Date published: 2026-1-10

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CMV UL146 Inhibitors

CMV UL146 inhibitors are a class of compounds designed to inhibit the function of the UL146 protein, which is encoded by the cytomegalovirus (CMV) genome. UL146 is classified as a viral chemokine-like protein, and its primary role involves mimicking host chemokines to modulate the immune response. Chemokines are signaling proteins that guide the migration of immune cells to sites of infection or inflammation, and UL146 is thought to interfere with this process by binding to chemokine receptors on immune cells, thus influencing their behavior. By mimicking the host's natural chemokines, UL146 plays a role in evading immune surveillance, helping CMV persist within the host by altering immune cell migration and function.

The study of CMV UL146 inhibitors is focused on blocking the interaction between the UL146 protein and its target receptors on immune cells. These inhibitors are typically designed to bind either to the UL146 protein itself or to the receptor it interacts with, preventing the protein from exerting its immune-modulating effects. By inhibiting UL146, researchers aim to dissect the precise mechanisms through which this viral protein manipulates immune responses, including its role in altering chemotactic signals and immune cell migration. Structural studies of UL146 and its inhibitors provide insights into how the viral protein interacts with host receptors and how inhibition can disrupt this interaction. These inhibitors are valuable tools for probing the function of viral chemokine-like proteins in the broader context of viral-host interactions and immune evasion strategies.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Hydroxyurea

127-07-1sc-29061
sc-29061A
5 g
25 g
$78.00
$260.00
18
(1)

Hydroxyurea may downregulate deoxyribonucleotide synthesis, leading to decreased availability for CMV DNA replication, ultimately reducing CMV UL146 expression.

5-Azacytidine

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

By incorporating into viral RNA, 5-Azacytidine could induce mutations or premature termination of transcription, decreasing CMV UL146 transcript levels.

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)

5-Aza-2′-Deoxycytidine's incorporation into viral DNA may disrupt methylation patterns, potentially decreasing transcriptional efficiency of CMV UL146.

Idoxuridine

54-42-2sc-205720
sc-205720A
500 mg
1 g
$104.00
$213.00
(1)

Idoxuridine could be integrated into CMV DNA, causing mutations which result in the synthesis of nonfunctional or unstable CMV UL146 mRNA.

Methotrexate

59-05-2sc-3507
sc-3507A
100 mg
500 mg
$94.00
$213.00
33
(5)

Methotrexate may inhibit the synthesis of thymidylate, a nucleotide required for DNA replication, thereby reducing CMV UL146 protein synthesis.

Mycophenolic acid

24280-93-1sc-200110
sc-200110A
100 mg
500 mg
$69.00
$266.00
8
(1)

Mycophenolic acid may deplete guanosine nucleotides, reducing the synthesis of viral RNA and DNA, resulting in decreased levels of CMV UL146.

Ribavirin

36791-04-5sc-203238
sc-203238A
sc-203238B
10 mg
100 mg
5 g
$63.00
$110.00
$214.00
1
(1)

By diminishing the pool of guanosine nucleotides, Ribavirin could decrease the synthesis of viral RNA and subsequent production of CMV UL146.

Cidofovir

113852-37-2sc-482141
50 mg
$135.00
(0)

Cidofovir may inhibit viral DNA polymerase, leading to decreased replication of CMV and consequent reduction in CMV UL146 expression.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

Epigallocatechin Gallate could interfere with the early stages of viral infection, potentially hindering the viral life cycle and decreasing CMV UL146 expression.

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 can elevate cellular cAMP levels, which might suppress CMV infection cycles and thereby reduce CMV UL146 expression.