| MPTP | 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine |
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| NMPTP | N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine |
| Ph | pharmacopeia; phenyl; Philadelphia [chromosome]; phosphate |
| PIH | periventricular-intraventricular hemorrhage; phenyl isopropylhydrazine; pregnancy-induced hypertensi... |
| PLA | peripheral laser angioplasty; phenyl lactate; phospholipase A; phospholipid antibody; placebo therap... |
| phenylethanolamine n-methyltransferase | <enzyme> A methyltransferase that catalyses the reaction of s-adenosyl-l-methionine and phenylethanolamine to yield s-adenosyl-l-homocysteine and n-methylphenylethanolamine. It can act on various phenylethanolamines and converts norepinephrine into epinephrine. Chemical name: S-Adenosyl-L-methionine:phenylethanolamine N-methyltransferase Registry number: EC 2.1.1.28 (12 Dec 1998) |
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| phenylethyl alcohol | <chemical> An antimicrobial, antiseptic, and disinfectant that is used also as an aromatic essence and preservative in pharmaceutics and perfumery. Pharmacological action: anti-infective agents, local, disinfectants, preservatives, pharmaceutical. Chemical name: Benzeneethanol (12 Dec 1998) |
| phenylethylamine oxidase | <enzyme> Contains a quinone cofactor, possibly topa quinone; isolated from arthrobacter globiformis; genbank u03517 Registry number: EC 1.4.3.- (26 Jun 1999) |
| phenylethylbarbituric acid | <chemical> A barbiturate used as a sedative and an anticonvulsant. It was used as an anti-anxiety agent but has been supplanted by benzodiazepines for that purpose. It may also be useful in the treatment of neonatal hyperbilirubinaemia and in the symptomatic treatment of opiate withdrawal in mothers and infants. Pharmacological action: anticonvulsants, gaba modulators, sedatives, barbiturate. Chemical name: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-phenyl- (12 Dec 1998) |
| phenylethylmalonamide | <chemical> 2-ethyl-2-phenylmalonamide. A metabolite of primidone. Chemical name: Propanediamide, 2-ethyl-2-phenyl- (12 Dec 1998) |
| phenylethylmalonylurea | <chemical> A barbiturate used as a sedative and an anticonvulsant. It was used as an anti-anxiety agent but has been supplanted by benzodiazepines for that purpose. It may also be useful in the treatment of neonatal hyperbilirubinaemia and in the symptomatic treatment of opiate withdrawal in mothers and infants. Pharmacological action: anticonvulsants, gaba modulators, sedatives, barbiturate. Chemical name: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-phenyl- (12 Dec 1998) |
| phenylglycolic acid | C6H5CHOHCOOH;a urinary antibacterial agent (both bactericidal and bacteriostatic). Synonym: hydroxytoluic acid, phenylglycolic acid. Origin: Ger. Mandel, almond (05 Mar 2000) |
| phenylglyoxal | <chemical> Alpha-oxo-benzeneacetaldehyde. A reagent that is highly selective for the modification of arginyl residues. It is used to selectively inhibit various enzymes and acts as an energy transfer inhibitor in photophosphorylation. Pharmacological action: enzyme inhibitors, indicators and reagents. Chemical name: Benzeneacetaldehyde, alpha-oxo- (12 Dec 1998) |
| phenylglyoxylate - acceptor oxidoreductase | <enzyme> Requires coenzyme a; converts phenylglyoxylate to benzoyl-CoA with release of co2 Registry number: EC 1.2.99.- Synonym: phenylglyoxylate oxidoreductase (acylating) (26 Jun 1999) |
| phenylhydrazine haemolysis | An in vitro test for G6PD deficiency; haemolysis resulting from in vitro addition of phenylhydrazine to blood with red cells which are deficient in glucose-6-phosphate dehydrogenase (G6PD), with the appearance of Heinz-Ehrlich bodies. (05 Mar 2000) |
| phenylhydrazines | Diazo derivatives of aniline, used as a reagent for sugars, ketones, and aldehydes. (12 Dec 1998) |
| phenylic | <chemistry> Pertaining to, derived from, or containing, phenyl. <chemistry> Phenylic alcohol, phenol. Source: Websters Dictionary (01 Mar 1998) |
| phenylindanedione | <chemical> An indandione that has been used as an anticoagulant. Phenindione has actions similar to warfarin, but it is now rarely employed because of its higer incidence of severe adverse effects. Pharmacological action: anticoagulant. Chemical name: 1H-Indene-1,3(2H)-dione, 2-phenyl- (12 Dec 1998) |
| phenylisopropyladenosine | <chemical> N-isopropyl-n-phenyl-adenosine. Antilipaemic agent. Synonym: th 162. Chemical name: Adenosine, N-(1-methylethyl)-N-phenyl- (12 Dec 1998) |
| phenylisothiocyanate | C6H5-N==C==S, a reagent that condenses with the free N-terminal amino group of a peptide chain to form a phenylthiohydantoin in the Edman method of identifying N-terminal amino acids. Synonym: Edman's reagent. Acronym: PITC (05 Mar 2000) |
Synonyms :
Synonyms : (R)-3-Hydroxy-alpha-((methylamino)methyl)benzenemethanol, Metaoxedrin, Metasympatol, Mezaton, Neo-Synephrine, Neosynephrine, Phenylephrine Hydrochloride, Phenylephrine Tannate, Neo Synephrine, Tannate, Phenylephrine
Synonyms : Noradrenalin N-Methyltransferase, Noradrenaline N-Methyltransferase, Norepinephrine Methyltransferase, Norepinephrine N-Methyltransferase, Methyltransferase, Norepinephrine, Noradrenalin N Methyltransferase, Noradrenaline N Methyltransferase
Synonyms : 2-Phenylethanol, beta-Phenylethanol, 2 Phenylethanol, Alcohol, Phenethyl, Alcohol, Phenylethyl, Carbinol, Benzyl, beta Phenylethanol
Synonyms : 2-Ethyl-2-Phenylmalonamide, 2 Ethyl 2 Phenylmalonamide
| phenylketonuria |
a hereditary disorder in which the enzyme that converts the amino acid phenylalanine into another amino acid is defective, meaning phenylalanine must be kept out of the diet
출처: www.american-depot.com/services/resources_gl_p.asp
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| phenylketonuria |
a disease that prevents the body from processing a specific part of protein called phenylalanine. The buildup of this substance in the body leads to mental retardation if the child does not have a special diet from birth.
출처: https://www.healthforums.com/library/1,1277,articl...
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| phenylketonuria |
A congenital condition in which the body lacks a specific enzyme. This causes abnormal metabolism that may result in brain damage.
출처: www.cnn.com/HEALTH/library/BN/00023.html
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| phenylketonuria |
An inherited disorder resulting in the inability to process the amino acid, phenylananine. If not treated, the disorder may result in mental retardation. Treatment is a diet low in phenylalanine. Newborns are screened for PKU, in order to determine the need for treatment before brain damage occurs.
출처: www.nutrabio.com/Definitions/definitions_p.htm
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| phenylketonuria |
an inherited (autosomal recessive) metabolic disorder, marked by the deficiency of the enzyme that converts phenylalanine (an amino acid) to tyrosine; accumulation of phenylalanine in the blood can lead to mental retardation and other neurologic problems; treatment includes a low-phenylalanine diet and a phenylalanine-free medical food
출처: depts.washington.edu/pwdlearn/web/glossary/glossar...
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