Gadodiamide Hydrate

Catalog No.S1751

Gadodiamide Hydrate Chemical Structure

Molecular Weight(MW): 591.67

Gadodiamide Hydrate, a nonionic Gd3+ chelate, is frequently injected i.v. into magnetic resonance imaging (MRI) to enhance contrast.

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Cited by 2 Publications

1 Customer Review

  • Solvent accessibility of Ubb+1. The solvent exposure of Ubb+1 has been probed by solvent PRE (A) or by measurement of water-amide proton exchange rates (B). In A) the 1HN-R2p rates of Ubb+1 obtained with 2 mM gadodiamide are plotted as a function of protein sequence. In B) the water-amide proton exchange rates (k) measured through a CLEANEX-PM-FHSQC experiment are reported versus the protein sequence. Error bars are standard errors obtained from data fitting. Residues affected by signal overlap or with insufficient signal-to-noise ratio were excluded from the analysis.

    International Journal of Biological Macromolecules, 2018, 108:24-31. Gadodiamide Hydrate purchased from Selleck.

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Biological Activity

Description Gadodiamide Hydrate, a nonionic Gd3+ chelate, is frequently injected i.v. into magnetic resonance imaging (MRI) to enhance contrast.
In vivo Gadodiamide results in half-life of 18, 38, and 75 minutes in rats, rabbits, and monkeys, respectively. Gadodiamide is shown to be excreted rapidly, primarily through the kidneys. [1] Gadodiamide, when administered i.v. as gadodiamide injection at a dosage of 0.3 mmol/kg, is stable in vivo and that the very major part of the dose (> 99%) is excreted in urine as an unchanged complex. [2] Gadodiamide produces focal and generalized myoclonus over several hours. Gadodiamide itself produces lesions in the central cerebellar regions resembling in character and severity those produced by the gadodiamide formulation, but not others. [3] Gadodiamide travels quickly throughout the ventricular system from the lateral ventricular site of injection to the fourth ventricle and foramina of Luschka and Magendie within 2 min. [4] Gadodiamide results in transient but statistically significant decreases in aortic pressure, left ventricular pressure, indices of left ventricular contractility and relaxation, and systemic and pulmonary vascular resistance, and increases in aortic blood flow in anesthetized dogs. Gadodiamide injection produces less severe alterations in hemodynamics than gadopentetate dimeglumine. [5]

Protocol

Solubility (25°C)

In vitro Water 100 mg/mL (169.01 mM)
DMSO Insoluble
Ethanol 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 591.67
Formula

C16H28GdN5O9C16H28GdN5O9.xH2O

CAS No. 122795-43-1
Storage powder
in solvent
Synonyms N/A

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