STING

STING

The ER-membrane protein Stimulator of Interferon Genes (STING) can be activated by the 2'3'-cGAMP produced by the enzyme Cyclic Guanosine Monophosphate-Adenosine Monophosphate Synthase (cGAS) in response to the binding of double-stranded DNA. To protect against microbial infection, it activates inflammatory cytokine and interferon (IFN) responses.

STING is an important cytosolic receptor for small nucleotides that is essential for both antiviral and anticancer immunity. The STING signaling pathway triggers anti-tumor immune responses and serves as a vital link between innate and adaptive immunity. In numerous studies for immunogenic tumor clearance, antiviral therapies, and vaccine adjuvants, STING agonists like endogenous cyclic dinucleotide (CDN) cyclic GMP-AMP (cGAMP) have been used.

STING related products

Structure Cat No. Product Name CAS No. Product Description
V74317 Dazostinag (TAK-676 free base) 2553413-86-6 Dazostinag (TAK-676 free base) is an agonist of stimulator of interferon genes (STING) protein and has anti-tumor activity.
V31646 diABZI STING agonist-1 2138299-33-7 diABZI STING agonist-1 is a novel, potent and selective STING (stimulator of interferon genes) receptor agonist, with an EC50s of 130 nM for human PBMCs.
V31645 diABZI STING agonist-1 trihydrochloride 2138299-34-8 diABZI STING agonist-1 (trihydrochloride) is a selective stimulator of interferon genes (STING) receptor agonist, with an EC50s of 130 for human PBMCs.
V74310 diABZI-C2-NH2 2137975-93-8 diABZI-C2-NH2 is an active analog containing primary amine function and a STING agonist.
V74311 E7766 diammonium salt 2242635-03-4 E7766 diammonium salt is a macrocyclic bridged STING agonist/activator with a Kd of 40 nM.
V79211 F-CRI1 F-CRI1 is a potent STING agonist/activator with a Kd of 40.62 nM.
V21450 G10 702662-50-8 STING agonist-1 (G10) is a human-specific STING agonist that elicits anti-viral effect against emerging alphaviruses.
V22028 H 151 (H-151) 941987-60-6 H151 (H-151) isa potent,selective andirreversible STING antagonist/inhibitor with the potential to be used for autoimmune diseases such as arthritis and other inflammatory conditions.
V76903 IACS-8803 diammonium IACS-8803 diammonium is a potent cyclic dinucleotide STING agonist with potent systemic anti-tumor effects.
V74309 IACS-8803 disodium 2243079-36-7 IACS-8803 disodium is a potent cyclic dinucleotide STING agonist with potent systemic anti-tumor effects.
V80542 LB244 LB244 is a homologue of BB-Cl-amidine, which is an orally bioactive STING inhibitor (EC50=0.8 μM) and may be utilized to inhibit STING-dependent inflammatory diseases.
V19990 m-Cl-CCP (CCCP) 555-60-2 m-Cl-CCP [555-60-2] is a protonophore (h+ ionophore) and uncoupler of oxidative phosphorylation in mitochondria, inhibiting secretion of hepatic lipase and partially inhibiting the ph gradient-activated cl- uptake and cl-/cl- exchange activities in brush-border membrane vesicles
V2470 MSA-2 129425-81-6 MSA 2 (MSA2;MSA-2) is a novel, orally bioactive and potent non-nucleotide agonist of stimulator of interferon genes (STING) with potential antitumor activity.
V74312 MSA-2 dimer 2377881-92-8 MSA-2 dimer is a selective and orally bioactive non-nucleotide STING agonist (Kd=145 μM) with long-term anti-tumor and immunogenic activity.
V78866 NVS-STG2 NVS-STG2 is a molecular glue targeting STING and can activate STING-mediated immune signaling.
V79086 SAP-04 SAP-04 is a potent orally bioactive STING agonist.
V74314 SN-008 2249106-01-0 SN-008 is a low activity analog of SN-011 and can be used as a negative control (NC).
V41902 SP-23 2762552-74-7 SP-23 (SP23) is a novel, first-in-class and potent STING-targeting PROTAC degrader based on C-170 (STING inhibitor) with anti-inflammatory effects.
V51740 SR-717 2375420-34-9 SR-717 free acid is a non-nuclear STING-like agonist/activator with EC50s of 2.1 μM and 2.2 μM in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cells, respectively.
V2205 SR-717 lithium 2375421-09-1 SR-717 lithium is a novel, potent and non-nucleotide STING (stimulator of interferon genes) agonist with anticancer activities.
Contact Us Back to top