N-(2-(3-Fluorophenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).
Catalog Number | Size | Price | Quantity | |
---|---|---|---|---|
BADC-00532 | -- | $-- | Inquiry |
N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide is a compound that has garnered interest in the field of pharmaceutical research due to its potential as a bioactive molecule. One of the primary applications of this compound is in the development of therapeutics targeting inflammatory diseases. Its molecular structure allows it to interact with specific enzymes and receptors that play a crucial role in the inflammatory process. By modulating these interactions, N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide can potentially reduce the expression of pro-inflammatory cytokines, thus providing relief from symptoms associated with chronic inflammation. This property makes it a promising candidate for the treatment of conditions such as rheumatoid arthritis and inflammatory bowel disease.
In addition to its anti-inflammatory potential, N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide has shown promise as an anti-cancer agent. The compound has been studied for its ability to selectively induce apoptosis in cancer cells, sparing normal healthy cells, which is a significant advantage over traditional chemotherapy. This specificity is achieved through its interaction with certain cellular pathways that are often deregulated in cancerous cells. Researchers are particularly interested in its applications in treating breast and lung cancers, where preliminary studies have shown that it can inhibit tumor growth significantly. The development of N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide as a targeted cancer therapy could lead to more effective and less toxic treatment options for patients.
Furthermore, the compound's potential application extends into the realm of neuropharmacology. Recent studies suggest that N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide may have neuroprotective properties. Its ability to cross the blood-brain barrier and modulate neural pathways presents opportunities for developing treatments for neurodegenerative disorders such as Alzheimer's and Parkinson's disease. By reducing oxidative stress and inflammation in neural tissues, this compound could help in preserving cognitive function and slowing the progression of neurodegeneration. These findings offer hope for new therapeutic strategies in managing disorders that currently have limited treatment options.
Finally, N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide is also being explored for its antimicrobial properties. With the rise of antibiotic-resistant strains of bacteria, there is an urgent need for novel antimicrobial agents. This compound has demonstrated inhibitory effects against several pathogenic bacteria, potentially offering a new mechanism of action that could be exploited in antimicrobial drug design. Researchers are optimistic that with further development and clinical trials, N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide could contribute to the next generation of antibiotics, offering safe and effective treatment options for resistant infections.
Customer Support
Providing excellent 24/7 customer service and support
Project Management
Offering 100% high-quality services at all stages
Quality Assurance
Ensuring the quality and reliability of products or services
Global Delivery
Ensuring timely delivery of products worldwide
BOC Sciences offers comprehensive services for ADC manufacturing, including antibody modification, linker chemistry, payload conjugation, and formulation development. In particular, our payload-linker customization service offers a convenient and fast raw material channel for many ADC researchers.
BOC Sciences provides one-stop site-specific conjugation services for amino acids, glycans, unnatural amino acids, and short peptide tags. In addition, cysteine conjugation, lysine conjugation, enzymatic conjugation, thio-engineered antibody can also be obtained quickly.
BOC Sciences offers a full range of linkers, including peptide linkers, PEG linkers, click chemistry, PROTAC linkers, non-cleavable linkers, etc. We also provide custom development services for chemically labile linkers and enzymatically cleavable linkers.