“…Overall, the pool of metabolites found to be distinct between normal and CRC patients included (a) 3-hydroxybutyric acid, L-valine, L-threonine, 1-deoxyglucose, and glycine [141]; (b) a panel consisting of citrate, hippurate, p -cresol, 2-aminobutyrate, myristate, putrescine, and kynurenate [142]; (c) alanine, citrate, creatine, glutamine, peptide NHs, lactate, leucine, pyruvate, tyrosine, 3-hydroxybutyrate, acetate, formate, glycerol, lipid (−CH 2 –OCOR), the N-acetyl signal of glycoproteins, phenylalanine, and proline [143]; (d) hydroxylated polyunsaturated ultra long-chain fatty acid metabolites [144]; (e) glucose, inositol, hypoxanthine, xanthine, uric acid, and deoxycholic acid [145]; (f) L-valine, 5-oxo-L-proline, 1-deoxyglucose, D-turanose, D-maltose, arachidonic acid, hexadecanoic acid, and L-tyrosine [146]; (g) proline, cysteine, acetate, and butyrate [147]; and (h) L-alanine, glucuronic lactone, and L-glutamine [148]. Most of these metabolites are yet to be validated but might serve as tools for the early detection, prediction, and prognosis of CRC [149–152]. …”