Adefovir 20μM R07 exp332

Nucleoside reverse transcriptase inhibitor (NRTI), active against HBV and HSV

  • Class / Subclass 1: Infectious Disease / Antiviral
  • Class / Subclass 2: DNA Damage, Repair and Replication / Reverse Transcriptase Inhibitor
  • Class / Subclass 3: Metabolism / Antimetabolite

Compound References

  • PubChem Name: Adefovir
  • Synonyms: GS-0393; PMEA
  • CAS #: 106941-25-7
  • PubChem CID: 60172
  • IUPAC: 2-(6-aminopurin-9-yl)ethoxymethylphosphonic acid
  • INCHI Name: InChI=1S/C8H12N5O4P/c9-7-6-8(11-3-10-7)13(4-12-6)1-2-17-5-18(14,15)16/h3-4H,1-2,5H2,(H2,9,10,11)(H2,14,15,16)
  • INCHI Key: SUPKOOSCJHTBAH-UHFFFAOYSA-N
  • Molecular Weight: 273.19
  • Canonical SMILES: C1=NC(=C2C(=N1)N(C=N2)CCOCP(=O)(O)O)N
  • Isomeric SMILES: N/A
  • Molecular Formula: C8H12N5O4P

Compound Supplier

  • Supplier Name: Ark Pharm Inc.
  • Catalog #: AK-75903
  • Lot #: WG0017455-170306001

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C8H12N5O4P 274.06997; found 274.06966

Dose Response Curve

  • Platform ID: Adefovir
  • Min: -8.5475; Max: 70.4919





IC Concentration (µM)
IC10 N/A
IC20 0.0648
IC30 0.1411
IC40 0.3040
IC50 0.7276
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 07
  • Dose: 20µM
  • Days of incubation: 8
  • Doublings: 6.3
  • Numbers of reads: 22625883
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