diABZI STING agonist-1 (Tautomerism)
CAS No. 2138498-18-5
diABZI STING agonist-1 (Tautomerism)( —— )
Catalog No. M32885 CAS No. 2138498-18-5
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
Purity : >98% (HPLC)
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Datasheet
HNMR
HPLC
MSDS
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| Size | Price / USD | Stock | Quantity |
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| 5MG | 477 | Get Quote |
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| 10MG | 644 | Get Quote |
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| 25MG | 1311 | Get Quote |
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| 50MG | 2162 | Get Quote |
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| 100MG | 3204 | Get Quote |
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Biological Information
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Product NamediABZI STING agonist-1 (Tautomerism)
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NoteResearch use only, not for human use.
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Brief DescriptiondiABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
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DescriptiondiABZI STING agonist-1 Tautomerism (compound 3) is a selective stimulator of interferon genes (STING) receptor agonist,with EC50s of 130, 186 nM for human and mouse, respectively.
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In VitrodiABZI STING agonist-1 (Tautomerism) 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.
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In VivodiABZI STING agonist-1 (Tautomerism) (subcutaneous injection; 2.5 mg/kg) induces STING-dependent activation of type-I interferon and pro-inflammatory cytokines in vivo.diABZI STING agonist-1 (Tautomerism) (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 (Tautomerism) (intravenous injection; 1.5 mg/kg; 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.
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Synonyms——
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PathwayImmunology/Inflammation
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TargetSTING
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RecptorSTING
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Research Area——
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Indication——
Chemical Information
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CAS Number2138498-18-5
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Formula Weight849.94
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Molecular FormulaC42H51N13O7
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Purity>98% (HPLC)
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Solubility——
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SMILESC(/C=C/CN1C=2C(N=C1NC(=O)C=3N(CC)N=C(C)C3)=CC(C(N)=O)=CC2OC)N4C=5C(N=C4NC(=O)C=6N(CC)N=C(C)C6)=CC(C(N)=O)=CC5OCCCN7CCOCC7
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Ramanjulu JM, et al. Design of amidobenzimidazole STING receptor agonists with systemic activity. Nature. 2018 Nov 7.?
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