Temsirolimus
Chemical Name: Rapamycin 42-[3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate]
Purity: ≥98%
Biological Activity
Temsirolimus is a mTOR inhibitor; inhibits tumor growth in breast cancer cell lines (IC50 values are 1.6 and 4.3 nM for SKBr3 and BT474, respectively). Inhibits HIF-1α-mediated VEGF production in breast cancer cell lines (BT474 and MDA-MB-231). Directly inhibits serum and VEGF mediated endothelial cell proliferation and morphogenesis in vitro and vessel formation in vivo. Causes G1/S cell cycle arrest in multiple cancer cell lines. Antiangiogenic. Activates autophagy.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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Inhibition of mammalian target of rapamycin signaling by CCI-779 (temsirolimus) induces growth inhibition and cell cycle arrest in Cashmere goat fetal fibroblasts (Capra hircus).
Wang et al.
DNA Cell Biol., 2012;31:1095 -
Effects of the mammalian target of rapamycin inhibitor CCI-779 used alone or with chemotherapy on human prostate cancer cells and xenografts.
Wu L et al.
Cancer Res., 2005;65:2825 -
The novel mTOR inhibitor CCI-779 (temsirolimus) induces antiproliferative effects through inhibition of mTOR in Bel-7402 liver cancer cells.
Li et al.
Cancer Cell Int., 2013;13 -
Pharmacological modulation of autophagy: therapeutic potential and persisting obstacles.
Galluzzi et al.
Nat.Rev.Drug.Discov., 2017; -
Antiangiogenic potential of the Mammalian target of rapamycin inhibitor temsiro.
Del Bufalo et al.
Cancer Res., 2006;66:5549
Product Datasheets
Citations for Temsirolimus
The citations listed below are publications that use Tocris products. Selected citations for Temsirolimus include:
3 Citations: Showing 1 - 3
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RNA N6-Methyladenosine Methyltransferase METTL3 Facilitates Colorectal Cancer by Activating the m6A-GLUT1-mTORC1 Axis and Is a Therapeutic Target.
Authors: Jun Et al.
Gastroenterology 2021;160:1284-1300.e16
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In vivo brain GPCR signaling elucidated by phosphoproteomics.
Authors: Liu
Science 2018;360(6395):eaao4927
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Combined CDK4/6 and mTOR Inhibition Is Synergistic against Glioblastoma via Multiple Mechanisms.
Authors: Olmez Et al.
Clin Cancer Res 2017;23:6958
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