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| Product | Description | |
|---|---|---|
| Desfesoterodine | Desfesoterodine (PNU-200577) is a potent and selective muscarinic receptor (mAChR) antagonist with a K B and a pA 2 of 0.84 nM and 9.14, respectively [1]. Desfesoterodine is a major pharmacologically active metabolite of Tolterodine (PNU-200583; HY-A0024) and Fesoterodine (HY-70053) [2] [3]. Desfesoterodine improves cerebral infarction induced detrusor overactivity in rats [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PNU-200577; 5-Hydroxymethyl Tolterodine. CAS No. 207679-81-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-76569. |  |
| Desfesoterodine fumarate | Desfesoterodine is the active metabolite of fesoterodine as its isobutyrate ester. Uses: Muscarinic m3 receptor antagonists. Synonyms: PNU-200577 fumarate; (R)-2-[3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)phenol fumaric acid salt. Grades: ≥98%. CAS No. 380636-50-0. Molecular formula: C22H31NO2. Mole weight: 341.5. |  |
| (R)-5-Hydroxymethyl tolterodine | 5-hydroxymethyl tolterodine produces a competitive and concentration-dependent inhibition of carbachol-induced contraction of guinea-pig isolated urinary bladder strips. Synonyms: Desfesoterodine. Grades: >98%. CAS No. 207679-81-0. Molecular formula: C22H31NO2. Mole weight: 341.49. | |
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