Talk:Bexlosteride

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Name/Structure mismatch

The names imply that bexlosteride has R-configuration at both stereocentres, however, the image is S-configuration at both stereocentres. --The chemistds (talk) 00:15, 9 November 2011 (UTC)[reply]

I have corrected the infobox data to consistently match the correct stereoisomer. -- Ed (Edgar181) 11:48, 24 November 2016 (UTC)[reply]

Moved from article

I have moved the following content here because it lacks context/explanation. If anyone wants to use it to improve the article, here it is. -- Ed (Edgar181) 21:54, 23 November 2016 (UTC)[reply]

[[File:Bexlosteride synthesis.svg|thumb|700px|center|Preparation of Bexlosteride:<ref>{{Cite journal | doi = 10.1021/jo9601425| pmid = 11667351| title = Resolution of δ-Lactams Provides Access to Nonracemic Benzoquinolinones: The Synthesis of LY300502 and LY300503| journal = The Journal of Organic Chemistry| volume = 61| issue = 13| pages = 4450–4454| year = 1996| last1 = Astleford | first1 = B. A. | last2 = Audia | first2 = J. E. | last3 = Deeter | first3 = J. | last4 = Heath | first4 = P. C. | last5 = Janisse | first5 = S. K. | last6 = Kress | first6 = T. J. | last7 = Wepsiec | first7 = J. P. | last8 = Weigel | first8 = L. O. }}</ref>]] A QSAR model was developed (1993):<ref>{{Cite journal | doi = 10.1016/S0960-894X(00)80306-6| title = QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase| journal = Bioorganic & Medicinal Chemistry Letters| volume = 3| issue = 6| pages = 1157| year = 1993| last1 = Wikel | first1 = J. H. | last2 = Bemis | first2 = K. G. | last3 = Audia | first3 = J. E. | last4 = McQuaid | first4 = L. A. | last5 = Jones | first5 = C. D. | last6 = Pennington | first6 = P. A. | last7 = Lawhorn | first7 = D. E. | last8 = Hirsch | first8 = K. R. | last9 = Stamm | first9 = N. B.}}</ref>