CAS 552309-42-9

T16Ainh-A01

CAS: 552309-42-9

T16Ainh-A01 is a potent TMEM16A chloride channel inhibitor with a 1 μM IC50, targeting CaCC.

Fórmula: C₁₉H₂₀N₄O₃S₂

Pureza: 97.18% - 98.15%

Forma y color: Solid

Peso molecular: 416.52

Ref: TM-T13059

TMEM16AInhibitorsRevealTMEM16A(T16Ainh-A01)

CAS: 552309-42-9

Fórmula: C₁₉H₂₀N₄O₃S₂

Pureza: 97%

Forma y color: Solid

Peso molecular: 416.5171

Ref: IN-DA00DF68

2-((5-Ethyl-4-Methyl-6-Oxo-1,6-Dihydropyrimidin-2-Yl)Thio)-N-(4-(4-Methoxyphenyl)Thiazol-2-Yl)Acetamide

CAS: 552309-42-9

2-((5-Ethyl-4-Methyl-6-Oxo-1,6-Dihydropyrimidin-2-Yl)Thio)-N-(4-(4-Methoxyphenyl)Thiazol-2-Yl)Acetamide

Pureza: 98%

Peso molecular: 416.52g/mol

Ref: 54-OR1009623

T16Ainh-A01

CAS: 552309-42-9

T16Ainh-A01

Pureza: ≥95%

Peso molecular: 416.52g/mol

Ref: 54-BUP06175

2-((5-Ethyl-4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio)-N-(4-(4-methoxyphenyl)thiazol-2-yl)acetamide

CAS: 552309-42-9

Pureza: 98%

Peso molecular: 416.5100098

Ref: 10-F869769

TMEM16A Inhibitor, T16Ainh-A01

CAS: 552309-42-9

Tmem16a Inhibitor, T16Ainh-A01 is a pharmacological agent that has been shown to be effective against human cells in vivo. It inhibits the membrane hyperpolarization and intracellular calcium concentration. This drug is a potent activator of the epidermal growth factor receptor (EGFR). The compound also activates cellular signaling pathways, such as the phosphatidylinositol 3-kinase (PI3K) pathway. T16Ainh-A01 inhibits cellular functions by inhibiting cation channels and gland cells.

Fórmula: C₁₉H₂₀N₄O₃S₂

Pureza: Min. 95%

Peso molecular: 416.52 g/mol

Ref: 3D-CXA30942