Eribulin

CAS No. 253128-41-5

Eribulin( B1939 | E7389 | ER-086526 )

Catalog No. M13751 CAS No. 253128-41-5

Eribulin (B1939, E7389, ER-086526) is a macrocyclic ketone analogue of halichondrir B.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 606 In Stock
5MG 376 In Stock
10MG 603 In Stock
25MG 1074 In Stock
50MG 1469 In Stock
100MG 2065 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Eribulin
  • Note
    Research use only, not for human use.
  • Brief Description
    Eribulin (B1939, E7389, ER-086526) is a macrocyclic ketone analogue of halichondrir B.
  • Description
    Eribulin (B1939, E7389, ER-086526) is a macrocyclic ketone analogue of halichondrir B, shows sub-nM growth inhibitory activities in vitro against numerous human cancer cell lines via inhibition of tubulin polymerization; induces G2-M cell cycle arrest and disruption of mitotic spindles, demonstrates marked in vivo activities at 0.1-1 mg/kg against human xenografts: MDA-MB-435 breast cancer, COLO 205 colon cancer, LOX melanoma, and NIH: OVCAR-3 ovarian cancer.Breast Cancer Approved.
  • In Vitro
    Eribulin (1-100 nM; 72 h) inhibits cells proliferation, with IC50s of 22.8 and 21.5 nM for LM8 and Dunn cells, respectively.Eribulin (10-50 nM; 12-72 h) increases early apoptosis significantly after 24 h treatment at the dose of 50 nM in LM8 cells.Eribulin (10-50 nM; 12-72 h) induces G2/M arrest by 12 h treatment with at the dose of 50 nM, but not by long-term treatment (72 h) with 10 nM in LM8 cells.Eribulin (1-50 nM; 12 h) does not induce senescence in LM8 cells.Eribulin (1-10 nM; 16 h) induces morphological change and suppresses cell migration in a low concentration in LM8 cells. Cell Proliferation Assay Cell Line:LM8 cells and Dunn cells Concentration:0, 1, 10, 100 n MIncubation Time:72 hours Result:Inhibited cells proliferation in a dose-dependent manner.Apoptosis Analysis Cell Line:LM8 cells Concentration:0, 10, 50 nMIncubation Time:12, 24, 48, 72 hours Result:Induced early apoptosis after 12 h at the concentration of 50 nM.Cell Cycle Analysis Cell Line:LM8 cells Concentration:0, 10, 50 nMIncubation Time:12, 24, 48, 72 hours Result:Induced G2/M arrest by 12 h treatment with 50 nM.No G2/M arrest was induced by10 nM treatment.
  • In Vivo
    Eribulin (1 mg/kg; i.v. once a week for 2 weeks) reduces primary tumor growth and lung metastasis of osteosarcoma in mice.Eribulin (1 mg/kg; once i.v.) suppresses circulating tumor cells (CTC) appearance in the low-concentration phase. Animal Model:C3H/HeN mice (4-week-old) are injected LM8 cells Dosage:1 mg/kg Administration:I.v. once a week for 2 weeks Result:Suppressed primary tumor growth and induced apoptosis in tumor cells.
  • Synonyms
    B1939 | E7389 | ER-086526
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Microtubule/Tubulin
  • Recptor
    Microtubule/Tubulin
  • Research Area
    Cancer
  • Indication
    Breast Cancer

Chemical Information

  • CAS Number
    253128-41-5
  • Formula Weight
    729.8965
  • Molecular Formula
    C40H59NO11
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    CC1CC2CCC3C(=C)CC(O3)CCC45CC6C(O4)C7C(O6)C(O5)C8C(O7)CCC(O8)CC(=O)CC9C(CC(C1=C)O2)OC(C9OC)CC(CN)O
  • Chemical Name
    11,15:18,21:24,28-Triepoxy-7,9-ethano-12,15-methano-9H,15H-furo[3,2-i]furo[2',3':5,6]pyrano[4,3-b][1,4]dioxacyclopentacosin-5(4H)-one, 2-[(2S)-3-amino-2-hydroxypropyl]hexacosahydro-3-methoxy-26-methyl-20,27-bis(methylene)-, (2R,3R,3aS,7R,8aS,9S,10aR,11S,1

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Towle MJ, et al. Cancer Res. 2001 Feb 1;61(3):1013-21. 2. Vahdat LT, et al. J Clin Oncol. 2009 Jun 20;27(18):2954-61. 3. Okouneva T, et al. Mol Cancer Ther. 2008 Jul;7(7):2003-11. 4. Zheng W, et al. Bioorg Med Chem Lett. 2004 Nov 15;14(22):5551-4.
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