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  • ¿µ¹®
    ÇѱÛ
  • exothermic compound
    ¹ß¿­È­ÇÕ¹°
  • heterocyclic compound
    ÇìÅ×·Î°í¸®È­ÇÕ¹°, ÀÌÁ¾¿øÀÚ°í¸®È­ÇÕ¹°
  • high energy compound
    °í¿¡³ÊÁöÈ­ÇÕ¹°
  • high energy phosphate compound
    °í¿¡³ÊÁöÀλ꿰ȭÇÕ¹°
  • impression compound
    Àλó¿ëÄÞÆÄ¿îµå
  • inorganic compound
    ¹«±âÈ­ÇÕ¹°
  • molecular compound
    ºÐÀÚÈ­ÇÕ¹°
  • moulding compound impression
    ¿¬¼ºÀçÀλó
  • nonpolar compound
    ºñ±Ø¼ºÈ­ÇÕ¹°, ¹«±Ø¼ºÈ­ÇÕ¹°
  • open-chain compound
    ¿­¸°»ç½½È­ÇÕ¹°
  • organic compound
    À¯±âÈ­ÇÕ¹°
  • polyfunctional compound
    ´Ù±â´ÉÈ­ÇÕ¹°
  • potentially toxic compound
    ÀáÀçµ¶¼º¹°Áú
  • radioactive luminous compound
    ¹æ»ç¼º¹ß±¤È­ÇÕ¹°
  • ring compound
    °í¸®È­ÇÕ¹°
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  • ¿µ¹®
    ÇѱÛ
  • compound scan motion
    º¹ÇÕ½ºÄµ¿îµ¿
  • conjugated compound
    º¹ÇÕÈ­ÇÕ¹°
  • contact compound scan
    Á¢Ã˺¹ÇÕ½ºÄµ
  • coordination compound
    ¹èÀ§È­ÇÕ¹°
  • cryoprotective compound
    µ¿°á¹æÁöÁ¦
  • cyclic compound
    (¢¡closed chain) ´ÝÈù»ç½½
  • exothermic compound
    ¿Ü¿­¼ºÈ­ÇÕ¹°
  • heterocyclic compound
    ÇìÅ×·Î°í¸®È­ÇÕ¹°, ÀÌÁ¾¿øÀÚ°í¸®È­ÇÕ¹°
  • heteropolar compound
    À̱ØÈ­ÇÕ¹°
  • homocyclic compound
    °°Àº°í¸®È­ÇÕ¹°, µ¿¼Òȯ½ÄÈ­ÇÕ¹°
  • homopolar compound
    µ¿±ØÈ­ÇÕ¹°
  • impression compound
    Àλó¿ëÄÄÆÄ¿îµå
  • inorganic compound
    ¹«±âÈ­ÇÕ¹°
  • interstitial compound
    °£ÁúÈ­ÇÕ¹°
  • levorotary compound
    Á¼±È­ÇÕ¹°
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  • ¿µ¹®
    ÇѱÛ
  • antimuscarinic action
    Ç×¹«½ºÄ«¸°(¼º) ÀÛ¿ë(ù÷¡­(àõ) íÂéÄ).
  • antimuscarinic action
    Ç×¹«½ºÄ«¸°ÀÛ¿ë(ù÷¡­íÂéÄ).
  • antipyretic action
    ÇØ¿­ÀÛ¿ë(¡­íÂéÄ).
  • antispasmodic action
    Áø°æÀÛ¿ë(¡­íÂéÄ)
  • galvanic action
    °¥¹Ù´ÏÀÛ¿ë.
  • ganglionic blocking action
    ½Å°æÀýÂ÷´ÜÀÛ¿ë.
  • germicidal action
    »ì±ÕÀÛ¿ë(߯жíÂéÄ).
  • gestagenic action
    ÇÁ·ÎÁ¦½ºÅ×·ÐÀÛ¿ë(¡­íÂéÄ).
  • immediate action
    Áï°¢ÀÛ¿ë, Áï½ÃÀÛ¿ë.
  • indirect action
    °£Á¢ÀÛ¿ë.
  • indirect action
    °£Á¢ÀÛ¿ë
  • inhibitory action
    ÀúÁöÀÛ¿ë(îÁò­íÂéÄ).
