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Chemical Structure
Chemical Structure
Chemical Structure

Everolimus Solution [159351-69-6]

Research Use Only
CDX-E0574
Chemodex
CAS Number159351-69-6
Product group Chemicals
Estimated Purity>99%
Molecular Weight958.22
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Everolimus Solution [159351-69-6]
  • Delivery Days Customer
    10
  • ADR Class
    3
  • CAS Number
    159351-69-6
  • Certification
    Research Use Only
  • Estimated Purity
    >99%
  • Formulation
    Liquid
  • Hazard Information
    Danger,Excepted quantity
  • Molecular Formula
    C53H83NO14
  • Molecular Weight
    958.22
  • Scientific Description
    Chemical. CAS: 159351-69-6. Formula: C53H83NO14. MW: 958.22. Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the activation of the mammalian target of rapamycin (mTOR). More selective for the mTORC1 protein complex, with little impact on the mTORC2 complex, compared to Rapamycin. Anticancer agent. Inhibition of mTOR reduces the activity of effectors downstream, which leads to a blockage in the progression of cells from G1 into S phase, and subsequently inducing cell growth arrest, apoptosis and autophagy, resulting in reduction of cell proliferation, angiogenesis and glucose uptake. Inhibits tumor proliferation in vitro and in vivo. This compound can be used as a reference material. - Macrolide antibiotic, inhibiting bacterial protein synthesis. Potent immunosuppressant. Binds with high affinity to the FK506 binding protein-12 (FKBP-12) to generate an immunosuppressive complex that inhibits the activation of the mammalian target of rapamycin (mTOR). More selective for the mTORC1 protein complex, with little impact on the mTORC2 complex, compared to Rapamycin. Anticancer agent. Inhibition of mTOR reduces the activity of effectors downstream, which leads to a blockage in the progression of cells from G1 into S phase, and subsequently inducing cell growth arrest, apoptosis and autophagy, resulting in reduction of cell proliferation, angiogenesis and glucose uptake. Inhibits tumor proliferation in vitro and in vivo. This compound can be used as a reference material.
  • SMILES
    OCCO[C@H]1[C@H](OC)C[C@H](C[C@@H](C)[C@H](CC([C@H](C)/C=C(C)/[C@@H](O)[C@H]2OC)=O)OC([C@@H]3CCCCN3C(C([C@@]4(O)[C@H](C)CC[C@@H](C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C2=O)O4)=O)=O)=O)CC1
  • Storage Instruction
    -20°C,2°C to 8°C
  • UN Number
    1648
  • UNSPSC
    12352200