TMEM145 inhibitors are a class of compounds designed to interact with and inhibit the activity of the transmembrane protein 145 (TMEM145). TMEM proteins, in general, are a large and diverse group of proteins that span the cellular membrane and are involved in a variety of cellular processes such as transport, cell signaling, and maintaining structural integrity. While the specific biological role of TMEM145 may be less characterized, inhibitors that target this protein would likely be created with the intent to alter its normal function within the cellular membrane environment. The development of TMEM145 inhibitors would thus require a deep exploration of the protein's structure, the identification of its active or regulatory sites, and a clear understanding of its interaction with other cellular components.
Creating specific inhibitors for TMEM145 would involve a multifaceted approach, integrating computational modeling, biochemistry, and molecular biology techniques. Researchers would utilize computational tools to predict the protein's structure and potential druggable pockets where small molecules could bind. Subsequent in vitro studies, such as ligand binding assays or functional screens, would be employed to validate these computational predictions and to understand the binding kinetics and affinity of potential inhibitors. The specificity of TMEM145 inhibitors is paramount, as off-target effects could disrupt other TMEM proteins or membrane-associated processes, leading to undesirable cellular consequences. Therefore, the design of these inhibitors must be precise, ensuring that they are selective for TMEM145 without cross-reacting with other proteins in the transmembrane protein family. The process of inhibitor design is a meticulous one, often involving iterative cycles of synthesis and testing to optimize the compounds for the desired level of interaction with the target protein.
SEE ALSO...
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
Could inhibit DNA methyltransferases, potentially leading to hypomethylation and reduced expression of TMEM145. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Histone deacetylase inhibitor that may increase histone acetylation, potentially changing TMEM145 expression. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Binds to DNA and may interfere with transcription factor binding, potentially reducing TMEM145 transcription. | ||||||
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 | |
Another DNA methyltransferase inhibitor that could affect the methylation and expression of the TMEM145 gene. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
Inhibits RNA polymerase II, potentially reducing mRNA synthesis of genes, including TMEM145. | ||||||
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 | |
Intercalates in DNA and might inhibit RNA polymerase, thereby decreasing TMEM145 mRNA synthesis. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
Non-nucleoside DNA methyltransferase inhibitor, which may affect the methylation and expression of TMEM145. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Histone deacetylase inhibitor that could alter chromatin structure and TMEM145 gene expression. | ||||||
Chaetocin | 28097-03-2 | sc-200893 | 200 µg | $120.00 | 5 | |
Histone methyltransferase inhibitor that could affect histone methylation status and gene expression. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Can inhibit the proteasome, potentially affecting protein degradation and indirectly gene expression. | ||||||