Latrunculin-B 10μM R07 exp374

Binds actin monomers, inhibits actin polymerization

  • Class / Subclass 1: Cell Cycle / Cytokinesis Inhibitor
  • Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor
  • Class / Subclass 3: Environmental Stresses / Toxin

Compound References

  • PubChem Name: Latrunculin B
  • Synonyms: N/A
  • CAS #: 76343-94-7
  • PubChem CID: 6436219
  • IUPAC: (4R)-4-[(1R,4Z,8Z,10S,13R,15R)-15-hydroxy-5,10-dimethyl-3-oxo-2,14-dioxabicyclo[11.3.1]heptadeca-4,8-dien-15-yl]-1,3-thiazolidin-2-one
  • INCHI Name: InChI=1S/C20H29NO5S/c1-13-5-3-4-6-14(2)9-18(22)25-16-10-15(8-7-13)26-20(24,11-16)17-12-27-19(23)21-17/h3,5,9,13,15-17,24H,4,6-8,10-12H2,1-2H3,(H,21,23)/b5-3-,14-9-/t13-,15-,16-,17+,20-/m1/s1
  • INCHI Key: NSHPHXHGRHSMIK-JRIKCGFMSA-N
  • Molecular Weight: 395.5
  • Canonical SMILES: CC1CCC2CC(CC(O2)(C3CSC(=O)N3)O)OC(=O)C=C(CCC=C1)C
  • Isomeric SMILES: C[C@H]/1CC[C@@H]2C[C@H](C[C@@](O2)([C@@H]3CSC(=O)N3)O)OC(=O)/C=C(\\CC/C=C1)/C
  • Molecular Formula: C20H29NO5S

Compound Supplier

  • Supplier Name: Abcam
  • Catalog #: ab144291
  • Lot #: GR3184664-5

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+Na)+ Calcd for C20H29NO5S 418.16586; found 418.16584

Dose Response Curve

  • Platform ID: Latrunculin_B
  • Min: -3.9960; Max: 98.0418





IC Concentration (µM)
IC10 N/A
IC20 2.0673
IC30 4.2107
IC40 7.7555
IC50 13.8130
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 07
  • Dose: 10µM
  • Days of incubation: 8
  • Doublings: -0.2
  • Numbers of reads: 21695338
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
1/95ScoresViewViewViewViewView

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