| PDMP | D,L-threo-1-phenyl-2- decanoylamino-3-morpholino-1-propanol |
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| D-PIA | D-N6-(2-phenyl-isopropyl)adenosine |
| D-PDMP | D-Threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol |
| BIPM | N-(p(2-Benzimidazolyl)phenyl)maleimide |
| fMLP | N-formyl-methionine-leucine-phenyl-alanine |
| phenylketonuria | <disease> Congenital absence of phenylalanine hydroxylase (an enzyme that converts phenylalanine into tyrosine). Phenylalanine accumulates in blood and seriously impairs early neuronal development. The defect can be controlled by diet and is not serious if treated in this way. Incidence: highest in Caucasians. Acronym: PKU Origin: Gr. Ouron = urine (15 Oct 1997) |
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| phenylketonuria, maternal | Phenylketonuria in a pregnant woman. The maternal disease puts the foetus at great risk of mental retardation and other congenital diseases. (12 Dec 1998) |
| phenyllactic acid | C6H5CH2CHOH==COOH;a product of phenylalanine catabolism, appearing prominently in the urine in individuals with phenylketonuria. (05 Mar 2000) |
| phenylmercuric acetate | <chemical> A phenyl mercury compound used mainly as a fungicide. Has also been used as a herbicide, slimicide, and bacteriocide. Pharmacological action: fungicides, industrial, pharmaceutic aid. Chemical name: Mercury, (acetato-O)phenyl- (12 Dec 1998) |
| phenylmercuric nitrate | Basic phenylmercuric nitrate;a mixture of phenylmercuric nitrate and phenylmercuric hydroxide; an antiseptic used for the prophylactic disinfection of the intact skin or of minor wounds. (05 Mar 2000) |
| phenylmercury compounds | <chemical> Organic mercury compounds in which the mercury is attached to a phenyl group. Often used as fungicides and seed treatment agents. Pharmacological action: fungicides, industrial. (12 Dec 1998) |
| phenylmethylsulfonyl fluoride | <chemical> Alpha-toluenesulfonyl fluoride. An enzyme inhibitor that inactivates irc-50 arvin, subtilisin, and the fatty acid synthetase complex. Pharmacological action: enzyme inhibitors, protease inhibitors. Chemical name: Benzenemethanesulfonyl fluoride (12 Dec 1998) |
| phenylpropanolamine | <chemical> A sympathomimetic that acts mainly by causing release of norepinephrine but also has direct agonist activity at some adrenergic receptors. It is most commonly used as a nasal vasoconstrictor and an appetite depressant. Pharmacological action: adrenergic alpha-agonists, adrenergic agents, appetite depressants, nasal decongestants, sympathomimetic. Chemical name: Benzenemethanol, alpha-(1-aminoethyl)-, (R*,S*)-(+-)- (12 Dec 1998) |
| phenylpyruvate oligophrenia | <disease> Congenital absence of phenylalanine hydroxylase (an enzyme that converts phenylalanine into tyrosine). Phenylalanine accumulates in blood and seriously impairs early neuronal development. The defect can be controlled by diet and is not serious if treated in this way. Incidence: highest in Caucasians. Acronym: PKU Origin: Gr. Ouron = urine (15 Oct 1997) |
| phenylpyruvate oxidase | <enzyme> Phenylpyruvate is converted to o-hydroxyphenyl-acetic acid Registry number: EC 1.- (26 Jun 1999) |
| phenylpyruvic acid | C6H5-CH2COCOOH;the transaminated product of the action of phenylalanine aminotransferase; elevated in the urine in individuals with phenylketonuria. (05 Mar 2000) |
| phenylpyruvic acids | A group of compounds that are derivatives of phenylpyruvic acid which has the general formula c6h5ch2cocooh, and is a metabolite of phenylalanine. (12 Dec 1998) |
| phenylpyruvic amentia | Amentia accompanied by the appearance of phenylpyruvate in the urine. (05 Mar 2000) |
| phenylthiazolylthiourea | <chemical> 1-phenyl-3-(2-thiazolyl)-2-thiourea. A dopamine-beta-hydroxylase inhibitor. Synonym: u-14,624. Chemical name: Thiourea, N-phenyl-N'-2-thiazolyl- (12 Dec 1998) |
| phenylthiocarbamide | <chemical> Chemical name: Thiourea, phenyl- (12 Dec 1998) |
Synonyms :
Synonyms :
Synonyms : L-Phenylisopropyladenosine, N(6)-Phenylisopropyl-Adenosine, L Phenylisopropyladenosine
Synonyms : Maternal Phenylketonuria, PKU, Maternal, Phenylalanine-Hydroxylase Deficiency Disease, Maternal, Phenylketonuria, Pregnancy in, Phenylketonurias, Pregnancy in, Pregnancy in Phenylketonurias, in Phenylketonuria, Pregnancy, in Phenylketonurias, Pregnancy
Synonyms : Deficiency Disease, Dihydropteridine Reductase, Deficiency Disease, Phenylalanine Hydroxylase, Deficiency Disease, Phenylalanine Hydroxylase, Severe, Folling Disease, Folling's Disease, Hyperphenylalaninaemia, Phenylketonuria, Phenylketonuria I
| phenylketonuria |
an inherited disease in which the body cannot metabolize a protein called phenylalanine. phototherapy - special lights used to treat jaundice. port wine stain - a flat, pink, red, or purple colored birthmark.
출처: www.chw.org/display/PPF/DocID/3336/router.asp
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| phenylketonuria |
A genetic disorder in which the body cannot break down the amino acid phenylalanine; abbreviated PKU.
출처: www.nigms.nih.gov/news/science_ed/chemhealth/gloss...
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| phenylketonuria |
Category: Baby's health A genetic liver enzyme disorder that may be regulated by a careful diet. In the US, all babies are screened for PKU at birth. Women with an inborn error of body chemistry called phenylketonuria (PKU) also are at high risk of having a baby with a heart defect Find out more about Phenylketonuria: Articles | Books/products
출처: pregnancyandbaby.com/read/articles/2455.htm
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| phenylpropanolamine |
A decongestant and appetite suppressant.
출처: www.third-plateau.org/faq/dxm_glossary.shtml
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| phenylketonuria |
A disease in which the enzyme that metabolizes the amino acid phenylalanine is not expressed, resulting in abnormally high levels of phenylalanine. If left untreated, PKU can lead to severe, progressive mental retardation.
출처: www.knowledgene.com/public/glossary_content.php3
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