Nitric oxide biosynthesis-inhibiting anti-inflammatory and anti-microbial compounds of Formula (3) and Formula (4) wherein R1 and R2 are independently selected from optionally substituted thienyl, optionally substituted furyl, optionally substituted —CH═CH-thienyl and optionally substituted provided that R2 is substituted with as nitro group
Treatment methods utilizing the compounds, and methods of synthesis of the compounds are also disclosed.
氮氧化物
生物合成抑制抗炎和抗微
生物化合物的公式(3)和公式(4),其中R1和R2分别选自可选择取代
噻吩基、可选择取代
呋喃基、可选择取代-CH═CH-
噻吩基和可选择取代,前提是R2被取代为硝基。还公开了利用这些化合物的治疗方法,以及合成这些化合物的方法。