A-395N 10μM R05 exp219

Mechanism of Action

Inactive analog of A-395 EED inhibitor

  • Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

Compound References

  • PubChem Name: (3S,4R)-1-Benzyl-N,N-dimethyl-4-(4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)pyrrolidin-3-amine
  • Synonyms: N/A
  • CAS #: 2096983-62-7
  • PubChem CID: 123132222
  • IUPAC: (3S,4R)-1-benzyl-N,N-dimethyl-4-[4-(4-methylsulfonylpiperazin-1-yl)phenyl]pyrrolidin-3-amine
  • INCHI Name: InChI=1S/C24H34N4O2S/c1-25(2)24-19-26(17-20-7-5-4-6-8-20)18-23(24)21-9-11-22(12-10-21)27-13-15-28(16-14-27)31(3,29)30/h4-12,23-24H,13-19H2,1-3H3/t23-,24+/m0/s1
  • INCHI Key: VEABDKBNQNHHCB-BJKOFHAPSA-N
  • Molecular Weight: 442.6
  • Canonical SMILES: CN(C)C1CN(CC1C2=CC=C(C=C2)N3CCN(CC3)S(=O)(=O)C)CC4=CC=CC=C4
  • Isomeric SMILES: CN(C)[C@@H]1CN(C[C@H]1C2=CC=C(C=C2)N3CCN(CC3)S(=O)(=O)C)CC4=CC=CC=C4
  • Molecular Formula: C24H34N4O2S

Compound Supplier

  • Supplier Name: Structural Genomics Consortium
  • Catalog #: N/A
  • Lot #: N/A

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C24H34N4O2S 443.24752; found 443.24819

Dose Response Curve

  • Platform ID: A395N
  • Min: -0.0177; Max: 13.6402





IC Concentration (µM)
IC10 N/A
IC20 N/A
IC30 N/A
IC40 N/A
IC50 N/A
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


Screen Summary

  • Round: 05
  • Dose: 10µM
  • Days of incubation: 8
  • Doublings: 7.1
  • Numbers of reads: 15266833

Screen Results

Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
2/0ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1