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  • ¿µ¹®
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  • chain compound
    »ç½½È­ÇÕ¹°
  • exothermic compound
    ¹ß¿­È­ÇÕ¹°
  • heterocyclic compound
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  • high energy compound
    °í¿¡³ÊÁöÈ­ÇÕ¹°
  • high energy phosphate compound
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  • impression compound
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  • inorganic compound
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  • molecular compound
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  • moulding compound impression
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  • nonpolar compound
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  • open-chain compound
    ¿­¸°»ç½½È­ÇÕ¹°
  • organic compound
    À¯±âÈ­ÇÕ¹°
  • polyfunctional compound
    ´Ù±â´ÉÈ­ÇÕ¹°
  • potentially toxic compound
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  • radioactive luminous compound
    ¹æ»ç¼º¹ß±¤È­ÇÕ¹°
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  • ¿µ¹®
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  • contact compound scan
    Á¢Ã˺¹ÇÕ½ºÄµ
  • coordination compound
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  • cryoprotective compound
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  • cyclic compound
    (¢¡closed chain) ´ÝÈù»ç½½
  • exothermic compound
    ¿Ü¿­¼ºÈ­ÇÕ¹°
  • heterocyclic compound
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  • 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°
  • molecular compound
    ºÐÀÚÈ­ÇÕ¹°
  • nonpolar compound
    ºñ±Ø¼ºÈ­ÇÕ¹°, ¹«±Ø¼ºÈ­ÇÕ¹°
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  • ¿µ¹®
    ÇѱÛ
  • compound eye
    º¹ÇÕ¾È
  • compound fracture =open f.
    º¹Àâ °ñÀý(~Íéï¹), °³¹æ¼º °ñÀý(ËÒÛ¯àõÍéï¹)
  • compound gland
    º¹ÇÕ»ù
  • compound intercellular junction
    º¹ÇÕ¼¼Æ÷»çÀÌ¿¬Á¢
  • compound joint
    º¹ÇÕ°üÀý
  • compound lens
    º¹ÇÕ·»Áî
  • compound microscope
    º¹ÇÕÇö¹Ì°æ
  • compound monster
    ÀÏ¹Ý º¹Ã¼±âÇü(ÜÜô÷ѱû¡).
  • compound nevus
    º¹ÇÕ(ÜÜùê) ¸ð¹Ý(Ù½Úè)
  • compound nucleus
    º¹ÇÕÇÙ, °ãÇÙ
  • compound pepsin elixir
    º¹ÇÕÆé½Å¿¤¸¯½Ã¸£.
  • compound presentation
    º¹ÇÕÀ§(ÜÜùêêÈ).
  • compound scan
    º¹ÇÕ(ÜÜùê)½ºÄµ.
  • compound scan
    º¹ÇÕ ½ºÄµ
  • compound scan
    º¹ÇÕ (ÜÜùê) ½ºÄµ
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  • ¿µ¹®
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  • energy-rich compound
    ºÎ(Ý£)¿¡³ÊÁö È­ÇÕ¹°(ûùùêÚª)
  • enzyme-substrate compound
    È¿¼Ò-±âÁú È­ÇÕ¹° (ý£áÈÐñòõûùùêÚª)
  • high-energy compound
    °í(ÍÔ)¿¡³ÊÁö È­ÇÕ¹°(ûùùêÚª)
  • Kendall's compound
    ÄË´Þ È­ÇÕ¹°(ûùùêÚª)
  • labeled compound
    Ç¥ÁöÈ­ÇÕ¹°(øöò½ûùùêÚª)
  • low-energy compound
    Àú(î¸)¿¡³ÊÁöÈ­ÇÕ¹°(ûùùêÚª)
  • meso compound
    ¸Þ¼ÒÈ­ÇÕ¹°(ûùùêÚª)
  • nodal compound
    ¿ËÀÌ È­ÇÕ¹°(ûùùêÚª)
  • prochiral compound
    ۶ö Àü±¸È­ÇÕ¹°(îñÏÌûùùêÚª)
  • quaternary ammonium compound
    »çÂ÷(ÞÌó­) ¾Ï¸ð´Ï¾ÆÈ­ÇÕ¹°(ûùùêÚª).
  • Reichstein's compound
    ¶óÀÌÅ©½ºÅ¸ÀÎ È­ÇÕ¹°(ûùùêÚª)
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VG van Gieson [stain]; ventricular gallop; volume of gas
ALEC artificial lung-expanding compound
CAP camptodactyly-arthropathy-pericarditis [syndrome]; Canada Assistance Plan; capsule; captopril; catab...
CC calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card...
CCF cancer coagulation factor; cardiolipin complement fixation; carotid-cavernous fistula; centrifuged c...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
CMAP Compound motor action potential
CMAP Compound muscle action potential
CNAP Compound nerve action potential
OP organophosphorus compound
OLC Ouabainlike compound
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  • ¿µ¹®
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    ¼³¸í
  • open chain compound
    ¿­¸° »ç½½ È­ÇÕ¹°
  • organometallic compound
    À¯±â ±Ý¼Ó È­ÇÕ¹°
    À¯±â ±â¿Í °áÇÕµÈ ±Ý¼ÓÀ¸·Î ÀÌ·ç¾îÁø È­ÇÕ¹°.
