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NO 711(NNC-711 free acid) is a potent and selective inhibitor of GABA transporter 1 (GAT-1), which increases GABAergic transmission, enhances non-rapid eye movement sleep, and prevents and treats paclitaxel-induced neuropathic pain.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $293 | - | In Stock | |
| 5 mg | $722 | - | In Stock | |
| 10 mg | $987 | - | In Stock | |
| 25 mg | $1,520 | - | In Stock | |
| 50 mg | $1,980 | - | In Stock | |
| 100 mg | $2,500 | - | In Stock |
| Description | NO 711(NNC-711 free acid) is a potent and selective inhibitor of GABA transporter 1 (GAT-1), which increases GABAergic transmission, enhances non-rapid eye movement sleep, and prevents and treats paclitaxel-induced neuropathic pain. |
| In vitro | Treatment of microglia with NO 711 (1 μM, 0-15 minutes) significantly reduced Na+-dependent GABA uptake. [2] |
| In vivo | Methods: 12-, 18-, and 25-day-old rat pups with implanted electrodes were used. Epileptic foci were induced by local application of dithiothreitol methyl iodide (BMI) via an implanted cannula over the sensorimotor cortical area, and cortical afterepileptic discharges (ADs) were induced by low-frequency stimulation (8 Hz) of the same cortical area. Epileptic foci were formed after pretreatment with NO 711 (1 or 10 mg/kg, i.p.), and epileptic ADs were induced in a second experimental series. NNC-711 was then applied at the same dose, and stimulation was repeated. Results: NO 711 did not block the formation of epileptogenic foci, but it significantly inhibited the spontaneous transition of interictal focal to ictal activity in all age groups. In 18- and 25-day-old rats, the intensity of movements accompanying sensorimotor cortical stimulation was smaller under the influence of NNC-711. [1] |
| Synonyms | NO711, NNC-711 free acid |
| Molecular Weight | 350.41 |
| Formula | C21H22N2O3 |
| Cas No. | 159094-94-7 |
| Smiles | OC(=O)C1=CCCN(CCON=C(c2ccccc2)c2ccccc2)C1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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