Chk2 Inhibitor

Chk2 Inhibitor Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:SC-203885
CAS:724708-21-8
Package:1mg;968USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Hu Bei Jiutian Bio-medical Technology CO.,Ltd
Tel: 027-88013699 17354350817
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Products Intro: Product Name:Chk2 Inhibitor
CAS:724708-21-8
Purity:0.99 Package:25kg,50kg,180kg,200kg,250kg,1000kg,as your needs Remarks:as your needs
Company Name: Aladdin Scientific
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Products Intro: Product Name:Chk2 inhibitor
CAS:724708-21-8
Purity:>=95% Package:$435.9/500μg;$783.9/1mg;$3524.9/5mg;Bulk package Remarks:95%
Company Name: VDM Biochemicals   
Tel: 0330-2528181
Email: sales@vdmbio.com
Products Intro: Product Name:Chk2 Inhibitor
CAS:724708-21-8
Purity:>=95%
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Products Intro: Product Name:Chk2 Inhibitor
CAS:724708-21-8
Remarks:Reach out to us for more information about custom solutions.

Chk2 Inhibitor manufacturers

  • SC-203885
  • SC-203885 pictures
  • $968.00 / 1mg
  • 2024-10-24
  • CAS:724708-21-8
  • Min. Order:
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  • Supply Ability: 10g
Chk2 Inhibitor Basic information
Product Name:Chk2 Inhibitor
Synonyms:Chk2 Inhibitor;Chk2 Inhibitor - CAS 724708-21-8 - Calbiochem;Azepino[3,4-b]indol-1(2H)-one, 5-(2-amino-1,5-dihydro-5-oxo-4H-imidazol-4-ylidene)-3,4,5,10-tetrahydro-, (5Z)-;SC 203885;SC203885;SC-203885
CAS:724708-21-8
MF:C15H13N5O2
MW:295.3
EINECS:
Product Categories:Cholinergics
Mol File:724708-21-8.mol
Chk2 Inhibitor Structure
Chk2 Inhibitor Chemical Properties
storage temp. -20C
solubility DMSO: Soluble
form Pale yellow solid
color pale yellow
Safety Information
MSDS Information
Chk2 Inhibitor Usage And Synthesis
UsesChk2 Inhibitor is a checkpoint kinase inhibitor that mediates apoptosis and cell cycle arrest.
General DescriptionA cell-permeable, ATP competitive, and reversible indoloazepine compound that displays anti-proliferative and anti-inflammatory properties. Acts as a potent inhibitor of Chk2 (IC50 = 8 nM) that targets the ATP binding pocket. Exhibits selectivity for Chk2 over MEK1, Chk1, CK1δ, PKCα, PKCβII and CK2 (IC50 = 89 nM, 237 nM, 1.352 μM, 2.539 μM, 3.381 μM, and >10.0 μM, respectively). Blocks the production of IL-2 and TNF-α by preventing the transcriptional activation of NF-κB (IC50 = 3.55 μM for IL-2 production in PMA-stimulated Jurkat T cells; 8.16 μM for TNF-α production in LPS-stimulated THP-1 cells). Also reported to suppress the growth of leukemic T cells (GI50 = 1.73 μM).
Biochem/physiol ActionsPrimary TargetChk2
IC 50Chk2: 13.5 nM (IC50); Chk1: 220.4 nM (IC50)
Chk2 Inhibitor Preparation Products And Raw materials
Tag:Chk2 Inhibitor(724708-21-8) Related Product Information
2-[(6-Amino-9H-purin-9-yl)methyl]-5-methyl-3-(2-methylphenyl)-4(3H)-quinazolinone N-[4-[5-(1,3-BENZODIOXOL-5-YL)-3-METHOXY-1H-1,2,4-TRIAZOL-1-YL]PHENYL]-2-(PHENYLTHIO)ACETAMIDE NSC 23766 TETRAHYDROCHLORIDE NSC697923 MIF Antagonist, ISO-1 GSK-3β Inhibitor XVIII Pictilisib JNJ-10198409 Trolox C2 CERAMIDE Motesanib PD 173074 Compound 28 Glycogen Phosphorylase Inhibitor MMP-9 INHIBITOR I Compound 23 ERK Inhibitor 6-HYDROXY-2,5,7,8-TETRAMETHYLCHROMAN-2-CARBOXYLIC ACID

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