Imidazoles
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![Medchemexpress LLC 2-[4-[[4-hydroxy-3-[2-(4-nitrophenyl)ethynyl]-5-propan-2-ylphenyl]methyl]-3,5-dimethylphenoxy]aceti | 447415-26-1 | 99.4% | C28H27NO6 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000258815.png-250.jpg)
Medchemexpress LLC 2-[4-[[4-hydroxy-3-[2-(4-nitrophenyl)ethynyl]-5-propan-2-ylphenyl]methyl]-3,5-dimethylphenoxy]aceti | 447415-26-1 | 99.4% | C28H27NO6 | 10MG
NH-3 is an orally active, reversible thyroid hormone receptor (THR) antagonist that inhibits hormone binding and cofactor recruitment; it shows potent THR inhibition (IC50 55 nM) and contains an alkyne group enabling copper-catalyzed azide-alkyne cycloaddition for click chemistry applications.
- Orally active, reversible thyroid hormone receptor antagonist.
- Potent THR inhibition with reported IC50 of 55 nM.
- Contains an alkyne group for copper-catalyzed click chemistry.
- High purity suitable for research use (≈99.4%).
- Available as powder and DMSO solution formats for flexibility in assays.
- Recommended storage conditions provided to preserve stability.
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Medchemexpress LLC Ca inhibitor 1 (GS-6207 analog) | 2189684-45-3 | 99.8% | 958.34 g·mol^-1 | C41H36ClF8N7O5S2 | 10MM 1ML
CA inhibitor 1 is a synthetic HIV capsid inhibitor and alkyne-containing small molecule supplied as a ready-to-use 10 mM solution in DMSO for research and chemical biology applications, including copper-catalyzed azide-alkyne cycloaddition workflows.
- Supplied as 10 mM solution in DMSO
- High purity: 99.8%
- Molecular weight 958.34 g·mol⁻¹
- Molecular formula C41H36ClF8N7O5S2
- Contains terminal alkyne for click chemistry applications
- Recommended storage: powder -20 °C; in solvent -80 °C for long-term storage