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

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1476074-39-1, vx984Related Search:

VX-745 VX-222 VX-661 1H-Pyrrole-2-carboxaMide, 4-[2-[(2-chloro-4-fluorophenyl)aMino]-5-Methyl-4-pyriMidinyl]-N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]- VX 702

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