PF-4800567 HCl

PF-4800567 HCl Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:PF 4800567 hydrochloride
CAS:1391052-28-0
Package:10 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:PF 4800567 hydrochloride
CAS:1391052-28-0
Purity:98% Package:$102.9/5mg;$183.9/10mg;$412.9/25mg;$743.9/50mg;$1339.9/100mg;Bulk package Remarks:98%
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Products Intro: Product Name:PF-4800567 HCl
CAS:1391052-28-0
Company Name: Shenzhen SUNGENING Bio-Medical Co., Ltd.  
Tel: 0755-28967200 13631290199
Email: wxf@sungening.com
Products Intro: Product Name:PF-4800567 Hydrochloride
CAS:1391052-28-0
Purity:99% HPLC or More Package:10MG;25MG;50MG;100MG
Company Name: Shanghai Biopharmaleader Co., Ltd.  
Tel: +86 18721201413
Email: sales@biopharmaleader.com
Products Intro: Product Name:PF-4800567 HCl
CAS:1391052-28-0
Purity:98%HPLC Package:10g,100g
PF-4800567 HCl Basic information
Product Name:PF-4800567 HCl
Synonyms:PF-4800567 HCl;3-[(3-chlorophenoxy)methyl]-1-(oxan-4-yl)pyrazolo[3,4-d]pyrimidin-4-amine:hydrochloride;PF-4800567 hydrochloride >=98% (HPLC)
CAS:1391052-28-0
MF:C17H19Cl2N5O2
MW:396.27
EINECS:
Product Categories:
Mol File:1391052-28-0.mol
PF-4800567 HCl Structure
PF-4800567 HCl Chemical Properties
storage temp. Desiccate at RT
solubility Soluble to 100 mM in DMSO
form Powder
color white to beige
Safety Information
MSDS Information
PF-4800567 HCl Usage And Synthesis
UsesPF 4800567 is a selective casein kinase 1ε inhibitor; displays 22-fold greater potency towards CK1ε than CK1δ (IC50 values are 32 and 711 nM for CK1ε and CK1δ respectively). ATP competitive. Displays minimal effect on the circadian clock.
Biological ActivityPF-4800567 is a casein kinase 1e (CK1e) selective inhibitor (IC50 = 32 nM) th at is 20 fold selective for the CK1e isoform over CK1d. PF-4800567 blockes CK1e-mediated PER3 nuclear translocation, but does not effect the circadian clock in animal studies.', 'PF-4800567 is also known as (3-[(3-Chlorophenoxy)methyl]-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine hydrochloride). It can block the epidermal growth factor receptor (EGFR) at micromolar concentrations. PF-4800567 helps to improve the locomotor stimulant reaction to methamphetamine (MA) and fentanyl.
storageDesiccate at RT
PF-4800567 HCl Preparation Products And Raw materials
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