fbpx
Wikipedia

Taleranol

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.[1][2] It is the β epimer of zeranol (α-zearalanol) and is a major metabolite of zeranol but with less biological activity.[1][3][2]

Taleranol
Clinical data
Other namesP-1560; Teranol; β-Zearalanol
Identifiers
  • (7S,11S)-7,15,17-Trihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),15,17-trien-13-one
CAS Number
  • 42422-68-4
PubChem CID
  • 65434
UNII
  • HUN219N434
ChEBI
  • CHEBI:35071
ChEMBL
  • ChEMBL491510
CompTox Dashboard (EPA)
  • DTXSID3022532
ECHA InfoCard100.164.729
Chemical and physical data
FormulaC18H26O5
Molar mass322.401 g·mol−1
3D model (JSmol)
  • Interactive image
  • C[C@H]1CCC[C@@H](O)CCCCCc2cc(O)cc(O)c2C(=O)O1
  • InChI=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
  • Key:DWTTZBARDOXEAM-JSGCOSHPSA-N

See also edit

References edit

  1. ^ a b J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 350–. ISBN 978-1-4757-2085-3.
  2. ^ a b Yildiz F (16 December 2009). Advances in Food Biochemistry. CRC Press. pp. 233–. ISBN 978-1-4200-0769-5.
  3. ^ Yu L, Wang S, Sun BG (28 October 2014). Food Safety Chemistry: Toxicant Occurrence, Analysis and Mitigation. CRC Press. pp. 240–. ISBN 978-1-4665-9795-2.



taleranol, usan, developmental, code, name, 1560, teranol, also, known, zearalanol, synthetic, nonsteroidal, estrogen, resorcylic, acid, lactone, group, related, mycoestrogens, found, fusarium, which, never, marketed, epimer, zeranol, zearalanol, major, metabo. Taleranol INN USAN developmental code name P 1560 or teranol also known as b zearalanol is a synthetic nonsteroidal estrogen of the resorcylic acid lactone group related to mycoestrogens found in Fusarium spp which was never marketed 1 2 It is the b epimer of zeranol a zearalanol and is a major metabolite of zeranol but with less biological activity 1 3 2 TaleranolClinical dataOther namesP 1560 Teranol b ZearalanolIdentifiersIUPAC name 7S 11S 7 15 17 Trihydroxy 11 methyl 12 oxabicyclo 12 4 0 octadeca 1 14 15 17 trien 13 oneCAS Number42422 68 4PubChem CID65434UNIIHUN219N434ChEBICHEBI 35071ChEMBLChEMBL491510CompTox Dashboard EPA DTXSID3022532ECHA InfoCard100 164 729Chemical and physical dataFormulaC 18H 26O 5Molar mass322 401 g mol 13D model JSmol Interactive imageSMILES C C H 1CCC C H O CCCCCc2cc O cc O c2C O O1InChI InChI 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 s1Key DWTTZBARDOXEAM JSGCOSHPSA NSee also edita Zearalenol b Zearalenol Zearalanone ZearalenoneReferences edit a b J Elks 14 November 2014 The Dictionary of Drugs Chemical Data Chemical Data Structures and Bibliographies Springer pp 350 ISBN 978 1 4757 2085 3 a b Yildiz F 16 December 2009 Advances in Food Biochemistry CRC Press pp 233 ISBN 978 1 4200 0769 5 Yu L Wang S Sun BG 28 October 2014 Food Safety Chemistry Toxicant Occurrence Analysis and Mitigation CRC Press pp 240 ISBN 978 1 4665 9795 2 nbsp This drug article relating to the genito urinary system is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Taleranol amp oldid 1145821883, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.