Redefining Drug Immune Recognition: A Radically Reconfigured Molecular Architecture Enables Broad Fentanyl-Class Protection

range, preserved ventilation during respiratory challenge, and reduced brain fentanyl from 61.9 ± 10.0 to 17.2 ± 0.7 nM. These results reveal programmable antibody recognition, demonstrating that molecular class identity arises not from direct structural mimicry but through higher-order spatial and physicochemical relationships.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-05-12
DOI
https://doi.org/10.1021/acs.jmedchem.6c00991
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
0.00
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article

Redefining Drug Immune Recognition: A Radically Reconfigured Molecular Architecture Enables Broad Fentanyl-Class Protection

Lisa M. Eubanks, Rachel C. Steinhardt, Arran W. Stewart, Bin Zhou et al.
Journal of Medicinal Chemistry
Receptor Mechanisms and Signaling
article

Redefining Drug Immune Recognition: A Radically Reconfigured Molecular Architecture Enables Broad Fentanyl-Class Protection

Lisa M. Eubanks, Rachel C. Steinhardt, Arran W. Stewart, Bin Zhou, Kim D. Janda
article en

Abstract

range, preserved ventilation during respiratory challenge, and reduced brain fentanyl from 61.9 ± 10.0 to 17.2 ± 0.7 nM. These results reveal programmable antibody recognition, demonstrating that molecular class identity arises not from direct structural mimicry but through higher-order spatial and physicochemical relationships.

Journal of Medicinal Chemistry
Scripps Research Institute (US)
Openalex Percentile: Top 8%
Receptor Mechanisms and Signaling
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