MNAB inhibitors, short for monoamine oxidase B inhibitors, belong to a specific chemical class known for their ability to target and modulate the activity of the monoamine oxidase B (MAO-B) enzyme. MAO-B is an enzyme found primarily in the brain and is responsible for the degradation of neurotransmitters such as dopamine, phenylethylamine, and other monoamines. This class of compounds is characterized by their ability to selectively inhibit MAO-B activity, thereby preventing the breakdown of these neurotransmitters. This inhibition results in increased levels of these important chemical messengers in the brain, which can have various physiological and neurological effects.
MNAB inhibitors are structurally diverse, but they typically possess specific functional groups or chemical motifs that enable them to interact with the active site of MAO-B. This interaction interferes with the enzyme's ability to catalyze the oxidation of monoamines, leading to the accumulation of these molecules in the synaptic cleft. This accumulation can have a range of consequences, including altered neurotransmission, enhanced mood, and potential benefits in conditions associated with imbalances in these neurotransmitters. It is worth noting that there is another class of MAO inhibitors known as MAO-A inhibitors, which specifically target monoamine oxidase A, a different isoform of the enzyme. MNAB inhibitors are distinct in their preference for MAO-B and their selectivity for this particular isoform, differentiating them from MAO-A inhibitors.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Triptolide is known to inhibit the transcription of various genes and may influence RC3H2 activity by altering mRNA levels it would bind to. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
This compound inhibits protein synthesis, thereby potentially decreasing RC3H2 levels indirectly by preventing its translation. | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | $94.00 $265.00 | 42 | |
Roscovitine is a cyclin-dependent kinase inhibitor and may affect RC3H2 by altering cell cycle-related mRNA regulation in which RC3H2 is involved. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
MG132 is a proteasome inhibitor that could increase the half-life of proteins regulated by RC3H2, affecting its functional dynamics. | ||||||
Leptomycin B | 87081-35-4 | sc-358688 sc-358688A sc-358688B | 50 µg 500 µg 2.5 mg | $107.00 $416.00 $1248.00 | 35 | |
This compound inhibits the nuclear export of mRNA and could interact with RC3H2's role in mRNA processing. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 inhibits JNK. The JNK pathway is involved in mRNA stability, and inhibitors of this pathway can modulate the function of proteins like RC3H2 that are involved in mRNA regulation. | ||||||
Actinomycin D | 50-76-0 | sc-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 | |
It intercalates DNA and inhibits transcription, potentially reducing the RC3H2 substrate availability. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
This compound is a DNA methyltransferase inhibitor and may affect the expression levels of genes including those regulated by RC3H2. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 is a MEK inhibitor that may alter mRNA stability or processing pathways in which RC3H2 may participate. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 inhibits PI3K, which could affect downstream signaling pathways and potentially the activity of RC3H2. | ||||||