Raltitrexed
| Storage | Store at -20°C |
| M.Wt | 458.49 |
| Cas No. | 112887-68-0 |
| Formula | C21H22N4O6S |
| Solubility | insoluble in H2O; ≥154 mg/mL in DMSO; ≥10.62 mg/mL in EtOH with ultrasonic |
| Chemical Name | (2S)-2-[[5-[methyl-[(2-methyl-4-oxo-1H-quinazolin-6-yl)methyl]amino]thiophene-2-carbonyl]amino]pentanedioic acid |
| SDF | Download SDF |
| Canonical SMILES | CC1=NC(=O)C2=C(N1)C=CC(=C2)CN(C)C3=CC=C(S3)C(=O)NC(CCC(=O)O)C(=O)O |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |
| Cell experiment [1]: | |
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Cell lines |
2 wild-type (wt) p53 (Lovo and LS174T) and 4 mutant (mt) p53 (WiDr, WiDr/F, HT29 and SW948) colon carcinoma cell lines |
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Preparation method |
The solubility of this compound in DMSO is > 154mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months. |
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Reacting condition |
50 and 100 nM; 24 and 48 hrs |
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Applications |
Raltitrexed up-regulated p53 and p21 expression in wt p53 cells, but not in mt p53 cells. In the mt p53 cells HT29 and WiDr/F, the highest induction of thymidylate synthase (6 ~ 10 folds) was observed after Raltitrexed treatment. Moreover, Raltitrexed increased Bax expression up to 5 folds in wt p53 cells, but with only a very slight induction of Bax expression in mt p53 cells. In wt p53 cells, Raltitrexed treatment hardly changed Bcl-2 expression. |
| Animal experiment [2]: | |
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Animal models |
C57BL/6J-ApcMin/+ mice |
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Dosage form |
3 or 5 mg/kg; twice a week or five times a week |
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Applications |
In C57BL/6J-ApcMin/+ mice, Raltitrexed (3 mg/kg; twice a week) increased the average tumor number in the small intestine by 4 folds. When the dose of Raltitrexed was elevated to 5 mg/kg, five times a week, it resulted in a 10-fold increase in the average tumor number. Under all administration schedules, Raltitrexed was well-tolerated with only few treatment-related deaths occurring. Raltitrexed-induced tumors commonly occurred in the duodenum and jejunum, with few in the ileum and none in the colon. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: [1]. Peters GJ, van Triest B, Backus HH, Kuiper CM, van der Wilt CL, Pinedo HM. Molecular downstream events and induction of thymidylate synthase in mutant and wild-type p53 colon cancer cell lines after treatment with 5-fluorouracil and the thymidylate synthase inhibitor raltitrexed. Eur J Cancer. 2000 May;36(7):916-24. [2]. Murphy JT, Tucker JM, Davis C, Berger FG. Raltitrexed increases tumorigenesis as a single agent yet exhibits anti-tumor synergy with 5-fluorouracil in ApcMin/+ mice. Cancer Biol Ther. 2004 Nov;3(11):1169-76. |
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Quality Control & MSDS
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Chemical structure
Related Biological Data
