| Name | Tetrandrine |
| Description | Tetrandrine (Sinomenine A) is a naturally occurring biphenylisoquinoline alkaloid, a calcium channel inhibitor. Tetrandrine inhibits voltage-gated calcium channels (ICa) and Ca2+-activated potassium channels. |
| In vitro | METHODS: Leukemia cell lines K562, THP-1, U937, and HL60 were treated with Tetrandrine (1-3 µM) for 24-72 h, and cell numbers were measured.
RESULTS: 2 µM and 3 µM Tetrandrine significantly inhibited cell proliferation. [1]
METHODS: A panel of GFP-LC3-expressing tumor cell lines MCF-7, PLC-5, SK-Hep1, HeLa, and PC3 cells were treated with Tetrandrine (5 µM) for 16 h and GFP-LC3 spots were detected.
RESULTS: Tetrandrine significantly induced GFP-LC3 spot formation with similar potency (5 µM) in all cell lines tested.Tetrandrine induced autophagy in multiple cell lines. [2] |
| In vivo | METHODS: To detect anti-tumor activity in vivo, athymic nude mice bearing THP-1 xenografts were administered Tetrandrine (25-50 mg/kg, 0.5% methylcellulose) by gavage once daily for 13 days.
RESULTS: Tetrandrine treatment reduced tumor growth. [1] |
| Storage | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 0.7 mg/mL (1.12 mM), Solution. DMSO : 12.45 mg/mL (19.99 mM), Sonication and heating are recommended.
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| Keywords | Tetrandrine | PotassiumChannel | Potassium Channel | NSC77037 | NSC 77037 | KcsA | Inhibitor | inhibit | CalciumChannel | Calcium Channel | Ca2+ channels | Ca channels |
| Inhibitors Related | 2,4,6-Tri-tert-butylphenol | Gum arabic | Kojic acid | Hydroxychloroquine | Metronidazole | Avermectin B1a | 2-Amino-2-methyl-1-propanol | Doxycycline | 1,8-Cineole | Fenpyroximate | Methylene Blue trihydrate | Magnesium Chloride Hexahydrate |
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