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"glutamic acid dehydrogenase"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
  • ¿µ¹®
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  • isometric coefficient of lactic acid
    ¶ôÆ®»ê µî¿ë°è¼ö(¡­ß«Ôõé»Ìõâ¦).
  • isonicotinic acid hydrazide
    À̼ҴÏÄÚÆ¾»êÈ÷µå¶óÁöµå.
  • isothiocyanic acid
    ¾ÆÀÌ¼ÒÆ¼¿À½Ã¾È»ê.
  • ketoadipic acid
    ÄÉÅ侯µðÇÉ»ê(¡­ß«).
  • ketobutyric acid
    ÄÉÅäºÎƼ¸£»ê(¡­ß«).
  • ketonic acid
    ÄÉÅæ»ê(¡­ß«).
  • kinotannic acid
    Ű³ëź´Ñ»ê(¡­ß«).
  • kynurenic acid
    Ű´©·»»ê(¡­ß«).
  • laccainic acid
    ¶óÄ«Àλê(¡­ß«).
  • lactic acid
    ¶ôÆ®»ê(¡­ß«), Á¥»ê, À¯»ê.
  • lactic acid
    À¯»ê
  • lactic acid bacterium
    ¶ôÆ®±Õ(¡­Ð¶).
  • lactic acid bacterium
    ¶ôÆ®±Õ(¡­Ð¶).
  • lactic acid formation
    À¯»êÇü¼º
  • lactic acid milk
    ¶ôÆ®À¯(¡­êá).
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  • primary bile acid
    ÀÏÂ÷ ´ãÁó»ê(ìéó­ÓÅñðß«)
  • prostanoic acid
    ÇÁ·Î½ºÅº»ê(ß«)
  • protonic acid
    ÇÁ·ÎÅæ»ê(ß«)
  • pseudouridylic acid
    ½´µµÀ¯¸®µô»ê(ß«)
  • PTC-amino acid
    PTC ¾Æ¹Ì³ë»ê(ß«)
  • pteroic acid
    Å׷λê(ß«)
  • pteroylglutamic acid
    Å×·ÎÀϱ۷玻ê(ß«)
  • PTH-amino acid
    PTH ¾Æ¹Ì³ë»ê(ß«)
  • pyroglutamic acid
    ÇǷα۷玻ê(ß«)
  • pyruvic acid
    ÆÄÀÌ·çºê»ê(ß«)
  • radical amino acid replacement
    ¶óµðÄ® ¾Æ¹Ì³ë»ê ġȯ(öÇüµ)
  • rare amino acid
    Èñ±Í(ýüÏþ) ¾Æ¹Ì³ë»ê
  • reductive carboxylic acid cycle
    ȯ¿ø¼º(ü½êªàõ) Ä«¸£º¹½Ç»ê(ß«) ȸ·Î(üÞÖØ)
  • reductive tricarboxylic acid cycle
    ȯ¿ø¼º(ü½êªàõ) Æ®¸®Ä«¸£º¹½Ç»ê(ß«) ȸ·Î(üÞÖØ)
  • resin acid
    ¼öÁö»ê(â§ò·ß«)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 19
MCAD medium chain acyl-CoA dehydrogenase
MD Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major...
MDH malate dehydrogenase; medullary dorsal horn
OGDH oxoglutarate dehydrogenase
OHSD hydroxysteroid dehydrogenase
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GLDH Glutamate dehydrogenase
G3PD Glyceraldehyde-3-phosphate dehydrogenase
G3PDH Glyceraldehyde-3-phosphate dehydrogenase
GPDH Glycero-3-phosphate dehydrogenase
G-3-PDH Glycerol-3-phosphate dehydrogenase
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 19
long-chain-acyl-CoA dehydrogenase <enzyme> Flavoprotein; forms with another flavoprotein plus EC 1.5.5.1 a system reducing ubiquinone and other acceptors
Registry number: EC 1.3.99.-
Synonym: lc-acyl-CoA dehydrogenase, long-chain-acyl-coenzyme a dehydrogenase, very-long-chain acyl-CoA dehydrogenase, vlcad
(26 Jun 1999)
long-chain-alcohol dehydrogenase <enzyme> Catalyses reversibly the oxidation of a long-chain alcohol in the presence of nad to a long-chain acid anion and NADH
Registry number: EC 1.1.1.192
Synonym: fatty alcohol-nad+ oxidoreductase
(26 Jun 1999)
L-sorbosone dehydrogenase <enzyme> Converts l-sorbosone to 2-keto-l-gulonic acid.
