CAS 1404437-62-2

ML281

Description:

ML281, with the CAS number 1404437-62-2, is a chemical compound that has garnered attention in the field of medicinal chemistry, particularly for its role as a selective inhibitor of the enzyme protein kinase C (PKC). This compound is characterized by its ability to modulate various cellular processes, including cell proliferation and differentiation, making it a subject of interest in cancer research and other therapeutic areas. ML281 exhibits a specific binding affinity for certain PKC isoforms, which can lead to distinct biological effects depending on the cellular context. Its chemical structure typically includes functional groups that contribute to its pharmacological properties, enhancing its selectivity and potency. Additionally, ML281's solubility, stability, and metabolic profile are important factors that influence its potential as a drug candidate. Ongoing studies aim to further elucidate its mechanism of action and therapeutic applications, highlighting its significance in the development of targeted therapies.

2-Thiophenecarboxamide, N-[2-(3,4-dihydro-3-oxo-2-quinoxalinyl)-4-(1-methylethyl)phenyl]-

CAS: 1404437-62-2

Formula: C₂₂H₁₉N₃O₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 389.4702

Ref: IN-DA001CG0

N-(4-Isopropyl-2-(3-Oxo-3,4-Dihydroquinoxalin-2-Yl)Phenyl)Thiophene-2-Carboxamide

CAS: 1404437-62-2

N-(4-Isopropyl-2-(3-Oxo-3,4-Dihydroquinoxalin-2-Yl)Phenyl)Thiophene-2-Carboxamide

Purity: 99%

Molecular weight: 389.47g/mol

Ref: 54-OR1023281

ML281

CAS: 1404437-62-2

ML281

Purity: ≥98%

Molecular weight: 389.47g/mol

Ref: 54-BUP07209

ML281

CAS: 1404437-62-2

ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM.

Formula: C₂₂H₁₉N₃O₂S

Purity: 99.12% - 99.87%

Color and Shape: Solid

Molecular weight: 389.47

Ref: TM-T3423

ML281

CAS: 1404437-62-2

Purity: 99%

Molecular weight: 389.12

Ref: 10-F861829

ML 281

CAS: 1404437-62-2

ML 281 is a molecule being studied for its anti-cancer properties. It has been shown to inhibit tumor growth in vivo and to induce apoptosis in vitro. ML281 binds to the histamine H1 receptor, which inhibits tumor cell proliferation by blocking the mitochondrial pathway of oncogenesis. It also has bactericidal activity against bacteria via inhibition of protein synthesis. The chemical structure of ML281 is a cetirizine derivative that contains an amide linkage between two amino-acid residues.

Formula: C₂₂H₁₉N₃O₂S

Purity: Min. 95%

Molecular weight: 389.47 g/mol

Ref: 3D-EGC43762