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I5784

Sigma-Aldrich

Ibandronate sodium salt

≥97% (NMR), solid

Synonym(s):

(1-Hydroxy-3-(methylpentylamino)propylidene)bisphosphonic acid sodium, Bondronat

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1 L
₩108,301

About This Item

Empirical Formula (Hill Notation):
C9H22NNaO7P2
CAS Number:
Molecular Weight:
341.21
MDL number:
UNSPSC Code:
41106300
PubChem Substance ID:
NACRES:
NA.77

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Quality Level

Assay

≥97% (NMR)

form

solid

storage condition

protect from light

color

white

solubility

H2O: >10 mg/mL

originator

Roche

storage temp.

2-8°C

SMILES string

[Na+].CCCCCN(C)CCC(O)(P(O)(O)=O)P(O)([O-])=O

InChI

1S/C9H23NO7P2.Na/c1-3-4-5-7-10(2)8-6-9(11,18(12,13)14)19(15,16)17;/h11H,3-8H2,1-2H3,(H2,12,13,14)(H2,15,16,17);/q;+1/p-1

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bp

101 °C/1013 hPa

bp

-

bp

109 °C/1013 hPa

bp

-

mp

-1 °C

mp

-

mp

-5 °C

mp

-

grade

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certified reference material

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certified reference material

application(s)

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

application(s)

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

application(s)

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

application(s)

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

Application

Ibandronate sodium salt has been used to study its effect on the proliferation and ultrastructure of Leishmania and Giardia by the generation of concentration curves.[1] It has also been used to elucidate the route by which nitrogen-containing bisphosphonates (N-BPs) enter the cytosol and inhibit their molecular target.[2]

Biochem/physiol Actions

Ibandronate is a nitrogen-containing bisphosphonate (N-BP).[1] It potentially inhibits mevalonate pathway in osteoclasts. Thus, ibandronate is effectively used to treat osteoporosis and other bone-related diseases.[2]
Ibandronate sodium inhibits farnesyl diphosphate synthase (IC50 = 20 nM). Ibandronate sodium is also a bone resorption inhibitor. It has been investigated for in vitro anti-tumor effects, such as apoptosis induction, inhibitor of cell growth, inhibition of invasive behavior, and inhibition of angiogenesis and for its in vivo role in various cancers including breast and prostate cancers.
Ibandronate sodium is a farnesyl diphosphate synthase inhibitor (IC50 = 20 nM); also a bone resorption inhibitor.

Features and Benefits

This compound was developed by Roche. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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