Date published: 2026-2-23

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TLR6 Inhibitors

TLR6 Inhibitors represent a class of chemicals that play a pivotal role in the regulation of Toll-like Receptor 6 (TLR6), a critical component of the innate immune system responsible for recognizing microbial pathogens. These inhibitors can either directly target TLR6 or indirectly modulate its activity by influencing specific signaling pathways. Understanding the mechanisms by which TLR6 inhibitors operate is essential for unraveling the complex regulation of innate immune responses. Direct TLR6 inhibitors, such as ODN 2088 and Pellino1 Inhibitor, directly interfere with TLR6 activation. ODN 2088, a synthetic oligonucleotide, binds to and blocks TLR6, disrupting its engagement in downstream signaling pathways. Pellino1 Inhibitor disrupts the interaction between Pellino1 and TLR6, inhibiting the activation of downstream signaling events. These inhibitors directly target TLR6, inhibiting its ability to initiate immune responses.

Indirect TLR6 inhibitors, such as IRAK4 Inhibitor, modulate TLR6 activity by targeting related signaling pathways. RAK4 Inhibitor targets IRAK4, a key mediator of TLR6 signaling, thereby hindering downstream TLR6-induced inflammatory responses. These inhibitors indirectly inhibit TLR6 by interfering with signaling events downstream of TLR6 activation. Additionally, chemicals like TAK-242, BAY 11-7082, and BX795 target the TLR6 signaling pathway indirectly by affecting TLR4 signaling or components downstream of TLR6 activation. These compounds disrupt cross-talk between TLR4 and TLR6 signaling, leading to reduced TLR6-induced responses. In summary, TLR6 Inhibitors encompass a diverse range of chemicals that can either directly target TLR6 or indirectly modulate its activity by influencing related signaling pathways. These inhibitors play a crucial role in regulating innate immune responses by modulating TLR6 activation, thereby contributing to our understanding of host defense mechanisms against microbial pathogens.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Resatorvid

243984-11-4sc-476758
5 mg
$367.00
(0)

Resatorvid inhibits TLR6 indirectly by targeting TLR4 signaling. It specifically blocks TLR4-mediated MyD88-independent signaling, which can cross-talk with TLR6 signaling pathways.

BAY 11-7082

19542-67-7sc-200615B
sc-200615
sc-200615A
5 mg
10 mg
50 mg
$62.00
$85.00
$356.00
155
(1)

BAY 11-7082 inhibits TLR6 indirectly by targeting the NF-κB pathway, which is a downstream component of TLR6 signaling. By inhibiting NF-κB activation, it attenuates the effects of TLR6 stimulation.

BX 795

702675-74-9sc-281689
sc-281689A
sc-281689C
sc-281689B
sc-281689D
sc-281689E
2 mg
5 mg
10 mg
25 mg
50 mg
100 mg
$219.00
$273.00
$331.00
$495.00
$882.00
$1489.00
5
(1)

BX795 indirectly inhibits TLR6 by targeting the TBK1/IKKε pathway, which is a downstream component of TLR6 signaling. It inhibits TBK1/IKKε activity, leading to reduced TLR6-induced inflammatory responses.

IMD 0354

978-62-1sc-203084
5 mg
$199.00
3
(1)

IMD-0354 indirectly inhibits TLR6 by targeting the NF-κB pathway, a downstream component of TLR6 signaling. It inhibits the activation of NF-κB, reducing the effects of TLR6 stimulation.

BMS-345541

445430-58-0sc-221741
1 mg
$312.00
1
(1)

BMS-345541 inhibits TLR6 indirectly by targeting the IKKβ/NF-κB pathway, which is a downstream component of TLR6 signaling. It inhibits IKKβ, thereby attenuating the effects of TLR6 activation.

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$90.00
$204.00
13
(1)

Triptolide indirectly inhibits TLR6 by targeting the NF-κB pathway, a downstream component of TLR6 signaling. It inhibits the activation of NF-κB, reducing the effects of TLR6 stimulation.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin indirectly inhibits TLR6 by targeting the NF-κB pathway, a downstream component of TLR6 signaling. It inhibits the activation of NF-κB, leading to reduced TLR6-induced inflammatory responses.