  • inotropic action
    º¯·ÂÀÛ¿ë(ܨÕôíÂéÄ), ¼öÃàÃËÁøÀÛ¿ë(â¥õêõµòäíÂéÄ).³»°ú¼öÃà·Â
  • inotropic action
    º¯·ÂÀÛ¿ë, ¼öÃàÃËÁøÀÛ¿ë.[³»°ú]¼öÃà·Â º¯µ¿ÀÛ¿ë.
  • pharmacodynamic action
    ¾à¿ªÇÐ(Àû) ÀÛ¿ë(å·æ³ùÊ(îÜ) íÂéÄ).
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  • ¿µ¹®
    ÇѱÛ
  • iodine-125 compound
    ¿äµå 125 È­ÇÕ¹°
  • iodonium compound
    ¿äµå´½È­ÇÕ¹° (¡­ûùùêÚª).
  • levorotary compound
    Á¼±¼º È­ÇÕ¹°(ñ§àÁàõ ûùùêÚª).
  • molecular compound
    ºÐÀÚÈ­ÇÕ¹°(ÝÂí­ ûùùêÚª).
  • moulding compound impression
    ¿¬¼ºÀçÀλó(æèàõî§ìÔßÀ).
  • nitrogen compound
    Áú¼ÒÈ­ÇÕ¹°
  • non-protein nitrogenous compound
    ºñ´Ü¹é(Áú)Áú¼ÒÈ­ÇÕ¹°
  • nonpolar compound
    ºñ±Ø¼º È­ÇÕ¹°(ުпàõûùùêÚª), ¹«±Ø¼º È­ÇÕ¹°.
  • one compound system
    ´ÜÀÏÈ­ÇÕ¹°½Ã½ºÅÛ.
  • open chain compound
    ¿­¸°»ç½½È­ÇÕ¹° °³¼âÈ­ÇÕ¹°(ËÒáðûùùêÚª) .
  • organic compound
    À¯±âÈ­ÇÕ¹°(¡­ûùùêÚª).
  • organic molecular compound
    À¯±âºÐÀÚÈ­ÇÕ¹°(êóѦÝÂí­ûùùêÚª).
  • organolead compound
    À¯±â³³È­ÇÕ¹°
  • organomercury compound
    À¯±â¼öÀºÈ­ÇÕ¹°
  • organometallic compound
    À¯±â±Ý¼ÓÈ­ÇÕ¹°(ÊÙË»ËṴ̴̂ËÑ).
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  • ¿µ¹®
    ÇѱÛ
  • reduction potential
    ȯ¿ø ÀüÀ§(ü½êªï³êÈ)
  • resting potential
    ÈÞ½Ä ÀüÀ§(ï³êÈ)
  • sedimentation potential
    ħ°­Àü¾Ð (öØË½ï³äâ)
  • standard electrode potential
    Ç¥ÁØ Àü±ØÀüÀ§(øöñÞï³Ð¿ï³êÈ)
  • standard oxidation potential
    Ç¥ÁØ »êÈ­ÀüÀ§(øöñÞß«ûùï³êÈ)
  • standard potential
    Ç¥ÁØÀüÀ§(øöñÞï³êÈ)
  • standard reduction potential
    Ç¥ÁØ È¯¿øÀüÀ§(øöñÞü½êªï³êÈ)
  • starting potential
    ½ÃÀÛ ÀüÀ§ (ã·íÂï³êÈ)
  • Stern potential
    ½ºÅÏ ÀüÀ§(ï³êÈ)
  • streaming potential
    È帧 ÀüÀ§(ï³êÈ)
  • surface potential
    Ç¥¸éÀüÀ§ (øúØüï³êÈ)
  • threshold potential
    ¹®ÅÎÀüÀ§ (ï³êÈ)
  • transfer potential
    ÀüÀÌ´É(ï®ì¹Òö)
  • transmembrane potential
    ¸·È¾´ÜÀüÀ§(دüôÓ¨ï³êÈ)
  • zeta potential
    Á¦Å¸ ÀüÀ§(ï³êÈ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
SFAP single-fiber action potential
S-MUAP surface-detected motor unit action potential
SNAP sensory nerve action potential; S-nitroso-N-acetylpenicillamine
TAP transesophageal atrial pacing; transluminal angioplasty; transmembrane action potential; transporter...
AEP acute edematous pancreatitis; artificial endocrine pancreas; auditory evoked potential; average evok...
