Date published: 2025-9-11

1-800-457-3801

SCBT Portrait Logo
Seach Input

4921528O07Rik Inhibitors

The class of MROH9 Inhibitors would include chemicals that can indirectly influence the activity of MROH9 by modulating metabolic pathways and cellular energy homeostasis. Since MROH9 is presumed to be associated with lipid metabolism and related functions, agents that alter lipid synthesis, breakdown, or signaling can exert an influence on proteins that are part of these processes. For example, 2-Deoxy-D-glucose and AICAR, by affecting glucose metabolism and activating AMPK respectively, can alter the cellular energy state, potentially influencing the activity of proteins like MROH9 that may be involved in the cellular energy response.

Compounds such as rapamycin and etomoxir can have broader effects on cellular growth and metabolism. Rapamycin, by inhibiting mTOR, modulates a key signaling pathway that orchestrates cell growth in response to nutrient availability, while etomoxir impedes fatty acid oxidation, a crucial metabolic pathway. PPAR agonists such as WY-14643, GW501516, and fenofibrate specifically target nuclear receptors that play a central role in lipid metabolism and can modulate the expression and activity of a variety of proteins within this pathway. Through these mechanisms, these chemicals can indirectly influence the function of MROH9 by altering the lipid metabolic environment within the cell. Additionally, ALLN and oligomycin, by inhibiting protein degradation and mitochondrial ATP production respectively, can affect the stability and energy regulation of proteins implicated in cellular metabolism.

SEE ALSO...

Items 11 to 11 of 11 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Oligomycin A

579-13-5sc-201551
sc-201551A
sc-201551B
sc-201551C
sc-201551D
5 mg
25 mg
100 mg
500 mg
1 g
$175.00
$600.00
$1179.00
$5100.00
$9180.00
26
(1)

An ATP synthase inhibitor that disrupts mitochondrial ATP production, which can influence proteins involved in energy sensing and metabolism.