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Bioorg Med Chem ; 21(7): 1952-63, 2013 Apr 01.
Article in English | MEDLINE | ID: mdl-23415088

ABSTRACT

A number of novel imidazophenoxazine-4-sulfonamides have been designed as potential inhibitors of PDE4. All these compounds were readily prepared via an elegant multi-step method involving the initial construction of 1-nitro-10H-phenoxazine ring and then fused imidazole ring as key steps. Some of these compounds showed promising PDE4B and D inhibition when tested in vitro and good interactions with these proteins in silico. Three of these compounds showed dose dependent inhibition of PDE4B with IC50 value of 3.31 ± 0.62, 1.23 ± 0.18 and 0.53 ± 0.18 µM.


Subject(s)
Oxazines/chemistry , Oxazines/pharmacology , Phosphodiesterase 4 Inhibitors/chemistry , Phosphodiesterase 4 Inhibitors/pharmacology , Sulfonamides/chemistry , Sulfonamides/pharmacology , Animals , Cell Line , Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism , Molecular Docking Simulation , Oxazines/chemical synthesis , Sulfonamides/chemical synthesis
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