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"acid number"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • hydroxyindoleacetic acid
    È÷µå·Ï½ÃÀε¹¾Æ¼¼Æ®»ê
  • isothiocyanic acid
    ÀÌ¼ÒÆ¼¿À½Ã¾È»ê
  • inosinic acid
    À̳ë½Å»ê
  • ketonic acid
    ÄÉÅæ»ê
  • lauric acid
    ·Î¸£»ê
  • leuconic acid
    ·ùÄÜ»ê
  • lichenic acid
    ÁöÀÇ»ê
  • linoleic acid
    ¸®³î·¹»ê
  • linolenic acid
    ¸®³î·»»ê
  • linolic acid
    ¸®³î»ê
  • lipoic acid
    ¸®Æ÷»ê
  • lactic acid
    Á¥»ê
  • mixed acid
    È¥ÇÕ»ê
  • maleic acid
    ¸»·¹»ê
  • malic acid
    ¸»»ê
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  • ¿µ¹®
    ÇѱÛ
  • mucic acid
    ¹Â½Å»ê
  • muramic acid
    ¹Â¶ó¹Í»ê
  • mycolic acid
    ¹ÌÄÝ»ê
  • neuraminic acid
    ´º¶ó¹Î»ê
  • neurostearic acid
    ½Å°æÁö¹æ»ê
  • nicotinic acid
    ´ÏÄÚÆ¾»ê
  • nitric acid
    Áú»ê
  • nitrobenzoic acid
    ³ªÀÌÆ®·Îº¥Á¨»ê
  • nitrohydrochloric acid
    Áú¿°»ê, ¿Õ¼ö
  • nitrous acid
    Áú»ê
  • normal fatty acid
    Ç¥ÁØÁö¹æ»ê
  • nucleic acid
    ÇÙ»ê
  • oleic acid
    ¿Ã·¹»ê
  • organic acid
    À¯±â»ê
  • oxalic acid
    ¿Á»ì»ê
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  • ¿µ¹®
    ÇѱÛ
  • amino acid sequence
    ¾Æ¹Ì³ë»ê ¼­¿­.
  • aminoacetic acid<³ª> acidum aminoaceticum
    ¾Æ¹Ì³ë¾Æ¼¼Æ®»ê.
  • aminohippuric acid
    ¾Æ¹Ì³ë ¸¶´¢»ê
  • anaphylaxis,arachidonic acid metabolitesin
    ¾Æ¶ó۵·»ê ´ë»ç¹°Áú(¡­ß« ÓÛÞóÚªòõ)
  • anthranilic acid
    ¾ÈÆ®¶ó´Ò»ê.
  • apoascorbic acid
    ¾ÆÆ÷¾Æ½ºÄÚ¸£ºó»ê.
  • arachidonic acid
    ¾Æ¶ó۵·»ê
  • arachidonic acid
    ¾Æ¶ó۵·»ê(¡­ß«)
  • arachidonic acid metabolism
    ¾Æ¶ó۵·»ê´ë»ç
  • arachidonic acid metabolites
    ¾Æ¶ó۵·»ê ´ë»ç¹°Áú(¡­ÓÛÞóÚªòõ)
  • arginine-glycine-aspartic acid
    Arginine-glycine-aspartic acid
  • aromatic amino acid
    ¹æÇâÁ·¾Æ¹Ì³ë»ê.
  • arormatic amino acid
    ¹æÇâÁ·¾Æ¹Ì³ë»ê
  • arsenic acid
    ºñ»ê(Ý÷ß«).
  • arsenoacetic acid
    ¾Æ¸£¼¼³ë¾Æ¼¼Æ®»ê.
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  • ¿µ¹®
    ÇѱÛ
  • adenylic acid deaminase
    ¾Æµ¥´Ò»ê Å»¾Æ¹Ì³ëÈ¿¼Ò.
  • aliphatic acid
    Áö¹æÁ·»ê(ò·Û¸ðéß«).
  • aliphatic amino acid
    Áö¹æÁ·¾Æ¹Ì³ë»ê
  • allokainic acid
    ¾Ë·ÎÄ«Àλê(¡­ß«).
