Date published: 2025-12-24

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IFN-αR Inhibitors

Interferons (IFNs) are a group of proteins known for their ability to interfere with viral replication within host cells. Specifically, Interferon-alpha (IFN-α) is a type of interferon that plays a key role in the body's immune response to viral infections. IFN-α achieves this through its interaction with specific receptors on the cell surface, notably the IFN-α receptor (IFN-αR). Once activated, this receptor initiates a cascade of intracellular signaling pathways that result in a variety of cellular responses, including enhanced antiviral defenses.

IFN-αR inhibitors are molecules designed to specifically target and inhibit the activity of the IFN-α receptor. By doing so, they block the receptor's ability to recognize and respond to IFN-α, thereby interrupting the downstream signaling events it typically mediates. This inhibition is achieved through various chemical mechanisms, depending on the specific inhibitor in question. Some inhibitors may bind directly to the receptor's ligand-binding domain, preventing IFN-α from interacting with it. Others may interact with different regions of the receptor or its associated proteins, thereby altering its structural conformation and hampering its function. The exact mechanism of action, as well as the specificity and affinity of these inhibitors for the IFN-αR, can vary significantly between different molecules. The discovery and characterization of these inhibitors has deepened our understanding of the intricate molecular interactions underpinning the body's immune responses.

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Ruxolitinib

941678-49-5sc-364729
sc-364729A
sc-364729A-CW
5 mg
25 mg
25 mg
$246.00
$490.00
$536.00
16
(1)

Ruxolitinib is a Janus kinase (JAK) inhibitor, targeting JAK1 and JAK2. IFN-αR signaling works through the JAK-STAT pathway. By inhibiting JAK1 and JAK2, Ruxolitinib can prevent the downstream signaling initiated by IFN-αR activation.

Baricitinib

1187594-09-7sc-364730
sc-364730A
5 mg
25 mg
$196.00
$651.00
(1)

Another JAK inhibitor, Baricitinib specifically targets JAK1 and JAK2. Like Ruxolitinib, it can prevent the downstream signaling of IFN-αR by inhibiting these JAK kinases.

Sunitinib Malate

341031-54-7sc-220177
sc-220177A
sc-220177B
10 mg
100 mg
3 g
$193.00
$510.00
$1072.00
4
(1)

tyrosine kinase inhibitor. They can suppress IFN-α signaling, possibly by affecting the receptor itself or the downstream signaling molecules. Their broad kinase inhibition profile means they can impact multiple pathways, including the JAK-STAT pathway downstream of IFN-αR.

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

tyrosine kinase inhibitor. They can suppress IFN-α signaling, possibly by affecting the receptor itself or the downstream signaling molecules. Their broad kinase inhibition profile means they can impact multiple pathways, including the JAK-STAT pathway downstream of IFN-αR.

Leflunomide

75706-12-6sc-202209
sc-202209A
10 mg
50 mg
$20.00
$81.00
5
(1)

An immunomodulatory drug, Leflunomide can inhibit the enzyme dihydroorotate dehydrogenase (DHODH), impacting pyrimidine synthesis. This can reduce the production of IFN-α, which in turn can affect the activation of IFN-αR.

hydroxychloroquine

118-42-3sc-507426
5 g
$56.00
1
(0)

Originally an antimalarial drug, Hydroxychloroquine can affect endosomal pH and disrupt the endosomal signaling of toll-like receptors (TLRs). This can lead to a reduction in IFN-α production, thereby affecting IFN-αR signaling.

Mycophenolic acid

24280-93-1sc-200110
sc-200110A
100 mg
500 mg
$68.00
$261.00
8
(1)

An immunosuppressant, Mycophenolic acid inhibits inosine monophosphate dehydrogenase (IMPDH), affecting guanosine synthesis. This can lead to decreased IFN-α production, potentially affecting IFN-αR signaling.

Dexamethasone

50-02-2sc-29059
sc-29059B
sc-29059A
100 mg
1 g
5 g
$76.00
$82.00
$367.00
36
(1)

A corticosteroid, Dexamethasone can suppress various immune responses. Its broad anti-inflammatory effects can lead to a reduction in IFN-α production and, consequently, reduced IFN-αR signaling.