Date published: 2026-6-2

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OATP-C Activators

OATP-C Activators are a class of chemical compounds designed to modulate the activity of the organic anion-transporting polypeptide C (OATP-C), which is also known as solute carrier organic anion transporter 1C1 (SLCO1C1). OATP-C is a membrane-bound transporter protein found in various tissues, including the liver, brain, and blood-brain barrier. This transporter is responsible for the uptake and transport of a wide range of endogenous and exogenous substrates, including hormones, drugs, and xenobiotics, across cellular membranes. OATP-C Activators are synthesized to selectively interact with OATP-C, enhancing or inhibiting its transport functions, although the specific mechanisms can vary among different compounds within this chemical class.

The activation or modulation of OATP-C by these compounds can influence the cellular uptake and distribution of various molecules, impacting their pharmacokinetics and overall bioavailability. OATP-C is particularly important for the transport of endogenous compounds like bile acids and hormones, as well as a wide array of drugs. By targeting OATP-C, these activators can potentially enhance or inhibit the transport of specific substrates, affecting their absorption, distribution, and elimination. Consequently, OATP-C Activators serve as valuable tools in pharmacology and drug development research, allowing scientists to investigate the role of OATP-C in drug disposition and xenobiotic transport. However, it's essential to note that the specific mechanisms and potential outcomes of OATP-C activation or inhibition may vary depending on the context, the particular substrate, and the compound used within this chemical class, as OATP-C is involved in the transport of diverse molecules with distinct physicochemical properties.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Omeprazole

73590-58-6sc-202265
50 mg
$67.00
4
(1)

Omeprazole, a proton pump inhibitor, may enhance OATP-C expression, potentially through its interactions with liver enzymes and transporters.

Clofibrate

637-07-0sc-200721
1 g
$33.00
(1)

Clofibrate, a lipid-lowering agent, might induce OATP-C expression as part of its action in modifying lipid transport and metabolism.

Dexamethasone

50-02-2sc-29059
sc-29059B
sc-29059A
100 mg
1 g
5 g
$91.00
$139.00
$374.00
36
(1)

Dexamethasone, a corticosteroid, can potentially increase OATP-C levels, possibly through glucocorticoid receptor-mediated mechanisms.

Nifedipine

21829-25-4sc-3589
sc-3589A
1 g
5 g
$59.00
$173.00
15
(1)

Nifedipine, a calcium channel blocker, might affect OATP-C expression, potentially as part of its broader influence on cellular transport processes.

Benzo[a]pyrene

50-32-8sc-257130
1 g
$612.00
4
(1)

Benzo(a)pyrene, a polycyclic aromatic hydrocarbon, may increase OATP-C expression as part of the body's response to environmental toxins.

Troglitazone

97322-87-7sc-200904
sc-200904B
sc-200904A
5 mg
10 mg
25 mg
$110.00
$204.00
$435.00
9
(1)

Troglitazone, a thiazolidinedione, can potentially enhance OATP-C expression, possibly through peroxisome proliferator-activated receptor (PPAR) pathways.

Diethylstilbestrol

56-53-1sc-204720
sc-204720A
sc-204720B
sc-204720C
sc-204720D
1 g
5 g
25 g
50 g
100 g
$71.00
$287.00
$547.00
$1098.00
$2185.00
3
(1)

Diethylstilbestrol, a synthetic estrogen, can increase OATP-C expression, potentially through estrogen receptor-mediated mechanisms.