Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H21NO4 |
| Molecular Weight | 267.3208 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)NCC(O)COC1=CC=C(CC(O)=O)C=C1
InChI
InChIKey=PUQIRTNPJRFRCZ-UHFFFAOYSA-N
InChI=1S/C14H21NO4/c1-10(2)15-8-12(16)9-19-13-5-3-11(4-6-13)7-14(17)18/h3-6,10,12,15-16H,7-9H2,1-2H3,(H,17,18)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The influence of first pass metabolism on the development and validation of an IVIVC for metoprolol extended release tablets. | 2002 May |
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| In vivo biotransformation of metoprolol in the horse and on-column esterification of the aminocarboxylic acid metabolite by alcohols during solid phase extraction using mixed mode columns. | 2006 Jan 23 |
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| The effects of salvianolic acid B from radix salvia miltiorrhizae on the oral pharmacokinetics of metoprolol and metoprolol acid in rats. | 2010 Jun |
Patents
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Y6I8U8OX8P
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DTXSID70881080
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56392-14-4
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PARENT (METABOLITE INACTIVE)
SUBSTANCE RECORD
