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JC-171 (JC171)

JC-171 (JC171) Suppliers list
Company Name: TargetMol Chemicals Inc.
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Email: support@targetmol.com
Products Intro: Product Name:JC-171
CAS:2112809-98-8
Package:5mg;297USD
Company Name: Aladdin Scientific
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Email: tp@aladdinsci.com
Products Intro: Product Name:JC-171
CAS:2112809-98-8
Purity:99% Package:$300.9/5mg;$500.9/10mg;$1500.9/50mg;$2250.9/100mg;Bulk package Remarks:99%
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:JC-171
CAS:2112809-98-8
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: Beijing Jin Ming Biotechnology Co., Ltd.  
Tel: 010-60605840 15801484223;
Email: psaitong@jm-bio.com
Products Intro: Product Name:JC-171
CAS:2112809-98-8
Purity:98% Package:5mg
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Email: marketing@tsbiochem.com
Products Intro: Product Name:JC-171
CAS:2112809-98-8
Package:2mg/RMB 2130;5mg/RMB 2490;10mg/RMB 4160

JC-171 (JC171) manufacturers

  • JC-171
  • JC-171 pictures
  • $297.00 / 5mg
  • 2024-10-28
  • CAS:2112809-98-8
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  • Purity:
  • Supply Ability: 10g
JC-171 (JC171) Basic information
Product Name:JC-171 (JC171)
Synonyms:JC-171 (JC171);Benzamide, 5-chloro-N-[2-[4-[(hydroxyamino)sulfonyl]phenyl]ethyl]-2-methoxy-
CAS:2112809-98-8
MF:C16H17ClN2O5S
MW:384.83
EINECS:
Product Categories:
Mol File:2112809-98-8.mol
JC-171

(JC171) Structure
JC-171 (JC171) Chemical Properties
density 1.401±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 250 mg/mL (649.64 mM)
form Solid
pka6.43±0.69(Predicted)
color White to off-white
Safety Information
MSDS Information
JC-171 (JC171) Usage And Synthesis
UsesJC-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 50NLRP3
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
JC-171 (JC171) Preparation Products And Raw materials
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