N-(2-(3,4-dimethylphenoxy)ethyl)-4-formylbenzamide serves as a reactive aldehyde ADC linker for stable and selective conjugation to antibodies, improving payload attachment and targeted delivery in ADC therapeutics.
Structure of 1226096-54-3
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N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is gaining recognition in the pharmaceutical field due to its potentially broad range of therapeutic applications. Its chemical structure, characterized by the dimethylphenoxy and formylbenzamide moieties, allows for diverse biological interactions which are crucial for its function as a therapeutic agent. This compound is being extensively studied for its potential role in addressing several chronic conditions, thereby contributing significantly to drug discovery and development processes. Its chemical attributes make it a valuable candidate for further exploration in medicinal chemistry.
One of the critical applications of N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is in the development of novel analgesics. The compound's ability to modulate pain pathways makes it an attractive candidate for treating chronic pain conditions. By targeting specific receptors and enzymes implicated in pain transmission, it could offer a new mechanism of action distinct from traditional analgesics. This can be particularly beneficial in providing relief for patients who have not responded well to existing pain management therapies, as well as reducing the risk of dependency associated with opioid medications.
N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is also being investigated for its anti-inflammatory properties. Its potential to interfere with inflammatory mediators suggests that it could be effective in managing autoimmune diseases such as lupus and psoriasis. By inhibiting the production or action of pro-inflammatory cytokines, this compound could reduce the excessive immune response characteristic of these disorders. Researchers are focused on understanding its mode of action through clinical and preclinical studies, hoping to provide a new avenue for treatment that is both effective and has fewer side effects.
Furthermore, the compound has shown potential in neuroprotective applications. In diseases such as Alzheimer's and Parkinson’s, N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide may help protect nerve cells from the detrimental processes that lead to neurodegeneration. The compound might offer a mechanism to mitigate or even reverse neuronal damage, providing hope for new treatment paradigms in managing neurodegenerative disorders. This aligns with the growing need for innovative therapies that can address the root causes of these diseases rather than just alleviating symptoms, thereby improving the quality of life for affected individuals.
Catalog | Product Name | CAS | Inquiry |
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BADC-00523 | N-(2-(2-Chloroethoxy)ethyl)-4-Formylbenzamide | 1137575-49-5 | |
BADC-00531 | N-(2-(4-Fluorophenoxy)ethyl)-4-Formylbenzamide | 1225588-22-6 | |
BADC-00532 | N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide | 1225588-29-3 | |
BADC-00533 | N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide | 1225705-45-2 | |
BADC-00534 | N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide | 1225790-49-7 | |
BADC-00535 | N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide | 1225790-59-9 | |
BADC-00536 | N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide | 1225936-91-3 | |
BADC-00539 | N-(2-(2-Chlorophenoxy)ethyl)-4-Formylbenzamide | 1225972-65-5 | |
BADC-00540 | N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide | 1225979-81-6 | |
BADC-00541 | N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide | 1226006-03-6 |
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