产品
编 号：F196369
分子式：C15H11FN2
分子量：238.26
分子式：C15H11FN2
分子量：238.26
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
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1mg
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5mg
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10mg
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25mg
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50mg
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结构图
CAS No: 163239-22-3
产品详情
生物活性：
680C91 is an orally active, selective tryptophan 2,3-dioxygenase (TDO) inhibitor with a Ki of 51 nM. TDO is the key enzyme of tryptophan catabolism. 680C91 can be used for the research of cancer immunotherapy and Alzheimer’s Disease.
体内研究：
680C91 (a dose of 15 mg/kg for acute treatment ) elevates tryptophan in brain.Animal Model:Male C57Bl6/NCrl mice aged 13-18 weeks
Dosage:15 mg/kg
Administration:Administered per os
Result:Caused a significant increase in brain tryptophan.
体外研究：
680C91 is a potent (Ki=51 nM) and selective TDO inhibitor with no inhibitory activity against indoleamine 2,3-dioxygenase, monoamine oxidase A and B, 5-HT uptake and 5-HT1A,1D,2A and 2C receptors at a concentration of 10 μM.680C91 inhibits the catabolism of tryptophan by rat liver cells and rat liver perfused in situ. Tdo2 could regulate cell proliferation and stimulate the expression of decidual marker Dtprp in the uterine stromal cells and decidual cells. Tdo2 inhibitor 680C91 also inhibits the prolifer ation activity of uterine decidual cells at 24 h.Treatment of leiomyoma smooth muscle cell (LSMC) and myometrial smooth muscle cell (MSMC) spheroids with 680C91 (25 and 50 μM) significantly represses the expression of collagen type I (COL1A1) and type III (COL3A1) in a dose-dependent manner.
680C91 is an orally active, selective tryptophan 2,3-dioxygenase (TDO) inhibitor with a Ki of 51 nM. TDO is the key enzyme of tryptophan catabolism. 680C91 can be used for the research of cancer immunotherapy and Alzheimer’s Disease.
体内研究：
680C91 (a dose of 15 mg/kg for acute treatment ) elevates tryptophan in brain.Animal Model:Male C57Bl6/NCrl mice aged 13-18 weeks
Dosage:15 mg/kg
Administration:Administered per os
Result:Caused a significant increase in brain tryptophan.
体外研究：
680C91 is a potent (Ki=51 nM) and selective TDO inhibitor with no inhibitory activity against indoleamine 2,3-dioxygenase, monoamine oxidase A and B, 5-HT uptake and 5-HT1A,1D,2A and 2C receptors at a concentration of 10 μM.680C91 inhibits the catabolism of tryptophan by rat liver cells and rat liver perfused in situ. Tdo2 could regulate cell proliferation and stimulate the expression of decidual marker Dtprp in the uterine stromal cells and decidual cells. Tdo2 inhibitor 680C91 also inhibits the prolifer ation activity of uterine decidual cells at 24 h.Treatment of leiomyoma smooth muscle cell (LSMC) and myometrial smooth muscle cell (MSMC) spheroids with 680C91 (25 and 50 μM) significantly represses the expression of collagen type I (COL1A1) and type III (COL3A1) in a dose-dependent manner.
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