N-(3-Phenylpropionyl)glycine
CAS No. 56613-60-6
N-(3-Phenylpropionyl)glycine ( Phenylpropionylglycine )
Catalog No. M20154 CAS No. 56613-60-6
N-(3-Phenylpropionyl)glycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However the excretion of certain acyl glycines is increased in several inborn errors of metabolism.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
10MG | 30 | Get Quote |
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25MG | 45 | Get Quote |
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100MG | Get Quote | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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Biological Information
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Product NameN-(3-Phenylpropionyl)glycine
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NoteResearch use only not for human use.
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Brief DescriptionN-(3-Phenylpropionyl)glycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However the excretion of certain acyl glycines is increased in several inborn errors of metabolism.
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DescriptionN-(3-Phenylpropionyl)glycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However the excretion of certain acyl glycines is increased in several inborn errors of metabolism. Acyl glycines are produced through the action of glycine N-acyltransferase which is an enzyme that catalyzes the chemical reaction:acyl-CoA + glycine < -- > CoA + N-acylglycineThe detection of phenylpropionylglycine in urine after an oral load of phenylpropionic acid can be used to diagnose deficiency of medium-chain acyl-CoA dehydrogenase a frequent and treatable metabolic defect.
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SynonymsPhenylpropionylglycine
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number56613-60-6
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Formula Weight207.22
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Molecular FormulaC11H13NO3
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESOC(=O)CNCCC(=O)c1ccccc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Flath B et al. Simple high-performance liquid chromatographic method for the detection of phenylpropionylglycine in urine as a diagnostic tool in inherited medium-chain acyl-coenzyme A dehydrogenase deficiency. J Chromatogr B Biomed Sci Appl. 1997 Jun 20;694(1):227-32.
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