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S1R Agonist 1 (Compound 6b) hydrochloride is a selective S1R agonist, displaying K i values of 0.93 nM for S1R and 72 nM for S2R, and has demonstrated neuroprotective effects against ROS and NMDA-induced neurotoxicity [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $48 | 5 days | 5 days |
| Description | S1R Agonist 1 (Compound 6b) hydrochloride is a selective S1R agonist, displaying K i values of 0.93 nM for S1R and 72 nM for S2R, and has demonstrated neuroprotective effects against ROS and NMDA-induced neurotoxicity [1]. |
| In vitro | S1R agonist 1 (Compound 6b; 0.1-5 μM) hydrochloride significantly enhances neurite outgrowth induced by nerve growth factor (NGF) in a dose-dependent manner in PC12 cells and, at 1 μM for 24 hours, inhibits Rotenone-induced damage in SHSY5Y cells [1]. Additionally, it demonstrates neuroprotective effects against NMDA stimulation in SHSY5Y cells at 0.1-5 μM over 24 hours and shows no cytotoxicity in A549, LoVo, and Panc-1 cells at 0-10 μM over 24-72 hours [1]. |
| In vivo | Compound 6b, a selective S1R agonist at concentrations ranging from 0.1 to 50 μM, was administered over 120 hours, resulting in the death of 4 out of 8 zebrafish embryos at a 10 μM concentration [1]. |
| Molecular Weight | 331.88 |
| Formula | C20H26ClNO |
| Cas No. | 242487-82-7 |
| Smiles | Cl.O(C=1C=CC=CC1)CCN2CCC(CC=3C=CC=CC3)CC2 |
| 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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