vx984

vx984 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:VX-984;M9831
CAS:1476074-39-1
Purity:98.00% Package:1 mL * 10mM (in DMSO);10 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
Tel:
Email: tp@aladdinsci.com
Products Intro: Product Name:VX-984
CAS:1476074-39-1
Purity:97% Package:$9339.9/100mg;Bulk package Remarks:97%
Company Name: Suzhou ARTK Medchem Co., Ltd.
Tel: +86-512-68323658 +86-18168183658
Email: sales1@artkmedchem.com
Products Intro: Product Name:VX-984
CAS:1476074-39-1
Purity:0.98 Package:100KG;25KG;10KG;1KG
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Products Intro: Product Name:M9831 free base
CAS:1476074-39-1
Purity:98% Package:10g;1g;100mg
Company Name: Artis Biotech Co. Ltd.  
Tel: 19138486554 18108108965
Email: sales@artisbio.com
Products Intro: Product Name:VX-984 P1
CAS:1476074-39-1
Purity:99% HPLC Package:5mg 20mg 50mg 100mg 200mg 1g
vx984 Basic information
Product Name:vx984
Synonyms:vx984;VX-984 (M9831);(S)-N-Methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl-4',6'-d2)amino)propan-2-yl)quinoline-4-carboxamide;VX-984 (Synonyms: M9831);vx-984;M9831 free base;VX984,VX 984;VX-984, 10 mM in DMSO
CAS:1476074-39-1
MF:C23H23N7O
MW:413.49
EINECS:
Product Categories:
Mol File:1476074-39-1.mol
vx984 Structure
vx984 Chemical Properties
storage temp. Store at -20°C
solubility DMSO : 8.33 mg/mL (20.05 mM)
form Solid
color White to off-white
Safety Information
MSDS Information
vx984 Usage And Synthesis
UsesVX-984 is an orally active, potent, selective and BBB-penetrated DNA-PK inhibitor. VX-984 efficiently inhibits NHEJ (non-homologous end joining) and increases DSBs (DNA double-strand breaks). VX-984 can be used for glioblastomas (GBM) and non-small cell lung cancer (NSCLC) research. VX-984 is a de novo deuterium[1][2][3].
in vivo

VX-984 (0-100 mg/kg, Oral gavage, daily) inhibits radiation-induced DNA-PKcs phosphorylation in orthotopic brain tumor xenografts[1].
VX-984 (0-50 mg/kg, Oral gavage, twice a day for 2 days) enhances the radiosensitivity of brain tumor xenografts[1].

Animal Model:Athymic female nude mice (6-8 weeks old, 7-8 mice/group, U251 intracerebral xenografts)[1]
Dosage:0, 50, and 100 mg/kg
Administration:Oral gavage, daily, 1 or 4 hours before irradiation (10 Gy)
Result:Reduced the levels DNA-PKcs phosphorylation after irradiation.
Animal Model:Athymic female nude mice (6-8 weeks old, 7 mice/group, U251 intracerebral xenografts)[1]
Dosage:0, 50 mg/kg
Administration:Oral gavage, twice a day, 30 minutes before and 4 hours following local irradiation of the tumor (3 Gy) for 3 consecutive days (3×3 Gy)
Result:VX-984 treatment of U251 tumors alone had no significant effect on overall survival as compared with vehicle; radiation alone resulted in an increase in survival. VX-984 and radiation combination protocol increased tumor radiosensitivity, and significantly increased the survival of mice compared with radiation alone.
References[1] Timme CR, et al. The DNA-PK Inhibitor VX-984 Enhances the Radiosensitivity of Glioblastoma Cells Grown In Vitro and as Orthotopic Xenografts. Mol Cancer Ther. 2018 Jun;17(6):1207-1216. DOI:10.1158/1535-7163.MCT-17-1267
[2] Khan AJ, et al. VX-984 is a selective inhibitor of non-homologous end joining, with possible preferential activity in transformed cells. Oncotarget. 2018 May 25;9(40):25833-25841. DOI:10.18632/oncotarget.25383
[3] Diane Boucher, et al. Abstract 3716: Potent radiation enhancement with VX-984, a selective DNA-PKcs inhibitor for the treatment of NSCLC. Cancer Res (2016) 76 (14_Supplement): 3716.
[4] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
vx984 Preparation Products And Raw materials
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