144 Results for "

TLR7 agonist

" in MedChemExpress (MCE) Product Catalog:
Products (144)

144 Results for "TLR7 agonist" in MCE Product Catalog:

116
116 Publications Verification
Cat. No.: HY-13740
CAS No.: 144875-48-9
Purity:  99.87%
Synonyms: R848; S28463
Resiquimod is a Toll-like receptor 7 and 8 (TLR7/TLR8) agonist that induces the upregulation of cytokines such as TNF-α, IL-6 and IFN-α.
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60
60 Cited Publications
Cat. No.: HY-B0180
CAS No.: 99011-02-6
Synonyms: R 837
Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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60
60 Cited Publications
Cat. No.: HY-B0180A
CAS No.: 99011-78-6
Synonyms: R 837 hydrochloride
Imiquimod hydrochloride (R 837 hydrochloride), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod hydrochloride exhibits antiviral and antitumor effects in vivo. Imiquimod hydrochloride can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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60
60 Cited Publications
Cat. No.: HY-B0180B
CAS No.: 896106-16-4
Imiquimod maleate (R 837 maleate), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod maleate exhibits antiviral and antitumor effects in vivo. Imiquimod maleate can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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14
14 Cited Publications
Cat. No.: HY-15601
CAS No.: 1228585-88-3
Purity:  99.90%
Synonyms: GS-9620
Vesatolimod (GS-9620) is a potent, selective and orally active agonist of Toll-Like Receptor (TLR7) with an EC50 of 291 nM.
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11
11 Cited Publications
Cat. No.: HY-109104
CAS No.: 1359993-59-1
Purity:  98.44%
Synonyms: MEDI9197; 3M-052
Research Areas:  

Cancer

Telratolimod (MEDI9197) is a potent toll like receptors 7/8 (TLR7/8) agonist, with antitumor activity .
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4
4 Cited Publications
Cat. No.: HY-115400
CAS No.: 1062444-54-5
Purity:  99.67%
Synonyms: TLR7 agonist T7
Research Areas:  

Cancer

1V209 (TLR7 agonist T7) is a Toll-like receptor 7 (TLR7) agonist and has anti-tumor effects. 1V209 can be conjugated with various polysaccharides to improve its water solubility, and enhance its efficacy, and maintain low toxicity .
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3
3 Cited Publications
Cat. No.: HY-128799
CAS No.: 1026249-18-2
Purity:  99.90%
CL097, a potent TLR7 and TLR8 agonist, induces pro-inflammatory cytokines in macrophages . CL097 induces NADPH oxidase priming, resulting in an increase of the fMLF-stimulated ROS production .
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3
3 Cited Publications
Cat. No.: HY-128799A
CAS No.: 2990770-48-2
CL097, a potent TLR7 and TLR8 agonist, induces pro-inflammatory cytokines in macrophages . CL097 induces NADPH oxidase priming, resulting in an increase of the fMLF-stimulated ROS production .
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2
2 Cited Publications
Cat. No.: HY-118250
CAS No.: 1207629-49-9
Purity:  99.85%
GSK2245035 is a highly potent and selective intranasal Toll-Like receptor 7 (TLR7) agonist with preferential Type-1 interferon (IFN)-stimulating properties. GSK2245035 has pEC50s of 9.3 and 6.5 for IFNα and TFNα. GSK2245035 effectively suppresses allergen-induced Th2 cytokine production in human peripheral blood cell cultures. GSK2245035 is used for asthma .
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2
2 Cited Publications
Cat. No.: HY-W008634
CAS No.: 56741-95-8
Synonyms: U-54461; U-54461S; PNU-54461
Research Areas:  

Cancer

Bropirimine (U-54461; U-54461S; PNU-54461) is an orally active TLR7 agonist. Bropirimine inhibits RANKL-induced osteoclast differentiation of mouse bone marrow-derived macrophages (BMMs). Bropirimine exhibits dose-dependent direct inhibitory effects on colony formation of cultured KK-47 and 724 cells. Bropirimine can be used for the study of cancers and bone metabolic disorders such as osteoporosis .
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1
1 Cited Publications
Cat. No.: HY-103698A
CAS No.: 1620278-72-9
Purity:  99.70%
Research Areas:  

Inflammation/Immunology

TLR7/8 agonist 1 dihydrochloride is a toll-like receptor TLR7/TLR8 dual-agonistic imidazoquinoline .
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1
1 Cited Publications
Cat. No.: HY-117602
CAS No.: 1229024-78-5
Purity:  99.90%
TLR7 agonist 3 (compound 2) is a TLR7 agonist and can be used for the stuy of cancers .
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1
1 Cited Publications
Cat. No.: HY-103039
CAS No.: 1642857-69-9
Purity:  98.80%
Research Areas:  

Inflammation/Immunology

TLR7 agonist 2 is a potent and selective Toll-like Receptor 7 (TLR7) agonist with a LEC of 0.4 μM.
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1
1 Cited Publications
Cat. No.: HY-103698
CAS No.: 1258457-59-8
Purity:  98.42%
Research Areas:  

Inflammation/Immunology

TLR7/8 agonist 1 is a toll-like receptor (TLR7)/TLR8 dual-agonistic imidazoquinoline.
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1
1 Cited Publications
Cat. No.: HY-110120
CAS No.: 1059070-10-8
Purity:  99.32%
Research Areas:  

Cancer

DSR-6434 is a potent and selective Toll-like receptor 7 (TLR7) agonist, with EC50s of 7.2 nM and 4.6 nM for human and mice TLR7, respectively. DSR-6434 has a strong antitumor effect .
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1
1 Cited Publications
Cat. No.: HY-111269
CAS No.: 866269-28-5
Purity:  99.14%
Research Areas:  

Inflammation/Immunology

AZD8848 is a selective toll-like receptor 7 (TLR7) anteagent agonist which is developed for the research of asthma and allergic rhinitis .
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1
1 Cited Publications
Cat. No.: HY-13740S
CAS No.: 2252319-44-9
Purity:  99.84%
Synonyms: R848-d5; S28463-d5
Resiquimod-d5 is deuterium labeled Resiquimod. Resiquimod is a Toll-like receptor 7 and 8 (TLR7/TLR8) agonist that induces the upregulation of cytokines such as TNF-α, IL-6 and IFN-α .
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Cat. No.: HY-103697
CAS No.: 1020412-43-4
Purity:  99.91%
Research Areas:  

Cancer

Gardiquimod is an imidazoline TLR7/8 agonist. Gardiquimod inhibits HIV-1 infection of macrophages and activated peripheral blood mononuclear cells (PBMCs). Gardiquimod specifically activates TLR7 at concentrations below 10 μM.
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Cat. No.: HY-111358
CAS No.: 2178156-33-5
Purity:  98.19%
Research Areas:  

Inflammation/Immunology

TLR7 agonist 1 is a selective TLR7 agonist with an LEC value of 90 nM. TLR7 agonist 1 activates downstream immune regulation and shows no activity against TLR8. TLR7 agonist 1 induces endogenous IFN-α production in mice .
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