77140-72-8Relevant academic research and scientific papers
Synthesis of 4-oxotetrahydropyrimidine-1(2H)-carboxamides derivatives as capsid assembly modulators of hepatitis B virus
Hwang, Nicky,Ban, Haiqun,Chen, Junjun,Ma, Julia,Liu, Hui,Lam, Patrick,Kulp, John,Menne, Stephan,Chang, Jinhong,Guo, Ju-Tao,Du, Yanming
, p. 459 - 472 (2021)
We report herein the synthesis and evaluation of phenyl ureas derived from 4-oxotetrahydropyrimidine as novel capsid assembly modulators of hepatitis B virus (HBV). Among the derivatives, compound 27 (58031) and several analogs showed an activity of submi
6,7-DIHYDRO-4H-PYRAZOLO[1,5-A]PYRAZINE AND 6,7-DIHYDRO-4H-TRIAZOLO[1,5-A]PYRAZINE COMPOUNDS FOR THE TREATMENT OF INFECTIOUS DISEASES
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Page/Page column 23; 25, (2018/03/28)
The present invention relates to compounds of the formula (I), or pharmaceutically acceptable salts, enantiomer or diastereomer thereof, wherein R1 to R4 and Q are as described above. The compounds may be useful for the treatment or prophylaxis of hepatitis B virus infection.
CYCLOPROPANECARBOXAMIDO-SUBSTITUTE AROMATIC COMPOUNDS AS ANTI-TUMOR AGENTS
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Paragraph 0323; 0324, (2015/07/22)
Provided are cyclopropanecarboxamido-substituted aromatic compounds that inhibit protein kinases and their use in anti-tumor area. In particular, tyrosine-kinase inhibitors and Raf-kinase inhibitors as anti-tumor agents, their preparation, pharmaceutical composition, and their use in the treatment of cancer are also provided.
SPIROCYCLIC PIPERIDINE DERIVATIVES AS TRPM 8 MODULATORS
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Page/Page column 34, (2010/10/03)
The present invention provides Transient Receptor Potential subfamily M, member 8 (TRPM8) modulators of formula (I). In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPM8.
3-Arylhydantoine, a class of schistosomicidal compounds
Link,Stohler
, p. 261 - 265 (2007/10/02)
A series of derivatives of 3-arylhydantoin was synthesized and submitted to a broad pharmacological screening. Unexpectedly, some of the tested compounds showed interesting activity against infection with Schistosoma mansoni. From a study on structure-act
