>>Signaling Pathways>> Metabolism>> Inborn Errors of Metabolism>>N-(3-Phenylpropionyl)glycine

N-(3-Phenylpropionyl)glycine

Catalog No.GC49246

An acylglycine

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N-(3-Phenylpropionyl)glycine Chemical Structure

Cas No.: 56613-60-6

Size 가격 재고 수량
50 mg
US$37.00
재고 있음
100 mg
US$61.00
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250 mg
US$139.00
재고 있음
500 mg
US$205.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

N-(3-Phenylpropionyl)glycine is an acylglycine.1 Urinary levels of N-(3-phenylpropionyl)glycine are increased in patients with medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, an inborn error of metabolism characterized by intolerance to fasting, episodic vomiting, hypoketotic hypoglycemia, and dicarboxylic aciduria.

1.Rinaldo, P., O’Shea, J.J., Coates, P.M., et al.Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycineN. Engl. J. Med.319(20)1308-1313(1988)

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