Description
A inhibitor of endosomal trafficking; increases accumulation of fluorescently labeled EGF in early endosomes in HeLa cells at 20 μM; inhibits cell death induced by anthrax lethal toxin in RAW264.7 cells (IC50 = 1.7 μM) as well as by additional acid-dependent bacterial toxins, including diphtheria toxin, P. aeruginosa ExoA, and Hd-CDT, in various cell types; inhibits infection of Vero and HeLa cells by the low pH-dependent LCMV (Armstrong strain) and influenza A/WSN/33 viruses, respectively
Formal name: 2-[(4-bromophenyl)methylene]-N-(2,6-dimethylphenyl)-hydrazinecarboxamide
Synonyms:
Molecular weight: 346.2
CAS: 415687-81-9
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Research Area|Cell Biology|Endomembrane System & Vesicular Trafficking||Research Area|Immunology & Inflammation|Innate Immunity||Research Area|Infectious Disease|Bacterial Diseases||Research Area|Infectious Disease|Viral Diseases|Influenza