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EPZ015666

Base Information Edit
EPZ015666

Synonyms:EPZ015666;(S)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-6-(oxetan-3-ylamino)pyrimidine-4-carboxamide;GSK3235025;GSK-3235025;N-[(2S)-3-(3,4-Dihydro-2(1H)-isoquinolinyl)-2-hydroxypropyl]-6-(3-oxetanylamino)-4-pyrimidinecarboxamide;N-[(2S)-3-(3,4-dihydro-1H-isoquinolin-2-yl)-2-hydroxypropyl]-6-(oxetan-3-ylamino)pyrimidine-4-carboxamide

Suppliers and Price of EPZ015666
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • EPZ-015666
  • 1mg
  • $ 319.00
  • TRC
  • EPZ-015666
  • 25mg
  • $ 545.00
  • TRC
  • EPZ-015666
  • 10mg
  • $ 275.00
  • Tocris
  • EPZ015666 ≥98%(HPLC)
  • 5
  • $ 167.00
  • Tocris
  • EPZ015666 ≥98%(HPLC)
  • 25
  • $ 649.00
  • DC Chemicals
  • EPZ015666 >99%,chiralpurity>99%
  • 100 mg
  • $ 470.00
  • Crysdot
  • EPZ015666 98+%
  • 50mg
  • $ 958.00
  • Crysdot
  • EPZ015666 98+%
  • 10mg
  • $ 264.00
  • ChemScene
  • EPZ015666 99.83%
  • 100mg
  • $ 650.00
  • ChemScene
  • EPZ015666 99.83%
  • 5mg
  • $ 100.00
Total 54 raw suppliers
Chemical Property of EPZ015666 Edit
Chemical Property:
  • Boiling Point:686.4±55.0 °C(Predicted) 
  • PKA:12.40±0.46(Predicted) 
  • PSA:99.61000 
  • Density:1.331±0.06 g/cm3(Predicted) 
  • LogP:0.83810 
  • Storage Temp.:2-8°C 
  • Solubility.:Soluble in DMSO (up to 20 mg/ml) 
Purity/Quality:

98%,99%, *data from raw suppliers

EPZ-015666 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Description EPZ015666 (GSK3235025) is an orally available inhibitor of protein arginine methyltransferase-5 (PRMT5), which is involved in diverse cellular processes, including tumorigenesis, and its overexpression is observed in cell lines and primary patient samples derived from lymphomas, particularly mantle cell lymphoma (MCL).EPZ015666 showed dose-dependent antitumor activity in multiplein vitroandin vivomantle cell lymphoma (MCL) models with treatment of MCL cell lines leading to inhibition of SmD3 methylation and cell death. Therefore, it is a potential drug candidate for future cancer therapy. EPZ015666 (1616391-65-1) is a selective and potent (IC50?= 22nM) inhibitor of arginine methyltransferase 5 (PRMT5).1,2?PRMT5 inhibition with EPZ015666 potently suppressed?in vivo?glioblastoma tumors3?and significantly inhibited the growth of multiple myeloma cell lines4.
  • Uses Protein arginine methyltransferases (PRMTs) target nuclear and cytoplasmic substrates and can alter protein actions and gene expression. PRMT5, which can methylate histones H2A, H3, and H4, ribonucleoproteins, and other proteins, is upregulated in several human cancers, including lymphomas. Moreover, suppression of PRMT5 expression induces lymphoma cell death. EPZ015666 is a potent, orally bioavailable inhibitor of PRMT5 (Ki = 5 nM). It displays more than 20,000-fold selectivity for PRMT5 over other PMTs. EPZ015666 acts by blocking the association of PRMT5 with methylosome protein 50, which is necessary for the formation of an active methyltransferase complex. EPZ015666 (100 mg/kg twice daily) blocks the growth of mantle cell lymphoma Z-138 xenografts, without significant body weight loss, in mice.[Cayman Chemical] EPZ015666 is a potent, orally bioavailable inhibitor of Protein arginine methyltransferase 5 (PRMT5). It acts by blocking the association of PRMT5 with methylosome protein 50.
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