GPR33 inhibitors belong to a specific class of chemical compounds designed for the purpose of modulating the activity of the G-protein coupled receptor 33 (GPR33). G-protein coupled receptors (GPCRs) are a diverse and extensive family of cell surface receptors that play pivotal roles in signal transduction, enabling cells to respond to a wide array of external stimuli. GPR33, as a member of this receptor family, is expressed in various tissues and cells throughout the human body. The focus of GPR33 inhibitors is to interact with this receptor in a manner that can regulate or influence its activity, potentially affecting downstream cellular responses and signaling pathways associated with GPR33.
GPR33 inhibitors are typically small molecules or compounds that are designed to selectively bind to GPR33, affecting its function either by blocking its active site or by modulating its activity at allosteric sites. The aim is to modify the receptor's behavior, which may in turn impact the cellular responses and signaling cascades it mediates. Researchers in the field of molecular pharmacology and drug discovery are primarily interested in elucidating the roles and functions of GPR33, as well as the precise mechanisms by which GPR33 inhibitors interact with the receptor. This ongoing exploration helps expand our understanding of cellular signaling pathways and may have implications in various biological processes. The development of GPR33 inhibitors represents a promising avenue for advancing our knowledge of GPCR pharmacology and its potential applications in diverse physiological contexts.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $39.00 $59.00 $104.00 $206.00 | 8 | |
Geldanamycin binds to Hsp90 and can inhibit its chaperone function, potentially leading to reduced stability and expression of client proteins like GPR33. | ||||||
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 | |
Actinomycin D intercalates into DNA and inhibits RNA polymerase, which can reduce mRNA synthesis and potentially lower GPR33 expression. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis by interfering with ribosomal translocation, which could decrease overall protein levels including GPR33. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Triptolide is known to inhibit transcriptional activity by affecting multiple transcription factors, which could reduce the expression of GPR33. | ||||||
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 | |
MG-132 inhibits the proteasome, leading to altered protein turnover and potentially affecting the stability of proteins that regulate GPR33 expression. | ||||||
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 | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Curcumin can modulate various signaling pathways and transcription factors, potentially leading to a decrease in GPR33 transcription. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
Resveratrol has been shown to influence a range of signaling molecules and could affect transcription factors that regulate GPR33 expression. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of JNK signaling, which might modify transcription factor activity and reduce expression levels of GPR33. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine is a DNA methyltransferase inhibitor, which can lead to altered gene expression patterns, potentially including downregulation of GPR33. | ||||||
C646 | 328968-36-1 | sc-364452 sc-364452A | 10 mg 50 mg | $265.00 $944.00 | 5 | |
C646 is a selective inhibitor of the histone acetyltransferase p300, which could influence the acetylation status of chromatin and GPR33 expression. | ||||||