![]() Fesoterodine-d7 fumarate structure
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Common Name | Fesoterodine-d7 fumarate | ||
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CAS Number | 2747918-94-9 | Molecular Weight | 534.69 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C30H34D7NO7 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Fesoterodine-d7 fumarateFesoterodine-d7 (fumarate) is the deuterium labeled Fesoterodine fumarate[1]. Fesoterodine Fumarate is an orally active, nonsubtype selective, competitive muscarinic receptor (mAChR) antagonist with pKi values of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. Fesoterodine Fumarate is used for the overactive bladder (OAB)[2][3]. |
Name | Fesoterodine-d7 fumarate |
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Description | Fesoterodine-d7 (fumarate) is the deuterium labeled Fesoterodine fumarate[1]. Fesoterodine Fumarate is an orally active, nonsubtype selective, competitive muscarinic receptor (mAChR) antagonist with pKi values of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. Fesoterodine Fumarate is used for the overactive bladder (OAB)[2][3]. |
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Related Catalog | |
In Vitro | Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. |
References |
Molecular Formula | C30H34D7NO7 |
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Molecular Weight | 534.69 |