Date published: 2026-4-24

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FucT-l Activators

FucT-l activators represent a class of chemical agents that target the enzyme FucT-l, formally known as fucosyltransferase 1, which catalyzes the addition of fucose, a hexose deoxy sugar, to glycoproteins and glycolipids through an alpha-1,2 glycosidic bond. This enzymatic activity is crucial in the synthesis of H antigens, which are precursors to the ABO blood group antigens and have roles in cell adhesion and signal transduction.

Activators of FucT-l may operate via direct or indirect approaches to enhance the enzyme's catalytic function. Direct activators might interact with the enzyme's active site or allosteric sites, promoting a conformational change that increases its affinity for substrates or its catalytic efficiency. This interaction could mimic the natural allosteric regulation by the cell's own metabolites or by modifying the enzyme's structure to a more active form. Indirect activators of FucT-l could operate by increasing the transcription of the FUT1 gene that encodes FucT-l, by stabilizing its mRNA, or by inhibiting the degradation of the enzyme, thereby raising its levels within the cell. Alternatively, they might affect the cellular levels of substrates or cofactors necessary for the enzyme's activity, such as GDP-fucose, the fucosyl donor. They could also modulate the activity of signaling pathways that impact the enzyme's post-translational modifications, which can be critical for its localization, stability, and interaction with substrates.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-Acetyl-D-glucosamine

7512-17-6sc-286377
sc-286377B
sc-286377A
50 g
100 g
250 g
$94.00
$162.00
$306.00
1
(0)

UDP-GlcNAc is a substrate for O-GlcNAc transferase (OGT). OGT modifies proteins post-translationally by adding O-GlcNAc, which can enhance the activity of FucT-l by providing the necessary substrate for its action.

(Z)-Pugnac

132489-69-1sc-204415A
sc-204415
5 mg
10 mg
$224.00
$380.00
3
(1)

PUGNAc is an inhibitor of O-GlcNAcase (OGA), the enzyme that removes O-GlcNAc from proteins. Its inhibition leads to increased O-GlcNAcylation, providing more substrate for FucT-l to act on.

Thiamet G

1009816-48-1sc-224307
sc-224307A
1 mg
5 mg
$52.00
$96.00
1
(2)

Thiamet G is another OGA inhibitor, leading to increased O-GlcNAcylation and, consequently, a greater substrate for FucT-l.

TC-A 2317 hydrochloride

1245907-03-2sc-363291
sc-363291A
10 mg
50 mg
$218.00
$988.00
(0)

This compound enhances the production of sialic acid, which can be used by FucT-l as a substrate for the synthesis of complex carbohydrates.

N-Acetylneuraminic acid

131-48-6sc-281055A
sc-281055
sc-281055D
sc-281055B
sc-281055C
1 g
5 g
25 g
100 g
250 g
$84.00
$156.00
$326.00
$572.00
$1363.00
(1)

Neu5Ac is a form of sialic acid that stands as a substrate for FucT-l in the synthesis of complex carbohydrates.

2-Deoxy-D-glucose

154-17-6sc-202010
sc-202010A
1 g
5 g
$70.00
$215.00
26
(2)

This compound leads to increased O-GlcNAcylation, providing more substrate for FucT-l action.

Butyric acid

107-92-6sc-214640
sc-214640A
1 kg
10 kg
$64.00
$177.00
(0)

Butyrate is a histone deacetylase inhibitor that can lead to increased histone acetylation and open chromatin structure, potentially leading to enhanced FucT-l activity.

Sodium phenylbutyrate

1716-12-7sc-200652
sc-200652A
sc-200652B
sc-200652C
sc-200652D
1 g
10 g
100 g
1 kg
10 kg
$77.00
$166.00
$622.00
$5004.00
$32783.00
43
(1)

Sodium Phenylbutyrate is another histone deacetylase inhibitor that can potentially enhance FucT-l activity by opening the chromatin structure.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

Azacitidine is a DNA methyltransferase inhibitor that can lead to reduction in DNA methylation, potentially leading to increased FucT-l activity by loosening chromatin structure.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

Decitabine is another DNA methyltransferase inhibitor that can potentially enhance FucT-l activity by reducing DNA methylation and thereby opening chromatin structure.