| ¿µ¹® | penicillin | ÇÑ±Û | Æä´Ï½Ç¸° |
|---|---|---|---|
| ¼³¸í | Ç×»ýÁ¦ÀÇ ÀÏÁ¾. °¡Àå Ãʱ⿡ °³¹ßµÈ Ç×»ýÁ¦·Î ¸¹Àº Á¾·ùÀÇ º´±ÕÀ» Á×ÀÏ ¼ö ÀÖÀ¸¸ç, ºÎÀÛ¿ëÀº °ÅÀÇ ¾ø´Ù. ¾ÆÁ÷µµ °¡Àå ¸¹ÀÌ ¾²ÀÌ´Â Ç×»ýÁ¦ÀÇ ÇϳªÀÌÁö¸¸, ÀϺο¡¼ Æä´Ï½Ç¸°¼îÅ©(¾Ë·¹¸£±â¹ÝÀÀÀÇ ÀÏÁ¾À¸·Î »ý¸í¿¡ Å©°Ô À§ÇèÇÏ´Ù)°¡ ³ªÅ¸³ª±â ¶§¹®¿¡ ²¨¸®±âµµ ÇÑ´Ù. |
||
| BPO | Benzyl-Penicilloyl |
|---|---|
| 123I-MIBG | 123I-Meta-Iodo-Benzyl-Guanidine |
| 131I-MIBG | 131I-Meta-Iodo-Benzyl-Guanidine |
| MIBG | Meta-Iodo-Benzyl-Guanidine |
| ABNMP | alpha-benzyl-N-methyl phenethylamine |
| penicillin V | phenoxymethyl-penicillin |
|---|---|
| trimethoprim | 2,4-diamino)-5-(3,4,5-trimethoxy-benzyl)-pyrimidine |
| BA | Benzyl alcohol |
| BITC | Benzyl isothiocyanate |
| BSC | Benzyl selenocyanate |
| 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 | <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 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) |
| aluminum penicillin | The trivalent aluminum salt of an antibiotic substance or substances produced by the growth of the molds Penicillium notatum or P. Chrysogenum; used for oral or sublingual administration. (05 Mar 2000) |
| buffered crystalline penicillin G | Crystalline potassium penicillin G or crystalline sodium penicillin G buffered with not less than 4% and not more than 5% of sodium citrate. (05 Mar 2000) |
| penicillin | <drug> Probably the best known of the antibiotics, derived from the mould Penicillium notatum. It blocks the cross linking reaction in peptidoglycan synthesis and therefore destroys the bacterial cell wall making the bacterium very susceptible to damage. (18 Nov 1997) |
| penicillin amidase | <enzyme> An enzyme catalyzing the hydrolysis of penicillin to penicin and a carboxylic acid anion. Chemical name: Penicillin amidohydrolase Registry number: EC 3.5.1.11 (12 Dec 1998) |
| penicillin B | A penicillin preparation that is stable in gastric acid and is rapidly but only partially absorbed from the gastrointestinal tract. Synonym: alpha-phenoxyethylpenicillin potassium, penicillin B. (05 Mar 2000) |
| penicillin G | <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) |
| penicillin G benzathine | <chemical> Semisynthetic antibiotic that is a relatively insoluble preparation that may remain in the body for 1 to 2 weeks, and prepared by combining the sodium salt of penicillin G with n,n'-dibenzylethylenediamine. Pharmacological action: 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))-, compd. With N,N'-bis(phenylmethyl)-1,2-ethanediamine (2:1) (12 Dec 1998) |
| penicillin G hydrabamine | A dipenicillin compound, a mixture of penicillin G salts consisting chiefly of the salt of the diacidic base N,N '-bis-(dehydroabietyl) ethylenediamine. (05 Mar 2000) |
| benzyl penicillin potassium |
pG potassium.
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