KLHDC3 inhibitors constitute a specialized category of chemical compounds designed to specifically target and suppress the activity of the Kelch Domain Containing 3 (KLHDC3) protein. This protein is involved in various cellular processes, including the regulation of protein degradation pathways that are critical for maintaining cellular homeostasis. By inhibiting KLHDC3, these compounds can modulate the ubiquitin-proteasome system, potentially leading to the accumulation or reduction of specific substrates relevant to disease mechanisms. The strategic inhibition of KLHDC3 can offer insights into the protein's biological function and its contribution to various pathologies, including cancer, neurodegenerative diseases, and inflammatory conditions. The design and discovery of KLHDC3 inhibitors leverage advanced screening techniques, structural biology insights, and computational modeling to identify molecules that can bind to the KLHDC3 protein with high affinity and specificity, thereby blocking its functional activity.
The development of KLHDC3 inhibitors involves a multi-step process beginning with the identification of lead compounds through high-throughput screening (HTS) of chemical libraries. Following the identification of potential inhibitors, structure-activity relationship (SAR) studies are employed to optimize these leads for improved potency and selectivity. This optimization process is supported by detailed biochemical and biophysical assays to characterize the interaction between the inhibitors and KLHDC3, as well as cellular assays to assess the functional impact of inhibition on KLHDC3-mediated pathways. Throughout this development process, the aim is to elucidate the mechanistic basis of KLHDC3 inhibition. Importantly, the focus is on the biochemical and cellular mechanisms of action. This rigorous approach ensures that KLHDC3 inhibitors are thoroughly characterized, providing valuable tools for research associated with dysregulated protein degradation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG-132 [Z-Leu- Leu-Leu-CHO] inhibits the proteasome, potentially impacting the degradation pathway mediated by CRL2(KLHDC3) E3 ligase complex. | ||||||
Lactacystin | 133343-34-7 | sc-3575 sc-3575A | 200 µg 1 mg | $165.00 $575.00 | 60 | |
Lactacystin specifically inhibits the proteasome, which could affect the downstream degradation of proteins targeted by KLHDC3. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib, a proteasome inhibitor, may alter the degradation of proteins recognized by the CRL2(KLHDC3) complex. | ||||||
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | $280.00 | 1 | |
MLN 4924 inhibits NEDD8-activating enzyme, affecting neddylation, a modification crucial for the activity of cullin-RING E3 ligases, including CRL2 complexes. | ||||||
Carfilzomib | 868540-17-4 | sc-396755 | 5 mg | $40.00 | ||
Carfilzomib, a proteasome inhibitor, could impact the ubiquitin-proteasome pathway, influencing KLHDC3's function. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis, potentially affecting the pool of substrates available for KLHDC3-mediated degradation. | ||||||
Puromycin dihydrochloride | 58-58-2 | sc-108071 sc-108071B sc-108071C sc-108071A | 25 mg 250 mg 1 g 50 mg | $40.00 $210.00 $816.00 $65.00 | 394 | |
Puromycin dihydrochloride causes premature chain termination during protein synthesis, potentially influencing the substrate specificity of KLHDC3. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin has been shown to modulate various cellular pathways, including those related to protein degradation and could indirectly affect KLHDC3's activity. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine affects lysosomal function and autophagy, potentially influencing cellular pathways where KLHDC3 is involved. | ||||||