(2-Aminophenyl)(1-(3-isopropylphenyl)-1H-1,2,3-triazol-4-yl)methanone
98%
- Product Code: 36374
CAS:
1437325-71-7
| Molecular Weight: | 306.3617 g./mol | Molecular Formula: | C₁₈H₁₈N₄O |
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| Density: | Storage Condition: | room temperature |
Product Description:
(2-Aminophenyl)(1-(3-isopropylphenyl)-1H-1,2,3-triazol-4-yl)methanone is a compound with potential applications in medicinal chemistry and drug development. Its structure, featuring both an aminophenyl group and a triazole moiety, makes it a promising candidate for the design of biologically active molecules. The triazole ring is known for its role in enhancing binding affinity and metabolic stability, which is valuable in the development of pharmaceuticals targeting enzymes or receptors. This compound could be explored for its potential as an inhibitor in therapeutic areas such as cancer, inflammation, or infectious diseases, where triazole-based compounds have shown efficacy. Additionally, the isopropylphenyl group may contribute to improved pharmacokinetic properties, such as increased lipophilicity and membrane permeability, making it suitable for further optimization in drug discovery pipelines.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿20,862.00 |
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(2-Aminophenyl)(1-(3-isopropylphenyl)-1H-1,2,3-triazol-4-yl)methanone
(2-Aminophenyl)(1-(3-isopropylphenyl)-1H-1,2,3-triazol-4-yl)methanone is a compound with potential applications in medicinal chemistry and drug development. Its structure, featuring both an aminophenyl group and a triazole moiety, makes it a promising candidate for the design of biologically active molecules. The triazole ring is known for its role in enhancing binding affinity and metabolic stability, which is valuable in the development of pharmaceuticals targeting enzymes or receptors. This compound could be explored for its potential as an inhibitor in therapeutic areas such as cancer, inflammation, or infectious diseases, where triazole-based compounds have shown efficacy. Additionally, the isopropylphenyl group may contribute to improved pharmacokinetic properties, such as increased lipophilicity and membrane permeability, making it suitable for further optimization in drug discovery pipelines.
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