Date published: 2026-4-23

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CNT1 Inhibitors

CNT1 inhibitors, short for Concentrative Nucleoside Transporter 1 inhibitors, are a class of chemical compounds designed to selectively target and modulate the activity of the Concentrative Nucleoside Transporter 1 protein. CNT1 is a transmembrane protein that plays a crucial role in nucleoside transport across cell membranes. It is primarily responsible for the uptake of purine and pyrimidine nucleosides, including essential molecules like adenosine and cytidine, into cells. Inhibition of CNT1 can have profound effects on nucleoside homeostasis within cells and can influence various cellular processes.

CNT1 inhibitors are designed with the aim of regulating nucleoside transport by binding to CNT1 and altering its function. By blocking or reducing the activity of CNT1, these inhibitors can disrupt the normal flow of nucleosides into cells. This, in turn, can impact DNA and RNA synthesis, cell signaling, and energy metabolism. Researchers are particularly interested in CNT1 inhibitors because of their potential to selectively target specific cell types or diseases that rely heavily on nucleoside transport.

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Items 11 to 13 of 13 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Entecavir

142217-69-4sc-204738
sc-204738A
sc-204738B
1 mg
5 mg
25 mg
$77.00
$214.00
$632.00
11
(1)

Entecavir inhibits CNT1 by closely resembling natural nucleosides, leading to its competitive binding to CNT1. This binding prevents the transporter from effectively carrying out its role in nucleoside transport, resulting in inhibition.

Lamivudine

134678-17-4sc-221830
sc-221830A
10 mg
50 mg
$104.00
$218.00
1
(2)

Lamivudine, a drug, inhibits CNT1 and is studied in the research of HIV and hepatitis B virus (HBV) infections.

Adenosine

58-61-7sc-291838
sc-291838A
sc-291838B
sc-291838C
sc-291838D
sc-291838E
sc-291838F
1 g
5 g
100 g
250 g
1 kg
5 kg
10 kg
$34.00
$48.00
$300.00
$572.00
$1040.00
$2601.00
$4682.00
1
(0)

Adenosine acts as an inhibitor of CNT1 by directly competing with endogenous nucleosides for the transporter, thereby reducing the efficiency of nucleoside uptake and leading to inhibition of CNT1 functionality.