C-178
CAS No. 329198-87-0
C-178( —— )
Catalog No. M20739 CAS No. 329198-87-0
C-178 is a covalent inhibitor of STING binds to Cys91 on STING to block its palmitoylation and prevents recruitment and phosphorylation of TBK1 in HEK293T cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 58 | In Stock |
|
| 5MG | 56 | In Stock |
|
| 10MG | 92 | In Stock |
|
| 25MG | 187 | In Stock |
|
| 50MG | 276 | In Stock |
|
| 100MG | 427 | In Stock |
|
| 200MG | 612 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameC-178
-
NoteResearch use only, not for human use.
-
Brief DescriptionC-178 is a covalent inhibitor of STING binds to Cys91 on STING to block its palmitoylation and prevents recruitment and phosphorylation of TBK1 in HEK293T cells.
-
DescriptionC-178 is a covalent inhibitor of STING binds to Cys91 on STING to block its palmitoylation and prevents recruitment and phosphorylation of TBK1 in HEK293T cells.
-
In VitroWestern Blot Analysis Cell Line:Mouse bone marrow-derived macrophages (BMDMs)Concentration:0 μM; 0.125 μM; 0.25 μM; 0.5 μM; 1 μM Incubation Time:1 hour Result:Inhibited CMA-induced p-TBK1 expression as a does dependent manner.RT-PCR Cell Line:Mouse bone marrow-derived macrophages (BMDMs)Concentration:1 μM Incubation Time:1 hour Result:Downregulated Ifnb1 expression in BMDMs.
-
In Vivo——
-
Synonyms——
-
PathwayImmunology/Inflammation
-
TargetSTING
-
RecptormSTING
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number329198-87-0
-
Formula Weight322.27
-
Molecular FormulaC17H10N2O5
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 41.67 mg/mL (129.30 mM)
-
SMILES[O-][N+](=O)c1ccc(o1)C(=O)Nc1ccc2c(c1)oc1ccccc21
-
Chemical NameN-(Dibenzo[bd]furan-3-yl)-5-nitrofuran-2-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Haag S M Gulen M F Luc R et al. Targeting STING with covalent small-molecule inhibitors[J]. Nature 2018.
molnova catalog
related products
-
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.
-
diABZI STING agonist...
diABZI STING agonist-1 (trihydrochloride) is stimulator of interferon genes (STING) receptor agonist.
-
H-151
H-151 is a highly potent selective and covalent antagonist of?STING reduces TBK1 phosphorylation and suppresses human STING palmitoylation.
Cart
sales@molnova.com