Significats de chemical series en anglès

Here we describe our comprehensive structure-activity relationship (SAR) studies of this chemical series.

Identification, synthesis and structure-activity relationship of small-molecule VIPR1 antagonists encompassing two chemical series are described.

Although several chemical series of PHD inhibitors have been described, significant isoform selectivity has not been reported.

We describe two chemical series that bind to the myristoyl site of the c-Abl kinase domain and stimulate c-Abl activation.

Here, we further investigate the mechanisms of action of the most active of this chemical series, isopimpinellin, in our zebrafish model of neutrophilic inflammation.