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Year | Number of Results |
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2010 | 1 |
2011 | 5 |
2024 | 0 |
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Page 1
Selective inhibition of mitochondrial JNK signaling achieved using peptide mimicry of the Sab kinase interacting motif-1 (KIM1).
ACS Chem Biol. 2011 Aug 19;6(8):808-18. doi: 10.1021/cb200062a. Epub 2011 May 24.
ACS Chem Biol. 2011.
PMID: 21563797
Free PMC article.
Synthesis and SAR of novel quinazolines as potent and brain-penetrant c-jun N-terminal kinase (JNK) inhibitors.
He Y, Kamenecka TM, Shin Y, Song X, Jiang R, Noel R, Duckett D, Chen W, Ling YY, Cameron MD, Lin L, Khan S, Koenig M, LoGrasso PV.
He Y, et al.
Bioorg Med Chem Lett. 2011 Mar 15;21(6):1719-23. doi: 10.1016/j.bmcl.2011.01.079. Epub 2011 Jan 22.
Bioorg Med Chem Lett. 2011.
PMID: 21316221
Free PMC article.
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JNK Inhibition Protects Dopamine Neurons and Provides Behavioral Improvement in a Rat 6-hydroxydopamine Model of Parkinson's Disease.
Crocker CE, Khan S, Cameron MD, Robertson HA, Robertson GS, Lograsso P.
Crocker CE, et al.
ACS Chem Neurosci. 2011 Apr 20;2(4):207-212. doi: 10.1021/cn1001107.
ACS Chem Neurosci. 2011.
PMID: 21666838
Free PMC article.
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Small Molecule c-jun-N-terminal Kinase (JNK) Inhibitors Protect Dopaminergic Neurons in a Model of Parkinson's Disease.
Chambers JW, Pachori A, Howard S, Ganno M, Hansen D Jr, Kamenecka T, Song X, Duckett D, Chen W, Ling YY, Cherry L, Cameron MD, Lin L, Ruiz CH, Lograsso P.
Chambers JW, et al.
ACS Chem Neurosci. 2011 Apr 20;2(4):198-206. doi: 10.1021/cn100109k.
ACS Chem Neurosci. 2011.
PMID: 21666839
Free PMC article.
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Synthesis and SAR of 4-(pyrazol-3-yl)-pyridines as novel c-jun N-terminal kinase inhibitors.
Noël R, Shin Y, Song X, He Y, Koenig M, Chen W, Ling YY, Lin L, Ruiz CH, LoGrasso P, Cameron MD, Duckett DR, Kamenecka TM.
Noël R, et al.
Bioorg Med Chem Lett. 2011 May 1;21(9):2732-5. doi: 10.1016/j.bmcl.2010.11.104. Epub 2010 Dec 1.
Bioorg Med Chem Lett. 2011.
PMID: 21185177
Free PMC article.
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