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. 2001 Dec;45(12):3347–3354. doi: 10.1128/AAC.45.12.3347-3354.2001

FIG. 3.

FIG. 3

(A) Primary structure of butenafine; the torsion angles are annotated α1 to α9. (B and C) Selected structures of butenafine (probability, >15%) obtained by the Simplex energetic minimization procedure. The percentages of probability of the neutral form (B) and the protonated forms (R and S enantiomers) (C) are indicated for each structure.