NUBP1 inhibitors are a class of chemical compounds that specifically target and inhibit the activity of Nucleotide-binding protein 1 (NUBP1), a key component involved in cellular processes related to the regulation of cytoskeletal dynamics and iron-sulfur cluster biosynthesis. NUBP1 is an ATP-binding protein that functions as part of a complex system regulating the assembly and distribution of iron-sulfur (Fe-S) clusters, which are essential cofactors for various enzymes involved in electron transport and metabolic pathways. Fe-S cluster biosynthesis is vital for the activity of enzymes in processes like mitochondrial respiration, DNA repair, and ribosomal function. By inhibiting NUBP1, these compounds can disrupt its role in the Fe-S cluster machinery, leading to alterations in cellular metabolism and oxidative stress response mechanisms. The impact on the assembly of Fe-S clusters has broad implications for cellular homeostasis, particularly in cells with high metabolic rates and reliance on oxidative phosphorylation.
In addition to their role in Fe-S cluster regulation, NUBP1 inhibitors can also affect the cytoskeleton, as NUBP1 is implicated in microtubule dynamics and the regulation of spindle assembly during cell division. NUBP1 interacts with other nucleotide-binding proteins and molecular motors that help maintain the integrity of the mitotic spindle, ensuring proper chromosome segregation during mitosis. Inhibition of NUBP1 may therefore interfere with cytoskeletal functions, leading to defects in cell division and structural organization within the cell. This can cause a cascade of cellular responses, including disruptions in intracellular transport, signal transduction, and mechanical stability. The complex interplay between NUBP1's role in Fe-S cluster biogenesis and cytoskeletal regulation makes the study of NUBP1 inhibitors particularly intriguing in understanding fundamental biochemical pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ciclopirox | 29342-05-0 | sc-217893 | 25 mg | $207.00 | 2 | |
Chelates Fe2+ ions, possibly disrupting Fe-S cluster assembly where NUBP1 is involved. | ||||||
Deferiprone | 30652-11-0 | sc-211220 sc-211220A | 1 g 5 g | $124.00 $134.00 | 5 | |
Iron chelator that may affect Fe-S cluster biogenesis and NUBP1 function. | ||||||
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | $286.00 | 1 | |
Inhibits NEDD8 activating enzyme, affecting protein neddylation which could indirectly influence NUBP1 activity. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Proteasome inhibitor that can alter protein degradation pathways, potentially affecting NUBP1 levels. | ||||||
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 | |
Proteasome inhibitor that can lead to accumulation of misfolded proteins, possibly affecting NUBP1 function. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $69.00 | 2 | |
Lysosomotropic agent that can alter iron homeostasis, potentially impacting Fe-S cluster formation and NUBP1. | ||||||
Deferoxamine mesylate | 138-14-7 | sc-203331 sc-203331A sc-203331B sc-203331C sc-203331D | 1 g 5 g 10 g 50 g 100 g | $255.00 $1060.00 $2923.00 $4392.00 $8333.00 | 19 | |
Iron chelator that can disrupt iron availability, potentially influencing NUBP1-related Fe-S cluster assembly. | ||||||
3′-Azido-3′-deoxythymidine | 30516-87-1 | sc-203319 | 10 mg | $61.00 | 2 | |
Nucleoside reverse transcriptase inhibitor that can incorporate into DNA and disrupt cell division, potentially affecting NUBP1's role in the centrosome cycle. | ||||||
Auranofin | 34031-32-8 | sc-202476 sc-202476A sc-202476B | 25 mg 100 mg 2 g | $153.00 $214.00 $4000.00 | 39 | |
Thioredoxin reductase inhibitor that may influence redox homeostasis, potentially affecting NUBP1's function in Fe-S cluster assembly. | ||||||
PX 12 | 141400-58-0 | sc-358518 sc-358518A | 10 mg 50 mg | $133.00 $505.00 | 9 | |
Inhibits thioredoxin-1, which could disturb cellular redox states and indirectly impact NUBP1 activity. | ||||||