NMD670
Based on 1 Customer Validation
NMD670 is an orally active inhibitor of skeletal muscle specific chloride channel ClC-1 with an EC50 of 1.6 μM. NMD670 enhances neuromuscular transmission and improves muscle contraction and strength. NMD670 can be used in the study of muscle weakness and muscle fatigue.
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- Pureté: 99.60%
- CAS No.: 2354321-33-6
- Formule: C12H10BrNO4
- Masse moléculaire:312.12
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Stockage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Activité biologique
EC50: 1.6 μM (ClC-1)[1]
NMD670 (20 μM; 20-30 min) increases the amplitude of endplate potential, restores action potential excitation and enhances neuromuscular transmission in isolated muscle fibers of myasthenia gravis rats[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Pharmacokinetic Analysis in Rat and Dog[1]
| Species | Dose (mg/kg) | Oral Half-Life (h) | IV Half-Life (h) | IV distribution volume, VSS (L/kg) | Oral volume of distribution, terminal, VZ/F (L/kg) | Oral Cmax (ng/mL) | Tmax (h) | Oral AUC (ng·h/mL) | IV AUC (ng·h/mL) | Bioavailability, F (%) | IV Renal Clearance (mL/min/kg) |
| Female Rat | 10 | 5.15 | 2.90 | 0.418 | 2.04 | 19300 | 0.5 | 39900 | 36300 | 109.9 | 2.48 |
| Male Rat | 10 | 2.96 | 3.48 | 0.624 | 1.72 | 6780 | 0.5 | 24800 | 35300 | 70.25 | 1.94 |
| Male Beagle Dog | 2 | 7.46 | 7.74 | 0.208 | 0.817 | 12100 | 0.5 | 42200 | 34200 | 123.4 | 0.602 |