72337-27-0Relevant articles and documents
Bicyclic compounds as ring-constrained inhibitors of protein-tyrosine kinase p56(lck)
Burke Jr.,Lim,Marquez,Li,Bolen,Stefanova,Horak
, p. 425 - 432 (2007/10/02)
A study was undertaken to prepare inhibitors of the lymphocyte protein- tyrosine kinase p56(lck). Using the known p56(lck) inhibitor 3,4-dihydroxy- α-cyanocinnamamide (4) as a lead compound, bicyclic analogues were designed as conformationally constrained
Heterocyclic alkyl naphthols
-
, (2008/06/13)
Aminoalkylnaphthols and esters thereof, useful as cardiotonic or antibacterial agents, are prepared from the corresponding RO-naphthalenealkylamines, certain of which are also useful as cardiotonic agents.
5(OR 6)-[(Substituted-amino)alkyl]-2,3-naphthalenediols
-
, (2008/06/13)
Aminoalkylnaphthols and esters thereof, useful as cardiotonic agents, prepared from the corresponding RO-naphthalenealkylamines, certain of which are also useful as cardiotonic agents, are disclosed.