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SML4271

SN-011

≥98% (HPLC)

Synonym(s):

N-[3-[[(4-Fluorophenyl)sulfonyl]amino]-4-hydroxyphenyl][1,1′-biphenyl]-4-carboxamide, SN-11, GUN35901

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About This Item

Empirical Formula (Hill Notation):
C25H19FN2O4S
CAS Number:
Molecular Weight:
462.49
MDL number:
NACRES:
NA.21
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
powder
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Quality Segment

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Biochem/physiol Actions

Potent, selective, and non-cytotoxic STING inhibitor that blocks STING signaling and inflammation in both in vitro and in vivo.



SN-011 is a potent, specific, and non-cytotoxic STING antagonist that binds to the STING cyclic dinucleotide (CDN)-binding domain with higher affinity than endogenous 2’3’-cGAMP. It locks the STING dimer in an open, inactive conformation and stalls STING-dependent signaling. SN-011 inhibits 2′3′-cGAMP-induced Ifnb expression (IC50 = 127.5, 107.1, and 502.8 nM in MEFs, mouse bone marrow-derived macrophages (BMDMs), and human foreskin fibroblasts (HFFs), respectively. It also suppresses the secretion of pro-inflammatory molecules in vitro mouse and human models, including HSV-1 infection and Trex1 deficiency in mice. SN-011 blocks the spontaneous activation of GOF STING mutants that cause STING-associated vasculopathy with onset in infancy (SAVI).

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SML4208
SN-011 ≥98% (HPLC)

SML4271

SN-011

description

≥98% (HPLC)

description

≥98% (HPLC), powder, STING agonist

form

powder

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

-10 to -25°C

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: 2 mg/mL, clear

color

white to beige

color

white to beige


Pictograms

Exclamation mark

Signal Word

Warning

Hazard Codes

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable



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