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PF-06726304 acetate

PF-06726304 acetate Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:PF-06726304 acetate
CAS:2080306-28-9
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Email: support@targetmol.com
Products Intro: Product Name:PF-06726304 acetate
CAS:2080306-28-9
Package:10mg;540USD
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
Email: 3003855609@qq.com
Products Intro: Product Name:PF-06726304 acetate
CAS:2080306-28-9
Purity:HPLC≥98% Package:20mg/10
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:PF-06726304 acetate
CAS:2080306-28-9
Package:10mg/RMB 3780
Company Name: R&D Systems, Inc  
Tel: 18003437475
Email: rdname@qq.com
Products Intro: Product Name:PF 06726304 acetate
CAS:2080306-28-9

PF-06726304 acetate manufacturers

  • PF-06726304 acetate
  • PF-06726304 acetate pictures
  • $783.00 / 10mg
  • 2026-01-04
  • CAS:2080306-28-9
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  • Supply Ability: 10g
PF-06726304 acetate Basic information
Uses
Product Name:PF-06726304 acetate
Synonyms:PF 06726304 acetate,PF06726304 acetate
CAS:2080306-28-9
MF:C24H25Cl2N3O5
MW:506.38
EINECS:
Product Categories:
Mol File:2080306-28-9.mol
PF-06726304 acetate Structure
PF-06726304 acetate Chemical Properties
solubility Soluble to 100 mM in DMSO and to 100 mM in ethanol
Safety Information
MSDS Information
PF-06726304 acetate Usage And Synthesis
UsesPF 06726304 Acetate is a useful research chemical.
UsesPF-06726304 acetate is a potent and selective EZH2 inhibitor. PF-06726304 acetate inhibits wild-type and Y641N mutant EZH2 with Kis of 0.7 and 3.0 nM, respectively. PF-06726304 acetate displays robust antitumor growth activity[1].
in vivo

PF-06726304 (200 and 300 mg/kg; BID for 20 days) inhibits tumor growth and induces robust modulation of downstream biomarkers in a subcutaneous Karpas-422 xenograft model[1].

Animal Model:Female Scid beige mice (6-8 weeks old) with Karpas-422 xenograft model[1]
Dosage:200 and 300 mg/kg
Administration:Given BID for 20 days
Result:Inhibited tumor growth and induced robust modulation of downstream biomarkers in a subcutaneous Karpas-422 xenograft model.
IC 50EZH2 WT: 0.7 nM (Ki); EZH2 Y641N: 3.0 nM (Ki)
storageStore at RT
References[1] Kung PP, et al. Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors. J Med Chem. 2016 Sep 22;59(18):8306-25. DOI:10.1021/acs.jmedchem.6b00515
PF-06726304 acetate Preparation Products And Raw materials
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PF-06726304 PF-06726304 ACETATE

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