N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide - CAS 1225790-49-7

N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide - CAS 1225790-49-7 Catalog number: BADC-00534

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N-(2-(3-Ethylphenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide
CAS
1225790-49-7
Catalog Number
BADC-00534
Molecular Formula
C18H19NO3
Molecular Weight
297.35
N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00534 -- $-- Inquiry
Description
N-(2-(3-Ethylphenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
N-[2-(3-ethylphenoxy)ethyl]-4-formylbenzamide
Canonical SMILES
CCC1=CC(=CC=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C18H19NO3/c1-2-14-4-3-5-17(12-14)22-11-10-19-18(21)16-8-6-15(13-20)7-9-16/h3-9,12-13H,2,10-11H2,1H3,(H,19,21)
InChIKey
UQQYRINRJOIHKF-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

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.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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