Fenethazine References Navigation menu208-325-168223615268J97CUZ4HXD02602ChEMBL2106299100.007.570Interactive imageThe Dictionary of Drugs: Chemical Data: Chemical Data, Structures and BibliographiesLead Optimization for Medicinal Chemists: Pharmacokinetic Properties of Functional Groups and Organic CompoundsDrug Discovery: A Historyeeeexpanding ite

AstemizoleAzelastineBilastineEmedastineMizolastineTalastineAntazolineChloropyramineHistapyrrodineMepyramine (pyrilamine)MethapyrilenePhenbenzamineThenalidineTripelennamine (pyribenzamine)AntidepressantstrazodonePhenbenzamine2-PyridylethylamineBetahistineHistamineHTMTL-HistidineUR-AK494-MethyldiphenhydramineAlimemazineAntazolineAzatadineBamipineBenzatropine (benztropine)BepotastineBromazineBrompheniramineBuclizineCaptodiameCarbinoxamineChlorcyclizineChloropyramineChlorothenChlorphenamineChlorphenoxamineCinnarizineClemastineClobenzepamClocinizineCloperastineCyclizineCyproheptadineDacemazineDecloxizineDeptropineDexbrompheniramineDexchlorpheniramineDimenhydrinateDimetindeneDiphenhydramineDiphenylpyralineDoxylamineEmbramineEtodroxizineEtybenzatropine (ethylbenztropine)EtymemazineFenethazineFlunarizineHistapyrrodineHomochlorcyclizineHydroxyethylpromethazineHydroxyzineIsopromethazineIsothipendylMeclozineMedrylamineMepyramine (pyrilamine)MequitazineMethafuryleneMethapyrileneMethdilazineMoxastineOrphenadrineOxatomideOxomemazinePerlapinePhenindaminePheniraminePhenyltoloxaminePimethixenePiperoxanPipoxizinePromethazinePropiomazinePyrrobutamineTalastineThenalidineThenyldiamineThiazinamiumThonzylamineTolpropamineTripelennamineTriprolidineAcrivastineAlinastineAstemizoleAzelastineBamirastineBarmastineBepiastineBepotastineBilastineCabastinenCarebastineCetirizineClemastineClemizoleClobenztropineDesloratadineDorastineEbastineEfletirizineEmedastineEpinastineFexofenadineFlezelastineKetotifenLatrepirdineLevocabastineLevocetirizineLinetastineLoratadineMapinastineMebhydrolinMizolastineMoxastineNoberastineOctastineOlopatadinePerastinePibaxizinePiclopastineQuifenadine (phencarol)RocastineRupatadineSetastineSequifenadine (bicarphen)TalastineTemelastineTerfenadineVapitadineZepastineAtypical antipsychoticsaripiprazoleasenapinebrexpiprazoleclozapineiloperidoneolanzapinepaliperidonequetiapinerisperidoneRP-5063ziprasidonezotepinePhenylpiperazineantidepressantshydroxynefazodonenefazodonetrazodonetriazoledioneTetracyclic antidepressantsamoxapineloxapinemaprotilinemianserinmirtazapineoxaprotilineTricyclic antidepressantsamitriptylinebutriptylineclomipraminedesipraminedosulepin (dothiepin)doxepinimipramineiprindolelofepraminenortriptylineprotriptylinetrimipramineTypical antipsychoticschlorpromazineflupenthixolfluphenazineloxapineperphenazineprochlorperazinethioridazinethiothixeneAzanatorBelarizineElbanizineFlotrenizineGSK1004723NapactadineTagorizineTrelnarizineTrenizineα-MethylhistamineCipralisantHistamineImetitImmepipImmethridineL-HistidineMethimepipProxyfanA-349,821A-423,579ABT-239ABT-652AZD5213BavisantBetahistineBurimamideCiproxifanClobenpropitConessineEnerisantGSK-189,254ImpentamineIodophenpropitIrdabisantJNJ-5207852MK-0249NNC 38-1049PF-03654746PitolisantSCH-79687ThioperamideVUF-5681AcridineAnthraceneDibenzazepineDibenzocyclohepteneDibenzodiazepineDibenzothiazepineDibenzothiepinDibenzoxazepineDibenzoxepinPhenothiazinePyridazinobenzoxazinePyridinobenzodiazepineThioxantheneAzatadineBisulepinClobenzepamCyproheptadineDacemazineDeptropineDesloratadineEpinastineEtymemazineFenethazineHydroxyethylpromethazineIsopromethazineIsothipendylKetotifenLatrepirdineLoratadineMebhydrolinMequitazineMethdilazineOlopatadineOxomemazinePhenindaminePimethixenePromethazinePropiomazineRupatadineThiazinamiumCarbamazepineDizocilpineEslicarbazepineEslicarbazepine acetateEtazepineLicarbazepineOxcarbazepineOxitriptylineRispenzepine


AntihistaminesPhenothiazinesNervous system drug stubs


INNantihistaminephenothiazinePromethazinechlorpromazinephenbenzamine



























Fenethazine
Fenethazine.png
Clinical data
SynonymsPhenethazinum, Phenethazine, Phenetazine; RP-3015, SC-1627, WY-1143
Identifiers
CAS Number

  • 208-325-1 ☑Y

PubChem CID
  • 68223
ChemSpider

  • 61526 ☑Y
UNII
  • 8J97CUZ4HX
KEGG
  • D02602
ChEMBL

  • ChEMBL2106299 ☑Y
ECHA InfoCard
100.007.570 Edit this at Wikidata
Chemical and physical data
Formula
C16H18N2S
Molar mass270.39 g/mol g·mol−1
3D model (JSmol)
  • Interactive image

Fenethazine (INN) (brand names Anergen, Contralergial, Ethysine, Etisine, Lisergan, Lysergan; former developmental code names RP-3015, SC-1627, WY-1143), or phenethazine, is a first-generation antihistamine of the phenothiazine group.[1]Promethazine, and subsequently chlorpromazine, were derived from fenethazine.[2] Fenethazine, in turn, was derived from phenbenzamine.[3]



References




  1. ^ J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 434–. ISBN 978-1-4757-2085-3..mw-parser-output cite.citationfont-style:inherit.mw-parser-output .citation qquotes:"""""""'""'".mw-parser-output .citation .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-ws-icon abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center.mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-maintdisplay:none;color:#33aa33;margin-left:0.3em.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em


  2. ^ Florencio Zaragoza Dörwald (4 February 2013). Lead Optimization for Medicinal Chemists: Pharmacokinetic Properties of Functional Groups and Organic Compounds. John Wiley & Sons. pp. 301–. ISBN 978-3-527-64565-7.


  3. ^ Walter Sneader (23 June 2005). Drug Discovery: A History. John Wiley & Sons. pp. 404–. ISBN 978-0-471-89979-2.












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