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 |
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameEribulin
-
NoteResearch use only, not for human use.
-
Brief DescriptionEribulin (B1939, E7389, ER-086526) is a macrocyclic ketone analogue of halichondrir B.
-
DescriptionEribulin (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 VitroEribulin (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 VivoEribulin (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.
-
SynonymsB1939 | E7389 | ER-086526
-
PathwayCytoskeleton/Cell Adhesion Molecules
-
TargetMicrotubule/Tubulin
-
RecptorMicrotubule/Tubulin
-
Research AreaCancer
-
IndicationBreast Cancer
Chemical Information
-
CAS Number253128-41-5
-
Formula Weight729.8965
-
Molecular FormulaC40H59NO11
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESCC1CC2CCC3C(=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 Name11,15:18,21:24,28-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℃)
-
ShippingWith 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.
molnova catalog
related products
-
Briciclib
Briciclib is a small molecule that suppresses cyclin D1 accumulation in Y cells.
-
Decanoic Acid
Decanoic Acid acts as a non-competitive AMPA receptor antagonist.
-
Vinflunine ditartrat...
Vinflunine ditartrate is the first fluorinated microtubule inhibitor belonging to the Vinca alkaloids family. Vinflunine ditartrate has anti-angiogenic, vascular-disrupting and anti-metastatic activities.
Cart
sales@molnova.com