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Scoulerine HCl is a multi-target inhibitor with antibacterial, antitumor, and antioxidant activities. Scoulerine HCl targets GABA receptors and BACE1 and inhibits mitochondrial dehydrogenase activity, thereby suppressing cancer cell proliferation, migration, invasion, epithelial-mesenchymal transition, and stemness maintenance. Scoulerine HCl also disrupts microtubule structure by acting on the PI3K/Akt/mTOR signaling axis and α1D-adrenergic receptors, thereby inducing cell cycle arrest and apoptosis. Additionally, Scoulerine HCl regulates endoplasmic reticulum stress and mitochondrial function, and possesses various pharmacological activities, including anti-Plasmodium falciparum and antiemetic and antitussive effects.

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $195 | - | In Stock | |
| 5 mg | $483 | In Stock | In Stock | |
| 10 mg | $691 | In Stock | In Stock | |
| 25 mg | $1,080 | - | In Stock | |
| 50 mg | $1,490 | - | In Stock | |
| 100 mg | $1,960 | - | In Stock |
| Description | Scoulerine HCl is a multi-target inhibitor with antibacterial, antitumor, and antioxidant activities. Scoulerine HCl targets GABA receptors and BACE1 and inhibits mitochondrial dehydrogenase activity, thereby suppressing cancer cell proliferation, migration, invasion, epithelial-mesenchymal transition, and stemness maintenance. Scoulerine HCl also disrupts microtubule structure by acting on the PI3K/Akt/mTOR signaling axis and α1D-adrenergic receptors, thereby inducing cell cycle arrest and apoptosis. Additionally, Scoulerine HCl regulates endoplasmic reticulum stress and mitochondrial function, and possesses various pharmacological activities, including anti-Plasmodium falciparum and antiemetic and antitussive effects. |
| In vitro | Methods: A549 (lung cancer), A2780 (ovarian cancer), SK-BR-3, and MCF-7 (breast cancer) cells were treated with scoulerin HCl (6451-73-6, free base) at concentrations of 1, 5, 10, 20, and 50 μM for 72 consecutive hours, and cell proliferation was monitored using real-time impedance analysis. Results: Scoulerin HCl (6451-73-6 free base) exhibited concentration-dependent inhibition of adherent cancer cell proliferation, with significant inhibition observed at concentrations of 10 μM and above. [1] Methods: Jurkat and MOLT-4 leukemia cells were treated with Scoulerine HCl (2.5, 5, 10, 15, 20 μM) for 24 and 48 hours, and live cells were counted using the trypan blue exclusion assay. Results: Scoulerine HCl exhibited concentration- and time-dependent reductions in cell viability and proliferation. [1] Methods: OVCAR3 cells were treated with Scoulerine HCl (5, 10 μmol/L) were added to OVCAR3 cells and pretreated for 48 hours; after treatment, the cells were cultured for an additional 10 days, and cell cloning ability was assessed via crystal violet staining and spectrophotometry. Results: Scoulerine HCl exhibited a dose-dependent reduction in cell cloning ability, with an inhibition rate of approximately 78.3% at 10 μmol/L.[2] |
| In vivo | Methods: To investigate the in vivo antitumor efficacy of Scoulerine HCl (6451-73-6, free base), BALB/c nude mice were used. SK-OV-3 cells were implanted subcutaneously, and administration of Scoulerine HCl (6451-73-6, free base) (1, 2.5, 5, 10 mg/kg) until the end of the experiment. Results: Scoulerine HCl reduced tumor weight and volume in a dose-dependent manner; at 10 mg/kg, tumor weight decreased from approximately 2.1 g to approximately 0.7 g, and volume decreased from approximately 1800 mm³ to approximately 600 mm³. [2] |
| Synonyms | Scoulerine hcl (6451-73-6 free base), Discretamine hydrochloride, (-)-Scoulerine hydrochloride |
| Molecular Weight | 363.84 |
| Formula | C19H22ClNO4 |
| Cas No. | 51486-68-1 |
| Smiles | OC=1C=C2[C@]3(N(CC=4C(C3)=CC=C(OC)C4O)CCC2=CC1OC)[H].Cl |
| Relative Density. | no data available |
| 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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