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Coptisine

CAS No. : 3486-66-6

MCE 站：Coptisine

产品活性：Coptisine 是从黄连中分离到的生物碱，是一种有效的非竞争性的 IDO 抑制剂，K_i 值为 5.8 μM，IC₅₀ 值为 6.3 μM。

研究领域：Metabolic Enzyme/Protease

作用靶点：Indoleamine 2,3-Dioxygenase (IDO)

In Vitro: Coptisine is an efficient uncompetitive IDO inhibitor with a K_i value of 5.8 μM and an IC₅₀ value of 6.3 μM. Coptisine (0.1-100 μM) inhibits the proliferation of A549, H460, H2170, MDA-MB-231 and HT-29 cells, with IC₅₀s of 18.09, 29.50, 21.60, 20.15 and 26.60??M, respectively. Coptisine (12.5, 25, 50 μM) upregulates the expression of pH2AX and p21, reduces expression of cyclin B1, cdc2, and cdc25C, and induces G2/M arrest and apoptosis of A549 cells in a concentration-dependent manner. Coptisine (12.5, 25, 50 μM) also induces mitochondrial dysfunction and activates caspases activities in A549 cells. Furthermore, Coptisine (50 μM) increases ROS levels in a time-dependent manner (0.5, 1, 2, 4, 12, and 24?h).

In Vivo: Coptisine shows increased toxicity in mice in a concentration dependent manner, with LD₅₀ value of 880.18 mg/kg. Coptisine (154 mg/kg/day, 90 days) shows no toxicity on SD rats. Coptisine (23.35, 46.7, 70.05 mg/kg, p.o.) dose-dependently decreases the levels of TC, TG, and LDL-c and increases HDL-c content in serum of hamsters to different degree, slows down weight gain induced by the HFHC diet, and raises the level of cholesterol and TBA in feces dose-dependently in hamsters. Coptisine (70.05 mg/kg, p.o.) suppresses HMGCR protein expression level and induces the protein expression of SREBP-2, LDLR, and CYP7A1 involved in cholesterol metabolism.

相关产品：Necrostatin-1  |  Indoximod  |  Palmatine chloride  |  PF-06840003  |  Coptisine chloride  |  GNF-PF-3777  |  IDO-IN-3  |  IACS-8968 S-enantiomer  |  Coptisine Sulfate  |  Kushenol E  |  IDO-IN-11

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