507476-70-2Relevant academic research and scientific papers
NUCLEIC ACID-BINDING PHOTOPROBES AND USES THEREOF
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Paragraph 0042, (2019/06/17)
The present invention relates to photoactivatable compounds and methods of use thereof for determining binding site and other structural information about RNA transcripts. The invention also provides methods of identifying RNA transcripts that bind compounds and are thus druggable, methods of screening drug candidates, and methods of determining drug binding sites and/or accessible or reactive sites on a target RNA.
COMPOUNDS AND METHODS FOR MODULATING RNA FUNCTION
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Paragraph 0068; 00629, (2018/02/28)
The present invention provides compounds, compositions thereof, and methods of using the same.
POLYCYCLIC TLR7/8 ANTAGONISTS AND USE THEREOF IN THE TREATMENT OF IMMUNE DISORDERS
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Paragraph 00229; 00231, (2017/07/06)
The present invention relates to compounds of Formula (I) and pharmaceutically acceptable compositions thereof, useful as toll-like receptor 7/8 (TLR7/8) antagonists. In Formula (I), Ring A is aryl or heteroaryl; Ring B is aryl or heteroary; and X is C(R4)2, O, NR4, S, S(R4), or S(R4)2.
COMPOUNDS AND METHODS OF TREATING RNA-MEDIATED DISEASES
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Sheet 97/122, (2017/12/27)
The present invention provides compounds, compositions thereof, and methods of using the same.
CCR6 COMPOUNDS
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Paragraph 0114, (2015/06/18)
Compounds of formula (I) are provided which are useful in the treatment of diseases or conditions modulated at least in part by CCR6. Pharmaceutical compositions of the compounds of formula (I) are also provided. Further provided in the present disclosure
SELECTIVELY SUBSTITUTED QUINOLINE COMPOUNDS
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Paragraph 0069;0083; 0085, (2015/05/05)
Embodiments of the disclosure relate to selectively substituted quinoline compounds of formula (I) that act as antagonists or inhibitors for Toll -like receptors 7 and/or 8, and their use in pharmaceutical compositions effective for treatment of systemic
SELECTIVELY SUBSTITUTED QUINOLINE COMPOUNDS
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Paragraph 0168; 0184, (2015/04/21)
Embodiments of the disclosure relate to selectively substituted quinoline compounds that act as antagonists or inhibitors for Toll-like receptors 7 and/or 8, and their use in pharmaceutical compositions effective for treatment of systemic lupus erythematosus (SLE) and lupus nephritis.
PIPERAZINE DERIVATIVES AND THEIR USE AS MODULATORS OF NUCLEAR HORMONE RECEPTOR FUNCTION
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Page/Page column 79, (2010/02/11)
The present invention provides piperazine derivatives and methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders.
