Normetanephrine
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| Names |
| IUPAC name
4-(2-amino-1-hydroxy-ethyl)- 2-methoxy-phenol
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| Identifiers |
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97-31-4 Y |
| ChEMBL |
ChEMBL774 Y |
| ChemSpider |
1200 Y |
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6643 |
| Jmol 3D model |
Interactive image |
| MeSH |
Normetanephrine |
| PubChem |
1237 |
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InChI=1S/C9H13NO3/c1-13-9-4-6(8(12)5-10)2-3-7(9)11/h2-4,8,11-12H,5,10H2,1H3 Y
Key: YNYAYWLBAHXHLL-UHFFFAOYSA-N Y
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InChI=1/C9H13NO3/c1-13-9-4-6(8(12)5-10)2-3-7(9)11/h2-4,8,11-12H,5,10H2,1H3
Key: YNYAYWLBAHXHLL-UHFFFAOYAR
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| Properties |
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C9H13NO3 |
| Molar mass |
183.204 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Y verify (what is Y N ?) |
| Infobox references |
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Normetanephrine is a metabolite of norepinephrine created by action of catechol-O-methyl transferase on norepinephrine. It is excreted in the urine and found in certain tissues. It is a marker for catecholamine-secreting tumors such as pheochromocytoma.
Norepinephrine degradation. Normetanephrine is shown at top left. Enzymes are shown in boxes.
[1]
References[edit]
- ^ Figure 11-4 in: Flower, R.; Rang, H. P.; Dale, M. M.; Ritter, J. M. (2007). Rang & Dale's Pharmacology. Edinburgh: Churchill Livingstone. ISBN 0-443-06911-5.
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| Blood |
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| Endocrine |
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| Nervous system |
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Cardiovascular/
respiratory |
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| Digestive |
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Reproductive/
urinary/
breast |
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| General histology |
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| Musculoskeletal |
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