Colman P M
Biomolecular Research Institute, Parkville, Australia.
Curr Opin Struct Biol. 1994 Dec;4(6):868-74. doi: 10.1016/0959-440x(94)90268-2.
There are now many successful examples of the design of new ligands based on knowledge of target protein structures. In most cases those ligands are unsuitable as drugs because of problems of toxicity, stability or bioavailability. The past twelve months have also seen the description of the structures of many proteins which are either known to be targets for existing drugs or have clear potential to be utilized in therapy.
基于对靶蛋白结构的了解来设计新配体,现在已有许多成功的例子。在大多数情况下,由于毒性、稳定性或生物利用度问题,这些配体并不适合用作药物。在过去的十二个月里,还对许多蛋白质的结构进行了描述,这些蛋白质要么已知是现有药物的靶点,要么具有明显的治疗应用潜力。