N-(2-((2, 3-Dihydro-1H-inden-5-yl)oxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).
Catalog Number | Size | Price | Quantity | |
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BADC-00540 | -- | $-- | Inquiry |
Pharmaceutical Applications: N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide has gained attention in the pharmaceutical industry due to its potential as a therapeutic agent. Its unique structure, which combines a formylbenzamide group with an indenyl ether moiety, allows it to interact with various molecular targets. This compound has been explored for its anti-inflammatory properties, making it a candidate for treating conditions such as arthritis and other inflammatory diseases. By modulating key signaling pathways, it could help reduce tissue inflammation and mitigate pain associated with chronic inflammatory disorders. Additionally, its ability to influence cellular processes, such as apoptosis and cell proliferation, holds promise for cancer therapy research.
Chemical Biology and Drug Discovery: In chemical biology, N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide serves as a valuable tool for drug discovery. Its ability to serve as a molecular probe makes it useful for investigating biological systems and identifying potential therapeutic targets. The compound can be employed in high-throughput screening assays to identify new lead molecules for drug development. Furthermore, due to its structural features, it may exhibit specificity for certain enzymes or receptors, making it a candidate for developing more targeted therapies. By understanding how it interacts with biological molecules, researchers can gain insight into the molecular mechanisms of diseases, facilitating the discovery of novel drugs.
Materials Science and Synthesis: N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide also has potential applications in materials science, particularly in the synthesis of functional materials. The compound’s aromatic and heterocyclic components contribute to its ability to form stable bonds with other molecules, which can be leveraged in the development of polymers or composite materials with specialized properties. Its unique molecular structure allows it to serve as a building block in the creation of functionalized surfaces or coatings with specific chemical reactivity. These materials could find applications in areas such as sensors, electronics, and catalysis.
Cosmetic and Dermatological Uses: In addition to its pharmaceutical and chemical applications, N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide is being explored in the cosmetic and dermatological sectors. The compound’s potential to modulate inflammation and influence skin cell behavior makes it a candidate for skincare formulations. It could be used in products aimed at reducing signs of aging, such as wrinkles and fine lines, by promoting skin regeneration and enhancing elasticity. Additionally, its antioxidant properties may contribute to the prevention of oxidative stress-induced skin damage. The compound's gentle action on the skin could make it an ideal ingredient for sensitive skin formulations.
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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.