N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide is an aldehyde-bearing ADC linker designed for efficient conjugation to antibodies, enhancing payload delivery and targeted cytotoxicity in antibody-drug conjugates.
Structure of 1225790-49-7
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N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide is garnering interest within pharmaceutical research due to its unique chemical structure and potential across various therapeutic applications. The molecule comprises ethylphenoxy and formylbenzamide moieties, which endow it with distinctive biochemical properties. This structural sophistication allows for a range of biological interactions, positioning it as a promising candidate for further exploration in drug development. Scientific investigations are underway to assess its potential benefits and applications in addressing key health challenges, driving innovation in medical treatment paradigms.
One of the primary areas of focus for N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide is its prospective use in oncology. Researchers are studying its potential to inhibit tumor growth by targeting specific signaling pathways involved in the proliferation and survival of cancer cells. Its ability to discriminate between malignant and normal cells could result in a targeted therapy with minimized toxicity to healthy tissues. Such selectivity is vital for improving patient outcomes and quality of life during cancer treatment, as it aims to provide effective disease control while reducing side effects commonly associated with traditional chemotherapy.
Beyond cancer treatment, N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide is being explored for its anti-inflammatory properties. Chronic inflammatory conditions, such as arthritis and inflammatory bowel disease, could benefit from new treatments that effectively control inflammation without adverse effects. The compound's structure suggests it may interact with inflammatory mediators, potentially reducing inflammation and offering relief to individuals suffering from these debilitating conditions. Ongoing research includes preclinical and clinical studies to establish its efficacy and safety profile, with the hope of integrating it into standard treatment regimens.
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-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 | |
BADC-00543 | N-(2-(3-Ethoxyphenoxy)ethyl)-4-Formylbenzamide | 1226006-55-8 |
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