Metoprolol
Synonyms: metoprolol, Spesicor", "Beatrolol", "Toprol", "(RS)-Metoprolol", "dl-Metoprolol", "Lopressor", "37350-58-6", "Meijoprolol", "Metoprololum", "Preblok", "Presolol", "Metohexal", "Seroken", "Spesikor", "Lopresor", "Betalok", "Metoprolol succinate", "Selo-Zok", "Lopresoretic", "1-(Isopropylamino)-3-(4-(2-methoxyethyl)phenoxy)propan-2-ol", "1-[4-(2-methoxyethyl)phenoxy]-3-(propan-2-ylamino)propan-2-ol".
Source: Metoprolol is a selective ?1 (adrenergic) receptor blocker. Metoprolol has been used to treat various cardiovascular disorders including angina, arrhythmias, tachycardia, myocardial infarction, heart failure and hypertension.
Identifiers:
IUPAC Name: 1-[4-(2-methoxyethyl)phenoxy]-3-(propan-2-ylamino)propan-2-ol
CAS Number: 51384-51-1
PubChem ID: 4171
InChiKey: IUBSYMUCCVWXPE-UHFFFAOYSA-N
Canonical SMILES: CC(C)NCC(COC1=CC=C(C=C1)CCOC)O
Structural Properties:
Molecular Formula: C15H25NO3
Molecular Weight: 267.36
Pharmacophore Features:
Number of bond donors: 2
Number of bond acceptors: 4
Number of atoms different from hydrogen: 19
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Evidence Supporting This Chemical as an Emerging Contaminant
Lv, M., Lo, C., Hsu, C. C., Wang, Y., Chiang, Y. R., Sun, Q., ... & Yu, C. P. (2018). Identification of Enantiomeric Byproducts During Microalgae-Mediated Transformation of Metoprolol by MS/MS Spectrum Based Networking.?Frontiers in microbiology,?9, 2115.
Daneshkhah, M., Hossaini, H., & Malakootian, M. (2017). Removal of metoprolol from water by sepiolite-supported nanoscale zero-valent iron. Journal of environmental chemical engineering, 5(4), 3490-3499.
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