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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 |
| (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. Grade: ≥98%. CAS No. 581098-48-8. Molecular formula: C23H21FN4S. Mole weight: 404.5. |  |
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