AMAC1L1 inhibitors are a class of chemical compounds designed to specifically inhibit the activity of the AMAC1L1 enzyme, a member of the acyl-malonyl-coenzyme A (AMAC) family, which is involved in fatty acid metabolism and related biochemical processes. AMAC1L1 catalyzes reactions that are essential for lipid modification and energy production, particularly in the processing of fatty acyl groups. Inhibitors of AMAC1L1 function by binding to the enzyme's active site or allosteric regions, preventing the enzyme from catalyzing its normal biochemical reactions. These inhibitors are often designed to mimic the natural substrates or transition states of the enzymatic process, enabling them to bind competitively to the active site and block the enzyme's ability to process acyl-malonyl-CoA intermediates. The chemical structures of AMAC1L1 inhibitors generally include functional groups that interact with catalytic residues in the enzyme, such as carbonyl groups, hydroxyls, or hydrophobic regions that help form stable interactions through hydrogen bonding or hydrophobic contacts.
The design and development of AMAC1L1 inhibitors are informed by structural biology techniques like X-ray crystallography and cryo-electron microscopy, which provide detailed information about the enzyme's three-dimensional structure, including its active site configuration and binding pockets. This structural knowledge allows researchers to identify key interaction sites for inhibitor binding and design molecules with high specificity for AMAC1L1. Computational tools, such as molecular docking simulations, are frequently used to predict how potential inhibitors will interact with the enzyme and to optimize their binding efficiency and selectivity. Some AMAC1L1 inhibitors may also act through allosteric mechanisms by binding to regions of the enzyme distant from the active site, inducing conformational changes that reduce the enzyme's overall activity. These inhibitors are valuable tools for studying the role of AMAC1L1 in metabolic pathways, particularly in understanding its contribution to fatty acid metabolism and the regulation of lipid-related biochemical processes. By inhibiting AMAC1L1, researchers can explore the enzyme's specific functions in cellular metabolism and gain insights into how it influences broader metabolic networks.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $92.00 $209.00 | 33 | |
As a folate analog, Methotrexate inhibits dihydrofolate reductase, potentially decreasing "AMAC1L1" expression by disrupting folate metabolism. | ||||||
Azaserine | 115-02-6 | sc-29063 sc-29063A | 50 mg 250 mg | $306.00 $906.00 | 15 | |
Azaserine acts as a glutamine antagonist, potentially inhibiting "AMAC1L1" through its role in glutamine metabolism. | ||||||
Glyphosate | 1071-83-6 | sc-211568D sc-211568 sc-211568A sc-211568B sc-211568C | 250 mg 1 g 5 g 10 g 25 g | $45.00 $143.00 $408.00 $769.00 $1234.00 | 4 | |
Glyphosate inhibits the shikimate pathway, which could indirectly affect "AMAC1L1" expression by altering aromatic amino acid synthesis. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $76.00 $255.00 | 18 | |
Hydroxyurea disrupts ribonucleotide reductase, potentially reducing "AMAC1L1" expression by affecting DNA synthesis and repair mechanisms. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
As a pyrimidine analog, 5-Fluorouracil may decrease "AMAC1L1" expression by disrupting nucleotide synthesis. | ||||||
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, which may lead to a general decrease in "AMAC1L1" protein levels. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine disrupts lysosome function, which could indirectly lower "AMAC1L1" expression by affecting cellular autophagy and degradation processes. | ||||||
Sulfasalazine | 599-79-1 | sc-204312 sc-204312A sc-204312B sc-204312C | 1 g 2.5 g 5 g 10 g | $60.00 $75.00 $125.00 $205.00 | 8 | |
Sulphasalazine can influence the NF-κB pathway, which may lead to the downregulation of "AMAC1L1" 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 intercalates into DNA, inhibiting transcription and potentially decreasing "AMAC1L1" expression. | ||||||