  • aloetic acid
    ¾Ë·Î¿¡Æ¾»ê.
  • alpha-amino acid nitrogen
    ¾ËÆÄ-¾Æ¹Ì³ë»êÁú¼Ò
  • alpha1-acid glycoprotein
    ¾ËÆÄ-»ê´ç´Ü¹é
  • amino acid
    ¾Æ¹Ì³ë»ê
  • amino acid analyzer
    ¾Æ¹Ì³ë»êºÐ¼®±â
  • amino acid determination
    ¾Æ¹Ì³ë»ê°áÁ¤(̽ïÒ)
  • amino acid pattern
    ¾Æ¹Ì³ë»êÇüÅÂ
  • amino acid sequence
    ¾Æ¹Ì³ë»ê ¼­¿­.
  • aminoacetic acid<³ª> acidum aminoaceticum
    ¾Æ¹Ì³ë¾Æ¼¼Æ®»ê.
  • aminohippuric acid
    ¾Æ¹Ì³ë ¸¶´¢»ê
  • anaphylaxis,arachidonic acid metabolitesin
    ¾Æ¶ó۵·»ê ´ë»ç¹°Áú(¡­ß« ÓÛÞóÚªòõ)
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  • ¿µ¹®
    ÇѱÛ
  • choleic acid
    ÄÝ·¹»ê(ß«)
  • cholic acid
    ÄÝ»ê(ß«)
  • chorismic acid
    ÄÚ¸®½¿»ê(ß«)
  • citric acid
    ½ÃÆ®¸£»ê(ß«)
  • citric acid cycle
    ½ÃÆ®¸£»êȸ·Î(ß«üÞÖØ)
  • concerted acid-base catalysis
    Çùµ¿ »ê¿°±â Ã˸Å(úðÔÒß«ç¤ÐñõºØÚ)
  • conjugate acid-base pair
    ¦ÁöÀº »ê¿°±â½Ö(ß«ç¤Ðñäª)
  • conservative amino acid replacement
    "º¸Á¸¼º(ÜÁðíàõ) ¾Æ¹Ì³ë»ê ´ëÄ¡(ÓÛöÇ), (ÔÒ) conservative substitution"
  • cortoic acid
    ÄÚ¸£Æ¼¼Ö»ê(ß«)
  • cyclic adenylic acid °í¸® ¾Æµ¥´Ñ»ê(ß«)
    "(ÔÒ)(ÔÒ) adenosine-3',5'-cyclic monophosphate,"
  • cysteic acid
    ½Ã½ºÅ×ÀÎ »ê(ß«)
  • cytidylic acid
    »çÀÌÆ¼µò »ê(ß«)
  • acid dihydrouridine.
    dalton
  • dansyl amino acid
    ´í½Ç ¾Æ¹Ì³ë»ê(ß«)
  • dehydroascorbic acid
    Å»¼ö¼Ò(÷­â©áÈ)¾Æ½ºÄÚ¸£ºó»ê(ß«)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
NR do not repeat [Lat. non repetatur]; nerve root; neural retina; neutral red; noise reduction; nonreac...
NR Reynold's number
NSA Neurological Society of America; normal serum albumin; no salt added; no significant abnormality; no...
NUI number user identification
numc number concentration
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
12-H(P)ETE 12-hydro(pero)xy-eicosatetraenoic acid
HHT 12-Hydroxyheptadecatrienoic acid
BMIPP 123)I-beta-methyl-p-iodophenylpentadecanoic acid
13-cis-RA 13 cis retinoic acid
13-HPODE 13(S)-hydroperoxyoctadecadienoic acid
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • lysergic acid
    ¸®À縣±×»ê
    ¸Æ°¢ ¾ËÄ®·ÎÀ̵åÀÇ ¸ðü·Î, ±× À̼ºÃ¼ÀÎ ÀÌ¼Ò ¸®Á¦¸£±×»ê°ú ÇÔ²² Æ®¸®ÆéƼµå ¶Ç´Â ¾Æ¹Ì³ë ÇÁ·ÎÆÄ³î°ú °áÇÕÇÏ¿© ¸Æ°¢ ¾ËÄ®·ÎÀ̵å·ù¸¦ Çü¼ºÇÑ´Ù.
