
CAS 873080-25-2
:4-Pyrimidinecarboxamide, 5-chloro-N-[(4-chlorophenyl)methyl]-2-(ethylsulfonyl)-N-(2-furanylmethyl)-
Description:
4-Pyrimidinecarboxamide, 5-chloro-N-[(4-chlorophenyl)methyl]-2-(ethylsulfonyl)-N-(2-furanylmethyl)- is a synthetic organic compound characterized by its complex structure, which includes a pyrimidine ring, a carboxamide functional group, and multiple substituents such as chloro, ethylsulfonyl, and furanylmethyl groups. This compound is typically classified as a pharmaceutical intermediate or a potential drug candidate, often investigated for its biological activity, particularly in the context of medicinal chemistry. The presence of the chloro and sulfonyl groups may influence its solubility, stability, and reactivity, while the furanylmethyl moiety could contribute to its pharmacological properties. The compound's molecular interactions, including hydrogen bonding and hydrophobic interactions, are crucial for its biological efficacy. As with many synthetic compounds, safety and handling precautions are essential due to potential toxicity or reactivity. Further studies, including in vitro and in vivo evaluations, are necessary to fully understand its therapeutic potential and mechanism of action.
Formula:C19H17Cl2N3O4S
Synonyms:- 4-Pyrimidinecarboxamide, 5-chloro-N-[(4-chlorophenyl)methyl]-2-(ethylsulfonyl)-N-(2-furanylmethyl)-
- Inhibitor,autoimmune,ZAP-70,tyrosine,T-cell,ZAP 180013,ZAP180013,Tyrosinase,ZAP-180013,antigen,inhibit
- ZAP 180013
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Found 5 products.
5-Chloro-N-(4-Chlorobenzyl)-2-(Ethylsulfonyl)-N-(Furan-2-Ylmethyl)Pyrimidine-4-Carboxamide
CAS:<p>5-Chloro-N-(4-Chlorobenzyl)-2-(Ethylsulfonyl)-N-(Furan-2-Ylmethyl)Pyrimidine-4-Carboxamide</p>Purity:98%Molecular weight:454.33g/molZAP-180013
CAS:<p>ZAP-180013 is an inhibitor of zeta-chain-associated protein kinase 70 (ZAP70,IC50 : 1.8 μM).</p>Formula:C19H17Cl2N3O4SPurity:98.89%Color and Shape:SolidMolecular weight:454.33ZAP 180013
CAS:<p>ZAP 180013 is an advanced enzymatic reagent, which is derived from a recombinant source with specificity for targeted protein modification. It operates through a unique mechanism of action that involves the precise cleavage of peptide bonds at target sites identified by a specific amino acid sequence. This specificity allows for minimal off-target effects, making it a reliable tool in proteomics.</p>Formula:C19H17Cl2N3O4SPurity:Min. 95%Molecular weight:454.3 g/mol



