Date published: 2026-5-1

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CHT1 Activators

CHT1 (Solute Carrier Family 5 Member 7) activators belong to a distinct class of chemical compounds that have gained significance in the realm of molecular biology and pharmacology. CHT1, also known as the high-affinity choline transporter 1, is a membrane protein encoded by the SLC5A7 gene, and it plays a pivotal role in the transportation of choline, a crucial nutrient, across cell membranes. Choline is essential for a myriad of biological processes, including neurotransmitter synthesis, membrane structure maintenance, and one-carbon metabolism. The activation of CHT1 by specific ligands or activators has emerged as a subject of profound interest due to its implications in understanding cellular and molecular mechanisms related to choline uptake and transport.

CHT1 activators, through their interaction with the CHT1 protein, modulate choline transport, which can influence the availability of choline within cells. This, in turn, may have downstream effects on various cellular functions, such as acetylcholine synthesis in neurons, phospholipid production in cell membranes, and methylation reactions involved in gene regulation and overall metabolic processes. Understanding CHT1 activators is not only essential for unraveling the intricacies of choline metabolism but also for exploring their roles in the development of research tools. These compounds could serve as valuable molecular probes for investigating choline-related pathways and may offer insights into the broader field of membrane transport biology.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Forskolin

66575-29-9sc-3562
sc-3562A
sc-3562B
sc-3562C
sc-3562D
5 mg
50 mg
1 g
2 g
5 g
$78.00
$153.00
$740.00
$1413.00
$2091.00
73
(3)

Forskolin is a natural compound that directly activates SLC5A7 (CHT1) by increasing cAMP levels, which, in turn, enhances the transport of iodide into thyroid cells, ultimately activating thyroid function.

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
$260.00
$350.00
$500.00
34
(1)

IBMX indirectly activates SLC5A7 (CHT1) by inhibiting cAMP phosphodiesterase, leading to elevated cAMP levels that enhance the iodide transport function of SLC5A7 within thyroid cells.

L-Thyroxine, free acid

51-48-9sc-207813
sc-207813A
100 mg
500 mg
$35.00
$74.00
2
(0)

Levothyroxine directly activates SLC5A7 (CHT1) by providing a synthetic form of the thyroid hormone T4, thus increasing thyroid hormone production and iodide transport.

L-3,3′,5-Triiodothyronine, free acid

6893-02-3sc-204035
sc-204035A
sc-204035B
10 mg
100 mg
250 mg
$41.00
$77.00
$153.00
(1)

Liothyronine directly activates SLC5A7 (CHT1) by supplying a synthetic form of the thyroid hormone T3, enhancing the transport of iodide into thyroid cells and activating thyroid function.

Isoproterenol Hydrochloride

51-30-9sc-202188
sc-202188A
100 mg
500 mg
$28.00
$38.00
5
(0)

Isoproterenol indirectly activates SLC5A7 (CHT1) by activating beta-adrenergic receptors, activating thyroid function, and the activity of CHT1 through adrenergic pathways.

Dobutamine

34368-04-2sc-507555
100 mg
$295.00
(0)

Dobutamine indirectly activates SLC5A7 (CHT1) through beta-adrenergic activation, potentially activating the activity of CHT1 within thyroid cells.

Theophylline

58-55-9sc-202835
sc-202835A
sc-202835B
5 g
25 g
100 g
$20.00
$32.00
$85.00
6
(0)

Theophylline indirectly activates SLC5A7 (CHT1) by inhibiting cAMP phosphodiesterase, which elevates cAMP levels and indirectly activates the activity of CHT1 within the thyroid.

Rolipram

61413-54-5sc-3563
sc-3563A
5 mg
50 mg
$77.00
$216.00
18
(1)

Rolipram indirectly activates SLC5A7 (CHT1) by inhibiting cAMP phosphodiesterase, leading to increased cAMP levels that may indirectly activate CHT1 activity within thyroid cells.

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$41.00
$132.00
$214.00
$500.00
$948.00
119
(6)

PMA indirectly activates SLC5A7 (CHT1) by directly activating protein kinase C (PKC), potentially activating thyroid function and the activity of CHT1 through PKC signaling pathways.