6-Thio-2-deoxyguanosine 2μM R06 exp259

Nucleoside analog, incorporated into telomeric DNA by telomerase, impairs proliferation of telomerase-positive cells

  • Class / Subclass 1: Metabolism / Antimetabolite
  • Class / Subclass 2: DNA Damage, Repair and Replication / Helix-Distorting Adduct

Compound References

  • PubChem Name: 2'-Deoxythioguanosine
  • Synonyms: 6-thio-dG; β-TGdR; 6-thio-dG;β-TGdR
  • CAS #: 789-61-7
  • PubChem CID: 3000603
  • IUPAC: 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purine-6-thione
  • INCHI Name: InChI=1S/C10H13N5O3S/c11-10-13-8-7(9(19)14-10)12-3-15(8)6-1-4(17)5(2-16)18-6/h3-6,16-17H,1-2H2,(H3,11,13,14,19)/t4-,5+,6+/m0/s1
  • INCHI Key: SCVJRXQHFJXZFZ-KVQBGUIXSA-N
  • Molecular Weight: 283.31
  • Canonical SMILES: C1C(C(OC1N2C=NC3=C2NC(=NC3=S)N)CO)O
  • Isomeric SMILES: C1[C@@H]([C@H](O[C@H]1N2C=NC3=C2NC(=NC3=S)N)CO)O
  • Molecular Formula: C10H13N5O3S

Compound Supplier

  • Supplier Name: Selleck Chemicals
  • Catalog #: S7757
  • Lot #: N/A

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C10H13N5O3S 284.08119; found 284.07903

Dose Response Curve

Dose response curve not available.

  • Round: 06
  • Dose: 2µM
  • Days of incubation: 8
  • Doublings: 0.6
  • Numbers of reads: 8752501
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
0/28ScoresViewViewViewViewView

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