Date published: 2025-11-22

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LARS2 Inhibitors

Leucyl-tRNA synthetase 2 (LARS2) inhibitors are a diverse group of chemical compounds that can disrupt the normal function of the LARS2 enzyme. This enzyme plays a critical role in protein translation by catalyzing the attachment of leucine to its corresponding tRNA molecule, a process essential for incorporating this amino acid into elongating protein chains. Inhibition of LARS2 can result in the disruption of protein synthesis, particularly affecting the mitochondrial proteome where LARS2 is localized. Compounds that can inhibit LARS2 typically do so through various mechanisms, such as competing with the natural substrates of the enzyme-leucine and ATP-or by mimicking the products of the enzyme's catalytic action. This can prevent LARS2 from successfully binding to leucyl-tRNA or may even lead to the premature termination of protein synthesis. Additionally, some compounds can indirectly decrease the cellular demand for LARS2 activity by affecting upstream or downstream processes that are dependent on the enzyme's function.

The chemical structures of LARS2 inhibitors can vary widely, but their common goal is to alter the function of LARS2 within the cell. These compounds can include small molecules that interfere with the active site of the enzyme, preventing the normal catalytic activity from occurring. Others can interact with the enzyme or its tRNA substrate in a way that alters the conformation of the enzyme or the stability of the enzyme-tRNA complex. Beyond direct binding interactions, some compounds can affect the regulation of the LARS2 gene or the stability of its mRNA, reducing enzyme levels through non-competitive mechanisms. By intervening in the LARS2 pathway, these inhibitors can influence the rate of protein synthesis and the overall metabolic activity related to leucine utilization. As such, LARS2 inhibitors can serve as critical tools for probing the fundamental aspects of protein synthesis and mitochondrial function, providing insights into the complex network of biochemical pathways within the cell.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$97.00
$254.00
36
(2)

Although not targeting LARS2 directly, by inhibiting peptidyl transferase, it can reduce the functional demand on LARS2 by hindering protein elongation.

Puromycin dihydrochloride

58-58-2sc-108071
sc-108071B
sc-108071C
sc-108071A
25 mg
250 mg
1 g
50 mg
$40.00
$210.00
$816.00
$65.00
394
(15)

Mimics aminoacyl-tRNA structures and can cause premature chain termination, can decrease LARS2's role in translation.

Tetracycline

60-54-8sc-205858
sc-205858A
sc-205858B
sc-205858C
sc-205858D
10 g
25 g
100 g
500 g
1 kg
$62.00
$92.00
$265.00
$409.00
$622.00
6
(1)

While primarily targeting the 30S ribosomal subunit, can lead to reduced protein synthesis, which in turn can diminish the functional demand on LARS2.

Chloramphenicol

56-75-7sc-3594
25 g
$53.00
10
(1)

Inhibits the 50S ribosomal subunit, can indirectly cause a decrease in the amount of leucyl-tRNA required for protein synthesis.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

Inhibits the mTOR pathway, which is involved in protein synthesis, can result in a decreased need for LARS2 activity.

Gö 6976

136194-77-9sc-221684
500 µg
$223.00
8
(1)

Inhibits protein kinases, which can affect signaling pathways that regulate protein synthesis, potentially reducing LARS2's activity indirectly.

Cerulenin (synthetic)

17397-89-6sc-200827
sc-200827A
sc-200827B
5 mg
10 mg
50 mg
$158.00
$306.00
$1186.00
9
(1)

Inhibits fatty acid synthase, which can affect mitochondrial function, possibly leading to a decreased demand for LARS2.

Triacsin C Solution in DMSO

76896-80-5sc-200574
sc-200574A
100 µg
1 mg
$149.00
$826.00
14
(1)

Inhibits long-chain acyl-CoA synthetase, can affect lipid metabolism and mitochondria function, potentially affecting LARS2 indirectly.

Fluorouracil

51-21-8sc-29060
sc-29060A
1 g
5 g
$36.00
$149.00
11
(1)

As a uracil analog, can interfere with RNA processing and function, which can decrease the overall requirement for LARS2 activity.