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Everolimus
[CAS# 159351-69-6]

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Complete supplier list of Everolimus
Identification
Classification API >> Immune function drug >> Immunosuppressive drug
Name Everolimus
Synonyms (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
Molecular Structure CAS # 159351-69-6, Everolimus, (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
Molecular Formula C53H83NO14
Molecular Weight 958.22
CAS Registry Number 159351-69-6
EC Number 621-003-9
SMILES C[C@@H]1CC[C@H]2C[C@@H](/C(=C/C=C/C=C/[C@H](C[C@H](C(=O)[C@@H]([C@@H](/C(=C/[C@H](C(=O)C[C@H](OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@@]1(O2)O)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)OCCO)C)/C)O)OC)C)C)/C)OC
Properties
Density 1.2±0.1 g/cm3, Calc.*
Index of Refraction 1.548, Calc.*
Boiling Point 998.7±75.0 ºC (760 mmHg), Calc.*
Flash Point 557.8±37.1 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS08 Danger    Details
Hazard Statements H372-H412    Details
Precautionary Statements P260-P264-P270-P273-P319-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Specific target organ toxicity - repeated exposureSTOT RE1H372
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
CarcinogenicityCarc.2H351
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Reproductive toxicityRepr.1BH360Fd
Reproductive toxicityLact.-H362
Reproductive toxicityRepr.2H361
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
SDS Available
up Discovory and Applicatios
Everolimus, a derivative of rapamycin, was developed in the late 1990s by researchers at Novartis Pharmaceuticals. It was synthesized through modifications to the rapamycin molecule to enhance its pharmacokinetic properties and optimize its therapeutic efficacy. Everolimus belongs to the class of drugs known as mammalian target of rapamycin (mTOR) inhibitors, which selectively inhibit the mTOR pathway involved in cell growth, proliferation, and survival. The discovery of everolimus represented a significant advancement in targeted cancer therapy.

Everolimus is approved for the treatment of various advanced solid tumors, including renal cell carcinoma (RCC), pancreatic neuroendocrine tumors (pNET), and hormone receptor-positive, HER2-negative breast cancer. As an mTOR inhibitor, everolimus blocks aberrant signaling pathways implicated in tumor growth and angiogenesis, slowing disease progression and extending progression-free survival in patients with these malignancies. Everolimus is used in combination with other immunosuppressive agents for the prevention of organ rejection in transplant recipients. By inhibiting T-cell activation and proliferation, everolimus helps maintain graft function and reduce the risk of acute rejection episodes in kidney, liver, heart, and lung transplant recipients. Everolimus is indicated for the treatment of tuberous sclerosis complex (TSC), a rare genetic disorder characterized by the growth of benign tumors in multiple organs, including the brain, kidneys, and skin. By inhibiting the mTOR pathway, everolimus reduces tumor growth and alleviates symptoms associated with TSC, such as seizures, renal angiomyolipomas, and skin lesions. Everolimus has demonstrated efficacy in the treatment of lymphangioleiomyomatosis (LAM), a rare progressive lung disease characterized by abnormal smooth muscle cell proliferation in the lungs and lymphatic vessels. By inhibiting mTOR signaling, everolimus suppresses cell proliferation and stabilizes lung function in patients with LAM, reducing the risk of disease progression and improving quality of life.

References

2005. Adjusted indirect comparison of intracoronary drug-eluting stents: evidence from a metaanalysis of randomized bare-metal-stent-controlled trials. International Journal of Cardiology, 100(1), 119-123.
DOI: https://pubmed.ncbi.nlm.nih.gov/1582026

2009. Oral mTOR Inhibitor Everolimus in Patients With Gemcitabine-Refractory Metastatic Pancreatic Cancer. Journal of clinical oncology, 27/global2), 135-798.
DOI: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645085

2010. Updated recommendations from the Spanish Oncology Genitourinary Group on the treatment of advanced renal cell carcinoma. Cancer, 29(3), 2020-498.
DOI: https://pubmed.ncbi.nlm.nih.gov/206/10
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