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伊班膦酸钠单水合物

Ibandronate sodium monohydrate

CAS: 138926-19-9

Molecular Formula: C9H24NNaO8P2

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伊班膦酸钠单水合物 - Names and Identifiers

Name Ibandronate sodium monohydrate
Synonyms Boniva
Bonviva
Ibandrate
BM-21.0955
Ibadronate SodiuM
Ibandromate Monosodium
Ibandronate sodium monohydrate
[1-Hydroxy-3-(methylpentylamino)-propylidene]bisphosphonic acid sodium salt
[1-Hydroxy-3-(methylpentylamino)-propylidene]bisphosphonic acid sodium salt monohydrate
sodium hydrogen {1-hydroxy-3-[methyl(pentyl)amino]-1-phosphonopropyl}phosphonate hydrate
Sodium Trihydrogen (1-Hydroxy-3-(methylpenthylamino)propylidene)diphosphonate Monohydrate
CAS 138926-19-9
EINECS 639-757-2
InChI InChI=1/C9H23NO7P2.Na.H2O/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);;1H2/q;+1;/p-1

伊班膦酸钠单水合物 - Physico-chemical Properties

Molecular FormulaC9H24NNaO8P2
Molar Mass359.23
Melting Point840C (dec)
Boling Point587.8°C at 760 mmHg
Flash Point309.3°C
Solubility Soluble in water (72 mg/ml at 25 °C), ethanol (<1 mg/ml at 25 °C), and DMSO (<1 mg/
Vapor Presure2.88E-16mmHg at 25°C
AppearanceWhite crystalline powder
ColorWhite
Storage ConditionKeep in dark place,Inert atmosphere,2-8°C
StabilityStable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
SensitiveSensitive to light
Physical and Chemical PropertiesWhite crystalline powder, soluble in water, insoluble in alcohol.
UseFor the treatment of malignant hypercalcemia
In vitro studyIbronate (1.25-2 μm) significantly reduced endothelial cell growth, while ibronate (2 μm) also significantly reduced capillary-like lumen formation and increased endothelial cell apoptosis. Ibandronate (< 100 μm) dose-dependently increased VEGF expression in endothelial cells. Ibandronate (<100 μm) dose-dependently inhibited the growth of prostate cancer cell lines (LNCaP and PC-3).
In vivo studyIn women with osteoporosis treated for 3 years, Ibandronate is administered daily (2.5 mg) or intermittently (20 mg every other day for 12 doses every 3 months) significantly reduced the risk of new-form vertebral fractures by 62% and 50% (p = 0.0006), respectively. In women with osteoporosis treated for 3 years, Ibandronate is administered daily (2.5 mg) or intermittently (20 mg every other day for 12 doses every 3 months) significantly and progressively increased lumbar BMD by 6.5 and 5.7%, respectively. Ibandronate (< 125 mg/kg s.c.) caused a dose-dependent increase in bone density, cancellous bone volume, and trabecular bone number, failure load (Fmax), and yield load in long bones and vertebrae of ovariectomized rats, and the increased trabecular separation in ovariectomized rats could be completely prevented by any dose of Ibandronate.

伊班膦酸钠单水合物 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes40 - Limited evidence of a carcinogenic effect
Safety DescriptionS22 - Do not breathe dust.
S36 - Wear suitable protective clothing.
S24/25 - Avoid contact with skin and eyes.
HS Code29319090

伊班膦酸钠单水合物 - Reference Information

biological activity Ibandronate (BM-21.0955, BM-210955, RPR-102289A) is an efficient nitrogen-containing bisphosphonate used to treat osteoporosis.
use for the treatment of malignant hypercalcemia
Inhibits bone resorption as a sodium salt and complexed with technetium Tc 99m for bone imaging. The monophosphonates are not active. Biphosphonates are used in disorders affecting the skeleton such a
s asteoporosis, metastatic disease, and Paget holmium disease.
Last Update:2024-04-10 22:29:15
伊班膦酸钠单水合物
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View History
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