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Compound 8b hydrochloride, a selective S1R agonist, exhibits affinity with K i s of 1.1 nM for S1R and 88 nM for S2R. It demonstrates neuroprotective effects against ROS and NMDA-induced neurotoxicity [1].
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $97 | 5 days | 5 days |
| Description | Compound 8b hydrochloride, a selective S1R agonist, exhibits affinity with K i s of 1.1 nM for S1R and 88 nM for S2R. It demonstrates neuroprotective effects against ROS and NMDA-induced neurotoxicity [1]. |
| In vitro | S1R agonist 2 (Compound 8b; 0.1-5 μM) hydrochloride significantly enhances NGF-induced neurite outgrowth in a dose-dependent manner; at 1 μM over 24 hours, it markedly inhibits Rotenone-induced cellular damage in SHSY5Y cells. Additionally, it offers neuroprotection against NMDA stimulation in SHSY5Y cells at 0.1-5 μM over 24 hours. This compound exhibits no cytotoxicity in A549, LoVo, and Panc-1 cells at varying concentrations (0-10 μM) and durations (24-72 h) [1]. |
| In vivo | Compound 8b (S1R agonist 2; 0.1-50 μM; 120 h) hydrochloride at a concentration of 10 μM does not induce embryonic mortality (100% survival of embryos), yet at the highest dosage (50 μM), it induces death in all embryos [1]. |
| Molecular Weight | 345.91 |
| Formula | C21H28ClNO |
| 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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