We report a series of lipidated 伪-AApeptides that mimic the structure and function of natural antimicrobial lipopeptides. Several short lipidated 伪-AApeptides show broad-spectrum activity against a range of clinically related Gram-positive and Gram-negative bacteria as well as fungus. Their antimicrobial activity and selectivity are comparable or even superior to the clinical candidate pexiganan as well as previously reported linear 伪-AApeptides. The further development of lipidated 伪-AApeptides will lead to a new class of antibiotics to combat drug resistance.