CCR-9 inhibitors belong to a class of molecules designed to selectively bind to and inhibit the action of the chemokine receptor 9 (CCR-9). CCR-9 is a G protein-coupled receptor (GPCR) that is involved in the chemotactic responses of cells, meaning it plays a role in directing the migration of cells towards areas of the body where their presence is signaled by a gradient of chemokine ligands. CCR-9, in particular, has a specific ligand known as CCL25 or TECK (thymus-expressed chemokine). The interaction between CCR-9 and its ligand is a critical part of the mechanism by which certain cells are guided to specific tissues, which involves a complex cascade of intracellular signaling pathways following receptor-ligand binding.
The discovery and development of CCR-9 inhibitors would typically start with the identification of the receptor's structure and the characterization of its ligand-binding domain. Researchers would use a variety of biochemical and biophysical techniques, such as X-ray crystallography or cryo-electron microscopy, to determine the three-dimensional structure of the receptor. This structural information is crucial for understanding the binding interactions between CCR-9 and its natural ligand, CCL25. With this knowledge, scientists are able to design small molecules that can mimic or block the ligand's interaction with the receptor. These molecules can competitively bind to the ligand-binding site on CCR-9, which prevents the natural ligand from engaging with the receptor and initiating a cellular response.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide has been shown to inhibit the transcription of a wide range of genes by interfering with the activity of RNA polymerase II and other transcription factors. | ||||||
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 is a proteasome inhibitor. By inhibiting proteasome activity, it can lead to increased cellular stress and potentially downregulate the expression of various genes, including CCR9. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
Mitomycin C forms cross-links within DNA, inhibiting DNA replication and transcription, which could reduce the expression of multiple genes. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Camptothecin is a topoisomerase I inhibitor that causes DNA damage by stabilizing the DNA-topoisomerase complex, potentially reducing transcription of various genes. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine incorporates into RNA instead of cytidine and also inhibits DNA methyltransferases, altering gene expression patterns. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
Decitabine is a DNA methyltransferase inhibitor that can induce hypomethylation of DNA and affect gene expression. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol is a cyclin-dependent kinase inhibitor that may indirectly inhibit transcription and subsequently decrease gene expression. | ||||||
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 | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D inhibits RNA polymerase activity by binding to DNA, which can lead to a decrease in mRNA synthesis and downregulation of gene expression. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin is a potent inhibitor of RNA polymerase II and III, preventing mRNA and non-coding RNA synthesis, thus affecting gene expression. | ||||||
SN 38 | 86639-52-3 | sc-203697 sc-203697A sc-203697B | 10 mg 50 mg 500 mg | $117.00 $335.00 $883.00 | 19 | |
SN-38 is the active metabolite of the topoisomerase inhibitor irinotecan, capable of inhibiting DNA replication and transcription. |