  • lyxonic acid
    ¸¯¼Õ»ê
  • maleic acid
    ¸»·¹»ê, ¸»·¹Àλê
    ºÒÆ÷È­ ÀÌ¿°±â»ê.
  • malic acid
    ´É±Ý»ê
    µ¿ÀǾî=hydroxysuccinic acid. Æ®¶óÀÌÄ«¸£º¹½Ç»ê ȸ·ÎÀÇ Áß°£ ¹°Áú. ´ú ÀÍ°í ½Å »ç°ú¿Í ´Ù¸¥ ¸¹Àº °ú½Ç ¼Ó¿¡ µé¾îÀÖ´Ù. ±«Ç÷º´ÀÇ Ä¡·á¿¡ »ç¿ëµÇ±âµµ ÇÑ´Ù.
  • malonic acid
    ¸»·Ð»ê
    °áÁ¤¼ºÀÇ ÀÌ¿°±â»ê.
  • meclofenamic acid
    ¸ÞŬ·ÎÆä³ª¹Ìµå»ê
    °ñ°üÀý¿° ¹× ·ù¸¶ÅäÀÌµå °üÀý¿°ÀÇ Ä¡·á¿¡ meclofenamate sodiumÀ¸·Î »ç¿ëµÈ´Ù.
  • meconic acid
    ¸ÞÄÜ»ê
    ¹é»ö °áÁ¤¼º »ê.
  • mefenamic acid
    ¸ÞÆä³²»ê
    °áÁ¤¼º ºÐ¸», ÇÔ¿°ÁõÁ¦.
  • messenger ribonucleic acid
    Àü·É RNA
  • metabolic defect of amino acid
    ¾Æ¹Ì³ë»ê ´ë»ç °áÇÔ
    ¾Ëİſ ´¢Áõ.
  • metaphosphoric acid
    ¸ÞŸÀλê
    ÀλêÀÇ Çϳª. Çü»óÀ¸·Î º¸¾Æ À¯¸®»ó ÀÎ»ê ¶Ç´Â ºù»ó ÀλêÀ̶ó°íµµ ÇÑ´Ù. È­ÇÐ½Ä HPO. ¹Ì»ý¹°, °ïÃæ·ù ¶Ç´Â ¾î¶² Á¾·ùÀÇ µ¿¹°ÀÇ Á¶Á÷ µî¿¡ Á¸ÀçÇÑ´Ù. ¹«»ö Åõ¸íÇÑ À¯¸®»ó °íü ¶Ç´Â ºÎµå·¯¿î ºñ´Ü½Ç ¸ð¾çÀÇ ±«»ó ¹°Áú·Î, ºÐÀÚ·® 79.98, ºñÁß 2.2ÀÌ´Ù. Á¶ÇؼºÀ̸ç, ½ÀÇÑ °ø±â ¼Ó¿¡ ¹æÄ¡ÇÏ¸é ¿À¸£Åä Àλê HPO°¡ µÈ´Ù. ¹°, ¿¡Åº¿Ã¿¡ Àß ³ì´Â´Ù. °¡¿­ÇÏ¸é ¿ëÀ¶ÇÏ¿© Á¡¼ºµµ°¡ Áõ°¡ÇÏ°í ´õ¿í °¡¿­ÇÏ¸é ½ÂÈ­ÇÑ´Ù. ¼ö¿ë¾× ¼Ó¿¡¼­´Â ÁßÇÕü¸¦ Àß ¸¸µé°í, °£´ÜÇÑ °Íµµ »ïÇÕü³ª »çÇÕü°¡ µÇÁö¸¸, Àå½Ã°£ ¹æÄ¡ÇÏ¸é ¿À¸£ÅäÀλêÀ¸·Î º¯ÇÑ´Ù. ¸ÞŸÀÎ»ê ¿ë¾×¿¡ Áú»ê Àº ¿ë¾×À» °¡ÇÏ¸é ¹é»ö ħÀüÀÌ »ý±ä´Ù. ¸ÞŸÀλêÀº ¿À¸£ÅäÀÎ»ê ¶Ç´Â ÇÇ·ÎÀλê HPOÀ» 300 ¡É ÀÌ»óÀ¸·Î °¡¿­ÇÏ¸é »ý±ä´Ù. 2HPO 2j HPO+HO HPO 2j 2HPO+HO ¶Ç ¿À»êÈ­ÀÎÀ» 0 ¡É ÀÌÇÏ·Î ¼öÈ­ÇØµµ ¾ò´Â´Ù. Ä¡°ú¿ë ½Ã¸àÆ® , È­Çкм®¿ë ½Ã¾à, º¸ÀÏ·¯ ûÁ¤Á¦, ÀμâÁ¦ÆÇ, °¡Á×ÀÇ ¹«µÎÁú µî¿¡ ¾²À̸ç, Ä®·ý¿°Àº À¯Á¦Ç°ÀÇ Á¡¼ºµµ Áõ°¡Á¦, ¼¼Á¦, ÇÜ, ¼Ò½ÃÁöÀÇ Ã·°¡Á¦·Î »ç¿ëµÈ´Ù. ¶ÇÇÑ, ¸ÞŸÀλêÀº »ý¹°ÇлóÀ¸·Îµµ ¸Å¿ì Èï¹Ì·Î¿î ¼ºÁúÀ» °¡Áö°í Àִµ¥, È¿¸ð¿¡¼­´Â ÇÙ»êÀÇ ÇÕ¼º¿¡ ÇÊ¿äÇÑ Àΰú ¿¡³ÊÁö¸¦ ¸ÞŸÀλêÀÌ °ø±ÞÇÏ´Â °ÍÀ¸·Î »ý°¢µÈ´Ù.
