Biocatalytic synthesis of n-n and c-n heterobiaryl atropisomers - proposal summary atropisomerism is a type of chirality that arises from restricted rotation about a bond

Active Project Grant Awarded Last action

Award ID
F32GM157984
Recipient
Awarding agency
Obligated
$444,984

Award facts

Assistance listing
93.859 Biomedical Research and Research Training
Completion date 57% complete
Place of performance
Ann Arbor, MI 48109, USA

Award details come from USAspending.gov.

Description

Introduction of atropisomerism to small-molecule drug candidates can improve potency, selectivity, and adme (absorption, distribution, metabolism, and excretion) properties. An underexplored class of atropisomers are heterobiaryl atropisomers featuring an n-n or c-n atropisomeric axis. These classes of atropisomers have demonstrated potent pharmaceutical properties. However, as compared to c-c atropisomers, there are relatively few enantioselective methodologies for their synthesis. Most strategies rely on the derivatization of substrates already containing the n-x bond (where x = n or c). An underexplored approach is the direct coupling of two heteroarene fragments that form the n-x bond atroposelectively. However, known methods require the pre- functionalization of starting materials, thereby limiting the generality of these strategies. Nature, on the other hand, synthesizes heterobiaryl atropisomers by a direct oxidative coupling, wherein an n-h and x-h bond undergo direct conversion into an n-x bond under mild reaction conditions. Flavin- dependent aromatic hydroxylases (fdah) are an enzyme class with demonstrated n-n and c-n coupling reactivity. The research outlined in this proposal will draw upon this known reactivity to develop general strategies for the synthesis of n-n and c-n heterobiaryl atropisomers. Towards this goal, i will employ bioinformatic techniques to develop a library of fdah enzymes to explore this unique coupling reactivity. From the reactivity profile of this fdah enzyme library, i will identify features of these enzymes that contribute to the site-selectivity of this oxidative coupling approach. Employing both enzyme library reactivity profiling and protein engineering, i will develop atroposelective n-n and c-n biocatalytic coupling strategies. The methods developed herein will provide access to a class of medicinally relevant atropisomers that are difficult to obtain by other approaches.

Transactions

Action Obligated Date
Amendment $1,248
Amendment $75,052
Amendment $75,052
Amendment $73,408
Amendment $0
Amendment $73,408
Amendment $73,408
Amendment $0
Amendment $0
Original award $73,408

Quick answers

Who received award F32GM157984?

F32GM157984 was awarded to Regents Of The University Of Michigan by National Institute of General Medical Sciences (National Institutes of Health) on May 13, 2025.

How much is award F32GM157984 worth?

$444,984 has been obligated on F32GM157984.

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