Your request to link to MMDB for Mitogen-activated protein kinase 8
MMDB Description | |
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49816 | The C-jun N-terminal Kinase (Jnk3s) Complexed With Mgamp-pnp |
23780 | Crystal Structure of Jnk3 in Complex With an Imidazole- Pyrimidine Inhibitor |
23781 | The Structure of Jnk3 in Complex With an Imidazole- Pyrimidine Inhibitor |
23782 | The Crystal Structure of Jnk3 in Complex With a Phenantroline Inhibitor |
23783 | The Structure of Jnk3 in Complex With a Dihydroanthrapyrazole Inhibitor |
33136 | Structural Basis for the Selective Inhibition of Jnk1 by the Scaffolding Protein Jip1 and Sp600125 |
33137 | Structural Basis for the Selective Inhibition of Jnk1 by the Scaffolding Protein Jip1 and Sp600125 |
41320 | Inhibitor Complex of Jnk3 |
42705 | Inhibitor Complex of Jnk3 |
38771 | Pyrazoloquinolones as Novel, Selective Jnk1 Inhibitors |
39389 | Selective Aminopyridine-based C-jun N-terminal Kinase Inhibitors With Cellular Activity |
40539 | Discovery of Potent, Highly Selective, and Orally Bioavailable Pyridine Carboxamide C-jun Nh2-terminal Kinase Inhibitors |
45828 | Novel 4-anilinopyrimidines as Potent Jnk1 Inhibitors |
44637 | Crystal Structure of Human Jnk3 Complexed With N-{3-cyano-6-[3-(1- Piperidinyl)propanoyl]-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-2-yl}- 1-naphthalenecarboxamide |
44647 | Crystal Structure of Human Jnk3 Complexed With N-(3-cyano-4,5,6,7- Tetrahydro-1-benzothien-2-yl)-2-fluorobenzamide |
44222 | Crystal Structure of Jnk3 Bound to N-benzyl-4-(4-(3- Chlorophenyl)-1h-pyrazol-3-yl)-1h-pyrrole-2-carboxamide |
46949 | Synthesis and SAR of Aminopyrimidines as Novel C-jun N-terminal Kinase (Jnk) Inhibitors |
59670 | C-jun N-terminal Kinase 3 With 3,5-disubstituted Quinoline Inhibitor |
70511 | Crystal Structure of Human Jnk3 Complexed With a 1-aryl-3,4- Dihydroisoquinoline Inhibitor |
66867 | Crystal Structure of Human Jnk3 Complexed With an Isoquinolone Inhibitor |
66868 | Crystal Structure of Human Jnk3 Complexed With an Isoquinolone Inhibitor |
64784 | Irak-4 Inhibitors (Part Ii)- a Structure Based Assessment of Imidazo[1,2 A]pyridine Binding |
64785 | Irak-4 Inhibitors (Part Ii)- a Structure Based Assessment of Imidazo[1,2 A]pyridine Binding |
68867 | Crystal Structure of Human Jnk3 Complexed With N-(3-methyl- 4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy) Naphthalen-1-yl)-1h-benzo[d]imidazol-2-amine |
68814 | Jnk1 Complexed With a Bis-anilino-pyrrolopyrimidine Inhibitor |
69980 | Crystal Structure of Jnk3 With Amino-pyrazole Inhibitor, SR- 3451 |
69981 | Crystal Structure of Jnk3 With Indazole Inhibitor, Sr-3737 |
70712 | Jnk3 Bound to Piperazine Amide Inhibitor, Sr2774 |
69886 | Jnk-3 Bound to (Z)-5-fluoro-1-((6-fluoro-4h-benzo[d][1,3]dioxin-8-yl) Methyl)-3-(hydroxyimino)indolin-2-one |
71422 | Jnk3 Bound to (Z)-1-((6-fluoro-4h-benzo[d][1,3]dioxin-8-yl)methyl)-3- (Hydroxyimino)-4-styrylindolin-2-one |
69887 | Jnk3 Bound to (Z)-1-((6-fluoro-4h-benzo[d][1,3]dioxin-8-yl)methyl)-3- (Hydroxyimino)-4-phenylindolin-2-one |
78980 | Jnk3 Bound to Aminopyrimidine Inhibitor, Sr-3562 |
87855 | Crystal Structure of Jnk1-alpha1 Isoform |
87856 | Crystal Structure of Jnk1-alpha1 Isoform Complex With a Biaryl Tetrazol (A-82118) |
90299 | Design and Synthesis of Disubstituted Thiophene and Thiazole Based Inhibitors of JNK for the Treatment of Neurodegenerative Diseases |
88977 | Design and Synthesis of a Novel, Orally Efficacious Tri-substituted Thiophene Based JNK Inhibitor |