3032205-96-9
3032205-96-9
Chemical Structure
L-Hyoscyamine-d3
Synonym(s): Daturine-d3
- CAS No.: 3032205-96-9
- Formula:C17H20D3NO3
- Molecular Weight:292.39
IUPAC Name: (1R,3r,5S)-8-(methyl-d3)-8-azabicyclo[3.2.1]octan-3-yl (S)-3-hydroxy-2-phenylpropanoate
InChIKey: RKUNBYITZUJHSG-KHCPMMLOSA-N
SMILES: O=C([C@@H](C1=CC=CC=C1)CO)O[C@H]2C[C@H]3CC[C@H](N3C([2H])([2H])[2H])C2
Biological Activity: L-Hyoscyamine-d3 is the deuterium labeled L-Hyoscyamine. L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205)[1][2].
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L-Hyoscyamine-d3 | 98.87% | L-Hyoscyamine-d3 is the deuterium labeled L-Hyoscyamine. L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205). | ||||||||||||||||||||
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L-Hyoscyamine (Standard) | 99.63% | L-Hyoscyamine (Standard) is the analytical standard of L-Hyoscyamine. This product is intended for research and analytical applications. L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205). | ||||||||||||||||||||
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L-Hyoscyamine-d3-1 | L-Hyoscyamine-d3-1 (Hyoscyamine-d3) is the deuterium labeled L-Hyoscyamine (HY-N0471). L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205). | |||||||||||||||||||||
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L-Hyoscyamine | 99.96% | L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205). | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
- [2]. Lars Göran Axelsson, et al. Regulatory role of 5-HT and muscarinic receptor antagonists on the migrating myoelectric complex in rats. Eur J Pharmacol. 2003 Apr 25;467(1-3):211-8. [Content Brief]
