diABZI STING agonist-1

CAS No. 2138299-33-7

diABZI STING agonist-1( —— )

Catalog No. M36567 CAS No. 2138299-33-7

diABZI STING agonist-1 is a selective and potent interferon gene-stimulating receptor (STING) agonist with potential antitumor and anti-inflammatory activity for the study of cancer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 225 Get Quote
5MG 353 Get Quote
10MG 588 Get Quote
25MG 888 Get Quote
50MG 1178 Get Quote
100MG 1575 Get Quote
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Biological Information

  • Product Name
    diABZI STING agonist-1
  • Note
    Research use only, not for human use.
  • Brief Description
    diABZI STING agonist-1 is a selective and potent interferon gene-stimulating receptor (STING) agonist with potential antitumor and anti-inflammatory activity for the study of cancer.
  • Description
    diABZI STING agonist-1 is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
  • In Vitro
    diABZI STING agonist-1 is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively. At a concentration of 1 μM, diABZI STING agonist-1 (compound 3) demonstrates high selectivity against more than 350 kinases tested.
  • In Vivo
    diABZI STING agonist-1 (subcutaneous injection; 2.5 mg/kg) induces STING-dependent activation of type-I interferon and pro-inflammatory cytokines in vivo.?diABZI STING agonist-1 (intravenous injection; 3 mg/kg) exhibits systemic exposure with a half-life of 1.4 h and achieves systemic concentrations greater than the half-maximal effective concentration (EC50) for mouse STING (200 ng/ml).diABZI STING agonist-1 (intravenous injection; 1.5 mg/kg; days 1, 4 and 8; 43 days) results in significant tumour growth inhibition and significantly improves survival (P?0.001) with 8 out of 10 mice remaining tumor free at the end of the study on day 43.Animal Model:Wild and Sting?/? C57Blk6 mice Dosage:2.5 mg/kg Administration:Subcutaneous injection; 2.5 mg/kg Result:Activated secretion of IFNβ, IL-6, TNF, and CXCL1 in wild-type but not Sting?/? mice.Animal Model:Syngeneic mouse model of colorectal tumours (CT-26) in BALB/c mice Dosage:3 mg/kg Administration:Intravenous injection; 3 mg/kg Result:Exhibited a half-life of 1.4 hours and achieved systemic concentrations greater than EC50 for mouse STING (200 ng/ml).Animal Model:Syngeneic mouse model of colorectal tumours (CT-26) in BALB/c mice Dosage:1.5 mg/kg Administration: Intravenous injection; 1.5 mg/kg; 43 days Result:Resulted in significant tumour growth inhibition and improved survival.
  • Synonyms
    ——
  • Pathway
    Immunology/Inflammation
  • Target
    STING
  • Recptor
    STING
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2138299-33-7
  • Formula Weight
    849.94
  • Molecular Formula
    C42H51N13O7
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (117.66 mM; Ultrasonic )
  • SMILES
    O=C(C1=CC(C)=NN1CC)N=C2N(C3=C(OC)C=C(C(N)=O)C=C3N2)C/C=C/CN4C5=C(OCCCN6CCOCC6)C=C(C(N)=O)C=C5NC4=NC(C7=CC(C)=NN7CC)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Ramanjulu JM, et al. Design of amidobenzimidazole STING receptor agonists with systemic activity. Nature. 2018 Nov 7.?
molnova catalog
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