SGC0946 7μM R03 exp151

DOT1L methyltransferase inhibitor

  • Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Compound References

  • PubChem Name: 1-[3-[[(2R,3S,4R,5R)-5-(4-Amino-5-bromopyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxyoxolan-2-yl]methyl-propan-2-ylamino]propyl]-3-(4-tert-butylphenyl)urea
  • Synonyms: N/A
  • CAS #: 1561178-17-3
  • PubChem CID: 56962337
  • IUPAC: 1-[3-[[(2R,3S,4R,5R)-5-(4-amino-5-bromopyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxyoxolan-2-yl]methyl-propan-2-ylamino]propyl]-3-(4-tert-butylphenyl)urea
  • INCHI Name: InChI=1S/C28H40BrN7O4/c1-16(2)35(12-6-11-31-27(39)34-18-9-7-17(8-10-18)28(3,4)5)14-20-22(37)23(38)26(40-20)36-13-19(29)21-24(30)32-15-33-25(21)36/h7-10,13,15-16,20,22-23,26,37-38H,6,11-12,14H2,1-5H3,(H2,30,32,33)(H2,31,34,39)/t20-,22-,23-,26-/m1/s1
  • INCHI Key: IQCKJUKAQJINMK-HUBRGWSESA-N
  • Molecular Weight: 618.6
  • Canonical SMILES: CC(C)N(CCCNC(=O)NC1=CC=C(C=C1)C(C)(C)C)CC2C(C(C(O2)N3C=C(C4=C(N=CN=C43)N)Br)O)O
  • Isomeric SMILES: CC(C)N(CCCNC(=O)NC1=CC=C(C=C1)C(C)(C)C)C[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=C(C4=C(N=CN=C43)N)Br)O)O
  • Molecular Formula: C28H40BrN7O4

Compound Supplier

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

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C28H40BrN7O4 618.23979; found 618.24052

Dose Response Curve

  • Platform ID: SGC0946
  • Min: 1.1554; Max: 74.5033





IC Concentration (µM)
IC10 N/A
IC20 3.7421
IC30 5.9725
IC40 8.7616
IC50 12.4543
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 03
  • Dose: 7µM
  • Days of incubation: 8
  • Doublings: 7.2
  • Numbers of reads: 9543664
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
0/1ScoresViewViewViewViewView

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