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利尿药和降血糖药Medicinalchemistry利尿药和降血糖药Chapter10Diureticsand
SyntheticHypoglycemicDrugsSection1HypoglycemicDrugsSection2Diuretics利尿药和降血糖药Section1
HypoglycemicDrugsTheclassictriadofsymptomsindiabetesispolyphagia,polydypsia(thirst),andpolyuria(excessurine).Allthreeresultdirectlyfromexcessiveserumglucoselevels.Type1diabetesusuallydevelopsinanacutemanner,althoughthedestructiveautoimmuneprocessmayhavebeenunderwayforsometime.Type2diabeteshasamoreinsidious,oftenasymptomaticonsetanditspresenceisusuallydetectedbyroutinemedicalexaminations.利尿药和降血糖药Definitions
TypeIDiabetes.Insulin-dependentdiabetesmellitus(IDDM),thisconditionoccurswhentheβ-cellsofthepancreaticisletsofLangerhansaredestroyed,probablybyanautoimmuneprocess,suchthatinsulinproductionisdeficient.Type2Diabetes.Noninsulin-dependentdiabetesmellitus(NIDDM)isveryfrequentlyassociatedwithobesityinitsmainlyadultvictims.Seruminsulinlevelsarenormalorelevated,soinessencethisisadiseaseofinsulinresistance.利尿药和降血糖药BiochemistryandPathogenesisofDiabetes利尿药和降血糖药ClassificationsFirstGenerationSulfonylureas:tolbutamide.SecondGenerationSulfonylureas:glibenclamide.ThirdGenerationSulfonylureas:glimepiride,repaglinide.Biguanides:metformin.α-GlucosidaseInhibitors:Acarbose,Miglitol.利尿药和降血糖药
MechanismofActionSulfonylureasinteractwithreceptorsonpancreaticβ-cellstoblockATP-sensitivepotassiumchannels.Thisinturnleadstoopeningofvoltage-sensitivecalciumchannelswhichproducesaninfluxofcalcium;theinfluxofcalciumresultsinβ-cellsproductionofinsulin.Anadditionaleffectofsulfonylureasissuppressionofgluconeogenesisintheliver.利尿药和降血糖药
Physical-ChemicalPropertiesSulfonylureasareweakacidsduetothemarkeddelocalizationofthenitrogenloneelectronpairbythesulfonylgroup.TheirpKa'sclusteraround5.0andtheyarestronglyproteinbound.利尿药和降血糖药
Structure-activityRelationshipsTheremustbereasonablebulkontheureanitrogen;methylandethylcompoundsarenotactive.Usually,thereisonlyone(normallysubstituentpara)onthesulfonylaromaticring.利尿药和降血糖药Manysimplesubstituentsonthesulfonylaromaticringareactive.Thep-(β-arylcarboxamidoethyl)groupingseeninsecondgenerationcompoundsisconsistentwithhighpotency.Itisthoughtthatthespatialrelationshipbetweentheamidenitrogenofthesubstituentandthesulfonamidenitrogenisimportant.利尿药和降血糖药
TolbutamideN-[(Butylamino)carbonyl]-4-methylbenzene–sulfonamideButylgroupontheureanitrogen;Para-methylbenzeneonthesulfonylgroup.利尿药和降血糖药
Properties
Tolbutamidehavesulfonylureastructurewithweakacid,andthispropertymaybeusedforassay.利尿药和降血糖药Instability:Tolbutamideishydrolyzedtopara-toluenesulfonamidebyacids.Heatingofitsfiltratewithsodiumhydroxidesolutionproducesn-butylamineodour.利尿药和降血糖药Metabolism
Tolbutamideismetabolizedinthelivertop-hydroxyltolbutamide,retainingabout35%oftheactivityoftheparentcompound.itisconvertedveryrapidlytotheinactivetolbutamide4-carboxylicacid.利尿药和降血糖药Glibenclamide5-Chloro-N-[2-[4-[[[(cyclohexylamino)carbonyl]amino]sulfonyl]phenyl]-2-methoxybenzamideIntroductionofcyclohexaneontheureanitrogen;Introductionofsidechainonthesulfonylaromaticring.
