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Tipiracil
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Catalog No. T60343Cas No. 183204-74-2
Tipiracil is a pharmacological agent that inhibits the enzyme thymidine phosphorylase. Tipiracil is under research for combination effect with trifluridine in advanced or metastatic colorectal and gastric cancers. By inhibiting thymidine phosphorylase, Tipiracil enhances the bioavailability and efficacy of trifluridine, offering alternative in cancer research.
Tipiracil
🥰Excellent
Purity: 99.815%
Catalog No. T60343Cas No. 183204-74-2
Tipiracil is a pharmacological agent that inhibits the enzyme thymidine phosphorylase. Tipiracil is under research for combination effect with trifluridine in advanced or metastatic colorectal and gastric cancers. By inhibiting thymidine phosphorylase, Tipiracil enhances the bioavailability and efficacy of trifluridine, offering alternative in cancer research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 2 mg | $36 | In Stock | |
| 5 mg | $54 | In Stock | |
| 10 mg | $77 | In Stock | |
| 25 mg | $123 | In Stock | |
| 50 mg | $179 | In Stock | |
| 100 mg | $266 | In Stock | |
| 200 mg | $395 | In Stock |
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Purity:99.815%
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Product Introduction
Bioactivity
Chemical Properties
| Description | Tipiracil is a pharmacological agent that inhibits the enzyme thymidine phosphorylase. Tipiracil is under research for combination effect with trifluridine in advanced or metastatic colorectal and gastric cancers. By inhibiting thymidine phosphorylase, Tipiracil enhances the bioavailability and efficacy of trifluridine, offering alternative in cancer research. |
| In vitro | Tipiracil functions as a thymidine phosphorylase inhibitor, enhancing trifluridine's efficacy by impeding its metabolism via thymidine phosphorylase. This synergistic action facilitates the use of the Trifluridine-Tipiracil combination as an innovative oral treatment for metastatic colorectal cancer [2]. Additionally, Tipiracil fortifies the stability of FTD by mitigating its first-pass degradation through its inhibitory action on thymidine phosphorylase [3]. |
| Molecular Weight | 242.66 |
| Formula | C9H11ClN4O2 |
| Cas No. | 183204-74-2 |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||
| Solubility Information | H2O: 0.8 mg/mL (3.3 mM), Sonication is recommended. DMSO: < 1 mg/mL (insoluble) | ||||||||||
Solution Preparation Table | |||||||||||
H2O
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In Vivo Formulation Calculator (Clear solution)
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% Saline/PBS/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 μLSaline/PBS/ddH2O 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 μLSaline/PBS/ddH2O 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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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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