| scholarly article | Q13442814 |
| P2093 | author name string | John C Lee | |
| Jerry L Adams | |||
| Baoguang Zhao | |||
| Jeffrey C Boehm | |||
| Michael J Bower | |||
| Shouki Kassis | |||
| Zehong Wan | |||
| P2860 | cites work | A protein kinase involved in the regulation of inflammatory cytokine biosynthesis | Q24311139 |
| Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site | Q27638349 | ||
| Structural basis of inhibitor selectivity in MAP kinases | Q27765381 | ||
| 2-Alkynyl-8-aryl-9-methyladenines as novel adenosine receptor antagonists: their synthesis and structure-activity relationships toward hepatic glucose production induced via agonism of the A(2B) receptor | Q31916910 | ||
| p38 mitogen-activated protein kinase inhibitors--mechanisms and therapeutic potentials | Q33716182 | ||
| Anti-TNF agents for rheumatoid arthritis | Q34216181 | ||
| Tumor necrosis factor-alpha blockade in the treatment of rheumatoid arthritis | Q34276023 | ||
| p38 MAP kinase: molecular target for the inhibition of pro-inflammatory cytokines. | Q34483284 | ||
| Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase | Q41141283 | ||
| Pyrimidinylimidazole inhibitors of CSBP/p38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes. | Q42537136 | ||
| Conversion of SB 203580-insensitive MAP kinase family members to drug-sensitive forms by a single amino-acid substitution | Q42541263 | ||
| Cyclin-Dependent Kinase Inhibition by New C-2 Alkynylated Purine Derivatives and Molecular Structure of a CDK2−Inhibitor Complex | Q57899489 | ||
| 1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency | Q71591889 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1191-1194 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Bioorganic & Medicinal Chemistry Letters | Q2709483 |
| P1476 | title | N-Phenyl-N-purin-6-yl ureas: the design and synthesis of p38alpha MAP kinase inhibitors | |
| P478 | volume | 13 |
| Q34644067 | Radioiodinated O(6)-Benzylguanine derivatives containing an azido function | cites work | P2860 |
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