Table 2.
Chemical structures of metabolites referred to in this review article.
Compound Name | Chemical Structure | Detected Nuclei | References |
---|---|---|---|
N-acetyl aspartate |
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1H | 18 – 22 |
Citrate |
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1H | 18 – 22 |
Glucose, [1-13C]-/[U-13C]-glucose |
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1H, 13C, hyperpolarized 13C | 15–18,63–68,71 |
Lactate, [3-13C]-lactate |
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1H, 13C, hyperpolarized 13C | 15–18,63–68,71 |
Pyruvate |
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1H, hyperpolarized 13C | 70,71,196 |
[1,4-13C2]-fumarate |
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Hyperpolarized 13C | 70,196 |
Choline (Cho) |
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1H, 31P | 75 – 81 |
Phosphocholine (PC) |
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1H, 31P | 75 – 81 |
Glycerophosphocholine (GPC) |
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1H, 31P | 75 – 82 |
Phosphoethanolamine (PE) |
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1H, 31P | 82 – 84 |
Glycerophosphoethanolamine (GPE) |
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1H, 31P | 82 – 84 |
Triacylglycerides, example of C55H98O6, palmitic acid, oleic acid, alpha-linolenic acid (from top to bottom) |
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1H | 89 – 95 |
Nucleoside triphosphates (NTP), example of ATP |
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31P | 57,58,96–101 |
Nucleoside diphosphates (NDP), example of ADP |
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31P | 57,58,96–101 |
Phosphocreatine (PCr) |
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31P | 57,58,96–101 |
Inorganic phosphate (Pi) |
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31P | 57,58,96–101 |