Methicillin

PBP2a works in a similar manner to other PBPs, but it binds β-lactams with very low affinity, meaning they do not compete efficiently with the natural substrate of the enzyme and will not inhibit cell wall biosynthesis.[citation needed] These susceptibility data are given on a few medically significant bacteria: Like other beta-lactam antibiotics, methicillin acts by inhibiting the synthesis of bacterial cell walls.It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell wall of gram-positive bacteria.Methicillin and other β-lactam antibiotics are structural analogs of D-alanyl-alanine, and the transpeptidase enzymes that bind to them are sometimes called penicillin-binding proteins (PBPs).[4] It was previously used to treat infections caused by susceptible gram-positive bacteria, in particular, penicillinase-producing organisms such as Staphylococcus aureus that would otherwise be resistant to most penicillins.
metacyclineRoutes ofadministrationATC codeJ01CF03QJ51CF03PharmacokineticBioavailabilityMetabolismElimination half-lifeExcretionIUPAC nameCAS NumberDrugBankChemSpiderChEMBLCompTox DashboardECHA InfoCardFormulaMolar massSMILESnarrow-spectrumβ-lactam antibioticpenicillinantimicrobial resistanceβ-lactamaseinterstitial nephritisadverse effectsusceptibility testinglaboratoryStaphylococcus aureuscloxacillingenetic testinggram-positive bacteriapenicillin binding proteinmecA geneMethicillin resistant Staphylococcus aureuscell wallspeptidoglycantranspeptidasepenicillin-binding proteinspenicillinasebeta-lactamasesside-chainsteric hindranceBeechaminfectionsoxacillinflucloxacillindicloxacillinmethicillin-resistant Staphylococcus aureusAntibacterialscell wallenvelopeβ-lactamsD-alanyl-D-alaninetranspeptidasesPenicillinsPenamsBenzylpenicillin (G)Benzathine benzylpenicillinProcaine benzylpenicillinPhenoxymethylpenicillin (V)PropicillinPheneticillinAzidocillinClometocillinPenamecillinNafcillinExtendedspectrumAminopenicillinsAmoxicillinAmpicillinPivampicillinHetacillinBacampicillinLenampicillinMetampicillinTalampicillinEpicillinCarboxypenicillinsTicarcillinCarbenicillinCarindacillinTemocillinUreidopenicillinsPiperacillinAzlocillinMezlocillinMecillinamPivmecillinamSulbenicillinCarbapenemsPenemsErtapenemAntipseudomonalDoripenemImipenemMeropenemBiapenemPanipenemFaropenemRitipenemSulopenemCephemsCephalosporinsCephamycinsCarbacephemsCefazolinCefalexinCefadroxilCefapirinCefazedoneCefazaflurCefradineCefroxadineCeftezoleCefaloglycinCefacetrileCefaloniumCefaloridineCefalotinCefatrizineCefaclorCefprozilCefuroximeCefuroxime axetilCefamandoleCefonicidCeforanideCefuzonamCephamycinCefoxitinCefotetanCefminoxCefbuperazoneCefmetazoleCarbacephemLoracarbefCefiximeCeftriaxoneCefotaximeCeftazidimeCefoperazoneCefdinirCefcapeneCefdaloximeCeftizoximeCefmenoximeCefpiramideCefpodoximeCeftibutenCefditorenCefotiamCefetametCefodizimeCefpimizoleCefsulodinCefteramCeftioleneOxacephemFlomoxefLatamoxefCefepimeCefozopranCefpiromeCefquinomeCeftaroline fosamilCeftolozaneCeftobiproleSiderophoreCefiderocolVeterinaryCeftiofurCefovecinMonobactamsAztreonamTigemonamCarumonamNocardicin Aβ-lactamase inhibitorsSulbactamTazobactamClavamClavulanic acidAvibactamDurlobactamRelebactamVaborbactamAmoxicillin/clavulanic acidAmpicillin/flucloxacillinAmpicillin/sulbactamSultamicillinAztreonam/avibactamBenzathine benzylpenicillin/procaine benzylpenicillinCefepime/enmetazobactamCefoperazone/sulbactamCeftazidime/avibactamCeftolozane/tazobactamImipenem/cilastatinImipenem/cilastatin/relebactamMeropenem/vaborbactamPanipenem/betamipronPiperacillin/tazobactamSulbactam/durlobactamSulopenem/probenecidTicarcillin/clavulanic acidPolypeptidesLipopeptidesDaptomycinSurfactinRamoplaninFosfomycinCycloserinebactoprenolBacitracinlysozymeTyrothricinGramicidinTyrocidineIsoniazidTeixobactinWHO-EMWithdrawnClinical trials