¼±Åà - È­»ìǥŰ/¿£ÅÍŰ ´Ý±â - ESC

 
"2"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 10 ÆäÀÌÁö: 4
2-APH 2-Amino-7-phosphonoheptanoic acid
2-APV 2-Amino-5-phosphonovalerate
2-BP 2-Bromopropane
2-CA 2-Chloroadenosine
2-CADO 2-Chloroadenosine
2-CdA 2-Chloro-2'-deoxyadenosine
2-Cl-ado 2-chloro adenosine
2-ClA 2-Chloro-adenosine
2-CP 2-chlorophenol
2-D 2) two-dimensional
KMLE ¾àǰ/ÀǾàǰ ¸ÂÃã °Ë»ö °á°ú : 14 ÆäÀÌÁö: 4
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
2,6-diisopropyl phenol <chemical> 2,6-bis(1-methylethyl)phenol. An intravenous anaesthetic and a sedative for patients in the intensive care unit or under regional anaesthesia. Induction of anaesthesia is rapid and maintenance can be achieved by either continuous infusion or intermittent bolus injection. Recovery from propofol is rapid and the patient is clear-headed with almost no hangover effect or nausea following administration.
Pharmacological action: anaesthetics, intravenous, free radical scavengers, sedatives, nonbarbiturate.
Chemical name: Phenol, 2,6-bis(1-methylethyl)-
(12 Dec 1998)
2,6-dioxo-6-phenylhexa-3-enoate hydrolase <enzyme> Cleaves the product of EC 1.13.11.39 to form benzoate plus 2-oxopent-4-enoate
Registry number: EC 3.7.1.8
Synonym: hpda hydrolase, bphd gene product, 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid hydrolase, hohpda hydrolase, 2-hydroxy-6-oxo-6-(2-hydroxyphenyl)-2,4-hexadienoate hydrolase, bphf gene product
(26 Jun 1999)
2,8-dihydroxyadenine An insoluble minor product of adenine catabolism that is elevated in individuals with an absence of adenine phosphoribosyltransferase.
(05 Mar 2000)
2-acetolactate mutase <enzyme> An enzyme involved in the biosynthesis of isoleucine and valine. It converts 2-acetolactate into 3-hydroxy-2-oxo-isovalerate. Also acts on 2-hydroxy-2-acetobutyrate to form 2-hydroxy-2-oxo-3-methylvalerate.
Chemical name: 2-Acetolactate methylmutase
Registry number: EC 5.4.99.3
(12 Dec 1998)
2-acetylaminofluorene <chemical> N-fluoren-2-yl-acetamide. A hepatic carcinogen whose mechanism of activation involves n-hydroxylation to the arylhydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide.
Pharmacological action: carcinogens.
Chemical name: Acetamide, N-9H-fluoren-2-yl-
(12 Dec 1998)
2-amino-2-deoxy-D-galactose <chemical> Chemical name: D-Galactose, 2-amino-2-deoxy-
(12 Dec 1998)
2-amino-5-phosphonovalerate <chemical> A potent and specific antagonist of nmda receptors (receptors, nmda) in the d-enantiomeric form. The l form is inactive at nmda receptors but may affect the ap4 (2-amino-4-phosphonobutyrate; apb) excitatory amino acid receptors.
Pharmacological action: excitatory amino acid antagonists.
Chemical name: Norvaline, 5-phosphono-
(12 Dec 1998)
2-aminoadipic acid <chemical> 2-aminohexanedioic acid. An amino acid isolated from vibrio cholera.
Chemical name: Hexanedioic acid, 2-amino-
(12 Dec 1998)
2-aminobenzoate coenzyme A ligase <enzyme> From a denitrifying pseudomonas sp.; catalyses the formation of CoA thioester of 2-aminobenzoate with the formation of AMP and pyrophosphate from ATP
Registry number: EC 6.2.1.-
Synonym: 2-ab CoA ligase
(26 Jun 1999)
2-aminobenzoyl-CoA monooxygenase-reductase <enzyme> Flavoenzyme; contains fad; mechanism not known
Registry number: EC 1.14.99.-
Synonym: ab-CoA monooxygenase-reductase, 2-aminobenzoyl-coenzyme a monooxygenase-reductase
(26 Jun 1999)
2-aminodansyltyrosine 55 colipase <chemical> Sensitive probe of solvent polarity and viscosity but not of pH
Pharmacological action: fluorescent dye
Synonym: dnstyr55pc
(26 Jun 1999)
2-aminodansyltyrosine 59 colipase <chemical> Sensitive probe of solvent polarity and viscosity but not of pH
Pharmacological action: fluorescent dye
Synonym: dnstyr59pc
(26 Jun 1999)
2-aminoethanol A viscous, hygroscopic amino alcohol with an ammoniacal odour. It is widely distributed in biological tissue and is a component of lecithin. It is used as a surfactant, fluorimetric reagent, and to remove co2 and h2s from natural gas and other gases.
(12 Dec 1998)
2-aminophenol 1,6-dioxygenase <enzyme> From pseudomonas growing on 2-aminophenol; catalyses the oxidation of 2-aminophenol to 2-aminomuconic-6-saemialdehyde; made up of 2 subunits, alpha subunit (amna encoded) and beta subunit (amnb encoded); mw 140 kD (native enzyme); genbank d89855
Registry number: EC 1.13.-
(26 Jun 1999)
2-aminophenol oxidase <enzyme> Converts 4-methyl-3-hydroxyanthranilic acid or other aminophenols to phenoxazines
Registry number: EC 1.10.3.4
Synonym: isophenoxazine synthase, phenoxazinone synthetase, o-aminophenol oxidase, ortho-aminophenol oxidase
(26 Jun 1999)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 4
  • 2-Aminoadipic Acid - »õâ A metabolite in the principal biochemical pathway of lysine. It antagonizes neuroexcitatory activity modulated by the glutamate receptor, N-METHYL-D-ASPARTATE; (NMDA).
