Ipriflavone (Osteofix)

For research use only.

Catalog No.S2422

Ipriflavone (Osteofix) Chemical Structure

CAS No. 35212-22-7

Ipriflavone (7-Isopropoxyisoflavon) is used to inhibit bone resorption.

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Biological Activity

Description Ipriflavone (7-Isopropoxyisoflavon) is used to inhibit bone resorption.
advanced glycation end products (AGE) [2]
In vitro

Ipriflavone regulates the differentiation and biosynthetic properties of human bone marrow stromal osteoprogenitor cells (BMC) by enhancing the expression of some important matrix proteins and facilitating the mineralization process. [1] Ipriflavone treatment at 10 μM significantly inhibits advanced glycation end products (AGE) enhanced bone resorption in cultured mouse unfractionated bone cells. [2] In addition, Ipriflavone treatment potently enhances calcium uptake by duodenal cells. [3] Ipriflavone inhibits the proliferation and DNA synthesis of MDA-231 cells in a dose-dependent manner, and blocks the ligand-induced phosphorylation of Tyr845 of the EGFR. Ipriflavone treatment at 50 μM does not induce apoptosis of MDA-231 cells. [4]

In vivo Oral administration of Ipriflavone at 12 mg but not 6 mg significantly inhibits the development of new osteolytic bone metastases of MDA-231 cells, suppresses the progression of established osteolytic lesions, and reduces the number of osteoclasts adjacent to cancer cells in bone metastases. Consistent with the in vitro activity, Ipriflavone treatment at 6 or 12 mg/day significantly inhibits tumor growth of MDA-231 xenografts with 25% and 45% reductions by volume and 47% and 63% by weight, respectively, compared to untreated mice, and prolongs the life of tumor-bearing mice. [4] LD50: Mice >2.5g/kg (i.p.), >5g/kg (s.c.), >10g/kg (i.g.); Rats >2.5g/kg (i.p.), >5g/kg (s.c.), >10g/kg (i.g.) [5]


Cell Research:[4]
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  • Cell lines: MDA-231 cells
  • Concentrations: Dissolved in absolute ethanol, final concentrations ~50 μM
  • Incubation Time: 24, 48, 72 and 96 hours
  • Method: Cells are exposed to various concentrations of Ipriflavone for 24, 48, 72 and 96 hours. Cells are treated with trypan blue to estimate the number of viable cells. For thymidine incorporation analysis, [3H]Thymidine (1 μCi) is added, and cells are harvested onto glass fiber filters 4 hours later. Radioactivity is determined by scintillation counting.
    (Only for Reference)
Animal Research:[4]
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  • Animal Models: Male athymic nude mice (ICR-nu/nu) injected s.c. or intracardially with MDA-231 human breast cancer cells
  • Dosages: ~12 mg/day
  • Administration: Oral administration
    (Only for Reference)

Solubility (25°C)

In vitro DMSO 56 mg/mL (199.77 mM)
Ethanol 2 mg/mL (7.13 mM)
Water Insoluble

* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

Chemical Information

Molecular Weight 280.32


CAS No. 35212-22-7
Storage powder
in solvent
Synonyms N/A
Smiles CC(C)OC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=CC=C3

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Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID