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ChemicalBook--->CAS DataBase List--->2112809-98-8

2112809-98-8

2112809-98-8 Structure

2112809-98-8 Structure
IdentificationBack Directory
[Name]

JC-171 (JC171)
[CAS]

2112809-98-8
[Synonyms]

JC-171 (JC171)
Benzamide, 5-chloro-N-[2-[4-[(hydroxyamino)sulfonyl]phenyl]ethyl]-2-methoxy-
[Molecular Formula]

C16H17ClN2O5S
[MDL Number]

MFCD32708504
[MOL File]

2112809-98-8.mol
[Molecular Weight]

384.83
Chemical PropertiesBack Directory
[density ]

1.401±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 250 mg/mL (649.64 mM)
[form ]

Solid
[pka]

6.43±0.69(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

JC-171 is a selective NLRP3 inflammasome inhibitor, with an IC50 of 8.45 μM for inhibiting LPS/ATP-induced interleukin-1β (IL-1β) release from J774A.1 macrophages[1].
[in vivo]

JC-171 treatment delays the progression and reduces the severity of experimental autoimmune encephalomyelitis (EAE) in mouse[1].

Animal Model:Mice immunized subcutaneously with 200 μg Myelin oligodendrocyte glycoprotein (MOG) 35–55 peptide emulsified in Complete Freund’s Adjuvant (CFA) on day 0 followed by injection of 200 ng of pertussis toxin.
Dosage:100 mg/kg, 10 mg/kg.
Administration:IP days 0, 1 and 2; and every other days thereafter (100 mg/kg).
Initiated when the clinical scores of individual mice have reached 1 (flaccid tail), and given every other day (10 mg/kg).
Result:Efficiently suppressed EAE progression compared with vehicle treatment.
Resulted in a substantial decrease in the frequency of MOG35–55-specific Th17 cells in the spleens and spinal cords of EAE mice.
[IC 50]

NLRP3
[storage]

Store at -20°C
[References]

[1] Chunqing Guo, et al. Development and Characterization of a Hydroxyl-Sulfonamide Analogue, 5-Chloro-N-[2-(4-hydroxysulfamoyl-phenyl)-ethyl]-2-methoxy-benzamide, as a Novel NLRP3 Inflammasome Inhibitor for Potential Treatment of Multiple Sclerosis. ACS Chem Neurosci. 2017 Oct 18;8(10):2194-2201. DOI:10.1021/acschemneuro.7b00124
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