The enzyme A4GALT (alpha 1,4-galactosyltransferase) is involved in the synthesis of the P(k) antigen, also known as the P1 blood group antigen. A4GALT is responsible for transferring galactose to lactosylceramide and other glycoconjugates. The enzyme plays a critical role in blood transfusion medicine and is also implicated in other biological processes, such as cell adhesion and immune response. Activators in this class can operate through different mechanisms to enhance the catalytic activity of A4GALT. For instance, some activators might work by increasing the availability of the enzyme's natural substrates like UDP-galactose. Others could potentially influence cellular signaling pathways or epigenetic markers that lead to increased A4GALT expression or a more favorable enzymatic environment. Focusing on the substrate availability approach, certain small molecules might serve to increase the concentrations of UDP-galactose, thereby providing the A4GALT enzyme with more of its substrate and consequently elevating its activity.
Additional mechanisms by which these activators may function include indirect pathway modulation. Some molecules could inhibit the activity of pathways that oppose or limit A4GALT's natural functions. For instance, inhibitors of fucosyltransferases might tip the balance in favor of galactosylation, thereby indirectly increasing A4GALT activity. On a similar note, molecules that modulate intracellular signaling cascades or epigenetic markers could also serve to indirectly bolster A4GALT's activity. By targeting various upstream cellular events, these activators could induce a series of downstream effects that culminate in the increased activity of A4GALT.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
UDP-α-D-Galactose disodium salt | 137868-52-1 | sc-286849 sc-286849A | 10 mg 50 mg | $102.00 $194.00 | 1 | |
Availability of this substrate can naturally influence the enzymatic activity of A4GALT. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Compounds such as valproic acid and trichostatin A could affect the chromatin structure around the A4GALT gene, potentially influencing its transcription and thus enzyme activity. | ||||||
Ademetionine | 29908-03-0 | sc-278677 sc-278677A | 100 mg 1 g | $180.00 $655.00 | 2 | |
As a general methyl donor, SAM could potentially influence the methylation status of the A4GALT gene, thereby affecting its expression and activity. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
One of the first synthetic molecules identified to inhibit PI3K. Inhibition of PI3K could indirectly influence glycosylation processes and thus A4GALT activity. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
A steroidal metabolite of the fungi Penicillium funiculosum and is a potent, irreversible inhibitor of PI3K. Inhibition of PI3K could indirectly influence glycosylation processes and thus A4GALT activity. | ||||||
CAL-101 | 870281-82-6 | sc-364453 | 10 mg | $189.00 | 4 | |
A PI3Kδ isoform-specific inhibitor approved for certain types inhibition of PI3K could indirectly influence glycosylation processes and thus A4GALT activity. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $80.00 $212.00 $408.00 | 48 | |
A small molecule that inhibits the activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7, which are needed for TGF-β signaling. Its inhibition could lead to altered glycosylation pathways, thereby potentially influencing A4GALT activity. | ||||||
LY2109761 | 700874-71-1 | sc-396262 sc-396262A | 1 mg 5 mg | $87.00 $270.00 | 9 | |
An oral small molecule inhibitor that targets TGF-β type I and type II receptors. Its inhibition could lead to altered glycosylation pathways, thereby potentially influencing A4GALT activity. | ||||||
LY2157299 | 700874-72-2 | sc-391123 sc-391123A | 5 mg 10 mg | $209.00 $352.00 | 3 | |
Currently in research models for is a selective inhibitor of the TGF-β receptor I kinase. Its inhibition could lead to altered glycosylation pathways, thereby potentially influencing A4GALT activity. | ||||||