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  • ¿µ¹®
    ÇѱÛ
  • benzyl
    º¥Áú-, º¥Áú±â
  • bromide
    ºê·ÒÈ­¹°
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    ÇѱÛ
  • bromide
    ºê·ÒÈ­¹°
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  • ¿µ¹®
    ÇѱÛ
  • alumini(u)m bromide
    ºê·ÒÈ­¾Ë·ç¹Ì´½.
  • ammonium bromide
    ºê·ÒÈ­¾Ï¸ð´½.
  • phosphorus bromide
    ºê·ÒÈ­ÀÎ(¡­ûùìÝ).
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  • ¿µ¹®
    ÇѱÛ
  • benzyl benzoate
    ¾È½ÄÇâ»ê, º¥Áú º¥Á¶¿¡ÀÌÆ®
  • alumini(u)m bromide
    ºê·ÒÈ­¾Ë·ç¹Ì´½.
  • ammonium bromide
    ºê·ÒÈ­¾Ï¸ð´½.
  • bromide
    ÃëÈ­¹°, ºê·Î¸¶À̵å
  • bromide
    ÃëÇϹ°
  • bromide
    ºê·Î¹Î.
  • bromide intoxication
    ºê·Î¸¶À̵åÁßµ¶ (¡­ñéÔ¸).
  • cyanogen bromide
    ºê·ÒÈ­ ½Ã¾Æ³ë°Õ.
  • lauryl bromide
    ÃëÈ­<ºê·Ò»ê>¶ó¿ì¸±.
  • mercuric barium bromide
    ÃëÈ­¼öÀº(ö«ûùâ©ëÞ)¹Ù·ý.
  • mercuric barium bromide
    ÃëÈ­¼öÀº(̴̬ËàËô)¹Ù·ý.
  • nickel bromide
    ÃëÈ­(ö«ûù)´ÏÄÌ, ºê·ÒÈ­´ÏÄÌ.
  • nickel bromide
    ÃëÈ­(̴̬)´ÏÄÌ, ºê·ÒÈ­´ÏÄÌ.
  • phosphorus bromide
    ºê·ÒÈ­ÀÎ(¡­ûùìÝ).
  • tetraethylammonium bromide
    ÃëÈ­(ö«ûù)Åׯ®¶ó¿¡Æ¿¾Ï¸ð´½.
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  • ¿µ¹®
    ÇѱÛ
  • benzyl benzoate
    º¥Áúº¥Á¶¿¡ÀÌÆ®
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  • ¿µ¹®
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  • cyanogen bromide reaction
    ºê·ÒÈ­ ½Ã¾È ¹ÝÀÀ(Úãëë)
  • ethidium bromide
    ºê·Ò»ê(ß«) ¿¡Æ¼µð¿ò
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  • ¿µ¹®
    ÇѱÛ
  • bromide
    ÃëÈ­¹°
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brom bromide
CPB carboxypeptidase B; cardiopulmonary bypass; cetylpyridinium bromide; competitive protein binding
CTAB cetyltrimethyl-ammonium bromide
FAB fast atom bombardment; formalin ammonium bromide; fragment, antigen-binding [of immunoglobulins]; Fr...
MB Bachelor of Medicine [Lat. Medicinae Baccalaureus]; buccal margin; isoenzyme of creatine kinase cont...
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trimethoprim 2,4-diamino)-5-(3,4,5-trimethoxy-benzyl)-pyrimidine
BA Benzyl alcohol
BITC Benzyl isothiocyanate
BSC Benzyl selenocyanate
BBP Butyl benzyl phthalate
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    ¼³¸í
  • benzyl bromide
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    ¼³¸í
  • bromide
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  • decamethonium bromide
    Ƣȭµ¥Ä«¸ÞÅä´½
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  • benzyl
    º¥Áú±â
    º¥Áú ¾ËÄÝ ¹× ±âŸ ¿©·¯ °¡Áö È­ÇÕ¹°ÀÇ ÅºÈ­¼ö¼Ò±â.
  • benzyl fumarate
    Ǫ¸¶¸£»ê º¥Áú
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  • benzyl succinate
    È£¹Ú»ê º¥Áú
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benzyl <chemistry> A compound radical, C6H5.CH2, related to toluene and benzoic acid; commonly used adjectively.