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OLC Ouabainlike compound
OPIDN organophosphorous compound-induced delayed neurotoxicity
CAP cochlea action potentials
PAR Participatory Action Research
TRA Theory of Reasoned Action
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • antidiuretic action
    Ç×ÀÌ´¢ÀÛ¿ë
  • antimicrobial action
    Ç×±Õ ÀÛ¿ë
  • antinociception action
    Ç×Ä§ÇØ¼ö¿ë¼º ÀÛ¿ë, Ç×À¯ÇØ ¼ö¿ë¼º ÀÛ¿ë
  • antipyretic action
    ÇØ¿­ ÀÛ¿ë
  • antispasmodic action
    Áø°æÀÛ¿ë
  • bactericidal action
    »ì±Õ ÀÛ¿ë, »ì±Õ¼º
    1. ¹ÚÅ׸®¾Æ¸¦ Á×ÀÌ´Â Çö»ó. ÀÌ ¿ë¾î´Â Á¾Á¾ Ç×»ýÁ¦ÀÇ ¼º°ÝÀ» ¼³¸íÇϴµ¥ »ç¿ëµÈ´Ù. 2. È­Çпä¹ýÁ¦, ¼Òµ¶Á¦ Áß¿¡´Â ¹Ì»ý¹°À» ¼Ò¸ê½ÃŰ´Â ÀÛ¿ëÀÌ ÀÖ´Ù. ÀÌ¿¡ ´ëÇØ ¾î¶² ¾àÁ¦¿¡ ´ëÇØ ±ÕÀÇ Áõ½ÄÀÌ ¾ïÁ¦µÇ´Âµ¥ ¾àÁ¦¸¦ Á¦°ÅÇÏ¸é ´Ù½Ã Áõ½ÄÇÏ´Â °ÍÀ» Áõ±Õ ÀÛ¿ëÀ̶ó ÇÑ´Ù.
  • bacteriostatic action
    Á¤±Õ ÀÛ¿ë
    ¼¼±ÕÀÇ ¹ßÀ° ¶Ç´Â Áõ½ÄÀ» ¾ïÁ¦ÇÏ´Â ÀÛ¿ë.
  • biological action
    »ý¹° ÀÛ¿ë
  • buffer action
    ¿ÏÃæ ÀÛ¿ë
  • calorigenic action
    ¿­ »ý»ê ÀÛ¿ë
    À½½Ä¹° ¶Ç´Â À½½Ä¹° ¼ººÐ¿¡ ÀÇÇØ ü³»¿¡ ¹ß»ýÇÑ ÃÑ ¿¡³ÊÁö·®.
  • cause of action
    ¼Ò¼ÛÀÇ ¿øÀÎ
    ´ëºÎºÐ, ¹ýÀû Á¶Ä¡ÀÇ ¹è°æÀ̳ª ÀÌÀ¯¸¦ ÀǹÌÇÑ´Ù. ¹ýÀû ¹è»óÀ» ÇÏ¿©¾ß ÇÏ´Â À߸øµÈ ¿øÀÎ.
  • central action
    ÁßÃß ÀÛ¿ë
  • chronotropic action
    º¯µ¿ ÀÛ¿ë, º¯½Ã ÀÛ¿ë
  • ciliary action
    ¼¶¸ð ÀÛ¿ë
  • cleaning action
    ¼¼Á¤ ÀÛ¿ë
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
APC compound An analgesic tablet drug combination containing aspirin, phenacetin and caffeine. Very widely used in the 1940's through 1960's; original constituents of popular over-the-counter pain remedies. Use currently much diminished due to concerns about potential renal injury due to the phenacetin.
(05 Mar 2000)
aromatic compound Any compound in which the constituent atoms, or any part of them, form a ring. Used mainly in organic chemistry where: 1) numerous compound's contain rings of carbon atoms (carbocyclic compound's) or carbon atoms plus one or more atoms of other types (heterocyclic compound's), usually nitrogen, oxygen, or sulfur; 2) where the atoms in the ring are all of the same element (homocyclic or isocyclic compound); 3) where the ring is saturated or contains nonconjugated double bonds (alicyclic compound), the compound is similar in properties to the corresponding acyclic compound (e.g., cyclohexane resembles hexane); 4) where the ring contains conjugated double bonds in a closed loop in which there are 4n + 2 (where n is an integer) delocalised π electrons (Huckel's rule) (aromatic compound; e.g., benzene, pyridine), it is more stable than the corresponding saturated ring and exhibits unusual chemical properties characteristic of itself and not of other types of rings or of acyclic compound's. These aromatic compounds have the ability to sustain an induced ring current.
Synonym: closed chain compound, ring compound.
(05 Mar 2000)
binary compound <chemistry> This refers to any compound that is composed of only two elements.
