In one aspect, the invention relates to substituted 2-(1H-indol-3-yl)ethanol analogs and substituted 3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole analogs, derivatives thereof, and related compounds, which are useful as inhibitors of IL-6 mediated activation of the Jak2/STAT3 pathway; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating disorders of uncontrolled cellular proliferation associated with a IL6 dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
本发明涉及取代的2-(1H-
吲哚-3-基)乙
醇类似物和取代的3,3a,8,8a-四
氢-2H-
呋喃[2,3-b]
吲哚类似物、其衍
生物和相关化合物,它们可作为IL-6介导的Jak2/
STAT3途径激活的
抑制剂;制备这些化合物的合成方法;包含这些化合物的药物组合物;以及使用这些化合物和组合物治疗与IL6功能障碍相关的细胞无节制增殖疾病的方法。本摘要旨在作为特定领域的搜索工具,不限制本发明。