Taleranol

{{Short description|Chemical compound}}

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| IUPAC_name = (7S,11S)-7,15,17-Trihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),15,17-trien-13-one

| image = Taleranol.svg

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| CAS_number = 42422-68-4

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| PubChem = 65434

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| UNII = HUN219N434

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| ChEBI = 35071

| ChEMBL = 491510

| 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

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| StdInChIKey = DWTTZBARDOXEAM-JSGCOSHPSA-N

| synonyms = P-1560; Teranol; β-Zearalanol

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Taleranol (INN, USAN) (developmental code name P-1560), or teranol, also known as β-zearalanol, is a synthetic, nonsteroidal estrogen of the resorcylic acid lactone group related to mycoestrogens found in Fusarium spp which was never marketed.{{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–}}{{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–}} It is the β epimer of zeranol (α-zearalanol) and is a major metabolite of zeranol but with less biological activity.{{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–}}

See also

References

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{{Xenoestrogens}}

{{Estrogen receptor modulators}}

Category:Lactones

Category:Mycoestrogens

Category:Mycotoxins

Category:Resorcinols

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