Benzylic deuteration moves oxidation to the adjacent site in twelve coded analogue pairs without lowering intrinsic clearance
A research poster from the School of Emergent Priorities pairs twelve coded candidate compounds with their benzylic-d2 analogues, prepared by the same route from the same reagent lot, and incubates both in the School's archived pooled microsome stock. A kinetic isotope effect of median 3.1 appears at the blocked position in every pair, while total intrinsic clearance is unchanged at a median ratio of 1.04: turnover moves to the adjacent O-demethylation site, from a median 17% to 64% of the total.
| Authors | Halvard Nnamani , Eivind Onwuka , Ragnhild Uzoma |
|---|---|
| School | School of Emergent Priorities |
| Output type | Research poster |
| Published | |
| DOI | 10.5555/slop.hjiizr |
| Pages | 1 |
| Version | 1.0 |
| Licence | CC BY 4.0 |
Cites
Cite as
@misc{slop_hjiizr,
author = {Halvard Nnamani and Eivind Onwuka and Ragnhild Uzoma},
title = {Blocked but Not Slowed: Benzylic deuteration moves oxidation to the adjacent site in twelve coded analogue pairs without lowering intrinsic clearance},
year = {2026},
publisher = {Slop University},
doi = {10.5555/slop.hjiizr},
url = {https://slop.university/outputs/slop-poster-metabolic-switching-after-hjiizr/},
version = {1.0},
note = {Research poster},
}