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sCNH240

🥰Excellent
Catalog No. T204076Cas No. 1357746-77-0
Alias 2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide

sCNH240 (2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide) is a potential and selective Rv1625c/Cya activator with good cell permeability and oral activity, IC90=1.24 μM in cholesterol-supplemented 7H12 medium against Mycobacterium tuberculosis (Mtb) H37Rv strain, and inhibition of CYP2C19, CYP2C9 and hERG channels.

sCNH240

sCNH240

🥰Excellent
Purity: 98.46%
Catalog No. T204076Alias 2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamideCas No. 1357746-77-0
sCNH240 (2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide) is a potential and selective Rv1625c/Cya activator with good cell permeability and oral activity, IC90=1.24 μM in cholesterol-supplemented 7H12 medium against Mycobacterium tuberculosis (Mtb) H37Rv strain, and inhibition of CYP2C19, CYP2C9 and hERG channels.
Pack SizePriceAvailabilityQuantity
1 mg$940In Stock
5 mg$2,070In Stock
10 mg$3,110In Stock
25 mg$5,280In Stock
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Purity:98.46%
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Product Introduction

Bioactivity
Description
sCNH240 (2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide) is a potential and selective Rv1625c/Cya activator with good cell permeability and oral activity, IC90=1.24 μM in cholesterol-supplemented 7H12 medium against Mycobacterium tuberculosis (Mtb) H37Rv strain, and inhibition of CYP2C19, CYP2C9 and hERG channels.
Targets&IC50
M. tuberculosis H37Rv:1.24 μM (MIC₉₀), M. tuberculosis (Intracellular):2.93 μM (EC₅₀), Cytotoxicity:>40 μM (CC₅₀)
In vitro
sCNH240 showed potent anti-TB activity against M. tuberculosis H37Rv (MIC₉₀ = 1.24 μM) and intracellular efficacy (EC₅₀ = 2.93 μM) with low cytotoxicity (CC₅₀ > 40 μM). In a dormancy model, sCNH240 reduced CFU by 1 log₁₀ alone and 4 log₁₀ when combined with BPaL, likely via Rv1625c/Cya activation[1].
In vivo
After oral dosing (20 mg/kg) in mice, sCNH240 showed 78% bioavailability and maintained plasma levels above EC₅₀ for over 14 hours. IV dosing showed low clearance and no cardiotoxicity (hERG IC₅₀ > 30 μM)[1].
Alias2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide
Chemical Properties
Molecular Weight324.35
FormulaC13H9FN2O3S2
Cas No.1357746-77-0
SmilesO=S(=O)(NC=1ON=C(C1)C2=CSC=C2)C=3C=CC=CC3F
Relative Density.no data available
Storage & Solubility Information
Storagestore at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 16.66 mg/mL (51.36 mM), Sonication is recommended.
DMSO: 50 mg/mL (154.15 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM3.0831 mL15.4154 mL30.8309 mL154.1545 mL
5 mM0.6166 mL3.0831 mL6.1662 mL30.8309 mL
10 mM0.3083 mL1.5415 mL3.0831 mL15.4154 mL
20 mM0.1542 mL0.7708 mL1.5415 mL7.7077 mL
50 mM0.0617 mL0.3083 mL0.6166 mL3.0831 mL
DMSO
1mg5mg10mg50mg
100 mM0.0308 mL0.1542 mL0.3083 mL1.5415 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
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