CAS 587850-67-7

Benzenesulfonamide, 4-amino-N-(2-phenylethyl)-

Description:

Benzenesulfonamide, 4-amino-N-(2-phenylethyl)- is an organic compound characterized by the presence of a sulfonamide functional group attached to a benzene ring, along with an amino group and a phenylethyl substituent. This compound typically exhibits properties associated with sulfonamides, such as solubility in polar solvents and potential biological activity. The amino group can participate in hydrogen bonding, influencing its reactivity and interactions with biological targets. The phenylethyl moiety may contribute to the compound's lipophilicity, affecting its pharmacokinetic properties. As a sulfonamide derivative, it may also exhibit antibacterial or diuretic properties, although specific biological activities would depend on its structural nuances and the context of its use. The compound's molecular structure suggests it could be of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Formula: C₁₄H₁₆N₂O₂S

4-Amino-n-(2-phenylethyl)benzenesulfonamide

CAS: 587850-67-7

Formula: C₁₄H₁₆N₂O₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 276.3540

Ref: IN-DA00EAA7

C-7280948

CAS: 587850-67-7

C-7280948

Purity: ≥95%

Molecular weight: 276.35g/mol

Ref: 54-BUP13498

4-Amino-N-Phenethylbenzenesulfonamide

CAS: 587850-67-7

4-Amino-N-Phenethylbenzenesulfonamide

Purity: 98%

Molecular weight: 276.35g/mol

Ref: 54-OR1026280

C-7280948

CAS: 587850-67-7

C-7280948 is a PRMT1 inhibitor.

Formula: C₁₄H₁₆N₂O₂S

Purity: 99.55% - ≥95%

Color and Shape: Solid

Molecular weight: 276.35

Ref: TM-T2097

4-Amino-N-(2-phenylethyl)benzenesulfonamide

CAS: 587850-67-7

4-Amino-N-(2-phenylethyl)benzenesulfonamide (4APBS) is a histone deacetylase inhibitor. It has been shown to inhibit the histone methyltransferase activity of EZH2, which is important for regulating gene expression, in cells treated with 4APBS. This inhibition leads to increased levels of the transcriptional coactivator β-catenin and reduced levels of tumor suppressor genes. These changes ultimately lead to an increase in cancer cell proliferation and decreased apoptosis. 4APBS also interacts with hormone receptors that are found on the surface of cells and can regulate cellular functions such as proliferation, differentiation, or apoptosis.

Formula: C₁₄H₁₆N₂O₂S

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 276.36 g/mol

Ref: 3D-FA113793

4-amino-N-(2-phenylethyl)benzenesulfonamide

CAS: 587850-67-7

Formula: C₁₄H₁₆N₂O₂S

Purity: ≥98%

Molecular weight: 276.35

Ref: 10-F365215