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STING

STING (Stimulator of Interferon Genes) is a transmembrane protein localized to the endoplasmic reticulum that undergoes a conformational change in response to direct binding of cyclic dinucleotides (CDNs), resulting in a downstream signaling cascade involving TBK1 activation, IRF-3 phosphorylation, and production of IFN-β and other cytokines.

STING is a pattern recognition receptor of cyclic dinucleotides as well as an innate immune adaptor protein that enables signaling from cytoplasmic receptors to the transcription factor interferon regulatory factor 3. Initiation of these pathways leads to the expression of type I interferons and proteins associated with antiviral and antitumor immunity. Small molecules capable of triggering STING-dependent cellular processes are effective at blocking virus replication, enhancing vaccine efficacy, and facilitating immune response to cancer cells.

Targets for  STING

Products for  STING

  1. Cat.No. Product Name Information
  2. GC69959 STING agonist-20

    STING agonist-20 (compound 95) is an effective STING agonist used in the synthesis of XMT-2056. It can be used as a vaccine adjuvant for cancer, inflammation, and research on immune diseases.

    STING agonist-20  Chemical Structure
  3. GC69961 STING agonist-22

    STING agonist-22 (CF501) is an effective non-nucleotide STING agonist.

    STING agonist-22  Chemical Structure
  4. GC73407 STING agonist-26 STING agonist-26 (CF508) is a non-nucleotide small-molecule STING agonist. STING agonist-26  Chemical Structure
  5. GC37692 STING agonist-3

    CS-0029879, Diamidobenzimidazole STING Agonist, diABZI-3, EX-A3217, HY-103665, STING Agonist-3

    STING agonist-3, extracted from patent WO2017175147A1 (example 10), is a selective and non-nucleotide small-moleculeSTINGagonist with a pEC50 and pIC50 of 7.5 and 9.5, respectively. STING agonist-3 has durable anti-tumor effect and tremendous potential to improve treatment of cancer. STING agonist-3  Chemical Structure
  6. GC69962 STING agonist-3 trihydrochloride

    STING agonist-3 trihydrochloride is derived from patent WO2017175147A1 (Example 10) and is a selective and non-nucleotide small molecule STING agonist with pEC50 and pIC50 values of 7.5 and 9.5, respectively. It has long-lasting anti-tumor effects and holds great potential in improving cancer research.

    STING agonist-3 trihydrochloride  Chemical Structure
  7. GC37693 STING agonist-4

    CS-0087594, Diamidobenzimidazole STING Agonist-2, diABZI-4, HY-123943, STING Agonist-4, STING Agonist diABZI Compound 2

    A STING agonist STING agonist-4  Chemical Structure
  8. GC66008 STING agonist-7 STING agonist-7 is a non-nucleotide STING agonist. STING agonist-7 binds selectively to mouse STING but not human STING. STING agonist-7 penetrates cell membrane poorly. STING agonist-7  Chemical Structure
  9. GC69963 STING agonist-8 dihydrochloride

    STING agonist-8 dihydrochloride (5-AB) is an effective STING activator with an EC50 of 27 nM in THP1-Dual KI-hSTING-R232 cells.

    STING agonist-8 dihydrochloride  Chemical Structure
  10. GC34322 STING ligand-1 STING ligand-1 is a lead STING ligand with an IC50 of 68 nM for HAQ STING. STING ligand-1  Chemical Structure
  11. GC78685 STING-IN-15 STING-IN-15 is a potent STING inhibitor with an IC50 value of 116nM. STING-IN-15  Chemical Structure
  12. GC71186 STING-IN-4 STING-IN-4 (Compound 1) is a STING inhibitor that inhibits STING expression and hence reducing activation of STING and nuclear factor-κB (NF-κB) signaling. STING-IN-4  Chemical Structure
  13. GC71189 STING-IN-5 STING-IN-5 is a potent STING inhibitor, inhibiting LPS-induced NO synthesis in macrophages with an IC50 value of 1.15 μM. STING-IN-5  Chemical Structure
  14. GC73186 STING-IN-6 STING-IN-6 (compound 50) is a potent STING inhibitor with a pIC50 of 8.9. STING-IN-6  Chemical Structure
  15. GC73647 STING-IN-7 STING-IN-7 (compound 21) is a potent STING inhibitor with an IC50 of 11.5 nM. STING-IN-7  Chemical Structure
  16. GC46227 STING18 A competitive STING ligand STING18  Chemical Structure
  17. GC79068 Telomeric G4s ligand 2 Telomeric G4s ligand 2 is an orally active, selective ligand of telomeric G-quadruplex (G4), with an IC50 of 0.4 μM. Telomeric G4s ligand 2  Chemical Structure
  18. GC79431 UM-259 hydrochloride UM-259 hydrochloride is a STING inhibitor with activity against both murine and human STING (including the STING R232 mutant). UM-259 hydrochloride  Chemical Structure
  19. GC52084 YSK05 YSK05 is a pH-sensitive cationic lipid. YSK05 improves the intracellular trafficking of non-viral vectors. YSK05-MEND shows significantly good gene silencing activity and hemolytic activity. YSK05 overcomes the suppression of endosomal escape by PEGylation. YSK05 effectively enhances siRNA delivery both in vitro and in vivo. YSK05  Chemical Structure

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