利尿药和降血糖药Properties
Itisnotstabletomoistureandishydrolyzedtosulfamidederivate.利尿药和降血糖药MetabolismGlibenclamideaffordstrans-4'-hydroxy-glyburideasthemajorproduct.The3'-hydroxymetaboliteretainsabout15%oftheactivityoftheparentcompound.利尿药和降血糖药TherapeuticApplicationIngeneral,theeffectsofthefirst-andsecond-generationsulfonylureasaresimilar.Allproducereliablehypoglycemiaintype2diabetics.Theseagentsworkbestinpatientswhosetype2diabetesisrelativelymild.利尿药和降血糖药SyntheticRoute利尿药和降血糖药Third-generationsulfonylureaGlimepirideisasulfonylureawithaquickonsetofactionandalongdurationofaction.Itmaybindtoadifferentproteinintheputativesulfonylureareceptorthanearlierdrugs,andmayexertitshypoglycemiceffectwithlesssecretionofinsulin.利尿药和降血糖药
Metforminhydrochloride
N,N-DimethylimidodicarbonimidicdiamidehydrochlorideMetformin,Biguanides,hasbeeninusethroughouttheworld,withtheexceptionoftheU.S.,fordecades.利尿药和降血糖药
MechanismofActionMetforminisusuallysaidtobeanantihyperglycemicratherthanahypoglycemicagent.Overall,thedrugappearstoincreaseglucoseutilization.Inhibitionofgluconeogenesisappearstobeanimportantcomponentofthedrug'sactivity.利尿药和降血糖药
ActionsandUsesUnlikesulfonylureas,Metforminisnotproteinbound,isnotmetabolized,andisrapidlyeliminatedbythekidney.Itiswidelyusedasmonotherapyorincombinationwithasulfonylureaintype2diabetes,particularlywhenthepatientisobeseandinsulin-resistant.利尿药和降血糖药
α-GlucosidaseInhibitorsTobeabsorbedfromthegastrointestinaltractintothebloodstream,thecomplexcarbohydratesweingestaspartofourdietmustfirstbehydrolyzedtomonosaccharides.Therationalefortheα-glucosidaseinhibitoristhatbypreventingthehydrolysisofcarbohydratestheirabsorptioncouldbereduced.利尿药和降血糖药Metabolismofcomplexcarbohydrades
利尿药和降血糖药
Section2DiureticsDiureticsarechemicalsthatincreasetherateofurineformation.Diureticusageleadstotheincreasedexcretionofelectrolytes(especiallysodiumandchlorideions)andwaterfromthebodywithoutaffectingprotein,vitamin,glucoseoraminoacidreabsorption.利尿药和降血糖药
StructureClassificationThediureticscurrentlyinusetodayareclassifiedasfollows:Thiazides(bytheirchemicalclasses);Carbonicanhydraseinhibitors,osmotics(bymechanismofaction);Loopdiuretics(bysiteofaction);Potassium-sparingdiuretics(byeffectsonurinecontents).利尿药和降血糖药Furosemide5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoicacidFurosemideisanexampleofahigh-ceilingdiureticandmayberegardedasaderivativeofanthranilicacids.利尿药和降血糖药
Structure-activityRelationshipsThechlorineandsulfonamidesubstitutionsarefeaturesofthisclassdrugs.Furosemideisastrongeracidthanthethiazidediuretics(pKa3.9).Thisdrugisexcretedprimarilyunchanged.Asmallamountofmetabolism,however,cantakeplaceonthefuranring.利尿药和降血糖药
TherapeuticApplicationsFurosemidehasasalureticeffect8-10timesthatofthethiazidediuretics,however,ithasashorterdurationofaction,about6-8hours.Itiseffectiveforthetreatmentofedemasconnectedwithcardiac,hepatic,andrenalsites.Clinicaltoxicityoffurosemideinvolvesabnormalitiesoffluidandelectrolytebalance.利尿药和降血糖药Hydrochlorothiazide6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide1,1-dioxideThethiazidediureticsareweaklyacidicwithabenzothiadiaze1,1-dioxidenucleus.利尿药和降血糖药
MechanismofActionThemajorsiteofactionofthesecompoundsisinthedistaltubule,wherethesedrugscompeteforthechloridebindingsiteoftheNa+-C1-symporterandinhibitthereabsorptionofsodiumandchlorideions.Theyalsoinhibitthereabsorptionofpotassiumandbicarbonateionsbuttoalesserdegree.利尿药和降血糖药
Structure-activityRelationshipThehydrogenatomatthe2-Nisthemostacidic.Theseacidicprotonsmakepossibletheformationofawater-solublesodiumsalt.Anelectron-withdrawinggroupisnecessaryatposition6fordiureticactivity.Replacementorremovalofthesulfonamideatposition7yieldscompoundswithlittleornodiureticactivity.利尿药和降血糖药Saturationofthedoublebondtogivea3,4dihydroderivativeproducesadiureticthatis10timesmorethantheunsaturatedderivative.Substitutionlipophilicgroupatposition3givesamarkedinthediureticpotencywithalongerdurationofaction.Alkylsubstitutiononthe2-Npositionalsodecreasesthepolarityandincreasesthedurationofdiureticaction.利尿药和降血糖药TherapeuticApplicationsHydrochlorothiazideisindicatedinthemanagementofhypertensioneitherasthesoletherapeuticagent,orincombinationwithotherantihypertensives.利尿药和降血糖药AcetazolamideN-[5-(Aminosulfonyl)1,3,4-thiadiazol-2-yl]acetamideAcetazolamidewasthefirstofthecarbonicanhydraseinhibitorswithadiureticeffectthatlastsabout8-12hours.Itisusedprimarilyforthetreatmentofglaucomaandabsenceseizures.利尿药和降血糖药MechanismofActionTheactionoftheenzymecarbonicanhydrasecatalyzestheformationofcarbonicacidfromcarbondioxideandwater.Carbonicanhydraseinhibitorsinducediuresisbyinhibitingtheformationofcarbonicacidwithinproximalanddistaltubularcellstolimitthenumberofhydrogenionsavailabletopromotesodiumreabsorption.利尿药和降血糖药SpironolactoneTheadrenal(7β-17α)-7(Acetylthio)-17-hydroxy-3-oxopregn-4ene-21-carboxylicacid
-lactone
Spironolactoneisacompetitiveantagonisttothemineralocorticoidssuchasaldosterone.利尿药和降血糖药
MechanismofActionTheadrenalcortexsecretesapotentmineralocorticoidcalledaldosteronewhichpromotessaltandwaterretentionandpotassiumandhydrogenionexcretion.Spironolactoneinhibitsreabsorptionofsodiumandchlorideionandincreasedpotassiumionexcretion.利尿药和降血糖药
Metabolism
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