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CITCO
🥰Excellent
Catalog No. T14973Cas No. 338404-52-7
CITCO inhibits growth and expansion of brain tumour stem cells (BTSCs) and has an EC50 of 49 nM over pregnane X receptor (PXR), and no activity on other nuclear receptors. CITCO is an imidazothiazole derivative and it also is a selective Constitutive androstane receptor (CAR) agonist.
CITCO
🥰Excellent
Purity: 99.24%
Catalog No. T14973Cas No. 338404-52-7
CITCO inhibits growth and expansion of brain tumour stem cells (BTSCs) and has an EC50 of 49 nM over pregnane X receptor (PXR), and no activity on other nuclear receptors. CITCO is an imidazothiazole derivative and it also is a selective Constitutive androstane receptor (CAR) agonist.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $57 | In Stock | |
| 10 mg | $91 | In Stock | |
| 25 mg | $166 | In Stock | |
| 50 mg | $266 | In Stock | |
| 100 mg | $397 | In Stock | |
| 200 mg | $597 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $63 | In Stock |
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CitedSelect Batch
Purity:99.24%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | CITCO inhibits growth and expansion of brain tumour stem cells (BTSCs) and has an EC50 of 49 nM over pregnane X receptor (PXR), and no activity on other nuclear receptors. CITCO is an imidazothiazole derivative and it also is a selective Constitutive androstane receptor (CAR) agonist. |
| In vitro | CITCO (1-50 μM; 48 hours) results in dose-dependent inhibition of viable cell count and proliferation in T98G, U87MG glioma, and BTSCs. CITCO (0-25 μM; 48 hours) significantly increases CAR protein expression in T98G, U87MG glioma, and BTSCs. CITCO (2.5-10 μM; 48 hours) induces apoptosis in BTSCs in a dose-dependent manner, but not in normal astrocytes. CITCO (2.5, 5 μM; 48 hours) induces differential cell cycle arrest in various BTSCs in culture, but not in normal astrocytes[1]. |
| In vivo | CITCO (intraperitoneal; 25?μg; on days 22, 24, 26, 30 and 36) results a significant decrease in tumour growth. After treatment with 100?μg CITCO, it further decreases to an undetectable level [1]. |
| Molecular Weight | 436.74 |
| Formula | C19H12Cl3N3OS |
| Cas No. | 338404-52-7 |
| Smiles | C(=NOCC1=CC(Cl)=C(Cl)C=C1)C2=C(N=C3N2C=CS3)C4=CC=C(Cl)C=C4 |
| Relative Density. | 1.48g/cm3 |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
| Solubility Information | H2O: insoluble DMSO: 11 mg/ml (25.19 mM)  | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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