Date published: 2025-11-1

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Everolimus (CAS 159351-69-6)

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See product citations (7)

Alternate Names:
40-O-(2-Hydroxyethyl)rapamycin; 42-O-(2-Hydroxy)ethyl Rapamycin; Afinitor
Application:
Everolimus is an immunosuppresive inhibitor of FRAP (mTOR)
CAS Number:
159351-69-6
Purity:
≥98%
Molecular Weight:
958.22
Molecular Formula:
C53H83NO14
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Everolimus is a macrolide derived from rapamycin (sc-3504) with immunosuppressant properties shown to inhibit cell proliferation induced by growth factors. Macrolides belong to a group of antibiotics that bind to the 50S ribosomal subunit and inhibit protein synthesis. Studies indicate that everolimus is a mTOR (FRAP) inhibitor that displays high affinity toward the intracellular receptor FKBP12. Additionally, the Everolimus-FKBP12 complex decreases the activity of the S6K1 and 4EBP by binding to FRAP.


Everolimus (CAS 159351-69-6) References

  1. Everolimus. Novartis.  |  Dumont, FJ. 2001. Curr Opin Investig Drugs. 2: 1220-34. PMID: 11717808
  2. Early clinical experience with a novel rapamycin derivative.  |  Nashan, B. 2002. Ther Drug Monit. 24: 53-8. PMID: 11805723
  3. Potent antifibrotic activity of mTOR inhibitors sirolimus and everolimus but not of cyclosporine A and tacrolimus in experimental liver fibrosis.  |  Patsenker, E., et al. 2011. J Hepatol. 55: 388-98. PMID: 21168455
  4. Everolimus - a new approach in the treatment of renal cell carcinoma.  |  Anandappa, G., et al. 2010. Cancer Manag Res. 2: 61-70. PMID: 21188097
  5. Therapeutic potential and adverse events of everolimus for treatment of hepatocellular carcinoma - systematic review and meta-analysis.  |  Yamanaka, K., et al. 2013. Cancer Med. 2: 862-71. PMID: 24403259
  6. Everolimus in postmenopausal, hormone receptor-positive advanced breast cancer: summary and results of an austrian expert panel discussion.  |  Gnant, M., et al. 2013. Breast Care (Basel). 8: 293-9. PMID: 24415983
  7. [Exemestane-everolimus in HER2-negative, hormonal receptor-positive, post-menopausal metastatic breast cancer with resistance to non-steroidal aromatase inhibitor: a new option].  |  Gilabert, M., et al. 2014. Bull Cancer. 101: 325-33. PMID: 24691195
  8. Everolimus.  |  Hasskarl, J. 2014. Recent Results Cancer Res. 201: 373-92. PMID: 24756805
  9. Targeting the mammalian target of rapamycin pathway with everolimus: implications for the management of metastatic breast cancer.  |  Ng, VC., et al. 2015. J Oncol Pharm Pract. 21: 433-42. PMID: 24964967
  10. Durable polymer everolimus-eluting stents: history, current status and future prospects.  |  Rodríguez-Arias, JJ., et al. 2020. Expert Rev Med Devices. 17: 671-682. PMID: 32543934
  11. Everolimus ameliorates Helicobacter pylori infection-induced inflammation in gastric epithelial cells.  |  Liu, J., et al. 2022. Bioengineered. 13: 11361-11372. PMID: 35506423
  12. Everolimus reduces BK polyomavirus infection by suppressing its replication and spread of infection.  |  Sato, N., et al. 2022. Antiviral Res. 208: 105456. PMID: 36328070
  13. Inducible erythromycin resistance in bacteria.  |  Weisblum, B. 1984. Br Med Bull. 40: 47-53. PMID: 6442874

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Everolimus, 5 mg

sc-218452
5 mg
$128.00

Everolimus, 50 mg

sc-218452A
50 mg
$638.00

What is the solubility of everolimus in aqueous solutions?

Asked by: Debbie
Thank you for your question. As indicated above, Everolimus is soluble in chloroform, methanol, DMSO (100 mg/ml), water (<1 mg/ml at 25° C), and ethanol (100 mg/ml).
Answered by: Tech Support Europe
Date published: 2022-12-13

What is the appearance of the compound?

Asked by: two2igm05
Thank you for your question. Everolimus, sc-218452, is in white to off-white powder form.
Answered by: Chemical Support 4
Date published: 2022-08-28
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Rated 5 out of 5 by from PatsenkerPatsenker, E. et al. (PubMed 21168455) wanted to test the potential of Everolimus, a macrolide derived from Rapamycin, in halting experimental liver fibrosis progression in rats. Everolimus decreased fibrosis up to 70%, improved portal pressure, reduced ascites, and showed potent down-regulation of pro-fibrogenic genes, paralleled by a strong increase in matrix degradation (collagenase) activity. -SCBT Publication Review
Date published: 2015-04-28
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Everolimus is rated 5.0 out of 5 by 1.
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