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Taleranol
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{{Short description|Chemical compound}} {{Drugbox | Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (7''S'',11''S'')-7,15,17-Trihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),15,17-trien-13-one | image = Taleranol.svg | width = 250 <!--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 = | CAS_number = 42422-68-4 | CAS_supplemental = | ATC_prefix = | ATC_suffix = | ATC_supplemental = | PubChem = 65434 | IUPHAR_ligand = | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = | UNII = HUN219N434 | KEGG = | ChEBI = 35071 | ChEMBL = 491510 <!--Chemical data--> | C=18 | H=26 | O=5 | SMILES = C[C@H]1CCC[C@@H](O)CCCCCc2cc(O)cc(O)c2C(=O)O1 | StdInChI_Ref = | StdInChI = 1S/C18H26O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h10-12,14,19-21H,2-9H2,1H3/t12-,14-/m0/s1 | StdInChIKey_Ref = | StdInChIKey = DWTTZBARDOXEAM-JSGCOSHPSA-N | synonyms = P-1560; Teranol; β-Zearalanol }} '''Taleranol''' ([[International Nonproprietary Name|INN]], [[United States Adopted Name|USAN]]) (developmental code name '''P-1560'''), or '''teranol''', also known as '''β-zearalanol''', is a [[synthetic compound|synthetic]], [[nonsteroidal]] [[estrogen]] of the [[resorcylic acid lactone]] group related to [[mycoestrogen]]s found in ''[[Fusarium|Fusarium spp]]'' which was never marketed.<ref name="Elks2014">{{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA350|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=350–}}</ref><ref name="Yildiz2009">{{cite book| vauthors = Yildiz F |title=Advances in Food Biochemistry|url=https://books.google.com/books?id=orwY4Nd_t1wC&pg=PA233|date=16 December 2009|publisher=CRC Press|isbn=978-1-4200-0769-5|pages=233–}}</ref> It is the β [[epimer]] of [[zeranol]] (α-zearalanol) and is a major [[metabolite]] of zeranol but with less [[biological activity]].<ref name="Elks2014" /><ref name="YuWang2014">{{cite book| vauthors = Yu L, Wang S, Sun BG |title=Food Safety Chemistry: Toxicant Occurrence, Analysis and Mitigation|url=https://books.google.com/books?id=rs3MBQAAQBAJ&pg=PA240|date=28 October 2014|publisher=CRC Press|isbn=978-1-4665-9795-2|pages=240–}}</ref><ref name="Yildiz2009" /> ==See also== * [[α-Zearalenol]] * [[β-Zearalenol]] * [[Zearalanone]] * [[Zearalenone]] ==References== {{Reflist}} {{Xenoestrogens}} {{Estrogen receptor modulators}} [[Category:Lactones]] [[Category:Mycoestrogens]] [[Category:Mycotoxins]] [[Category:Resorcinols]] {{genito-urinary-drug-stub}}
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