IDH-889

IDH-889 Suppliers list
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: Shanghai XinKai Chemical Technology Co., Ltd.  
Tel: 021-58930698 15921516558
Email: zhangyichao84@126.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com

IDH-889 manufacturers

  • IDH889
  • IDH889 pictures
  • $247.00
  • 2026-07-14
  • CAS:1429179-07-6
  • Purity: ≥98%
  • Supply Ability: 10g
IDH-889 Basic information
Product Name:IDH-889
Synonyms:IDH889;IDH-889;IDH889;IDH-889;IDH 889;Inhibitor,inhibit,Isocitrate Dehydrogenase (IDH),IDH889,IDH 889,IDH-889;2-Oxazolidinone, 3-[2-[[(1S)-1-[5-(4-fluoro-3-methylphenyl)-2-pyrimidinyl]ethyl]amino]-4-pyrimidinyl]-4-(1-methylethyl)-, (4S)-;IDH889, 10 mM in DMSO;IDH889 (IDH 889
CAS:1429179-07-6
MF:C23H25FN6O2
MW:436.48
EINECS:
Product Categories:
Mol File:1429179-07-6.mol
IDH-889 Structure
IDH-889 Chemical Properties
Boiling point 589.5±60.0 °C(Predicted)
density 1.284±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Solid
pka4.15±0.10(Predicted)
color White to off-white
Safety Information
MSDS Information
IDH-889 Usage And Synthesis
DescriptionIDH889 is a potent and selective inhibitors of IDH1. IDH899 shows IDH (R132H) IC50 = 20 nM; Cell 2-HG IC50 = 14 nM. IDH889 demonstrates significantly improved plasma exposure in mice vs IDH662 (AUC 3.6 μM·h, Cmax 1.7 μM at 10 mg/kg; AUC 55.5 μM·h, Cmax 14.2 μM at 100 mg/kg). IDH889 also has excellent permeability and no efflux in the Caco-2 and human MDR1-MDCK cell lines, supporting the hypothesis that potent inhibition of mutant IDH1 function by binding at the allosteric binding site is compatible with brain penetration.
UsesIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1). IDH889 has potent selectivity for IDH1 R132* mutations, with IC50s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1R132H, IDH1R132C and IDH1wt, respectively. IDH889 shows potent cellular inhibition of R-2-hydroxyglutarate (2-HG) production with an IC50 of 0.014 μM[1].
References[1] Levell JR, et al. Optimization of 3-Pyrimidin-4-yl-oxazolidin-2-ones as Allosteric and Mutant Specific Inhibitors of IDH1. ACS Med Chem Lett. 2016 Dec 16;8(2):151-156. DOI:10.1021/acsmedchemlett.6b00334
IDH-889 Preparation Products And Raw materials
Tag:IDH-889(1429179-07-6) Related Product Information
2-Oxazolidinone, 3-[2-[[(1R)-1-[5-(4-fluoro-3-methylphenyl)-2-pyrimidinyl]ethyl]amino]-4-pyrimidinyl]-4-(1-methylethyl)-, (4S)- NA IDH-889 Mutant IDH1 inhibitor Olutasidenib Anti-cancer compound library