  • methacrylic acid
    ¸ÞŸ ¾ÆÅ©¸¯ »ê
  • morrhuate sodium : °£À¯ÀÇ Áö¹æ»ê ³ªÆ®·ý¿°. °æÈ­Á¦·Î¼­ ƯÈ÷ Á¤¸Æ·ù ¹× Ä¡ÁúÀÇ Ä¡·á¿¡ »ç¿ëµÇ¸ç Á¤¸Æ·ù ³»·Î ¿ë¾×À» ÁÖ»çÇÑ´Ù.

    morrhuic acid

    ¸ð·çÀλê
  • mucosal barrier to acid back-diffusion

    mucosal bleeding (Á¡¸· ÃâÇ÷

  • mycolic acid
    ¹ÌÄÝ»ê.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
aldaric acid One of a group of sugar acids characterised by the formula HOOC-(CHOH)n-COOH; e.g., saccharic acid.
(05 Mar 2000)
aldehydic acid <biochemistry> Dicarboxylic acids in which one of the carboxyl groups (-cooh) has been replaced by an aldehyde group (-cho).
(12 Dec 1998)
aldobiuronic acid Condensation products of an aldose and a uronic acid; such groupings occur among the components of various mucopolysaccharides, notably hyaluronic acid.
(05 Mar 2000)
allantoic acid Diureidoacetic acid;a degradation product of allantoin.
(05 Mar 2000)
allodeoxycholic acid 3a,12alpha-dihydroxy-5alpha-cholan-24-oic acid, one of the bile acids.
(05 Mar 2000)
allomaleic acid Trans-Butanedioic acid;an unsaturated dicarboxylic acid occurring as an intermediate in the tricarboxylic acid cycle.
Synonym: allomaleic acid.
(05 Mar 2000)
allophanic acid NH2CONHCOOH; urea carbonic acid;its amide is biuret (allophanamide).
Synonym: carbamoylcarbamic acid, N-carboxyurea.
(05 Mar 2000)
alpha-acetolactic acid An intermediate in pyruvic acid catabolism and valine biosynthesis; CH3COC(OH)(CH3)-COOH.
