N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide is an aldehyde-functionalized ADC linker supporting efficient site-specific conjugation, enhancing antibody-drug conjugate stability and therapeutic performance.
Structure of 1226006-03-6
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N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide is a chemical compound with a unique structure that incorporates a benzo[d][1,3]dioxole group, a well-known pharmacophore with various bioactive properties. The benzo[d][1,3]dioxole ring system has been extensively studied for its potential in drug design due to its ability to interact with multiple biological targets. When combined with the formylbenzamide group, this compound presents an exciting opportunity for the development of novel therapeutic agents, particularly in the fields of cancer treatment, enzyme inhibition, and drug discovery.
One of the primary applications of N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide lies in its potential as an anticancer agent. The benzo[d][1,3]dioxole structure is known for its ability to interact with enzymes and receptors involved in cancer cell signaling, such as kinases and growth factor receptors. The formylbenzamide component may also play a critical role in targeting specific cellular pathways that are dysregulated in cancer. By modulating these pathways, the compound could inhibit tumor growth and proliferation, offering a promising strategy for the treatment of various cancers, including breast, lung, and colon cancers. The selectivity provided by the unique structure could reduce off-target effects, making it a valuable candidate for further development as a targeted cancer therapeutic.
In addition to its potential as an anticancer agent, N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide could be explored as a modulator of enzyme activity, particularly in relation to enzymes involved in cell signaling and metabolism. The benzo[d][1,3]dioxole ring is known to exhibit inhibitory activity against various enzymes, such as protein kinases, which are often overactive in cancer cells. The formylbenzamide group may enhance the binding affinity of the compound to these enzymes, allowing for more effective inhibition. By selectively inhibiting enzymes involved in cancer cell growth and survival, this compound could offer a therapeutic approach for treating cancer and other diseases linked to abnormal enzyme activity, such as autoimmune disorders or inflammatory diseases.
Furthermore, N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide has significant potential in drug discovery and molecular biology research. Due to its distinctive structure, it could serve as a valuable tool for studying drug-receptor interactions and cellular signaling mechanisms. The compound can be labeled with fluorescent or radioactive markers to track its distribution within cells or tissues. This capability makes it an excellent candidate for developing molecular probes that could aid in high-throughput screening assays, providing researchers with critical insights into how small molecules interact with biological targets. This research could lead to the identification of more effective drug candidates for treating various diseases.
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-00543 | N-(2-(3-Ethoxyphenoxy)ethyl)-4-Formylbenzamide | 1226006-55-8 |
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