Combretastatin A4 0.002 to 0.003μM day4 R04 exp179

Inhibits microtubule polymerization

  • Class / Subclass 1: Cell Cycle / Microtubule Poison
  • Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor

Compound References

  • PubChem Name: Combretastatin A4
  • Synonyms: CRC 87-09
  • CAS #: 117048-59-6
  • PubChem CID: 5351344
  • IUPAC: 2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenol
  • INCHI Name: InChI=1S/C18H20O5/c1-20-15-8-7-12(9-14(15)19)5-6-13-10-16(21-2)18(23-4)17(11-13)22-3/h5-11,19H,1-4H3/b6-5-
  • INCHI Key: HVXBOLULGPECHP-WAYWQWQTSA-N
  • Molecular Weight: 316.3
  • Canonical SMILES: COC1=C(C=C(C=C1)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
  • Isomeric SMILES: COC1=C(C=C(C=C1)/C=C\\C2=CC(=C(C(=C2)OC)OC)OC)O
  • Molecular Formula: C18H20O5

Compound Supplier

  • Supplier Name: Abcam
  • Catalog #: AB120925
  • Lot #: N/A

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C18H20O5 317.13835; found 317.13863

Dose Response Curve

  • Platform ID: Combretastatin_A4
  • Min: -2.6499; Max: 88.5172





IC Concentration (µM)
IC10 N/A
IC20 0.0017
IC30 0.0019
IC40 0.0022
IC50 0.0024
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 04
  • Dose: 0.002-0.003µM
  • Days of incubation: 8
  • Doublings: 5.7
  • Numbers of reads: 23260964
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
23/5ScoresViewViewViewViewView

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