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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H23N7O
Molecular Weight 415.4873
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VX-984

SMILES

[2H]C1=NC(C)=NC([2H])=C1C2=CC(NC[C@@H](C)C3=C4N=CC=C(C(=O)NC)C4=CC=C3)=NC=N2

InChI

InChIKey=PEACIOGDEQRHFA-KIYKJNLWSA-N
InChI=1S/C23H23N7O/c1-14(17-5-4-6-18-19(23(31)24-3)7-8-25-22(17)18)10-28-21-9-20(29-13-30-21)16-11-26-15(2)27-12-16/h4-9,11-14H,10H2,1-3H3,(H,24,31)(H,28,29,30)/t14-/m1/s1/i11D,12D

HIDE SMILES / InChI

Molecular Formula C23H23N7O
Molecular Weight 415.4873
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets
PubMed

PubMed

TitleDatePubMed
The DNA-PK Inhibitor VX-984 Enhances the Radiosensitivity of Glioblastoma Cells Grown In Vitro and as Orthotopic Xenografts.
2018 Jun
VX-984 is a selective inhibitor of non-homologous end joining, with possible preferential activity in transformed cells.
2018 May 25
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:43:30 GMT 2025
Edited
by admin
on Mon Mar 31 23:43:30 GMT 2025
Record UNII
0C33IBK195
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VX-984
Code English
M-9831
Preferred Name English
4-QUINOLINECARBOXAMIDE, N-METHYL-8-((1S)-1-METHYL-2-((2'-METHYL(4,5'-BIPYRIMIDIN)-6-YL-4',6'-D2)AMINO)ETHYL)-
Systematic Name English
N-METHYL-8-((2S)-1-((6-(2-METHYL(2H2)PYRIMIDIN-5-YL)PYRIMIDIN-4-YL)AMINO)PROPAN-2-YL)QUINOLINE-4-CARBOXAMIDE
Common Name English
Code System Code Type Description
CAS
1476074-39-1
Created by admin on Mon Mar 31 23:43:30 GMT 2025 , Edited by admin on Mon Mar 31 23:43:30 GMT 2025
PRIMARY
FDA UNII
0C33IBK195
Created by admin on Mon Mar 31 23:43:30 GMT 2025 , Edited by admin on Mon Mar 31 23:43:30 GMT 2025
PRIMARY
PUBCHEM
72188357
Created by admin on Mon Mar 31 23:43:30 GMT 2025 , Edited by admin on Mon Mar 31 23:43:30 GMT 2025
PRIMARY
NCI_THESAURUS
C129061
Created by admin on Mon Mar 31 23:43:30 GMT 2025 , Edited by admin on Mon Mar 31 23:43:30 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY