Nifurtimox 1μM R03 exp141

Nitrofuran derivative, forms nitro-anion radical metabolite, induces ROS

  • Class / Subclass 1: Infectious Disease / Antitrypanosomal

Compound References

  • PubChem Name: Nifurtimox
  • Synonyms: N/A
  • CAS #: 23256-30-6
  • PubChem CID: 6842999
  • IUPAC: (E)-N-(3-methyl-1,1-dioxo-1,4-thiazinan-4-yl)-1-(5-nitrofuran-2-yl)methanimine
  • INCHI Name: InChI=1S/C10H13N3O5S/c1-8-7-19(16,17)5-4-12(8)11-6-9-2-3-10(18-9)13(14)15/h2-3,6,8H,4-5,7H2,1H3/b11-6+
  • INCHI Key: ARFHIAQFJWUCFH-IZZDOVSWSA-N
  • Molecular Weight: 287.29
  • Canonical SMILES: CC1CS(=O)(=O)CCN1N=CC2=CC=C(O2)[N+](=O)[O-]
  • Isomeric SMILES: CC1CS(=O)(=O)CCN1/N=C/C2=CC=C(O2)[N+](=O)[O-]
  • Molecular Formula: C10H13N3O5S

Compound Supplier

  • Supplier Name: Sigma-Aldrich
  • Catalog #: N3415
  • Lot #: N/A

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+COOH)- Calcd for C10 H13 N3 O5 S 332.05579; found 332.05672

Dose Response Curve

  • Platform ID: RC-NFN5
  • Min: -7.4928; Max: 14.3019





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


  • Round: 03
  • Dose: 1µM
  • Days of incubation: 8
  • Doublings: 8.0
  • Numbers of reads: 9780191
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
0/0ScoresViewViewViewViewView

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