67058-76-8Relevant academic research and scientific papers
Regioselective halogenation of 6-azaindoles: Efficient synthesis of 3-halo-2,3-disubstituted-6-azaindole derivatives
Gallou, Fabrice,Reeves, Jonathan T.,Tan, Zhulin,Song, Jinhua J.,Yee, Nathan K.,Campbell, Scot,Jones, Paul-James,Senanayake, Chris H.
, p. 2400 - 2402 (2005)
A mild and efficient synthesis of 3-halo-2-substituted-6-azaindoles was developed by regioselective halogenation of 6-azaindole systems. The transformation was achieved with copper(II) bromide in acetonitrile at room temperature. Georg Thieme Verlag Stutt
PIM KINASE INHIBITOR COMPOSITIONS AND USES THEREOF
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Paragraph 0233, (2020/11/12)
This disclosure relates to compounds and compositions useful as inhibitors of PIM kinases. Also provided are methods of synthesis and methods of use of PIM inhibitors in treating individuals suffering from cancerous malignancies.
Discovery and optimization of a novel series of dyrk1b kinase inhibitors to explore a MEK resistance hypothesis
Kettle, Jason G.,Ballard, Peter,Bardelle, Catherine,Cockerill, Mark,Colclough, Nicola,Critchlow, Susan E.,Debreczeni, Judit,Fairley, Gary,Fillery, Shaun,Graham, Mark A.,Goodwin, Louise,Guichard, Sylvie,Hudson, Kevin,Ward, Richard A.,Whittaker, David
, p. 2834 - 2844 (2015/04/14)
Potent and selective inhibitors of Dyrk1B kinase were developed to explore the hypothesis, based on siRNA studies, that Dyrk1B may be a resistance mechanism in cells undergoing a stress response.
Practical regioselective bromination of azaindoles and diazaindoles
Gallou, Fabrice,Reeves, Jonathan T.,Tan, Zhulin,Song, Jinhua J.,Yee, Nathan K.,Harcken, Christian,Liu, Pingrong,Thomson, David,Senanayake, Chris H.
, p. 211 - 214 (2007/10/03)
A mild and efficient synthesis of various 3-brominated azaindoles and diazaindoles was developed by regioselective halogenation of the parent systems. This practical and high-yielding transformation was achieved with copper(II) bromide in acetonitrile at
Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. 6. 2-Indol-3-yl- and 2-azaindol-3-yl- dipyridodiazepinones
Kelly,McNeil,Rose,David,Shih,Grob
, p. 2430 - 2433 (2007/10/03)
Modification of the non-nucleoside inhibitor of HIV-1 reverse transcriptase nevirapine (Viramune) by incorporation of a 2-indolyl substituent confers activity against several mutant forms of the enzyme.
