4-(2-(methoxymethyl)-1-((R)-1-phenylethyl)-8-(((S)-pyrrolidin-3-yl)methoxy)-1H-imidazo[4,5-c]quinolin-7-yl)-3,5-dimethylisoxazole
98%
- Product Code: 228759
CAS:
2451862-42-1
Molecular Weight: | 511.2583 g./mol | Molecular Formula: | C₃₀H₃₃N₅O₃ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 679.6±55.0 °C(Predicted) | |
Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | -20°C |
Product Description:
Used as a potent immunomodulatory agent in research settings, particularly in the development of treatments for viral infections and certain cancers. It functions as a Toll-like receptor 7 (TLR7) agonist, stimulating the innate immune system to produce cytokines such as interferon-alpha, which enhances antiviral and antitumor responses. Its selective activation of TLR7 makes it valuable in studying immune activation pathways and designing targeted therapies with reduced systemic inflammation. Due to its complex stereochemistry and targeted activity, it is primarily used in preclinical studies to evaluate immune stimulation and optimize dosing regimens for related drug candidates.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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5mg | 10-20 days | ฿27,900.00 |
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10mg | 10-20 days | ฿45,330.00 |
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25mg | 10-20 days | ฿68,000.00 |
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4-(2-(methoxymethyl)-1-((R)-1-phenylethyl)-8-(((S)-pyrrolidin-3-yl)methoxy)-1H-imidazo[4,5-c]quinolin-7-yl)-3,5-dimethylisoxazole
Used as a potent immunomodulatory agent in research settings, particularly in the development of treatments for viral infections and certain cancers. It functions as a Toll-like receptor 7 (TLR7) agonist, stimulating the innate immune system to produce cytokines such as interferon-alpha, which enhances antiviral and antitumor responses. Its selective activation of TLR7 makes it valuable in studying immune activation pathways and designing targeted therapies with reduced systemic inflammation. Due to its complex stereochemistry and targeted activity, it is primarily used in preclinical studies to evaluate immune stimulation and optimize dosing regimens for related drug candidates.
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