  • paraffin compound
    ÆÄ¶óÇÉÁ· È­ÇÕ¹°
  • phenolic compound
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  • racemic compound
    ¶ó¼¼¹Ì È­ÇÕ¹°
  • SH compound
    SH È­ÇÕ¹°
    SH±â¸¦ °¡Áö´Â °Í, ½Ã½ºÅ×ÀÎ, ÆÇÅäÅ×ÀÎ µîÀÌ ÀÖ´Ù.
  • unsaturated compound
    ºÒÆ÷È­ È­ÇÕ¹°, ºÒÆ÷È­¹°
    ºÐÀÚ ¾È¿¡ ź¼Ò ¿øÀÚ »çÀÌÀÇ ÀÌÁß °áÇÕ ¶Ç´Â »ïÁß °áÇÕÀ» Æ÷ÇÔÇÏ´Â À¯±â È­ÇÕ¹°.
  • vitamin compound
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    ºñŸ¹ÎÀ» ÁÖ¼ººÐÀ¸·Î ÇÏ´Â ¿µ¾çÁ¦·Î¼­ ºñŸ¹Î °áÇÌÁõÀÇ Ä¡·á¿Í ¿¹¹æ¿¡ »ç¿ëµÇ´Â ÀǾàǰ. ÇöÀç ºñŸ¹Î B2¸¦ Á¦¿ÜÇÑ ´ëºÎºÐÀÇ ºñŸ¹ÎµéÀº ÇÕ¼ºÇÒ ¼ö ÀÖ°í È­Çлê¾÷¿¡ ÀÇÇØ ´Ù·®À¸·Î Á¦Á¶°¡ °¡´ÉÇϹǷΠ´ëºÎºÐÀÇ ºñŸ¹ÎÁ¦´Â ÇÕ¼ºÇ°À¸·Î ¸¸µé¾îÁø´Ù. ´ÜÀÏ Á¦Á¦ Áß¿¡ ÇÑ Á¾·ùÀÇ ºñŸ¹ÎÀ» Æ÷ÇÔÇϵµ·Ï ¸¸µç ´ÜÀÏ ºñŸ¹ÎÁ¦, Áö¿ë¼º ÈæÀº ¼ö¿ë¼º ºñŸ¹Î ¸î Á¾·ù¸¸À» º¹ÇÕ½ÃÄÑ ¸¸µç º¹ÇÕ ºñŸ¹ÎÁ¦, °ÅÀÇ ¸ðµç ºñŸ¹ÎÀ» Æ÷ÇÔÇϵµ·Ï ¸¸µç Á¾ÇÕ ºñŸ¹ÎÁ¦°¡ ÀÖ¾î ¿ëµµ¿¡ µû¶ó »ç¿ëµÈ´Ù. ºñŸ¹ÎÁ¦´Â Áúº´, ¾Ë·¹¸£±â, ½Ä»çÀÇ Á¦ÇÑ µî ¾î¶² ÀÌÀ¯¿¡¼­ ÀûÀýÇÑ ½Ä»ç¸¦ ÇÏÁö ¸øÇÏ´Â »ç¶÷¿¡°Ô´Â ¸Å¿ì À¯¿ëÇϳª Á¤±Ô½Ä»ç¸¦ ÇÏ´Â °Ç°­ÇÑ »ç¶÷ÀÌ ºñŸ¹ÎÀ» ´õ º¸Ãæ¼·ÃëÇϱâ À§ÇÏ¿© »ç¿ëÇÏ´Â °ÍÀº ³¶ºñÀ̰ųª ÇØ°¡ µÇ´Â °æ¿ìµµ ÀÖÀ¸¹Ç·Î »ï°¡¾ß ÇÑ´Ù. 5°¡Áö ±âÃʽÄǰ±º¿¡ ±âº»À» µÐ ±ÕÇü½Ä»ç´Â ¸öÀÌ ÇÊ¿ä·Î ÇÏ´Â ¸ðµç ºñŸ¹ÎÀ» °ø±ÞÇϱ⿡ ÃæºÐÇϸç, Çʿ䷮ ÀÌ»óÀÇ ºñŸ¹ÎÀÌ °Ç°­¿¡ ÇØ·Ó±â ¶§¹®ÀÌ´Ù. Á¤±Ô½Ä»ç¸¦ ÅëÇÑ ºñŸ¹ÎÀÇ ¼·Ãë´Â °áÄÚ °úÀ× µ¶¼º¼öÁرîÁö °¡Áö ¾ÊÁö¸¸, ³óÃàµÈ ºñŸ¹ÎÁ¦¸¦ °è¼Ó ¸ÔÀ¸¸é °úÀ× µ¶¼º ¼öÁرîÁö À̸£°Ô µÈ´Ù. ½Ä»ç¸¦ ÅëÇÏ¿© °Ç°­À¯Áö¿Í Áúº´¿¹¹æ¿¡ ÇÊ¿äÇÑ ¸ðµç ºñŸ¹ÎÀ» ¼·ÃëÇØ¾ß ÇÑ´Ù.
