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|
| Mechanism of Action |
Cefmetazole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The bactericidal activity of cefmetazole results from the inhibition of cell wall synthesis via affinity for penicillin-binding proteins (PBPs).
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| Pharmacology |
Cefmetazole¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cefmetazole is a second-generation cephalosporin. The cephalosporins are bactericidal drugs with both gram-positive and gram-negative activity. They inhibit bacterial cell wall synthesis in a way similar to the penicillins. Cefmetazole is more active than 1st-generation cephalosporins against indole-positive Proteus, Serratia, anaerobic gram-negative bacilli (including B. fragilis), and some E. coli, Klebsiella, and P. mirabilis, but is less active than cefoxitin or cefotetan against most gram-negative bacilli.
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| Metabolism |
Cefmetazole¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Cefmetazole¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Cefmetazole¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1.50 ¡¾0.14 hours
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| Absorption |
Cefmetazole¿¡ ´ëÇÑ Absorption Á¤º¸ Bioavailability is approximately 100% following intramuscular injection.
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| Biotransformation |
Cefmetazole¿¡ ´ëÇÑ Biotransformation Á¤º¸ No appreciable metabolism.
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| Toxicity |
Cefmetazole¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in rats is 3,204 mg/kg. With other b-lactam antibiotics, adverse effects following overdosage have included nausea, vomiting, epigastric distress, diarrhea, and convulsions.
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| Drug Interactions |
Cefmetazole¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
|
| Description |
Cefmetazole¿¡ ´ëÇÑ Description Á¤º¸ A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. [PubChem]
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| Drug Category |
Cefmetazole¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial Agents
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| Smiles String Canonical |
Cefmetazole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1(NC(=O)CSCC
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| Smiles String Isomeric |
Cefmetazole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CO[C@]1(NC(=O)CSCC
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| InChI Identifier |
Cefmetazole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H17N7O5S3/c1-21-14(18-19-20-21)30-6-8-5-29-13-15(27-2,17-9(23)7-28-4-3-16)12(26)22(13)10(8)11(24)25/h13H,4-7H2,1-2H3,(H,17,23)(H,24,25)/t13-,15+/m1/s1/f/h17,24H
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| Chemical IUPAC Name |
Cefmetazole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7S)-7-[[2-(cyanomethylsulfanyl)acetyl]amino]-7-methoxy-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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The database contains the following fields: The generic name of each chemical For module A10 (liver enzyme composite module): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method) Number of endpoints at which each compound is marginally active (M) Number of endpoints at which each compound is active (A) For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method) Number of ADR reports for each compound, given as <4 or ¡Ã4 Reporting Index value for each compound, except where no shipping units were available (NSU) Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period. CEFMETAZOLE[GGT Increase][Composite Activity](Score) I(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) I(Number of Rpts) <4(Index value) 0.1[SGOT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[SGPT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[LDH Increase](Activity Score) I(Number of Rpts) <4(Index value) 25.5[GGT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0
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