ErSO

CAS No. 2407860-35-7

ErSO( —— )

Catalog No. M28247 CAS No. 2407860-35-7

ErSO is a selective activator of anticipatory unfolded protein response (UPR) via ERα receptor. ErSO can be used in studies about anti-cancer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 260 In Stock
10MG 417 In Stock
25MG 687 In Stock
50MG 963 In Stock
100MG 1287 In Stock
500MG 2601 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ErSO
  • Note
    Research use only, not for human use.
  • Brief Description
    ErSO is a selective activator of anticipatory unfolded protein response (UPR) via ERα receptor. ErSO can be used in studies about anti-cancer.
  • Description
    ErSO is a selective activator of anticipatory unfolded protein response (UPR) via ERα receptor. ErSO can be used in studies about anti-cancer.(In Vitro):In MCF-7 cells, ErSO (1-1000 nM) inhibits cell viability with an IC50 of 20.3 nM. ErSO (1 μM) rapidly kills ERα-positive breast cancer cells in TYS and TDG cells and induces rapid killing of ERα-positive MCF-7 human breast cancer cells.(In Vivo):ErSO (10 and 40 mg/kg; p.o.) induces >100000-fold regression (to undetectable amounts) within 14 days and >10000-fold regression of TYS-luciferase-expressing breast tumors in all five mice. In Nu/J mice, ErSO (10 or 40 mg/kg; p.o.) eliminates tumors with >90% reduction in all cases.
  • In Vitro
    Cell Viability Assay Cell Line:MCF-7 cells Concentration:1~1000 nM Incubation Time:24 hours Result: Showed that IC50 value is 20.3 nM in MCF-7 cells and inhibited cell viability.
  • In Vivo
    Animal Model:Nu/J mice Dosage:10 or 40 mg/kg Administration:P.o.; 21 days Result:Resulted in elimination of these tumors, with >90% reduction in all cases.Animal Model:Mice Dosage:0.5~40 mg/kg Administration:P.o.; 3 weeks Result:Sufficient for a robust response.Animal Model:Mice Dosage:40 mg/kg Administration:I.p.; 14 days Result:Metastatic burden was greatly reduced
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    γ secretase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2407860-35-7
  • Formula Weight
    453.33
  • Molecular Formula
    C22H13F6NO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 120 mg/mL (264.71 mM)
  • SMILES
    O=C1[C@@](C=2C(N1)=C(C(F)(F)F)C=CC2)(C3=CC=C(OC(F)(F)F)C=C3)C4=CC=C(O)C=C4
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Baumann, et al. Preparation of 4,5,6,7-tetrahydrobenzothiazolyl- or 5,6,7,8-tetrahydroquinazolinylphenylamine derivatives as modulators for amyloid beta. WO2009087127A1
molnova catalog
related products
  • [Sar1, Ile8]-Angiote...

    [Sar1, Ile8]-Angiotensin II is a peptide that has multiple effects on vascular smooth muscle, including contraction of normal arteries and hypertrophy or hyperplasia of cultured cells or diseased vessels. The biological activities of angiotensin II antagonists upon basal and angiotensin II-stimulated aldosterone production were evaluated in an isolated canine glomerulosa cell preparation.

  • MBP MAPK Substrate

    MBP MAPK Substrate is used as an exogenous substrate for MAPK.

  • Dalvastatin

    Dalvastatin (RG-12561) is an orally available inhibitor of HMG-CoA reductase and cholesterol-lowering synthesis.Dalvastatin competitively inhibits rat hepatic HMG-CoA reductase with an IC50 value of 3.4 nmol / l.