252882-61-4Relevant articles and documents
Discovery of 3,3′-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection
Shi, Weihua,Jiang, Zhigan,He, Haiying,Xiao, Fubiao,Lin, Fusen,Sun, Ya,Hou, Lijuan,Shen, Liang,Han, Lixia,Zeng, Minggao,Lai, Kunmin,Gu, Zhengxian,Chen, Xinsheng,Zhao, Tao,Guo, Li,Yang, Chun,Li, Jian,Chen, Shuhui
supporting information, p. 94 - 97 (2018/02/19)
A new series of 3,3′-spirocyclic-2-oxo-indoline derivatives was synthesized and evaluated against respiratory syncytial virus (RSV) in a cell-based assay and animal model. Extensive structure-activity relationship study led to a lead compound 14h, which e
RSV ANTIVIRAL COMPOUNDS
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Page/Page column 36, (2014/05/07)
Inhibitors of RSV replication of formula RI including stereochemically isomeric forms, and salts or solvates thereof, wherein R22, W, Q, V, Z p,s,and Het have the meaning as defined herein. The present invention also relates to processes for preparing said compounds, pharmaceutical compositions containing them and their use, alone or in combination with other RSV inhibitors, in RSV therapy.
SPIROINDALONES
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Page/Page column 29, (2009/01/20)
The present invention relates to spiroindalone compounds useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.
NOVEL SPIROOXYINDOLE COMPOUNDS AND DRUGS CONTAINING SAME
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, (2009/01/20)
A Spiro oxindole compound represented by formula (1) of the present invention or salt thereof, or their solvate shows a superior inhibitory effect of 11β-hydroxysteroid dehydrogenasel, and is useful as an agent for preventing or treating a disease that involves 11β-hydroxysteroid dehydrogenasel (in particular, diabetes, insulin resistance, diabetes complication, obesity, dyslipidemia, hypertension, fatty liver, or metabolic syndrome).
FUSED AND SPIROCYCLE COMPOUNDS AND THE USE THEREOF
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Page/Page column 96, (2008/06/13)
The invention relates to fused and spirocycle compounds of Formula (I), or a pharmaceutically acceptable salt, prodrug, or solvate thereof, wherein R1, R2, Q1-Q3, and Z are defined as set forth in the specification. The invention is also directed to the use of compounds of Formula (I) to treat, prevent or ameliorate a disorder responsive to the blockade of calcium channels, and particularly N-type calcium channels. Compounds of the present invention are especially useful for treating pain.
Inhibitors of prenyl-protein transferase
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, (2008/06/13)
The present invention is directed to conformationally constrained compounds which inhibit prenyl-protein transferase and the prenylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting prenyl-protein transferase and the prenylation of the oncogene protein Ras.