Zoledronic Acid

CAS No. 118072-93-8

Zoledronic Acid( Orazol | Reclast | Zoledronate | Zoledronic acid )

Catalog No. M10613 CAS No. 118072-93-8

Zoledronic acid induces apoptosis in osteoclasts by inhibiting enzymes of the mevalonate pathway and preventing the isoprenylation of small GTP-binding proteins such as Ras and Rho.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 30 In Stock
25MG 45 In Stock
50MG 72 In Stock
100MG 118 In Stock
200MG 175 In Stock
500MG 295 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Zoledronic Acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Zoledronic acid induces apoptosis in osteoclasts by inhibiting enzymes of the mevalonate pathway and preventing the isoprenylation of small GTP-binding proteins such as Ras and Rho.
  • Description
    Zoledronic acid induces apoptosis in osteoclasts by inhibiting enzymes of the mevalonate pathway and preventing the isoprenylation of small GTP-binding proteins such as Ras and Rho.(In Vitro):Zoledronic Acid (0.1-1 μM; 48 hours) increases receptor activator of nuclear factor kB ligand (RANKL) and sclerostin mRNA expressions in osteocyte-like MLO-Y4 cells.Zoledronic Acid increases the expression of osteoclastogenesis supporting factor from MLO-Y4 cells.Zoledronic Acid enhances the RANKL expression via IL-6/ JAK2/STAT3 pathway in MLO-Y4 cells.Zoledronic acid inhibits osteoclast differentiation and function through the regulation of NF-κB and JNK signalling pathways.Zoledronic Acid (10-100 μM; 1-7 days) markedly reduces the viability of MC3T3-E1 cells.Zoledronic Acid (10-100 μM; 1-7 days) induces apoptosis in MC3T3-E1 cells.Zoledronic Acid (10-100 μM; 4 days) inhibits cell viability due to the induction of apoptosis.Zoledronic Acid exerts inhibitory effects on the differentiation and maturation of MC3T3-E1 cells at concentrations <1 μM.(In Vivo):Zoledronic Acid (0.05 mg/kg; i.p.; weekly; for 3 weeks) increases bone mineral density and content.Zoledronic Acid (0.5-1 mg/kg; i.p.; weekly; for 3 weeks) inhibits both osteoclast and osteoblasts function and bone remodeling in vivo interfering with bone mechanical properties.
  • In Vitro
    Zoledronic Acid (0.1-1 μM; 48 hours) increases receptor activator of nuclear factor kB ligand (RANKL) and sclerostin mRNA expressions in osteocyte-like MLO-Y4 cells.Zoledronic Acid increases the expression of osteoclastogenesis supporting factor from MLO-Y4 cells.Zoledronic Acid enhances the RANKL expression via IL-6/ JAK2/STAT3 pathway in MLO-Y4 cells.Zoledronic acid inhibits osteoclast differentiation and function through the regulation of NF-κB and JNK signalling pathways.Zoledronic Acid (10-100 μM; 1-7 days) markedly reduces the viability of MC3T3-E1 cells.Zoledronic Acid (10-100 μM; 1-7 days) induces apoptosis in MC3T3-E1 cells.Zoledronic Acid (10-100 μM; 4 days) inhibits cell viability due to the induction of apoptosis.Zoledronic Acid exerts inhibitory effects on the differentiation and maturation of MC3T3-E1 cells at concentrations <1 μM.Cell Viability Assay Cell Line:MC3T3-E1 cells Concentration:0.01 μM , 0.1 μM, 1 μM, 10 μM, 100 μMIncubation Time:1 day, 3 days, 5 days, 7 days Result:Reduced cells viability at 10 μM and 100 μM.Apoptosis Analysis Cell Line:MC3T3-E1 cells Concentration:0.01 μM , 0.1 μM, 1 μM, 10 μM, 100 μM Incubation Time:1 days, 4 days, 7 days Result:Increased the number of early apoptotic cells and late apoptotic or necrotic cells at dose-dependent and time-dependent (high concentrations).Western Blot Analysis Cell Line:MC3T3-E1 cells Concentration:0.01 μM , 0.1 μM, 1 μM, 10 μM, 100 μM Incubation Time:4 days Result:Down-regulated the protein level of inactive caspase-3 and up-regulated the protein level of active caspase-3 at the concentrations of 10 and 100 μM.
  • In Vivo
    Zoledronic Acid (0.05 mg/kg; i.p.; weekly; for 3 weeks) increases bone mineral density and content.Zoledronic Acid (0.5-1 mg/kg; i.p.; weekly; for 3 weeks) inhibits both osteoclast and osteoblasts function and bone remodeling in vivo interfering with bone mechanical properties. Animal Model:Five-week-old C57BL6 mice Dosage:0.05 mg/kg, 0.5 mg/kg, 1 mg/kg Administration:Intraperitoneal injection, weekly, for 3 weeks Result:Inhibited both osteoclast and osteoblasts function and bone remodeling at 0.5 mg/kg and 1 mg/kg.
  • Synonyms
    Orazol | Reclast | Zoledronate | Zoledronic acid
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Rho
  • Recptor
    Rho
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    118072-93-8
  • Formula Weight
    272.09
  • Molecular Formula
    C5H10N2O7P2
  • Purity
    >98% (HPLC)
  • Solubility
    0.1M NaOH (aq): 40 mg/ml; DMSO: 0.004 mg/mL (0.01 mM)
  • SMILES
    OC(P(O)(O)=O)(P(O)(O)=O)CN1C=CN=C1
  • Chemical Name
    Phosphonic acid, (1-hydroxy-2-(1H-imidazol-1-yl)ethylidene)bis-

Shipping & Storage Information

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

Reference

1. Jagdev SP, et al. Br J Y, 2001, 84(8), 1126-1134.
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