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Temsirolimus is a dihydroxymethyl propionic acid ester of rapamycin with improved solubility that specifically inhibits mTOR signaling with a potency similar to that of rapamycin.1 Treatment with temsirolimus leads to cell cycle arrest in the G1 phase and also inhibition of tumor angiogenesis by reducing synthesis of VEGF.2,3 Temsirolimus demonstrates cytostatic activity in several xenograft models of human tumors in nude mice, including glioblastomas, prostate carcinoma, pancreatic, liver, and breast cancers, and medulloblastoma.2,4,3,1
WARNING This product is not for human or veterinary use.
1. Biochemical correlates of mTOR inhibition by the rapamycin ester CCI-
2. CCI-
3. mTOR, a novel target in breast cancer: The effect of CCI-
4. The novel mTOR inhibitor CCI-