Origin: Benzoic + -yl.
Source: Websters Dictionary
(01 Mar 1998)
benzyl alcohol <chemical> A colourless liquid with a sharp burning taste and slight odour. It is used as a local anaesthetic and to reduce pain associated with lidocaine injection. Also, it is used in the manufacture of other benzyl compounds, as a pharmaceutic aid, and in perfumery and flavoring.
Pharmacological action: anaesthetics, local, pharmaceutic aid.
(12 Dec 1998)
benzyl alcohol dehydrogenase <enzyme> Catalyses the oxidation of benzyl alcohol to yield benzaldehyde
Registry number: EC 1.1.1.-
(26 Jun 1999)
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)
benzyl carbinol <chemical> An antimicrobial, antiseptic, and disinfectant that is used also as an aromatic essence and preservative in pharmaceutics and perfumery.
Pharmacological action: anti-infective agents, local, disinfectants, preservatives, pharmaceutical.
Chemical name: Benzeneethanol
(12 Dec 1998)
benzyl cinnamate Trans-cinnamic benzyl ester;a constituent of balsams of Peru, Tolu, and styrax.
Synonym: cinnamein.
Benzyl fumarate, (C6H5CH2) OOCCHCHCOO(CH2C6H5; dibenzyl fumarate;used for the same purposes as benzyl benzoate.
Benzyl mandelate, the benzyl ester of mandelic acid, having an antispasmodic action similar to that of benzyl benzoate.
Benzyl succinate, (C6H5CH2)2(CH2CO2 )2; dibenzyl succinate;action and dosage are the same as those of benzyl benzoate.
(05 Mar 2000)
benzyl penicillin <chemical> (2s-(2 alpha,5 alpha,6 beta))-3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid. A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on gaba mediated synaptic transmission.
Pharmacological action: convulsants, gaba modulators, penicillins.
Chemical name: 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)- (2S-(2alpha,5alpha,6beta))-
(12 Dec 1998)
benzyl viologen <chemical> 1,1'-bis(phenylmethyl)4,4'-bipyridinium dichloride. Oxidation-reduction indicator.
Chemical name: 4,4'-Bipyridinium, 1,1'-bis(phenylmethyl)-
(12 Dec 1998)
ammonium bromide A sedative.
(05 Mar 2000)
azamethonium bromide A ganglionic blocking agent.
Chemical name: [(Methylimino)diethylene]bis-[ethyldimethylammonium bromide].
(05 Mar 2000)
benzpyrinium bromide 1-benzyl-3-hydroxypyridinium bromide diethylcarbamate;a cholinergic drug with action and uses similar to those of neostigmine.
Synonym: benzstigminum bromidum.
(05 Mar 2000)
bromide <chemistry> A compound of bromine with a positive radical.
Source: Websters Dictionary
(01 Mar 1998)
bromide acne Follicular eruption on face, trunk, and extremities, due to bromide ingestion.
See: bromoderma.
(05 Mar 2000)
butylscopolammonium bromide <chemical> Antimuscarinic quaternary ammonium derivative of scopolamine used to treat cramps in gastrointestinal, urinary, uterine, and biliary tracts, and to facilitate radiologic visualization of the gastrointestinal tract.
Pharmacological action: muscarinic antagonists, parasympatholytics.
Chemical name: 3-Oxa-9-azoniatricyclo(3.3.1.02,4)nonane, 9-butyl-7-(3-hydroxy-1-oxo-2-phenylpropoxy)-9-methyl-, bromide, (7(S)-(1alpha,2beta,4beta,5alpha,7beta))-
(12 Dec 1998)
calcium bromide Used to meet the same indications as potassium bromide.
(05 Mar 2000)
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benzyl bromide Benzyl bromide (C 7 H 7 Br) is a colorless to yellow liquid with a pungent odor. The Germans used it as a war gas in March 1915, but later completely abandoned it. Benzyl bromide usually is prepared in a laboratory by the action of bromine on toluene. Effects of short-term exposure include severe irritation of the eyes, skin, and respiratory tract. Chemical names: alpha-Bromotoluene Bromophenylmethanel [118]
Ãâó: www.gulflink.osd.mil/asp_orch_ii/asp_orch_ii_taba....
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