专利号:US-7884125-B2 优先权日:2008-04-30 标 题:Straightforward entry to 7-azabicyclo[2.2.1]heptane-1-carbonitriles and subsequent synthesis of epibatidine analogues 发明人:STEVENS CHRISTIAN; HEUGEBAERT THOMAS 权利人:UNIV GENT 摘要:The present invention relates to a group of substituted-7-azabicyclo-[2.2.1]heptyl derivatives with biological activity. The present invention also relates to synthetic methods for producing said substituted-7-azabicyclo-[2.2.1]heptyl derivatives. The present invention also relates to certain intermediates for producing such substituted-7-azabicyclo-[2.2.1]heptyl derivatives, as well as a synthetic method for producing such intermediates. The present invention also relates to pharmaceutical compositions comprising such substituted-7-azabicyclo-[2.2.1]heptyl derivatives, as well as their use as medicaments for the treatment of diseases mediated by a Nicotinic Acetylcholine Receptor or a receptor being a member of the Neurotransmitter-gated Ion Channel Superfamily, such as pain, Alzheimer's disease, Parkinson's disease, schizophrenia, epilepsy and nicotine addiction.
专利号:US-2009275616-A1 优先权日:2008-04-30 标 题 :Straightforward entry to 7-azabicyclo[2.2.1]heptane-1-carbonitriles and subsequent synthesis of epibatidine analogues
专利号:US-2024116909-A1 优先权日:2021-01-12 标题 :Novel compounds useful as sting agonists and uses thereof 发明人:YE YANG; LI XIUWEI; YANG GUIQUN; YAN FASHUN; WANG YANPING; LONG WEI 权利人:JACOBIO PHARMACEUTICALS CO LTD 摘要:Compounds of general Formula I, II, III, IV, V and their pharmaceutically acceptable salts, that may be useful as inductors of type I interferon production, specifically as STING active agents, are provided. Also provided are synthesis, compositions, and uses of such compounds.
专利号:US-2025026766-A1 优先权日:2022-01-12 标题 :Thiazolopyridyl Amide Derivatives as DNA Polymerase Theta Inhibitors 发明人:LI JING; XU WENQING; WANG ZHIWEI 权利人:BEIGENE LTD 摘要:The present invention relates to compounds containing thiazolopyridyl amide structure, the process for their synthesis, as well as the use of such compounds for inhibiting DNA Polymerase Theta (Pol Theta), and in the treatment of various diseases including cancers.
专利号:US-2025108123-A1 优先权日:2021-12-17 标 题:Compound-linker constructs comprising novel compounds useful as sting agonists and uses thereof 发明人:YE YANG; LI XIUWEI; YANG GUIQUN; WANG HONGLING; FANG XIONG; CUI YANKAI; YAN FASHUN; SONG BINHUA 权利人:JACOBIO PHARMACEUTICALS CO LTD 摘要:Provided herein are compound-linker constructs and antibody-drug-conjugates of compounds of formula (Y-1), (Y-2), (Y-3), (A), (B), (C), I, II, III, IV or V that are useful as modulators of STING (Stimulator of Interferon Genes). Also provided are synthesis, compositions and uses of such compound-linker constructs and antibody-drug-conjugates.
参考标题:Ruthenium-Catalyzed Site-Selective Intramolecular Silylation Of Primary C-H Bonds For Synthesis Of Sila-Heterocycles 作者:Huaquan Fang,Wenjun Hou,Guixia Liu,Zheng Huang |发布日期:2017.8.23 摘要:Medicinal Chemistry. Moreover, Organosilanes Are Valuable Synthetic Intermediates For Fine Chemicals And Materials. Transition Metal-Catalyzed C-H Silylation Has Become An Important Strategy For C-Si Bond Formations. However, Despite The Great Advances In Aromatic C(Sp2)-H Bond Silylations, Catalytic Methods For Aliphatic C(Sp3)-H Bond Silylations Are Relatively Rare. Here We Report A Pincer Ruthenium