Combinatorial chemistry techniques can generate extensive libraries of potential enzyme activators and inhibitors. These
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Combinatorial chemistry techniques can generate extensive libraries of potential enzyme activators and inhibitors. These
Combinatorial chemistry techniques can generate extensive libraries of potential enzyme activators and inhibitors. These libraries can be screened by "high throughput screening" (HTS). Briefly explain what HTS is. Compare/contrast HTS to "rational drug design"? Which do you think is more likely to yield a viable drug candidate? Why?