosine kinase: Synthesis, molecular modeling, and biological studies
Butini, Stefania,Gemma, Sandra,Brindisi, Margherita,Borrelli, Giuseppe,Lossani, Andrea,Ponte, Anna Maria,Torti, Andrea,Maga, Giovanni,Marinelli, Luciana,La Pietra, Valeria,Fiorini, Isabella,Lamponi, Stefania,Campiani, Giuseppe,Zisterer, Daniela M.,Nathwani, Seema-Maria,Sartini, Stefania,La Motta, Concettina,Da Settimo, Federico,Novellino, Ettore,Focher, Federico
, p. 1401 - 1420 (2011/04/24)
Adenosine kinase (AK) catalyzes the phosphorylation of adenosine (Ado) to AMP by means of a kinetic mechanism in which the two substrates Ado and ATP bind the enzyme in a binary and/or ternary complex, with distinct protein conformations. Most of the desc
ANTIULCER BENZIMIDAZOLE DERIVATIVES
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, (2008/06/13)
Compounds of formula I STR1 in which R 1 and R 2, which may be the same or different, are hydrogen, a C 1 to C 3 alkyl group or R 1 and R 2 together with the nitrogen to which they are attached form an optionally substituted heterocyclic ring; R 3 and R. sub.4, which may be the same or different are hydrogen, a C 1 to C. sub.3 alkyl or an optionally substituted C 3 to C 6 cycloalkyl group, or R 3 and R 4 together with the nitrogen to which they are attached form an optionally substituted heterocyclic ring; m is 0, 1 or 2; p is 0, 1 or 2; E is an alkylene group connected to or interrupted by an oxygen or a sulphur atom; J is hydrogen or a substituent group; and their pharmaceutically acceptable salts have utility as histamine H 2-receptor antagonists.