Registry number: EC 1.2.99.-
(26 Jun 1999)
LTDH short chain dehydrogenase <enzyme> Has been sequenced; responsible for methotrexate resistance; isolated from leishmania sp.
Registry number: EC 1.3.-
Synonym: ltdh gene product, pteridine reductase 1, ptr1 gene product, hmtx(r) gene product
(26 Jun 1999)
lysine epsilon-dehydrogenase <enzyme> From agrobacterium tumefaciens; forms alpha-aminoadipate delta-saemialdehyde which is spontaneously converted to delta 1-piperideine-6-carboxylate
Registry number: EC 1.4.1.-
Synonym: l-lysine epsilon-dehydrogenase
(26 Jun 1999)
a1-acid glycoprotein <biology> Plasma protein of mammals and birds, 38% carbohydrate. In humans a single chain glycoprotein of 39 kD. Increased levels are associated with inflammation, pregnancy and various diseases.
(18 Nov 1997)
abscisic acid <biochemistry> A lipid hormone that inhibits cell growth in plants, it is associated with fruit drop, leaf death and seed dormancy. It is synthesised in the plastids from carotenoids. This hormone helps plants deal with water loss, and its effects can be reversed with gibberellins.
(06 May 1997)
abscisic acid 8'-hydroxylase <enzyme> Catalyses conversion of abscisic acid to 8'-hydroxyabscisic acid, which rearranges to phaseic acid
Registry number: EC 1.14.99.-
Synonym: aba 8'-hydroxylase
(26 Jun 1999)
acetic acid <chemical> The acid most commonly associated with vinegar, it is the most commercially important organic acid and is used to manufacture a wide range of chemical products, such as plastics and Acetobacter but, except for making vinegar, is usually made through synthetic processes.
Derivatives of acetic acid which may be formed by substitution reactions. Mono- and di-substituted, as well as, halogenated compounds have been synthesised.
Experimentally, alpha- and n2- substituted acetic acids have been examined for their anti-inflammatory activity and effect on the central nervous system respectively. Additionally, limited exposure data has been collected on dibromo and dichloroacetic acids to determine whether they pose health effects.
Synonym: ethanoic acid.
(26 Jun 1999)
acetoacetic acid CH3COCH2COOH;one of the ketone bodies, formed in excess and appearing in the urine in starvation or diabetes.
Synonym: diacetic acid.
(05 Mar 2000)
acetohydroxamic acid C2H5NO2; N-Hydroxyacetamide;an inhibitor of urease, used as adjunctive therapy in chronic urea-splitting urinary infections.
(05 Mar 2000)
acetrizoic acid <chemical> A water-soluble, iodinated radiographic contrast medium, used as sodium acetrizoate in hysterosalpingography.
Pharmacological action: contrast media.
Chemical name: Benzoic acid, 3-(acetylamino)-2,4,6-triiodo-
(12 Dec 1998)
acetylsalicylic acid <drug> An odourless, white, slightly bitter drug used to reduce pain, fever, inflammation and sometimes to prevent blood clotting. Also called aspirin. Some people cannot tolerate it because it can cause stomach bleeding, however. It is soluble in both water and alcoholand melts at 132 to 136 degrees C.
(06 May 1997)
acetyltannic acid An astringent used for treatment of diarrhoea.
Synonym: diacetyltannic acid, tannylacetate.
(05 Mar 2000)
acid <chemical, chemistry> A fundamental category of many compounds whose water-based solutions have a sour taste, turn blue litmus paper red and can combine with metals to form salts.
They are chemical compounds which yield hydrogen ions or protons when dissolved in water, whose hydrogen can be replaced by metals or basic radicals, or which react with bases to form salts and water (neutralization).
An extension of the term includes substances dissolved in media other than water. Specific types of acids include:
Arrhenius acid: any chemical that increases the number of free hydrogen ions (H+) when added to a water-based solution. The more free hydrogens produced, the stronger the acid.
Bronsted or Bronsted-Lowry acid: any chemical that acts as a proton donor in a chemical reaction.
Lewis acid: any chemical that accepts two electrons to form a covalent bond during a chemical reaction.
(13 Nov 1997)
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