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NMD670 is a first-in-class potent, specific and orally bioavailable ClC-1 chloride channel inhibitor with EC50 of 1.6 uM.
NMD670 (20 mg/kg) enhances neuromuscular transmission and restores muscle function in experimental autoimmune myasthenia gravis (MG) rats. NMD670 improves running performance in a passive immunization MG rat model.
| Molecular Weight | 312.12 |
| Formula | C12H10BrNO4 |
| CAS Number | 2354321-33-6 |
| Form | Solid |
| Solubility (25°C) | DMSO 10 mM |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
| Related Chloride Channel Products |
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| Atractyloside potassium salt
Atractyloside potassium salt is a highly effective and specific inhibitor of mitochondrial ADP/ATP transport. Atractyloside potassium salt inhibited the chloride channel in rat heart mitochondrial membrane. Atractyloside potassium salt is a toxic diterpenoid glycoside, which can be isolated from the fruit of Atractyloside. |
| CaCCinh-A01
CaCCinh-A01 is a calcium-activated chloride channel (CaCC) inhibitor. |
| Eact
Eact is a activator of Ca 2+-activated Cl - channel transmembrane protein 16A (TMEM16A). |
| NPPB
NPPB is a blocker of the outwardly rectifying chloride channel (ORCC) with IC50 of 80 nM. NPPB has been shown to activate the GPR35-Gαi/o and GPR35-Gα16 pathways in HEK293 cells, inducing intracellular calcium mobilization. |
| T16Ainh-A01
T16Ainh-A01 is a Ca2+-activated Cl- channel transmembrane protein 16A (TMEM16A) inhibitor. |
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