Compared to synthetic compounds, herbal monomers tend to have higher biological activity and structural diversity and are more likely to enter cells to exert their effects. In addition, for some specific challenging targets, there is a greater probability of obtaining their modulators from herbal monomers by screening. Lifeasible is dedicated to the isolation and activity evaluation of physiologically important natural products in herbal medicines, helping you elucidate the active substance base in herbal medication and providing strategies for developing new structural and highly functional target lead compounds for innovative medicines.
Figure 1. Schematic diagram of a new drug development model based on compatibility-combination theory.
We help you to identify and optimize lead compounds as drug candidates by applying high content analysis (HCA), network pharmacology, genomics, functional genomics, and other methods for the multi-target screening of new drugs. The series of new chemical entities obtained based on the above development concept, whether by isolation or synthesis, are derived from the efficacy of classical prescriptions, and therefore their efficacy evaluation is based on the clinical application of the herbal compound. The selection of pharmacological activity screening models based on the type of disease treated by the formulae can effectively reduce the blindness of pre-screening and allow for a more targeted pharmacodynamic evaluation of the obtained series of compounds.
Lifeasible applies traditional drug use thinking, principles of modern drug design, and other relevant methods of modern drug discovery to the design of innovative drugs from herbal medicines to help you obtain lead compounds that match the characteristics of herbal medicine's action (multi-component, multi-target, multi-pathway). Please feel free to contact us to create development strategies for different needs and to meet our customers' bespoke requirements.