(05 Mar 2000)
alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid <chemical> Alpha-amino-2,3-dihydro-5-methyl-3-oxo-4-isoxazolepropanoic acid. An ibotenic acid homolog and glutamate agonist. The compound is the defining agonist for the ampa subtype of glutamate receptors (receptors, ampa). It has been used as a radionuclide imaging agent but is more commonly used as an experimental tool in cell biological studies.
Pharmacological action: excitatory amino acid agonists.
Chemical name: 4-Isoxazolepropanoic acid, alpha-amino-2,3-dihydro-5-methyl-3-oxo-
(12 Dec 1998)
alpha-amino acid Typically, an amino acid of the general formula R-CHNH2-COOH (i.e., the NH2 in the a position); the l forms of these are the hydrolysis products of proteins. In rarer usages, this class of molecules also includes alpha-amino phosphoric acids and alpha-aminosulfonic acids.
(05 Mar 2000)
alpha-amino acid esterase <enzyme> Converts alpha-amino acid esters and water to alpha-amino acids and alcohol
Registry number: EC 3.1.1.43
Synonym: alpha-amino acid ester hydrolase
(26 Jun 1999)
alpha-aminoadipic acid 2-amino-1,6-hexanedioic acid;an intermediate of lysine biosynthesis in higher fungi and bacteria, but not in algae and higher plants. Also in degradation of lysine in mammals.
(05 Mar 2000)
alpha-amino-beta-ketoadipic acid 2-Amino-3-oxo-1,6-hexanedioic acid;an intermediate of porphobilinogen synthesis formed by d-aminolevulinic acid synthase from succinyl-CoA and glycine; it rapidly decarboxylates to d-aminolevulinic acid.
(05 Mar 2000)
alpha-aminoglutaric acid <amino acid> One of the 20 _ amino acids commonly found in proteins. Plays a central role in amino acid metabolism, acting as precursor of glutamine, proline and arginine. Also acts as amino group donor in synthesis by transamination of alanine from pyruvate and aspartic acid from oxaloacetate. Glutamate is also a neurotransmitter, the product of its decarboxylation is the inhibitory neurotransmitter amino butyrate (GABA).
(18 Nov 1997)
alpha-aminoisobutyric acid 2-amino-2-methylpropionic acid;a synthetic amino acid useful in the study of amino acid transport across cell membranes and in the study of cytokine effects; it is not metabolised by the cell.
(05 Mar 2000)
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  • ¿µ¹®
    ÇѱÛ
  • palmitic acid
    ÆÈ¹Ìƾ»ê
  • pantothenic acid
    ÆÇÅäÅÙ»ê;ºñŸ¹Î B º¹ÇÕüÀÇ Çϳª
  • paraaminobenzoic acid
    ÆÄ¶ó¾Æ¹Ì³ë ¾È½ÄÇâ»ê(ºñŸ¹Î Bº¹ÇÕüÀÇ Çϳª)
  • perchloric acid
    °ú¿°¼Ò»ê
  • periodic acid
    °ú¿Á¼Ò»ê
  • permanganic acid
    Åõ°ú¼º;Åõ¼ö¼º;ÅõÀÚÀ²;µµÀÚÀ²;»ïÃâ·®
  • phosphoric acid
    ¾ÆÀλê
  • picric acid
    ÇÇÅ©¸°»ê
  • polyadenylic acid
    Æú¸®¾Æµ¥´Ò»ê
  • propionic acid
    ÇÁ·ÎÇǿ»ê(°õÆÎÀÌ ¹æÁö ¿ëÀ¸·Î »§À» ¾¸)
  • prussic acid
    û»ê
  • pyruvic acid
    ÇÇ·çºê»ê
  • racemic acid
    ¶ó¼¼¹Ì(Æ÷µµ)»ê
  • ribonucleic acid
    ¸®º¸ ÇÙ»ê(RNA)
  • siliic acid n,
    ±Ô»ê
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
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    ±¸ºÐ/º¸Çè±Þ¿©
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