15726-38-2Relevant articles and documents
Synthesis and biological evaluation of clitocine analogues as adenosine kinase inhibitors
Lee, Chih-Hung,Daanen, Jerome F,Jiang, Meiqun,Yu, Haixia,Kohlhaas, Kathy L,Alexander, Karen,Jarvis, Michael F,Kowaluk, Elizabeth L,Bhagwat, Shripad S
, p. 2419 - 2422 (2007/10/03)
Adenosine kinase (AK) is the primary enzyme responsible for adenosine metabolism. Inhibition of AK effectively increases extracellular adenosine concentrations and represents an alternative approach to enhance the beneficial actions of adenosine as compared to direct-acting receptor agonists. Clitocine (3), isolated from the mushroom Clitocybe inversa, has been found to be a weak inhibitor of AK. We have prepared a number of analogues of clitocine in order to improve its potency and demonstrated that 5′-deoxy-5′-amino-clitocine (7) improved AK inhibitory potency by 50-fold.
A convenient synthesis of 4,6-dichloro-5-benzylthiopyrimidine
Thang,Watson,Best,Fam,Keep
, p. 2363 - 2369 (2007/10/02)
A practical and convenient two-step synthesis of the title compound 4,6-dichloro-5-benzylthiopyrimidine from 4,6-dihydroxypyrimidine is described.