An intermediate in the catabolism of L-tryptophan, L-lysine, and hydroxylysine
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2-Oxoadipic acid is an intermediate in the catabolism of L-tryptophan, L-lysine, and hydroxylysine.1,2 Urinary excretion of 2-oxoadipic acid is increased in patients with α-ketoadipic aciduria, a rare inborn error in the metabolism of 2-oxoadipic acid to glutaryl-coenzyme A (glutaryl-CoA).
1.Xia, Z.-W., Inoue, Y., Ohse, M., et al.A study on α-ketoadipic aciduria by gas chromatographic-mass spectrometryWorld J. Gastroenterol.6(5)766-769(2000) 2.Gray, R.G., O'Neill, E.M., and Pollitt, R.J.α-aminoadipic aciduria: Chemical and enzymatic studiesJ. Inherit. Metab. Dis.2(4)89-92(1980)
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