词条 | Cefmetazole |
释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 460023468 | IUPAC_name = (6R,7S)-7-(2-(cyanomethylthio)acetamido)-7-methoxy-3-((1-methyl-1H-tetrazol-5-ylthio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | image = Cefmetazole.svg | tradename = | Drugs.com = {{drugs.com|international|cefmetazole}} | MedlinePlus = a601206 | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 56796-20-4 | ATC_prefix = J01 | ATC_suffix = DC09 | PubChem = 42008 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = DB00274 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 38311 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 3J962UJT8H | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = D00910 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 3489 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 1201195 | C=15 | H=17 | N=7 | O=5 | S=3 | molecular_weight = 471.538 g/mol | smiles = O=C2N1/C(=C(\\CS[C@@H]1[C@]2(OC)NC(=O)CSCC#N)CSc3nnnn3C)C(=O)O | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/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 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = SNBUBQHDYVFSQF-HIFRSBDPSA-N }} Cefmetazole is a cephamycin antibiotic, usually grouped with the second-generation cephalosporins. Adverse effectsThe chemical structure of cefmetazole, like that of several other cephalosporins, contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain. As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase) and a reaction with ethanol similar to that produced by disulfiram, due to inhibition of aldehyde dehydrogenase.[1] Spectrum of bacterial susceptibilityCefmetazole is a broad-spectrum cephalosporin antimicrobial and has been effective in treating bacteria responsible for causing urinary tract and skin infections. The following represents MIC susceptibility data for a few medically significant microorganisms.
References1. ^{{cite book |author=Stork CM |veditors=Nelson LH, Flomenbaum N, Goldfrank LR, Hoffman RL, Howland MD, Lewin NA |title=Goldfrank's toxicologic emergencies |chapter=Antibiotics, antifungals, and antivirals |chapterurl=https://books.google.com/books?id=cvJuLqBxGUcC&pg=PA847 |publisher=McGraw-Hill |location=New York |year=2006 |pages=847 |isbn=0-07-143763-0 |accessdate=2009-07-03}} {{CephalosporinAntiBiotics}}{{antibiotic-stub}}2. ^http://www.toku-e.com/Assets/MIC/Cefmetazole%20free%20acid.pdf 5 : Acetaldehyde dehydrogenase inhibitors|Cephalosporin antibiotics|Tetrazoles|Nitriles|Carboxamides |
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