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Formula | C16H28GdN5O9C16H28GdN5O9.xH2O |
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Molecular Weight | 591.67 | CAS No. | 122795-43-1 | |
Solubility (25°C)* | In vitro | Water | 100 mg/mL (169.01 mM) | |
DMSO | Insoluble | |||
Ethanol | Insoluble | |||
* <1 mg/ml means slightly soluble or 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. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Gadodiamide Hydrate, a nonionic Gd3+ chelate, is frequently injected i.v. into magnetic resonance imaging (MRI) to enhance contrast. |
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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] |
Data from [Data independently produced by , , International Journal of Biological Macromolecules, 2018, 108:24-31]
Alzheimer's disease-associated ubiquitin mutant Ubb+1: Properties of the carboxy-terminal domain and its influence on biomolecular interactions [ Int J Biol Macromol, 2018, 108:24-31] | PubMed: 29175520 |
Solution Structure and Membrane Interaction of the Cytoplasmic Tail of HIV-1 gp41 Protein. [ Structure, 2017, 25(11):1708-1718] | PubMed: 29056482 |
Structural basis of dynamic membrane recognition by trans-Golgi network specific FAPP proteins. [Lenoir M, et al. J Mol Biol, 2015, 427(4):966-81] | |
Structural basis of dynamic membrane recognition by trans-Golgi network specific FAPP proteins [ J Mol Biol, 2015, 427(4):966-981] | PubMed: 25579996 |
HIV-1 Envelope Protein gp41: An NMR Study of Dodecyl Phosphocholine Embedded gp41 Reveals a Dynamic Prefusion Intermediate Conformation [Lakomek NA, et al Structure, 2014, 22(9):1311-21] | PubMed: 25132083 |
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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
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