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A series of novel stearoyl-CoA desaturase 1 (SCD1) inhibitors were identified by scaffold design based on known SCD1 inhibitors. Large structural changes were made leading to multiple analogs with comparable or improved potency. This approach is valuable for generation of proprietary compounds without conducting a costly high-throughput screening.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, name: 4-Phenoxypiperidine, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 3202-33-3
Reference:
Piperidine – Wikipedia,
Piperidine | C5H10730N – PubChem