Similar articles for PMID: 19303774

Year	Number of Results
1970	1
1975	1
2004	1
2005	7
2006	8
2007	5
2008	14
2009	54
2010	15
2011	10
2012	8
2013	8
2014	3
2015	7
2016	1
2017	6
2018	6
2019	3
2020	5
2021	2
2022	1
2023	2
2024	0

1

1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3.

Christopher JA, Atkinson FL, Bax BD, Brown MJ, Champigny AC, Chuang TT, Jones EJ, Mosley JE, Musgrave JR. Christopher JA, et al. Bioorg Med Chem Lett. 2009 Apr 15;19(8):2230-4. doi: 10.1016/j.bmcl.2009.02.098. Epub 2009 Feb 28. Bioorg Med Chem Lett. 2009. PMID: 19303774

2

Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3.

Swahn BM, Huerta F, Kallin E, Malmström J, Weigelt T, Viklund J, Womack P, Xue Y, Ohberg L. Swahn BM, et al. Bioorg Med Chem Lett. 2005 Nov 15;15(22):5095-9. doi: 10.1016/j.bmcl.2005.06.083. Bioorg Med Chem Lett. 2005. PMID: 16140012

3

N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3.

Angell RM, Atkinson FL, Brown MJ, Chuang TT, Christopher JA, Cichy-Knight M, Dunn AK, Hightower KE, Malkakorpi S, Musgrave JR, Neu M, Rowland P, Shea RL, Smith JL, Somers DO, Thomas SA, Thompson G, Wang R. Angell RM, et al. Bioorg Med Chem Lett. 2007 Mar 1;17(5):1296-301. doi: 10.1016/j.bmcl.2006.12.003. Epub 2006 Dec 15. Bioorg Med Chem Lett. 2007. PMID: 17194588

4

Biological evaluation and structural determinants of p38α mitogen-activated-protein kinase and c-Jun-N-terminal kinase 3 inhibition by flavonoids.

Goettert M, Schattel V, Koch P, Merfort I, Laufer S. Goettert M, et al. Chembiochem. 2010 Dec 10;11(18):2579-88. doi: 10.1002/cbic.201000487. Chembiochem. 2010. PMID: 21108268

5

Fluorescence polarization-based competition binding assay for c-Jun N-terminal kinases 1 and 2.

Ansideri F, Dammann M, Boeckler FM, Koch P. Ansideri F, et al. Anal Biochem. 2017 Sep 1;532:26-28. doi: 10.1016/j.ab.2017.05.022. Epub 2017 May 25. Anal Biochem. 2017. PMID: 28552758

6

Structure-based design and parallel synthesis of N-benzyl isatin oximes as JNK3 MAP kinase inhibitors.

Cao J, Gao H, Bemis G, Salituro F, Ledeboer M, Harrington E, Wilke S, Taslimi P, Pazhanisamy S, Xie X, Jacobs M, Green J. Cao J, et al. Bioorg Med Chem Lett. 2009 May 15;19(10):2891-5. doi: 10.1016/j.bmcl.2009.03.043. Epub 2009 Mar 17. Bioorg Med Chem Lett. 2009. PMID: 19361991

7

Fluorescence polarization-based assays for detecting compounds binding to inactive c-Jun N-terminal kinase 3 and p38α mitogen-activated protein kinase.

Ansideri F, Lange A, El-Gokha A, Boeckler FM, Koch P. Ansideri F, et al. Anal Biochem. 2016 Jun 15;503:28-40. doi: 10.1016/j.ab.2016.02.018. Epub 2016 Mar 5. Anal Biochem. 2016. PMID: 26954235

8

Design and synthesis of 1-aryl-5-anilinoindazoles as c-Jun N-terminal kinase inhibitors.

Jiang R, Frackowiak B, Shin Y, Song X, Chen W, Lin L, Cameron MD, Duckett DR, Kamenecka TM. Jiang R, et al. Bioorg Med Chem Lett. 2013 May 1;23(9):2683-7. doi: 10.1016/j.bmcl.2013.02.082. Epub 2013 Feb 27. Bioorg Med Chem Lett. 2013. PMID: 23518277

9

Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK.

Hom RK, Bowers S, Sealy JM, Truong AP, Probst GD, Neitzel ML, Neitz RJ, Fang L, Brogley L, Wu J, Konradi AW, Sham HL, Tóth G, Pan H, Yao N, Artis DR, Quinn K, Sauer JM, Powell K, Ren Z, Bard F, Yednock TA, Griswold-Prenner I. Hom RK, et al. Bioorg Med Chem Lett. 2010 Dec 15;20(24):7303-7. doi: 10.1016/j.bmcl.2010.10.066. Epub 2010 Oct 21. Bioorg Med Chem Lett. 2010. PMID: 21071223

10

A selective small-molecule inhibitor of c-Jun N-terminal kinase 1.

Yao K, Cho YY, Bode AM, Vummenthala A, Park JG, Liu K, Pang YP, Dong Z. Yao K, et al. FEBS Lett. 2009 Jul 7;583(13):2208-12. doi: 10.1016/j.febslet.2009.06.017. Epub 2009 Jun 13. FEBS Lett. 2009. PMID: 19527717 Free article.

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