SN-008
CAS No. 2249106-01-0
SN-008( —— )
Catalog No. M28759 CAS No. 2249106-01-0
SN-008 is a less active analog SN-011 which is a STING antagonist. SN-008 can be used as a negative control.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 126 | In Stock |
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| 2MG | 75 | In Stock |
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| 5MG | 116 | In Stock |
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| 10MG | 187 | In Stock |
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| 25MG | 432 | In Stock |
|
| 50MG | 625 | In Stock |
|
| 100MG | 889 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameSN-008
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NoteResearch use only, not for human use.
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Brief DescriptionSN-008 is a less active analog SN-011 which is a STING antagonist. SN-008 can be used as a negative control.
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DescriptionSN-008 is a less active analog SN-011 which is a STING antagonist. SN-008 can be used as a negative control.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayImmunology/Inflammation
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TargetSTING
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RecptorEndothelium dependent relaxation
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Research Area——
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Indication——
Chemical Information
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CAS Number2249106-01-0
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Formula Weight446.49
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Molecular FormulaC25H19FN2O3S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (223.97 mM)
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SMILESO=C(c(cc1)ccc1-c1ccccc1)Nc1cccc(NS(c(cc2)ccc2F)(=O)=O)c1
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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
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C-171
C-171 is an inhibitor of stimulator of interferon genes (STING).?It binds to STING, inhibits its palmitoylation, and prevents the recruitment and phosphorylation of TBK1.
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STING agonist-30
STING agonist-30 is a potent activator of STING-dependent immune responses, demonstrating broad-spectrum antiviral effects against viruses such as HSV (Herpes Simplex Virus), rotavirus, and SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2).
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MSA-2
MSA-2, a potent and orally available non-nucleotide STING agonist, has EC50s of 8.3 and 24 μM for human STING isoforms WT and HAQ, respectively. MSA-2 shows antitumor activity and stimulates interferon-β secretion in tumors, induces tumor regression with durable antitumor immunity, and synergizes with anti-PD-1 in syngeneic mouse tumor models.
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