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  • Relaxation of the rigid backbone of an oligoamide-foldamer-based α-helix mimetic: identification of potent Bcl-xL inhibitors.

Relaxation of the rigid backbone of an oligoamide-foldamer-based α-helix mimetic: identification of potent Bcl-xL inhibitors.

Organic & biomolecular chemistry (2012-03-08)
Jeremy L Yap, Xiaobo Cao, Kenno Vanommeslaeghe, Kwan-Young Jung, Chander Peddaboina, Paul T Wilder, Anjan Nan, Alexander D MacKerell, W Roy Smythe, Steven Fletcher
ABSTRACT

By conducting a structure-activity relationship study of the backbone of a series of oligoamide-foldamer-based α-helix mimetics of the Bak BH3 helix, we have identified especially potent inhibitors of Bcl-x(L). The most potent compound has a K(i) value of 94 nM in vitro, and single-digit micromolar IC(50) values against the proliferation of several Bcl-x(L)-overexpressing cancer cell lines.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Picolinamide, 98%