Xamoterol
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Systematic (IUPAC) name | |
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(RS)-N-(2-{[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino}ethyl)morpholine-4-carboxamide
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Identifiers | |
CAS Number | 81801-12-9 N |
ATC code | C01CX07 (WHO) |
PubChem | CID: 155774 |
IUPHAR/BPS | 538 |
ChemSpider | 137213 Y |
UNII | 7HE0JQL703 Y |
KEGG | D06328 Y |
ChEMBL | CHEMBL75753 Y |
Chemical data | |
Formula | C16H25N3O5 |
Molecular mass | 339.387 g/mol |
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NY (what is this?) (verify) |
Xamoterol is a cardiac stimulant. It works by binding to the β1 adrenergic receptor. It is a 3rd generation adrenergic β receptor partial agonist.[1] It provides cardiac stimulation at rest but it acts as a blocker during exercise.[2]
References
Cardiac stimulants excluding cardiac glycosides (C01C)
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Adrenergic and dopaminergic agents |
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Phosphodiesterase inhibitors (PDE3I) | |||||||||||||||
Other cardiac stimulants |
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This drug article relating to the cardiovascular system is a stub. You can help Wikipedia by expanding it. |
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Categories:
- Chemical articles having calculated molecular weight overwritten
- Infobox drug articles without a structure image
- Chemical pages without DrugBank identifier
- Drugs with no legal status
- Beta1-adrenergic agonists
- Cardiac stimulants
- Inotropic agents
- Morpholines
- Phenol ethers
- Phenols
- Cardiovascular system drug stubs