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TLR Toll-like Receptor

Cat.No.  Name Information
M4838 TAK-242 (Resatorvid) Resatorvid (TAK-242) is a selective TLR4 signaling inhibitor. Resatorvid inhibited the production of NO, TNF-α and IL-6 with IC50 values of 1.8 nM, 1.9 nM and 1.3 nM, respectively. Resatorvid down-regulates the expression of MyD88 and TRIF signaling molecules downstream of TLR4. Resatorvid inhibits autophagy and plays a key role in a variety of inflammatory diseases.
M11408 Hydroxychloroquine Hydroxychloroquine is a synthetic antimalarial agent that also inhibits Toll-like receptor 7/9 (TLR7/9) signaling. Hydroxychloroquine effectively inhibited SARS-COV-2 infection.
M9063 TLR2-IN-C29 C29 is a Toll-like receptor 2 (TLR2) inhibitor. C29 blocked HTLR2/1 and HTLR2/6 with IC50 values of 19.7 and 37.6 μM, respectively.
M42066 Polyinosinic acid Polyinosinic acid is a single stranded homonucleic acid, which is a Toll-like Receptor 3 (TLR3) agonist.
M5062 Polyinosinic:polycytidylic acid Polyinosinic:polycytidylic acid (poly I:C) is a synthetic polyinosinic-polycytidylic acid double-stranded RNA. Polyinosinic-polycytidylic acid (Poly (I:C)) is an agonist of toll-like receptor (TLR)-3. Polyinosinic-polycytidylic acid has protective effects against cerebral ischemia/reperfusion (I/R) injury and can be used as vaccine adjuvant to enhance innate and adaptive immune responses.
M54417 PSMα3 PSMα3 is a peptide for manipulating DCs to become tolerogenic for DC vaccination strategies.
M52830 Pam2CSK4 Pam2CSK4, a lipopeptide, is a TLR6-independent TLR2 ligand and agonist.
M49647 MAPK-IN-1 MAPK-IN-1 is a MAPK signaling pathway inhibitor.
M45111 Cobitolimod Cobitolimod is a first-of-its-kind (first-in-class), synthetic oligodeoxynucleotide (ODN) containing unmethylated CpG motifs that activates TLR9 in specific cells, including intestinal T and B lymphocytes as well as antigen-presenting cells (APCs), and can be used in studies related to inflammatory bowel disease (IBD).
M43824 Agatolimod Agatolimod is a class B ODN (Oligodeoxynucleotide) and also a TLR9 agonist that stimulates HD11 cells to produce NO2 and IL-6, which can be used in breast cancer related studies. Sequence: 5'-tcgtcgttttgtcgttttgtcgtt-3'.
M43823 Lefitolimod Lefitolimod is a DNA-based TLR9 agonist and immunosurveillance reactivator that induces HIV-specific immune responses for cancer and HIV-1 research.
M43822 SD-101 SD-101 is a TLR9 agonist that can be used in tumor-related studies.
M43821 Vidutolimod Vidutolimod is a CpG-A oligodeoxynucleotide. Vidutolimod is a Toll-like receptor 9 (TLR9) agonist, which activates plasmacytoid dendritic cells (pDCs) and triggers interferon alpha (IFNα) release, leading to a cascade of anti-tumor immune effects.
M42073 TLR7 agonist 9 TLR7 agonist 9 is an aonist of TLR7.
M42072 TLR8 agonist 6 TLR8 agonist 6 is a TLR8 agonist, with an EC50 of 0.052 μM.
M42071 TLR7/8/9 antagonist 2 TLR7/8/9 antagonist 2 is an orally active TLR7/8/9 antagonist.
M42070 Guretolimod hydrochloride Guretolimod hydrochloride is a Toll-like receptor 7 (TLR7) agonist.
M42069 RDR 02308 RDR 02308 is a TLR4-MyD88 binding inhibitor that inhibits full-length β-lactamase.
M42068 M62812 free base M62812 (free base) is a toll-like receptor 4 (TLR4) signal transduction inhibitor.
M42067 BMS905 BMS905 is an orally active TLR7 and TLR8 dual inhibitor (IC50s: 0.7 and 3.2 nM respectively).
M42065 TAT-CIRP TAT-CIRP is a a small peptide, refers to Trans-trans-activating (Tat)-cold-inducible RNA binding protein.
M42064 Tilsotolimod Tilsotolimod is a synthetic Toll-like receptor 9 (TLR9) agonist that has demonstrated antitumor activity in preclinical models.
M42063 TLR7/8 agonist 8 TLR7/8 agonist 8 is a potent toll-like receptor 7/8 (TLR7/8) dual agonist, with EC50s of 27 and 12 nM for hTLR7 and hTLR8, respectively.
M42062 Tilsotolimod sodium Tilsotolimod (sodium) is a synthetic Toll-like receptor 9 (TLR9) agonist that has demonstrated antitumor activity in preclinical models.
M40904 ODN TTAGGG ODN TTAGGG is an inhibitory oligodeoxynucleotide (ODN) as well as a TLR9, AIM2 and cGAS antagonist with immunosuppressive activity, which inhibits the activation of the AIM2 inflammasome by competing with DNA, as well as the activation of cGAS. It can be used in the study of autoimmune diseases such as lupus erythematosus. Sequence: 5'-T-T-T-A-G-G-G-T-T-T-T-A-G-G-G-T-T-T-A-G-G-G-T-T-T-A-G-G-G-T-T-T-A-G-G-G-3'.




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