Levormeloxifeneのソースを表示
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Levormeloxifene
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{{Short description|Chemical compound}} {{Drugbox | Verifiedfields = changed | Watchedfields = | verifiedrevid = 462091315 | IUPAC_name = 1-(2-[4-[(3''R'',4''R'')-7-Methoxy-2,2-dimethyl-3-phenyl-3,4-dihydro-2''H''-chromen-4-yl]phenoxy]ethyl)pyrrolidine | image = Levormeloxifene.svg | width = 225px <!--Clinical data--> | tradename = | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | pregnancy_US = <!-- A / B / C / D / X --> | pregnancy_category = | legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = <!--Pharmacokinetic data--> | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = <!-- Identifiers --> | CAS_number_Ref = {{cascite|changed|??}} | CAS_number = 78994-23-7 | CAS_supplemental = | class = | ATC_prefix = | ATC_suffix = | ATC_supplemental = | PubChem = 35805 | IUPHAR_ligand = | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 32935 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 9512UKZ352 | KEGG = | ChEBI = | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 301327 | synonyms = Levomeloxifene; 6720-CDRI; NNC-460020 <!--Chemical data--> | C=30 | H=35 | N=1 | O=3 | SMILES = O(c1ccc(cc1)[C@@H]3c4c(OC([C@H]3c2ccccc2)(C)C)cc(OC)cc4)CCN5CCCC5 | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C30H35NO3/c1-30(2)29(23-9-5-4-6-10-23)28(26-16-15-25(32-3)21-27(26)34-30)22-11-13-24(14-12-22)33-20-19-31-17-7-8-18-31/h4-6,9-16,21,28-29H,7-8,17-20H2,1-3H3/t28-,29+/m1/s1 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = XZEUAXYWNKYKPL-WDYNHAJCSA-N }} '''Levormeloxifene''' ({{abbrlink|INN|International Nonproprietary Name}}; developmental code names '''6720-CDRI''', '''NNC-460020''') is a [[selective estrogen receptor modulator]] (SERM) which was being developed as an alternative to [[hormone replacement therapy (menopause)|estrogen replacement therapy]] for the treatment and prevention of [[menopause|postmenopausal]] [[Osteoporosis|bone loss]] but did not complete development and hence was never marketed.<ref name="AdisInsight">{{Cite web | url=http://adisinsight.springer.com/drugs/800000737 |title = Levormeloxifene - AdisInsight}}</ref> The development was stopped because of a high incidence of [[gynecological]] [[side effect]]s during [[clinical trial]]s.<ref name="pmid16532904">{{cite journal | vauthors = Ravn P, Nielsen TF, Christiansen C | title = What can be learned from the levormeloxifene experience? | journal = Acta Obstet Gynecol Scand | volume = 85 | issue = 2 | pages = 135–42 | year = 2006 | pmid = 16532904 | doi = 10.1080/00016340500345691| s2cid = 12872469 | doi-access = free }}</ref> Levormeloxifene is the [[dextrorotation and levorotation|levorotatory]] [[enantiomer]] of [[ormeloxifene]], which, in contrast, has been marketed, though rather as a [[hormonal contraceptive]]. ==See also== * [[List of selective estrogen receptor modulators]] ==References== {{Reflist|2}} ==External links== * [http://adisinsight.springer.com/drugs/800000737 Levormeloxifene - AdisInsight] {{Estrogen receptor modulators}} [[Category:Abandoned drugs]] [[Category:Benzopyrans]] [[Category:Ethers]] [[Category:1-Pyrrolidinyl compounds]] [[Category:Selective estrogen receptor modulators]] {{genito-urinary-drug-stub}}
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