
CAS 552309-42-9
:Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
6 produits concernés.
T16Ainh-A01
CAS :T16Ainh-A01 is a potent TMEM16A chloride channel inhibitor with a 1 μM IC50, targeting CaCC.Formule :C19H20N4O3S2Degré de pureté :97.18% - 98.15%Couleur et forme :SolidMasse moléculaire :416.52TMEM16AInhibitorsRevealTMEM16A(T16Ainh-A01)
CAS :Formule :C19H20N4O3S2Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :416.51712-((5-Ethyl-4-Methyl-6-Oxo-1,6-Dihydropyrimidin-2-Yl)Thio)-N-(4-(4-Methoxyphenyl)Thiazol-2-Yl)Acetamide
CAS :2-((5-Ethyl-4-Methyl-6-Oxo-1,6-Dihydropyrimidin-2-Yl)Thio)-N-(4-(4-Methoxyphenyl)Thiazol-2-Yl)AcetamideDegré de pureté :98%Masse moléculaire :416.52g/mol2-((5-Ethyl-4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio)-N-(4-(4-methoxyphenyl)thiazol-2-yl)acetamide
CAS :Degré de pureté :98%Masse moléculaire :416.5100098TMEM16A Inhibitor, T16Ainh-A01
CAS :<p>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.</p>Formule :C19H20N4O3S2Degré de pureté :Min. 95%Masse moléculaire :416.52 g/mol




