Date published: 2025-9-17

1-800-457-3801

SCBT Portrait Logo
Seach Input

DDX50 Activators

DDX50 activators encompass a diverse group of compounds that interact with cellular energy balance, stress response, and RNA metabolism, indirectly influencing the activity of this RNA helicase. This set includes agents that increase intracellular ATP levels, such as adenosine triphosphate itself, ensuring the energy supply for the ATP-dependent helicase activity of DDX50. Compounds like actinomycin D and 5-azacytidine alter the transcription landscape, potentially creating a higher demand for RNA processing and, in turn, DDX50 function. Caffeine, by affecting cellular cAMP levels, may indirectly influence ATP availability and thereby DDX50 activity.

Moreover, inhibitors of nuclear export and protein folding such as Leptomycin B and MG132, respectively, could lead to an accumulation of RNA within the nucleus, thus necessitating increased DDX50 activity for RNA processing and management. Menadione and sodium arsenite, by inducing oxidative stress, may trigger a cellular response that involves the upregulation of RNA helicases including DDX50. Geldanamycin and its derivative 17-AAG target Hsp90 and provoke a heat shock response, which can include the activation of RNA helicases like DDX50 to manage stress-induced RNA dysregulation. Lastly, compounds that induce various forms of cellular stress, such as beta-lapachone and tunicamycin, might lead to enhanced DDX50 activity as the cell attempts to mitigate the effects of stress on RNA metabolism.

SEE ALSO...

Items 11 to 12 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

β-Lapachone

4707-32-8sc-200875
sc-200875A
5 mg
25 mg
$110.00
$450.00
8
(1)

Activates NQO1 and induces cellular oxidative stress, potentially increasing the need for DDX50 in RNA metabolism as part of the cellular response.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$169.00
$299.00
66
(3)

Induces ER stress by inhibiting N-glycosylation, which can lead to increased RNA misprocessing and a potential compensatory upregulation of DDX50 activity in an attempt to manage the stress-related RNA load.