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Coptisine

Catalog No. T5S0053   CAS 3486-66-6
Synonyms: Coptisin

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 Chemical Structure
Coptisine, CAS 3486-66-6
Pack Size Availability Price/USD Quantity
1 mg In stock $ 38.00
5 mg In stock $ 82.00
10 mg In stock $ 139.00
25 mg In stock $ 263.00
50 mg In stock $ 476.00
100 mg In stock $ 697.00
1 mL * 10 mM (in DMSO) In stock $ 108.00
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Purity: 99.91%
Purity: 98%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description 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.
Targets&IC50 IDO:6.3 μM.
Source
Synonyms Coptisin
Molecular Weight 320.32
Formula C19H14NO4
CAS No. 3486-66-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 10 mg/mL (31.22 mM)

TargetMolReferences and Literature

1. He K, et al. The safety and anti-hypercholesterolemic effect of coptisine in Syrian golden hamsters. Lipids. 2015 Feb;50(2):185-94. 2. Rao PC, et al. Coptisine-induced cell cycle arrest at G2/M phase and reactive oxygen species-dependent mitochondria-mediated apoptosis in non-small-cell lung cancer A549 cells. Tumour Biol. 2017 Mar;39(3):12010428317694565. 3. Yu D, et al. The IDO inhibitor coptisine ameliorates cognitive impairment in a mouse model of Alzheimer's disease. J Alzheimers Dis. 2015;43(1):291-302.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Traditional Chinese Medicine Monomer Library Natural Product Library Bioactive Compounds Library Max Bioactive Compound Library PBCRBS Traditional Chinese Medicine Compound Library Natural Product Library for HTS Selected Plant-Sourced Compound Library Anti-Fibrosis Compound Library Metabolism Compound Library

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Linrodostat IDO-IN-13 Navoximod 1-Isopropyltryptophan IDO1-IN-23 IDO1-IN-21 IDO1/TDO-IN-6 IDO-IN-1

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Keywords

Coptisine 3486-66-6 Metabolism Indoleamine 2,3-Dioxygenase (IDO) Inhibitor inhibit Coptisin inhibitor

 

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