[CAS NO. 159351-69-6]  Everolimus (RAD001)

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PRODUCTS SPECIFICATIONS [159351-69-6]

Catelog
SLK-S1120
Brand
Selleck
CAS
159351-69-6

DESCRIPTION [159351-69-6]

Overview

MDLMFCD00929329
Molecular Weight958.22
Molecular FormulaC53H83NO14
SMILESO=C1N2[C@](C(=O)O[C@]([C@@H](C[C@H]3C[C@@H](OC)[C@H](OCCO)CC3)C)(CC(=O)[C@H](C)/C=C(\C)/[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(/C)\[C@@H](OC)C[C@]4(O[C@@](O)(C1=O)[C@H](C)CC4)[H])[H])(CCCC2)[H]

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM1.0436 mL5.2180 mL10.4360 mL
5 mM0.2087 mL1.0436 mL2.0872 mL
10 mM0.1044 mL0.5218 mL1.0436 mL
50 mM0.0209 mL0.1044 mL0.2087 mL

Description

Everolimus (RAD001, SDZ-RAD, Afinitor) is an mTOR inhibitor of with of 1.6-2.4 nM in a cell-free assay. Everolimus induces cell and and inhibits tumor cells proliferation.

Targets

FKBP12 [1]
(Cell-free assay)
mTOR (FKBP12) [1]
(Cell-free assay)
1.6-2.4 nM1.6 nM-2.4 nM

In vitro

Everolimus exhibits the immunosuppressive activity which is comparable to that of rapamycin. Everolimus competes with immobilized FK 506 for binding to biotinylated FKBP12 and shows the inhibitory effect on a two-way MLR performed with spleen cells from BALB/c and CBA mice with IC50 of 0.12-1.8 nM. Everolimus also shows antiangiogenic/vascular effects in VEGF-induced HUVEC proliferation with IC50 of 0.12 nM and bFGF-induced HUVEC proliferation with IC50 of 0.8 nM, respectively. A recent study shows that Everolimus shows a dose-dependent inhibitory effects on both the total cells and the stem cells from the BT474 cell line and the primary breast cancer cells with IC50 of 156 nM in total cells of primary breast cancer cells and 71 nM in total cells of BT474 cells. In addition, combination treatment with Everolimus and trastuzumab produces the significantly increased inhibition on the growth of cancer stem cells with the inhibition rate increased by more than 50 %.

In vivo

Everolimus (0.1 to 10 mg/kg) dose-dependently inhibits growth of the primary (ear) and lymph node metastases of B16/BL6 melanoma, with decreased total number of vessels and reduced mature vessels. In a xenograft animal model of BT474 stem cells, Everolimus shows significant reductions in mean tumor sizes (590.6 mm), compared to the control group with a tumor size of 698 mm. Furthermore, combination treatment with Everolimus and trastuzumab significantly decreases the xenograft tumor size (410.8 mm) more than Everolimus treatment alone.


Synonyms

Rapamycin, 42-O-(2-hydroxyethyl)-
23,27-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclohentriacontine, rapamycin deriv.
42-O-(2-Hydroxyethyl)rapamycin
40-O-(2-Hydroxyethyl)rapamycin
SDZ-RAD
RAD 001
Everolimus
RAD
Certican
XIENCE V
Afinitor
Zortress
Xience
Afinitor Disperz
Votubia