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| Product | Description | |
|---|---|---|
| 4-(Methylthio)-1H-Imidazole | 4-(Methylthio)-1H-Imidazole. Group: Biochemicals. Grades: Highly Purified. CAS No. 83553-60-0. Pack Sizes: 50mg, 100mg, 250mg. US Biological Life Sciences. |  Worldwide |
| 4-(Methylthio)-1H-Imidazole ≥97% (NMR) | 4-(Methylthio)-1H-Imidazole ≥97% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| 4-[4-(4-Fluorophenyl)-2-[4-(methylthio)phenyl]-1H-imidazol-5-yl]pyridine | Potential inhibitor of glucagon receptors, also used in the synthesis of p38 MAP kinase inhibitors. Group: Biochemicals. Alternative Names: 4-[5-(4-Fluorophenyl)-2-[4-(methylthio)phenyl]-1H-imidazol-4-yl]pyridine. Grades: Highly Purified. CAS No. 152121-44-3. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| 4,5-Dihydro-2-(methylthio)-1H-imidazole-1-carboxylic Acid Methyl Ester | 4,5-Dihydro-2-(methylthio)-1H-imidazole-1-carboxylic Acid Methyl Ester is an intermediate in the synthesis of substituted imidazolidinethiones and thioimidazolines. Group: Biochemicals. Alternative Names: Methyl 2-(methylthio)-4,5-dihydro-1H-imidazole-1-carboxylate. Grades: Highly Purified. CAS No. 60546-77-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| ML3403 | ML 3403 is a potent and selective p38 mitogen-activated protein kinase (MAPK) inhibitor. MAPK is a key mediator in cytokine-induced signaling events and plays an integral role in disease states including oncogenesis, autoimmune diseases, and inflammatory processes. Therefore, MAPK inhibitors such as ML 3403 provides an attractive strategy for therapeutic intervention. Synonyms: ML 3403; ML-3403; p38 MAP Kinase Inhibitor III; 4-(4-(4-fluorophenyl)-2-(methylthio)-1H-imidazol-5-yl)-N-(1-phenylethyl)pyridin-2-amine. Grades: 98%. CAS No. 549505-65-9. Molecular formula: C23H21FN4S. Mole weight: 404.51. |  |
| (S)-p38 MAPK Inhibitor III | (S)-p38 MAPK inhibitor III is a methylsulfanylimidazole that inhibits p38 MAP kinase (IC50 = 0.90 μM in vitro). It is cell-permeable, potently blocking the release of TNF-α and IL-1β from human peripheral blood mononuclear cells (IC50s = 0.37 and 0.044 μM, respectively). Synonyms: (S)-p38 MAP Kinase Inhibitor III; 4-[5-(4-fluorophenyl)-2-(methylthio)-1H-imidazol-4-yl]-N-[(1S)-1-phenylethyl]-2-pyridinamin; (S)-p38 Mitogen-activated Protein Kinase Inhibitor III. Grades: ≥98%. CAS No. 581098-48-8. Molecular formula: C23H21FN4S. Mole weight: 404.5. | |
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