(09 Oct 1997)
calcium compound Inorganic compounds that contain calcium as an integral part of the molecule.
(12 Dec 1998)
carbamino compound Any carbamic acid derivative formed by the combination of carbon dioxide with a free amino group to form an N-carboxy group, -NH-COOH, as in haemoglobin forming carbaminohemoglobin.
(05 Mar 2000)
carbocyclic compound See: cyclic compound.
(05 Mar 2000)
genetic compound In medical genetics, the presence of two different mutant alleles at the same loci.
Synonym: genetic compound.
(05 Mar 2000)
Reichstein's compound One of several steroids; e.g., Reichstein's substance F (cortisone), Reichstein's substance H (corticosterone), Reichstein's substance M (cortisol), Reichstein's substance Q (cortexone), and Reichstein's substance S (cortexolone).
Synonym: Reichstein's compound.
(05 Mar 2000)
glycosyl compound The compound formed between a sugar and another organic substance in which the OH of the reducing (hemiacetal) group of the former is removed; e.g., the natural nucleosides, in which a heterocyclic N becomes linked directly to the C-1 of ribose (or deoxyribose) to yield ribosyl compounds.
Compare: glycoside.
(05 Mar 2000)
gold compound <pharmacology> A group of medications which act to suppress inflammation in synovial tissue.
Examples include gold sodium thiomalate, auranofin and aurothioglucose. These medications are indicated in the treatment of rheumatoid arthritis, psoriatic arthritis, Felty's syndrome and juvenile rheumatoid arthritis.
(27 Sep 1997)
meso compound <chemistry> A compound that has two or more chiral centres but does not rotate plane-polarized light because it has an internal plane of symmetry. These compounds are identical to their mirror images.
(09 Jan 1998)
chiral compound <chemistry> A molecule that has an asymmetric centre and can be found in twonon-superimposable mirror-image forms (enantiomers).
(05 Jan 1998)
ring compound Any compound in which the constituent atoms, or any part of them, form a ring. Used mainly in organic chemistry where: 1) numerous compound's contain rings of carbon atoms (carbocyclic compound's) or carbon atoms plus one or more atoms of other types (heterocyclic compound's), usually nitrogen, oxygen, or sulfur; 2) where the atoms in the ring are all of the same element (homocyclic or isocyclic compound); 3) where the ring is saturated or contains nonconjugated double bonds (alicyclic compound), the compound is similar in properties to the corresponding acyclic compound (e.g., cyclohexane resembles hexane); 4) where the ring contains conjugated double bonds in a closed loop in which there are 4n + 2 (where n is an integer) delocalised &pi; electrons (Huckel's rule) (aromatic compound; e.g., benzene, pyridine), it is more stable than the corresponding saturated ring and exhibits unusual chemical properties characteristic of itself and not of other types of rings or of acyclic compound's. These aromatic compounds have the ability to sustain an induced ring current.
Synonym: closed chain compound, ring compound.
(05 Mar 2000)
microscope, compound A microscope that consists of two microscopes in series, the first serving as the ocular lens (close to the eye) and the second serving as the objective lens (close to the object to be viewed). Credit for creating the compound microscope goes usually to the dutch spectaclemakers hans and zacharias janssen who in 1590 invented an instrument that could be used as either a microscope or telescope. The compound microscope evolved into the dominant type of optical microscope today.
(12 Dec 1998)
closed chain compound Any compound in which the constituent atoms, or any part of them, form a ring. Used mainly in organic chemistry where: 1) numerous compound's contain rings of carbon atoms (carbocyclic compound's) or carbon atoms plus one or more atoms of other types (heterocyclic compound's), usually nitrogen, oxygen, or sulfur; 2) where the atoms in the ring are all of the same element (homocyclic or isocyclic compound); 3) where the ring is saturated or contains nonconjugated double bonds (alicyclic compound), the compound is similar in properties to the corresponding acyclic compound (e.g., cyclohexane resembles hexane); 4) where the ring contains conjugated double bonds in a closed loop in which there are 4n + 2 (where n is an integer) delocalised &pi; electrons (Huckel's rule) (aromatic compound; e.g., benzene, pyridine), it is more stable than the corresponding saturated ring and exhibits unusual chemical properties characteristic of itself and not of other types of rings or of acyclic compound's. These aromatic compounds have the ability to sustain an induced ring current.
Synonym: closed chain compound, ring compound.
(05 Mar 2000)
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