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. Author manuscript; available in PMC: 2016 Mar 11.
Published in final edited form as: Curr Pharm Des. 2014;20(5):704–724. doi: 10.2174/138161282005140214163327

Figure 12. Chemical configurations of various toxophores.

Figure 12

(A) Illustration of s-cis and s-trans conformation of conjugated double bonds. (B) The oxazolidendione ring is oriented and its atoms are numbered (1–5) to optimally match the methoxy methyl acrylate (MOA) group to the left. The five-membered ring resembles a 'tied' back version of the MOA group.