    Synonyms : 2 Aminoadipic Acid, 2-Aminohexanedioic Acid, 2 Aminohexanedioic Acid, Acid, 2 Aminoadipic, Acid, 2-Aminoadipic, Acid, 2-Aminohexanedioic, Acid, alpha-Aminoadipic, Aminoadipic Acid, 2, alpha Aminoadipic Acid
  • 2-Aminopurine - »õâ A purine that is an isomer of ADENINE (6-aminopurine).
    Synonyms : 2 Aminopurine
  • 2-Chloroadenosine - »õâ 2-Chloroadenosine. A metabolically stable analog of adenosine which acts as an adenosine receptor agonist. The compound has a potent effect on the peripheral and central nervous system.
    Synonyms : 2 Chloroadenosine
  • 2-Hydroxy-5-nitrobenzyl Bromide - »õâ A chemical reagent that reacts with and modifies chemically the tryptophan portion of protein molecules. Used for 'active site' enzyme studies and other protein studies. Sometimes referred to as Koshland's reagent.
    Synonyms : Koshland Reagent, Koshlands Reagent, 2 Hydroxy 5 nitrobenzyl Bromide, Koshland Reagent I, Koshlands Reagent I, Reagent I, Koshland's, Reagent, Koshland, Reagent, Koshlands
  • 2-Hydroxyphenethylamine - »õâ Simple amine found in the brain. It may be modulator of sympathetic functions. Its derivatives are adrenergic agonists and antagonists. It is also used in chemical industry.
    Synonyms : 2 Hydroxyphenethylamine, 2 Phenylethanolamine, beta Hydroxyphenethylamine, beta Phenylethanolamine
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
2-acylglycerol O [EC 2.3.1.22] an enzyme of the transferase class that catalyzes the transfer of the acyl group from palmitoyl coenzyme A or other long chain acyl coenzyme A to a monoglyceride to form a diglyceride. The reaction occurs in the intestinal mucosa, synthesizing triglycerides from monoglycerides produced during digestion. Called also acylglycerol palmitoyltransferase and monoglyceride acyltransferase.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
2-CdA cladribine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
2-chlorodeoxyadenosine cladribine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
2-hydroxyethanesulfonate any salt of 2-hydroxyethanesulfonic acid; see also isethionate.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
2-hydroxyethanesulfonic acid see isethionic acid.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 4 ÆäÀÌÁö: 4
2 being nine more than twenty
2 coming next after the twenty-eighth in position
2 coming next after the first in position in space or time or degree or magnitude
2 coming next after the first in position in space or time or degree or magnitude
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
KMLE ÀÇÇоà¾î »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
KMLE ¾àǰ/ÀǾàǰ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • Á¦Ç°¸í
    ¼ººÐ/ÇÔ·®
    ±¸ºÐ/º¸Çè±Þ¿©
ÀÇÇÐ³í¹® ¾àÀÚ(Pubmed/Entrez) °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑÇØºÎÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѽŰæ¿Ü°úÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
    ÇÑÀÚ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇѱâ»ýÃæÇÐȸ ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
KI ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü ¸ÂÃã °Ë»ö (https://www.merriam-webster.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - Merriam-Webster's ÀÇÇлçÀü À¯»ç °Ë»ö (https://www.merriam-webster.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - MedlinePlus Health Topics ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - MedlinePlus Health Topics À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - µå·¯±×ÀÎÆ÷ ¾àÇÐ Á¤º¸ ¸ÂÃã °Ë»ö (http://www.druginfo.co.kr) °á°ú: 0 ÆäÀÌÁö: 4
Á¦Ç°¸í
ÆÇ¸Å»ç
º¸ÇèÄÚµå ¼ººÐ/ÇÔ·®
±¸ºÐ/º¸Çè±Þ¿©
¿ÜºÎ ¸µÅ© - µå·¯±×ÀÎÆ÷ ¾àÇÐ Á¤º¸ À¯»ç °Ë»ö (http://www.druginfo.co.kr) °á°ú: 0 ÆäÀÌÁö: 4
Á¦Ç°¸í
ÆÇ¸Å»ç
º¸ÇèÄÚµå ¼ººÐ/ÇÔ·®
±¸ºÐ/º¸Çè±Þ¿©
¿ÜºÎ ¸µÅ© - WebMD.com Drug Reference ¸ÂÃã °Ë»ö (http://www.webmd.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - WebMD.com Drug Reference À¯»ç °Ë»ö (http://www.webmd.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - Drug.com Drugs by Medical Condition ¸ÂÃã °Ë»ö (http://www.drugs.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - Drug.com Drugs by Medical Condition À¯»ç °Ë»ö (http://www.drugs.com) °á°ú: 0 ÆäÀÌÁö: 4
KMLE À¥ ¿ë¾î À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
ÇÑ¿µ/¿µÇÑ »çÀü ¸ÂÃã °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 0 ÆäÀÌÁö: 4
  • ¿µ¹®
    ÇѱÛ
¿ÜºÎ ¸µÅ© - American Heritage Dictionary ¿µ¿µ»çÀü ¸ÂÃã °Ë»ö (https://www.ahdictionary.com) °á°ú: 0 ÆäÀÌÁö: 4
¿ÜºÎ ¸µÅ© - American Heritage Dictionary ¿µ¿µ»çÀü À¯»ç °Ë»ö (https://www.ahdictionary.com) °á°ú: 0 ÆäÀÌÁö: 4
ÅëÇÕ°Ë»ö ¿Ï·á