Nocodazole 0.2μM R00 exp24

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

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

Compound References

  • PubChem Name: Nocodazole
  • Synonyms: Oncodazole; R17934
  • CAS #: 31430-18-9
  • PubChem CID: 4122
  • IUPAC: methyl N-[6-(thiophene-2-carbonyl)-1H-benzimidazol-2-yl]carbamate
  • INCHI Name: InChI=1S/C14H11N3O3S/c1-20-14(19)17-13-15-9-5-4-8(7-10(9)16-13)12(18)11-3-2-6-21-11/h2-7H,1H3,(H2,15,16,17,19)
  • INCHI Key: KYRVNWMVYQXFEU-UHFFFAOYSA-N
  • Molecular Weight: 301.32
  • Canonical SMILES: COC(=O)NC1=NC2=C(N1)C=C(C=C2)C(=O)C3=CC=CS3
  • Isomeric SMILES: N/A
  • Molecular Formula: C14H11N3O3S

Compound Supplier

  • Supplier Name: Sigma-Aldrich
  • Catalog #: M1404
  • Lot #: N/A

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C14H11N3O3S 302.05939; found 302.05966

Dose Response Curve

  • Platform ID: Nocodazole
  • Min: -9.8754; Max: 86.3481





IC Concentration (µM)
IC10 N/A
IC20 0.0313
IC30 0.0403
IC40 0.0496
IC50 0.0601
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 00
  • Dose: 200nM
  • Days of incubation: 8
  • Doublings: 0.2
  • Numbers of reads: 11500839
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
0/139ScoresViewViewViewViewView

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