4-(2-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamido)-2-hydroxybenzoic acid
95%
- Product Code: 46121
CAS:
4116-42-1
| Molecular Weight: | 305.2429 g./mol | Molecular Formula: | C₁₃H₁₁N₃O₆ |
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| EC Number: | MDL Number: | MFCD22495132 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.612 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry due to its structural similarity to uracil, a component of RNA. It is often explored for its potential as a building block in the synthesis of nucleoside analogs, which are critical in the development of antiviral and anticancer agents. Researchers investigate its ability to inhibit specific enzymes involved in nucleic acid metabolism, making it a candidate for targeted therapies. Additionally, its hydroxybenzoic acid moiety contributes to its potential use in designing prodrugs or drug delivery systems, enhancing solubility and bioavailability. The compound’s unique structure also makes it a subject of interest in biochemical studies to understand enzyme-substrate interactions and mechanisms of action.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $4,209.85 |
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4-(2-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamido)-2-hydroxybenzoic acid
This compound is primarily utilized in the field of medicinal chemistry due to its structural similarity to uracil, a component of RNA. It is often explored for its potential as a building block in the synthesis of nucleoside analogs, which are critical in the development of antiviral and anticancer agents. Researchers investigate its ability to inhibit specific enzymes involved in nucleic acid metabolism, making it a candidate for targeted therapies. Additionally, its hydroxybenzoic acid moiety contributes to its potential use in designing prodrugs or drug delivery systems, enhancing solubility and bioavailability. The compound’s unique structure also makes it a subject of interest in biochemical studies to understand enzyme-substrate interactions and mechanisms of action.
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