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  • unsaturated compound
    ºÒÆ÷È­È­ÇÕ¹°
  • unsaturated fatty acid
    ºÒÆ÷È­Áö¹æ»ê
  • unsaturated hydrocarbon
    ºÒÆ÷ȭźȭ¼ö¼Ò
  • unsaturated solution
    ºÒÆ÷È­¾×
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  • ¿µ¹®
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  • unsaturated fatty acid
    ºÒÆ÷È­Áö¹æ»ê
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  • unsaturated fatty acid
    ºÒÆ÷È­Áö¹æ»ê
  • unsaturated compound
    ºÒÆ÷È­È­ÇÕ¹°
  • unsaturated hydrocarbon
    ºÒÆ÷ȭźȭ¼ö¼Ò
  • unsaturated solution
    ºÒÆ÷È­¾×
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  • ¿µ¹®
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  • UIBC => unsaturated iron binding capacity
    ºÒÆ÷ȭö°áÇÕ´É
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  • unsaturated
    ºÒÆ÷È­(ÝÕøéûú)ÀÇ.
  • unsaturated compound
    ºÒÆ÷È­È­ÇÕ¹°(¡­ûùùêÚª).[¾à¸®]ºÒÆ÷È­¹°.
  • unsaturated fatty acid
    ºÒÆ÷È­Áö¹æ»ê (¡­ò·Û¸ß«).
  • unsaturated hydrocarbon
    ºÒÆ÷ȭźȭ¼ö¼Ò(ÝÕøéûú÷©ûýâ©áÈ).
  • unsaturated iron binding capacity
    ºÒÆ÷ȭö°áÇÕ´É(¡­ôÑÌ¿ùêÒö).
  • unsaturated iron binding capacity
    ºÒÆ÷ȭö°áÇÕ´É
  • unsaturated solution
    ºÒÆ÷È­¾×(¡­äû).
  • unsaturated vitamin B12 binding capacity
    ºÒÆ÷È­ºñŸ¹Î B12 °áÇÕ´É
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  • unsaturated fatty acid
    ºÒÆ÷È­(ÝÕøéûú) Áö¹æ»ê(ò·Û¸ß«)
  • unsaturated iron-binding capacity
    ºÒÆ÷È­(ÝÕøéûú) ö°áÇÕ´É(ôÑÌ¿ùêÒö)
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  • unsaturated fatty acid
    ºÒÆ÷È­Áö¹æ»ê
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UBBC unsaturated vitamin B12 binding capacity
UIBC unsaturated iron-binding capacity
unsat unsatisfactory; unsaturated
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MUFA Mono-unsaturated
ufa Unsaturated fatty acid
UBBC Unsaturated vitamin B12 binding capacity
PUFA poly-unsaturated
PUFA poly-unsaturated fat
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  • ¿µ¹®
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  • unsaturated compound
    ºÒÆ÷È­ È­ÇÕ¹°, ºÒÆ÷È­¹°
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  • unsaturated hydrocarbon
    ºÒÆ÷È­ źȭ ¼ö¼Ò
    ź¼Ò°£ °áÇÕ¿¡¼­ ±Ëµµ Áßø¿¡ ÀÇÇØ »ý±â´Â ÆÄÀÌ ÀüÀÚ¶ó°í ÇÏ´Â 2~3½ÖÀÇ °øÀ¯ ÀüÀÚ¸¦ °®°íÀÖ´Â »óÅÂ. ÀÌ·± È­ÇÕ¹°Àº ºÒÆ÷È­ °áÇÕ¿øÀÚ¿¡ ÀüÀÚ±ºÀ», °áÇÕ´ÉÀÇ ÇѰè, Áï Æ÷È­±îÁö °áÇÕÀÌ °¡´ÉÇÏ´Ù.
  • unsaturated solution
    ºÒÆ÷È­ ¾×
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
unsaturated alcohols Those alcohol's whose carbon chains contain one or more double or triple bonds.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 11 ÆäÀÌÁö: 1
fats, unsaturated Fats containing one or more double bonds, as from oleic acid, an unsaturated fatty acid.
(12 Dec 1998)
fatty acids, unsaturated Fatty acids containing one (monounsaturated) or multiple (polyunsaturated) double bonds. They predominate in most plant-derived fats. The number and position of each double bond can be specified, as in the systematic names, or the position of the double bond closest to the methyl group (omega) terminus can be specified to denote functional subdivisions of the overall group, e.g., omega-3 fatty acids. The numbers and positions of the double bonds have been linked to effects on plasma lipid, triglyceride, and cholesterol levels.
(12 Dec 1998)
unsaturated 1. Capable of absorbing or dissolving to a greater degree; as, an unsaturated solution.
2. <chemistry> Capable of taking up, or of uniting with, certain other elements or compounds, without the elimination of any side product; thus, aldehyde, ethylene, and ammonia are unsaturated.
Source: Websters Dictionary
(01 Mar 1998)
unsaturated fat <biochemistry> A fat that contains a carbon-carbon double bond, or a fat containing unsaturated fatty acids, such a fatty acid has double or triple covalent bonds and is thus able to add more atoms. Unsaturated fats are believed to lower blood cholesterol levels and are found at high levels in vegetable oils (olive oil, safflower oil, etc.) As a general rule, unsaturated fats are liquid at room temperature.
(09 Oct 1997)
unsaturated fatty acid <biochemistry> Fatty acid with one or more double bonds.
(18 Nov 1997)
alcohols Alkyl compounds containing a hydroxyl group. They are classified according to relation of the carbon atom: primary alcohols, r-ch2oh; secondary alcohols, r2-choh; tertiary alcohols, r3-coh.
(12 Dec 1998)
amino alcohols Compounds possessing both a hydroxyl (-oh) and an amino group (-nh2).
(12 Dec 1998)
benzyl alcohols Alcohols derived from the aryl radical (c6h5ch2-) and defined by c6h5choh. The concept includes derivatives with any substituents on the benzene ring.
(12 Dec 1998)
polyoxyethylene alcohols <chemistry> Used as emulsifying and wetting agents, antistats, solubilisers, defoamers, and other industrial applications. Laureth 9 as spermaticide; pharmaceutic aid (surfactant).
(05 Mar 2000)
sugar alcohols Polyhydric alcohols having no more than one hydroxy group attached to each carbon atom. They are formed by the reduction of the carbonyl group of a sugar to a hydroxyl group.
(12 Dec 1998)
fatty alcohols Usually high-molecular-weight, straight-chain primary alcohols, but can also range from as few as 4 carbons, derived from natural fats and oils, including lauryl, stearyl, oleyl, and linoleyl alcohols. They are used in pharmaceuticals, cosmetics, detergents, plastics, and lube oils and in textile manufacture.
(12 Dec 1998)
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  • unsaturated
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