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Your request to link to MMDB for c-Jun N-terminal kinase, JNK


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