Date published: 2026-3-31

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MCART1 Inhibitors

MCART1 inhibitors are a class of chemical compounds that target the mitochondrial carrier homolog 1 (MCART1), a protein integral to mitochondrial membrane function. MCART1, also known as SLC25A51, is a crucial member of the mitochondrial carrier family, which facilitates the transport of various metabolites across the inner mitochondrial membrane. This protein specifically plays a key role in the import of NAD+ (nicotinamide adenine dinucleotide) into mitochondria, a process vital for the proper functioning of mitochondrial metabolic pathways, particularly those involving redox reactions and energy production. The inhibition of MCART1 disrupts the delicate balance of NAD+ levels inside the mitochondria, thereby influencing the efficiency of metabolic processes such as oxidative phosphorylation, glycolysis, and the citric acid cycle.

MCART1 inhibitors are typically small molecules designed to interfere with the transporter's ability to carry NAD+ into the mitochondrial matrix. Such inhibition leads to a reduction in mitochondrial NAD+ pools, which in turn can alter mitochondrial bioenergetics, electron transport chain function, and ATP production. These inhibitors offer insight into the mechanistic underpinnings of mitochondrial NAD+ homeostasis, making them useful tools for studying mitochondrial metabolism and its broader role in cellular energy dynamics. The ability to modulate MCART1 activity provides researchers with a valuable means to explore how NAD+ depletion affects mitochondrial processes, including oxidative stress, redox balance, and the cellular response to metabolic changes.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

A cytidine analog that incorporates into DNA and RNA and inhibits DNA methyltransferases, potentially reducing SLC25A51 transcription.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

An analog of deoxycytidine that inhibits DNA methyltransferases, which may downregulate SLC25A51 expression by increasing DNA methylation.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$133.00
$275.00
37
(2)

A histone deacetylase inhibitor that could increase histone acetylation, potentially affecting the chromatin structure near the SLC25A51 gene and reducing its expression.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

Another histone deacetylase inhibitor, which could lead to altered chromatin conformation and decreased SLC25A51 gene expression.

Mithramycin A

18378-89-7sc-200909
1 mg
$55.00
6
(1)

An antitumor antibiotic that binds to GC-rich sequences in DNA, potentially preventing transcription factors from accessing the SLC25A51 promoter region.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$269.00
$1050.00
26
(2)

A potent inhibitor of RNA polymerase II, which could lead to the general inhibition of mRNA synthesis, including that of SLC25A51.

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Interacts with DNA and inhibits RNA polymerase, which could nonspecifically inhibit SLC25A51 mRNA synthesis.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$131.00
$515.00
2
(1)

A non-nucleoside DNA methyltransferase inhibitor, which may prevent methylation of the SLC25A51 gene, affecting its expression.

Chaetocin

28097-03-2sc-200893
200 µg
$126.00
5
(1)

A histone methyltransferase inhibitor, which could influence epigenetic marks associated with the SLC25A51 gene and reduce its expression.

Histone Lysine Methyltransferase Inhibitor Inhibitor

935693-62-2 (free base)sc-202651
5 mg
$151.00
4
(1)

An inhibitor of G9a histone methyltransferase, potentially altering the methylation status of histones near the SLC25A51 gene and decreasing its expression.