Begin with an sp2-hybridized nitrogen (N1) as the central point, which carries two substituents:
1. A benzene ring (Ring A) with three methyl groups.
   - Attach Ring A to N1 via a single bond to one of its carbons, labeled as A1.
   - Methyl groups (-CH3) are positioned at A2, A4, and A6, following consecutive numbering around the ring.
2. A double bond to an sp2-hybridized carbon (C2), which has two additional attachments:
   - A single-bonded hydroxyl (-OH) group.
   - A chain leading to a para-fluorophenyl (Ring B), described as follows:
     - From C2, proceed to a methylene (C3), which is bonded to a secondary amine (N4) which itself bears one methyl substituent.
     - N4 continues to another methylene (C5).
     - C5 is bonded to an sp2 carbon (C6).
     - C6 is single-bonded to a hydroxyl (-OH) group and double-bonded to a nitrogen (N7).
     - N7 is single-bonded to a methylene (C8).
     - C8 is bonded to a fluoro-substituted benzene ring (Ring B), where the fluorine is positioned para (B4) to the site of attachment (B1).

No stereogenic centers or double-bond (E/Z) stereochemistry are specified.