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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 Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $940 | - | In Stock | |
| 5 mg | $2,070 | - | In Stock | |
| 10 mg | $3,110 | - | In Stock | |
| 25 mg | $5,280 | - | In Stock |
| 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), Cytotoxicity:>40 μM (CC₅₀), M. tuberculosis (Intracellular):2.93 μM (EC₅₀) |
| 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]. |
| Synonyms | 2-Fluoro-N-[3-(3-thienyl)-5-isoxazolyl]benzenesulfonamide |
| Molecular Weight | 324.35 |
| Formula | C13H9FN2O3S2 |
| Cas No. | 1357746-77-0 |
| Smiles | O=S(=O)(NC=1ON=C(C1)C2=CSC=C2)C=3C=CC=CC3F |
| Relative Density. | no data available |
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| 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
DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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