The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
24831826 |
59 |
Small molecule inhibitors targeting activator protein 1 (AP-1). |
University of Texas Medical Branch |
24491635 |
4 |
Chemical constituents of Plectranthus amboinicus and the synthetic analogs possessing anti-inflammatory activity. |
National Defense Medical Center, Taiwan |
10937715 |
45 |
Novel inhibitors of AP-1 and NF-kappaB mediated gene expression: structure-activity relationship studies of ethyl 4-[(3-methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)++ +pyrimidi ne-5-carboxylate. |
Signal Pharmaceuticals |
19199792 |
3 |
Quassinoid inhibition of AP-1 function does not correlate with cytotoxicity or protein synthesis inhibition. |
National Cancer Institute-Frederick |
18077363 |
314 |
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. |
University of Oxford |
21806011 |
2 |
Grassypeptolides F and G, cyanobacterial peptides from Lyngbya majuscula. |
National Cancer Institute-Frederick |
21733691 |
2 |
Nothospondin, a new AP-1 inhibitory quassinoid from the Cameroonian plant Nothospondias staudtii. |
Nci-Frederick |
21458276 |
82 |
Design, synthesis, and structure-activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinase. |
Sanford-Burnham Medical Research Institute |
21306129 |
2 |
Inhibitors of the oncogenic transcription factor AP-1 from Podocarpus latifolius. |
National Cancer Institute-Frederick |
21316221 |
62 |
Synthesis and SAR of novel quinazolines as potent and brain-penetrant c-jun N-terminal kinase (JNK) inhibitors. |
The Scripps Research Institute |
20557982 |
7 |
Synthesis and evaluation of quinazolinone derivatives as inhibitors of NF-kappaB, AP-1 mediated transcription and eIF-4E mediated translational activation: inhibitors of multi-pathways involve in cancer. |
B.V. Patel Pharmaceutical Education and Research Development Centre |
17982447 |
1 |
Surveying polypeptide and protein domain conformation and association with FlAsH and ReAsH. |
Yale University |
20335039 |
1 |
Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kappaB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents. |
B.V. Patel Pharmaceutical Education and Research Development Centre |
19064304 |
4 |
Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-kappaB and AP-1 mediated transcription activation and as potential anti-inflammatory agents. |
B.V. Patel Pharmaceutical Education and Research Development Centre |
17531481 |
10 |
Structure-activity studies of phenanthroindolizidine alkaloids as potential antitumor agents. |
Yale University |
17459703 |
111 |
Synthesis and SAR of aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors. |
Ucb Pharma |
17055723 |
17 |
Hemodynamic effects of potent and selective JNK inhibitors in anesthetized rats: implication for targeting protein kinases in metabolic diseases. |
Abbott Laboratories |
16392794 |
13 |
Discovery of nonpeptidic small-molecule AP-1 inhibitors: lead hopping based on a three-dimensional pharmacophore model. |
Toyama Chemical |
15293995 |
17 |
Design, synthesis, and biological evaluation of new cyclic disulfide decapeptides that inhibit the binding of AP-1 to DNA. |
Toyama Chemical |
11052805 |
24 |
Inhibitors of NF-kappaB and AP-1 gene expression: SAR studies on the pyrimidine portion of 2-chloro-4-trifluoromethylpyrimidine-5-[N-(3', 5'-bis(trifluoromethyl)phenyl)carboxamide]. |
Signal Pharmaceuticals |
30525604 |
1 |
Melonoside B and Melonosins A and B, Lipids Containing Multifunctionalized ?-Hydroxy Fatty Acid Amides from the Far Eastern Marine Sponge Melonanchora kobjakovae. |
Far Eastern Branch of The Russian Academy of Sciences |