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  • Indoleamine 2,3-Dioxygenase (IDO)
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ido-in-9

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  • Inhibitors & Agonists
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IDO-IN-9
T116221888378-12-8
IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50 values of 0.011 μM for kinase and 0.0018 μM for Hela cells.
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8-10 weeks
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Coptisine
Coptisin
T5S00533486-66-6
1. Coptisine (Coptisin) treatment increases cell viability based on its reversal effect on the enhanced activity of Indoleamine 2, 3-dioxygenase . 2. Coptisine treats myocardial I R likely through suppressing myocardial apoptosis and inflammation by inhibiting the Rho ROCK pathway. 3. Coptisine is a potential anti-osteosarcoma drug candidate, via exerting a strong anti-osteosarcoma effect with very low toxicity . 4. Coptisine with a high dosage could inhibit cholesterol synthesis via suppressing the HMGCR expression and promoting the use and excretion of cholesterol via up-regulating LDLR and CYP7A1 expression. 5. Coptisine suppresses adhesion, migration and invasion of MDA-MB-231 breast cancer cells in vitro, the down-regulation of MMP-9 in combination with the increase of TIMP-1 possibly contributing to the anti-metastatic function for breast cancer.
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Coptisine chloride
Q-100696,NSC-119754
T5S00566020-18-4
1. Coptisine chloride (NSC-119754) can be absorbed across intestinal epithelial cells, and completely absorbed compounds.
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TargetMol | Inhibitor Sale
Coptisine sulfate
T4S00511198398-71-8
1. Coptisine sulfate has growth inhibitory activity against human cancer cell line in the NCI's anticancer drug screening program.
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TargetMol | Inhibitor Sale