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345 Possible Causes for 4 azido N glycyl 2 nitro , L Phenylalanine

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  • Phenylalanine Increased

    Name L-Phenylalanine (phenylethylamine, phenethylamine) L-Phenylalanine and Cognitive Function L-Phenylalanine confers a number of positive effects on cognitive function,[] My Personal Experience With DLPA and L-Phenylalanine I have taken l-tyrosine, DLPA, and l-phenylalanine. I personally react better to l-phenylalanine.[] Abstract L-Phenylalanine (L-Phe) is an important amino acid used in both food and medicinal applications.[]

    Missing: 4 azido N glycyl 2 nitro
  • Melphalan

    4-(Bis(2-chloroethyl)amino)-L-phenylalanine p-N,N-bis(2-chloroethyl)amino-L-phenylalanine P-N-Bis(2-chloroethyl)amino-L-phenylalanine P-Di-(2-chloroethyl)amino-L-phenylalanine[] […] mustard p-N-Bis(2-chloroethyl)amino-L-phenylalanine Phenylalanine mustard p-L-Sarcolysin p-Bis(beta-chloroethyl)aminophenylalanine p-Di-(2-chloroethyl)amino-L-phenylalanine[] From Wikidata Jump to navigation Jump to search chemical compound Alkeran CB-3025 L-phenylalanine mustard (L-PAM) L-sarcolysine melfalan Sarcolysin Phenylalanine nitrogen[]

    Missing: 4 azido N glycyl 2 nitro
  • Hyperphenylalaninemia

    This case report concerns a female infant born in 1976 with a presumptive positive PKU screening test on the third day of life of 240 mumol/L phenylalanine.[] Transient expression of mutant full-length cDNAs in human HEK293 cells yielded PAH variants whose l-phenylalanine hydroxylase activity was between 40% and 70% that of the[] […] concentrations 360 μmol/L or all patients with phenylalanine concentrations 600 μmol/L require treatment.[]

    Missing: 4 azido N glycyl 2 nitro
  • Phenylketonuria

    Differential pulse voltammetry were used for the quantitative l-Phenylalanine detection.[] If blood phenylalanine exceeded the target range, the CGMP-AA dose was reduced and replaced with Phe-free L-amino acids. The control group remained on Phe-free L-AAs.[] Before hospitalization, all but 1 of the patients had blood phenylalanine levels above 1,000 mumol/L; in 1 patient the blood phenylalanine level was 703 mumol/L.[]

    Missing: 4 azido N glycyl 2 nitro
  • Dianhydrogalactitol

    Abstract The incidence of hyponatremia in 34 patients following administration of high-dose L-phenylalanine mustard (L-PAM) and dianhydrogalactitol (DAG) was determined.[] Only a combination of L-phenylalanine mustard and dianhydrogalactitol produced a limited response in both the patient and the mice.[]

    Missing: 4 azido N glycyl 2 nitro
  • Classical Phenylketonuria

    Abstract Phenylketonuria (PKU) is a metabolic disorder due primarily to mutations in the PAH gene that impair both phenylalanine hydroxylase activity and disposal of l-phenylalanine[] Abstract Treatment of phenylketonuria (PKU, OMIM 261600) means a diet restricted in natural protein and supplemented with phenylalanine (Phe)-free L-amino acid mixtures.[] It seems essential to initiate diet early, and to keep blood phenylalanine levels 600 mumol/L and well controlled to at least age 10 to ensure satisfactory long-term development[]

    Missing: 4 azido N glycyl 2 nitro
  • Atypical Phenylketonuria

    Lehman WD, Heinrich HC (1985) Oral versus intravenous l -phenylalanine loading compared by simultaneous application of l -[-2H5] and l -[-15N]phenylalanine.[] The patients with the classical or typical form of PKU have phenylalanine levels above 1200 μ mol/L due to hepatic phenylalanine hydroxylase residual activity μ mol/L and[] The central reaction, L-phenylalanine oxidation - an essential amino acid which is not produced by the organism - for L-tyrosine, a nonessential amino acid, It is catalyzed[]

    Missing: 4 azido N glycyl 2 nitro
  • Levodopa

    3,4-Dihydroxy-L-phenylalanine, 98 % MDL MFCD00002598 EINECS 200-445-2 Chemische Eigenschaften Formel C 9 H 1 1 NO 4 Molmasse 197.19 Schmelzpunkt ca 295 dec.[] Levodopum β-(3,4-dihydroxyphenyl)alanine L-beta-(3,4-Dihydroxyphenyl)alanine 3,4-Dihydroxy-L-phenylalanine ( )-3-(3,4-dihydroxyphenyl)-L-alanine ( )-dopa Dihydroxy-L-phenylalanine[] , 3-hydroxy-; Alanine, 3-(3,4-dihydroxyphenyl)-, L-; β-(3,4-Dihydroxyphenyl)-L-alanine; β-(3,4-Dihydroxyphenyl)alanine; (-)-(3,4-Dihydroxyphenyl)alanine; (-)-Dopa; Dihydroxy-L-phenylalanine[]

    Missing: 4 azido N glycyl 2 nitro
  • Disorder of Catecholamine Synthesis

    ) 7-Tetrahydropterin 4-Chloro-DL-phenylalanine ( C6506 ) 4-Chloro-L-phenylalanine ( C8655 ) L-Tyrosine ( T2006 ) –––––––––––– Tyrosine-3-hydroxylase Oxygen Tetrahydrobiopterin[] Enzyme or Protein Biochemistry Syndromes Phenylalanine hydroxylase L-phenylalanine to L-tyrosine Phenylketonuria Tyrosine hydroxylase L-tyrosine to L-DOPA L-DOPA responsive[] Chem. 332, 1963 McGilvery, R.W., Cohen, P.P.; ''The decarboxylation of L-phenylalanine by Streptococcus faecalis R.''; J. Biol.[]

    Missing: 4 azido N glycyl 2 nitro
  • Tyrosine Increased

    For people with phenylketonuria who cannot synthesize L-Tyrosine from L-Phenylalanine, L-Tyrosine is an essential amino acid.[] L-tyrosine is created when its precursor amino acid, phenylalanine, is metabolized in the liver.[] The brain uses the amino acid l-phenylalanine as the source (precursor) for the production of dopamine.[]

    Missing: 4 azido N glycyl 2 nitro

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