1191280-48-4
1191280-48-4
Chemical Structure
(Rac)-Tolterodine-d14 tartrate
Synonym(s): (Rac)-PNU-200583-d14 tartrate
- CAS No.: 1191280-48-4
- Formula:C26H23D14NO7
- Molecular Weight:489.66
IUPAC Name: 2-(3-(bis(propan-2-yl-d7)amino)-1-phenylpropyl)-4-methylphenol (2R,3R)-2,3-dihydroxysuccinate
InChIKey: TWHNMSJGYKMTRB-GPSUCFBESA-N
SMILES: OC([C@H](O)[C@@H](O)C(O)=O)=O.OC(C=CC(C)=C1)=C1C(C2=CC=CC=C2)CCN(C(C([2H])([2H])[2H])([2H])C([2H])([2H])[2H])C(C([2H])([2H])[2H])([2H])C([2H])([2H])[2H]
Biological Activity: (Rac)-Tolterodine-d14 (tartrate) is the deuterium labeled (Rac)-Tolterodine tartrate[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(Rac)-Tolterodine-d14 tartrate | (Rac)-Tolterodine-d14 (tartrate) is the deuterium labeled (Rac)-Tolterodine tartrate. | |||||||||||||||||||||
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Tolterodine tartrate (Standard) | ≥98% | Tolterodine (tartrate) (Standard) is the analytical standard of Tolterodine tartrate. This product is intended for research and analytical applications. Tolterodine ((R)-(+)-Tolterodine) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine can be used for the research of urinary tract infections and overactive bladder. | ||||||||||||||||||||
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Tolterodine tartrate-d14 | Tolterodine tartrate-d14 (Kabi-2234-d14) is deuterium labeled Tolterodine tartrate. Tolterodine ((R)-(+)-Tolterodine) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine can be used for the research of urinary tract infections and overactive bladder. | |||||||||||||||||||||
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(Rac)-Tolterodine-d5 | (Rac)-Tolterodine-d5 is deuterium labeled (rac)-Tolterodine. | |||||||||||||||||||||
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Tolterodine tartrate | 98.64% | Tolterodine tartrate (Kabi-2234) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine tartrate competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine tartrate restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine tartrate ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine tartrate can be used for the research of urinary tract infections and overactive bladder. | ||||||||||||||||||||
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References