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van Horne, Johannes <person> Dutch anatomist, 1621-1670.
See: van Horne's canal.
(05 Mar 2000)
van Horne's canal <anatomy> The major efferent lymph duct into which lymph from most of the peripheral lymph nodes drains.
Recirculating lymphocytes that have left the circulation in the lymph node return to the blood through the thoracic duct.
(18 Nov 1997)
Van Slyke apparatus An apparatus for determining the amounts of respiratory gases in the blood.
(05 Mar 2000)
Van Slyke, Donald <person> U.S. Biochemist, 1883-1971.
See: slyke, Van Slyke apparatus, Van Slyke's formula.
(05 Mar 2000)
Van Slyke's formula The value obtained when the square root of the urine flow (when below 2 ml/min) is multiplied by the urine urea concentration and divided by the whole blood urea concentration; represents an old empirical adjustment for the effect of low urine flow on urea excretion; sometimes corrected for body size by dividing by some function of body weight or surface area. Later, plasma concentration was substituted for blood concentration in the calculation. The normal value is about 54 ml/min per 1.73 m2 in an adult person.
Synonym: Van Slyke's formula.
(05 Mar 2000)
van't Hoff, Jacobus <person> Dutch chemist and Nobel laureate, 1852-1911.
See: van't Hoff's equation, van't Hoff's law, van't Hoff's theory, Le Bel-van't Hoff rule.
(05 Mar 2000)
van't Hoff's equation Equation for osmotic pressure of dilute solutions.
See: van't Hoff's law.
For any reaction, d(ln Keq/d(1/T) equals -dH/R where Keq is the equilibrium constant, T the absolute temperature, R is the universal gas constant, and dH is the change in enthalpy; thus, plotting ln Keq vs. 1/T allows the determination of dH.
(05 Mar 2000)
van't Hoff's law In stereochemistry, all optically active substances have one or more multivalent atoms united to four different atoms or radicals so as to form in space an unsymmetrical arrangement, the osmotic pressure exerted by any substance in very dilute solution is the same that it would exert if present as gas in the same volume as that of the solution; or, at constant temperature, the osmotic pressure of dilute solutions is proportional to the concentration (number of molecules) of the dissolved substance; i.e., the osmotic pressure, &pi;, in dilute solutions is &pi; = RT&sigma;ci, where R is the universal gas constant, T is the absolute temperature, and ci is the molar concentration of solute i, the rate of chemical reactions increases between two-and three-fold for each 10°C rise in temperature.
(05 Mar 2000)
van't Hoff's theory That substances in dilute solution obey the gas laws.
Compare: van't Hoff's law.
(05 Mar 2000)
ellis-van creveld syndrome <radiology> Chondro-ectodermal dysplasia, hereditary (especially seen in Amish of Pennsylvania), polydactyly (100%), congenital heart disease (60%), abnormalities of cutaneous appendages (skin, hair, nails) More info: Ellis-van Creveld syndrome
(12 Dec 1998)
exon trapping vincent van buren <molecular biology, technique> A technique used to identify vector. The vector has two exons that are normal, splicedtogether in a transcript.Fragments of DNA can be inserted into the intron, and when the insert is an exon, the exon is splicedinto the transcript, thereby giving a longer transcript that can be detected by Northern blotanalysis.
(09 Oct 1997)
Le Bel-van't Hoff rule The number of stereoisomers of an organic compound is 2n where n represents the number of asymmetric carbon atoms (unless there is an internal plane of symmetry). A corollary of their simultaneously announced conclusions, in 1874, that the most probable orientation of the bonds of a carbon atom linked to four groups or atoms is toward the apexes of a tetrahedron, and that this accounted for all then-known phenomena of molecular asymmetry (which involved a carbon atom bearing four different atoms or groups).
See: stereoisomerism.
(05 Mar 2000)
Lobry de Bruyn-van Ekenstein transformation The conversion of glucose to fructose and mannose in dilute alkali by enolization adjacent to the carbonyl group to form an enediol, a reaction analogous to certain biochemical transformations.
(05 Mar 2000)
acetone compound <biochemistry> Any of the three compounds created by acetyl coenzyme A (acetoacetate, hydroxybutyrate, and acetone) which are water-soluble cellular fuels normally exported by the liver.
They can build up in the blood and body tissues because of starvation, untreated diabetes mellitus, or other disorders that interfere with carbohydrate metabolism. The body rids itself of ketones mainly through urine, but it rids itself of acetone through the lungs, which gives the breath a characteristic fruity odour. If ketones build up in the body long enough, they cause serious illness and coma (see ketoacidosis.)
(09 Oct 1997)
acyclic compound An organic compound in which the chain does not form a ring.
Synonym: aliphatic compound, open chain compound.
(05 Mar 2000)
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