N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide is an aldehyde-functionalized ADC linker that allows selective conjugation to antibody residues, enhancing antibody-drug conjugate targeting and payload stability.
Structure of 1226305-62-9
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N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide is an emerging compound in the field of medicinal chemistry, recognized for its unique structural attributes and potential therapeutic applications. By featuring both dimethylphenoxy and formylbenzamide groups, this compound is well-positioned to engage in various biochemical interactions which may be critical for its efficacy in diverse medical applications. The exploration of such compounds is crucial as researchers strive to discover new drugs that can tackle complex diseases with improved safety and efficacy profiles. As such, N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide represents a promising candidate in the pipeline of potential pharmacological innovations.
One of the foremost applications of N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide is its potential role in cancer therapy. The compound is being studied for its ability to selectively inhibit tumor growth by interfering with specific cellular pathways involved in cancer cell proliferation and survival. This characteristic makes it an attractive candidate for targeted cancer therapy, potentially reducing the side effects often associated with conventional chemotherapy. By contributing to the apoptosis of malignant cells while sparing normal, healthy cells, this compound could represent a significant advancement in the treatment of various cancers, including those resistant to existing therapeutic approaches.
Beyond oncology, N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide is also being investigated for possible applications in anti-inflammatory treatment. Its chemical structure suggests potential efficacy in modulating inflammatory responses, which could be beneficial in managing chronic inflammatory conditions such as rheumatoid arthritis and asthma. By dampening excessive inflammatory signals, the compound may provide relief from symptoms and help in the maintenance of normal tissue function. Ongoing research efforts aim to validate these effects through rigorous clinical trials, with the hope of developing it into a mainstream therapeutic option for inflammatory diseases.
Additionally, N-(2-(3,5-Dimethylphenoxy)ethyl)-4-Formylbenzamide holds promise as a neuroprotective agent, potentially offering therapeutic value in neurological disorders. In conditions like multiple sclerosis and neurodegenerative diseases, protecting neurons from damage is critical. The compound's ability to interact with pathways that mediate neuronal survival and repair gives it potential utility in protecting or restoring nerve function. Researchers are focused on elucidating the mechanisms by which this compound can exert its neuroprotective effects, aiming to pave the way for new treatments that can improve patient outcomes in neurodegenerative and neuroinflammatory diseases. This focus underscores the compound’s versatility and its potential to address several pressing medical challenges.
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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