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vx984

Product Name
vx984
CAS No.
1476074-39-1
Chemical Name
vx984
Synonyms
vx-984;vx984;VX984,VX 984;VX-984 (M9831);M9831 free base;VX-984, 10 mM in DMSO;VX-984 (Synonyms: M9831);(S)-N-Methyl-8-(1-((2'-methyl-[4,5'-bipyrimidin]-6-yl-4',6'-d2)amino)propan-2-yl)quinoline-4-carboxamide
CBNumber
CB83165816
Molecular Formula
C23H23N7O
Formula Weight
413.49
MOL File
1476074-39-1.mol
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vx984 Property

storage temp. 
Store at -20°C
solubility 
DMSO : 8.33 mg/mL (20.05 mM)
form 
Solid
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0017028
Product name
VX-984
Purity
99.36%
Packaging
5mg
Price
$550
Updated
2021/12/16
ChemScene
Product number
CS-0017028
Product name
VX-984
Purity
99.36%
Packaging
10mg
Price
$950
Updated
2021/12/16
ChemScene
Product number
CS-0017028
Product name
VX-984
Purity
99.36%
Packaging
50mg
Price
$3950
Updated
2021/12/16
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vx984 Chemical Properties,Usage,Production

Uses

VX-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

Raw materials

Preparation Products

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vx984 Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
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32435
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Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
52923
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AstaTech, Inc
Tel
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Fax
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Email
sales@astatechinc.com
Country
United States
ProdList
6371
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1476074-39-1, vx984Related Search:


  • vx984
  • vx-984
  • VX-984 (Synonyms: M9831)
  • 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
  • M9831 free base
  • VX984,VX 984
  • VX-984, 10 mM in DMSO
  • 1476074-39-1