Indole-4-carboxaldehyde

Indole-4-carboxaldehyde (ST-14C) (50-200 µM; 24 h) induces the proliferation of HepG2 cells at concentrations of 50 µM and 100 µM^[1].
Indole-4-carboxaldehyde (25-200 µM; 6-24 h) induces a dose-dependent increase in Glo-1 mRNA and protein expression, and enhances the fluorescence intensity of Glo-1 in HepG2 cells^[1].
Indole-4-carboxaldehyde reacts with 4-substituted thiosemicarbazides in refluxing ethanol to form thioformamide derivatives^[2].
Indole-4-carboxaldehyde shows significant upregulation and directly promotes fruit enlargement and fruit set of the pedicels of Summer Black grapes treated twice with exogenous gibberellin^[3].
Indole-4-carboxaldehyde (100 µM; 2 h pre-incubation prior to 4 h MGO exposure) attenuates the expression of TNF-α, IFN-γ and RAGE mRNA in MGO-induced HepG2 cells, and inhibits the nuclear translocation of NF-κB p65^[1].
Indole-4-carboxaldehyde (100 µM; 2 h pre-incubation prior to 24 h MGO exposure) reduces methylglyoxal-induced secretion of TNF-α and IFN-γ in HepG2 cells and attenuates the formation of AGE^[1].
Indole-4-carboxaldehyde (100 µM; 2 h pre-incubation prior to 4-24 h MGO exposure) fails to attenuate MGO-induced IFN-γ mRNA expression and AGE formation in Glo-1-knockdown HepG2 cells, indicating that these effects are mediated by Glo-1^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.