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Bioorg Med Chem ; 24(22): 5702-5716, 2016 11 15.
Article in English | MEDLINE | ID: mdl-27713015

ABSTRACT

Herein we report the synthesis, PDE-4B and TNF-α inhibitory activities of a few dibenzo[b,d]furan-1-yl-thiazole derivatives. The hydroxycyclohexanol amide derivatives 14, 18, 24, 29, 31 and 33 exhibited promising in vitro PDE-4B and TNF-α inhibitory activities. Compound 24 showed good systemic availability in preclinical animal models and was also found to be non-toxic (exploratory mutagenicity test). Further it exhibited promising results in in vivo asthma/COPD and Uveitis models.


Subject(s)
Cyclic Nucleotide Phosphodiesterases, Type 4/metabolism , Furans/pharmacology , Phosphodiesterase 4 Inhibitors/pharmacology , Thiazoles/pharmacology , Dose-Response Relationship, Drug , Furans/chemical synthesis , Furans/chemistry , Humans , Molecular Structure , Phosphodiesterase 4 Inhibitors/chemical synthesis , Phosphodiesterase 4 Inhibitors/chemistry , Structure-Activity Relationship , Thiazoles/chemical synthesis , Thiazoles/chemistry , Tumor Necrosis Factor-alpha/antagonists & inhibitors
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