LY500307

CAS No. 533884-09-2

LY500307( LY-500307 | LY 500307 | Erteberel | SERBA-1 )

Catalog No. M14897 CAS No. 533884-09-2

LY500307 (LY-500307, Erteberel, SERBA-1) is a potent, selective Estrogen Receptor β (ERβ) agonist with Ki/EC50 of 0.19/0.66 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 464 In Stock
5MG 432 In Stock
10MG 622 In Stock
25MG 938 In Stock
50MG 1265 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LY500307
  • Note
    Research use only, not for human use.
  • Brief Description
    LY500307 (LY-500307, Erteberel, SERBA-1) is a potent, selective Estrogen Receptor β (ERβ) agonist with Ki/EC50 of 0.19/0.66 nM.
  • Description
    LY500307 (LY-500307, Erteberel, SERBA-1) is a potent, selective Estrogen Receptor β (ERβ) agonist with Ki/EC50 of 0.19/0.66 nM, 12-fold higher affinity than ERα and exhibits 32-fold more functional potency; reduces proliferation and induces apoptosis in GBM cells, enhances ERβ signaling and expression, modulates the expression of genes involved in cell cycle, cell death, survival, and DNA damage response; also sensitizes GBM cells to chemotherapeutic agents, reduces GBM progression in an orthotopic model .Schizophrenia Phase 2 Clinical.
  • In Vitro
    Treatment with Erteberel (0.25-10 μM, 72 hours) significantly reduces the proliferation of GBM cells with no activity on normal astrocytes in vitro. Erteberel promotes apoptosis of GBM cells. Erteberel modulated several pathways related to apoptosis, cell cycle, and DNA damage response. Erteberel (0-1000 μM) sensitizes GBM cells to several FDA-approved chemotherapeutic drugs including cisplatin, lomustine and temozolomide.Cell Viability Assay Cell Line:U87, U251,T98G and normal astrocytesConcentration:0.25, 0.5, 1, 2, 4, 6, 8, and 10 μMIncubation Time:72 h Result:Treatment with Erteberel significantly reduces the viability of various GBM cell lines in a dose-dependent manner. In contrast, viability of normal astrocytes is not affected at the tested doses, suggesting that Erteberel has tumor cell–specific activity.
  • In Vivo
    Erteberel (5?mg/Kg body weight/day, oral, 28 days) treatment significantly reduces tumor growth and promotes apoptosis of GBM tumors in an orthotopic model.Erteberel (5?mg/Kg body weight/day, oral, 40-50 days) treatment improves the overall survival of tumor-bearing mice in the GL26 syngeneic glioma model. Animal Model:Athymic mice (5-7 weeks) inoculated with OVCAR-3 cells Dosage:5mg/Kg body weight Administration:Oral, daily for 28 days Result:Immunohistochemical analysis reveals that Erteberel treatment significantly reduces the number of proliferation marker Ki-67-positive cells and increases the number of TUNEL-positive apoptotic cells.
  • Synonyms
    LY-500307 | LY 500307 | Erteberel | SERBA-1
  • Pathway
    Endocrinology/Hormones
  • Target
    Estrogen Receptor/ERR
  • Recptor
    ERβ
  • Research Area
    Neurological Disease
  • Indication
    Schizophrenia

Chemical Information

  • CAS Number
    533884-09-2
  • Formula Weight
    282.339
  • Molecular Formula
    C18H18O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 30 mg/mL (106.26 mM)
  • SMILES
    OC1=CC=C2C([C@@](CCC3)([H])[C@@]3([H])[C@H](C4=CC=C(O)C=C4)O2)=C1
  • Chemical Name
    (3aS,4R,9bR)-1,2,3,3a,4,9b-Hexahydro-4-(4-hydroxyphenyl)cyclopenta[c][1]benzopyran-8-ol

Shipping & Storage Information

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

Reference

1. Sareddy GR, et al. Sci Rep. 2016 Apr 29;6:24185. 2. Norman BH, et al. 3. Zhao L, et al. Proc Natl Acad Sci U S A. 2018 Apr 17;115(16):E3673-E3681. 4. Reese JM, et al. Oncotarget. 2017 Oct 11;8(57):96506-96521.
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