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University of Texas Southwestern Medical Center

Precursor-Directed Identification of Natural Product Scaffolds

Abstract

dc:description

The rapid generation of natural product analogs is a fundamental challenge in both the optimization of medicinal potency and exploration of novel biological activity. Previous work with Streptomyces variabilis has demonstrated that natural products that incorporate non-enzymatic transformation can be exploited for the rapid generation of analogs. Herein we demonstrate a general methodology to use fluorinated or isotopically labeled substrates to identify natural product frameworks prone to non-enzymatic pathways. As proof of principle our precursor directed methodology was used in the study of discoipyrrole A formation, the guided isolation of a novel iminoquinone and the detection of a novel ammosamide analog via incorporation of a carbon-based nucleophile.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Brumley, David Anderson
Contributors dc:contributor
  • MacMillan, John

Subjects

dc:subject × 6

Rights

Language dc:language
en

Identifiers

dc:identifier.*
Identifier
1103324459
OAI identifier oai:identifier
oai:utswmed-ir.tdl.org:2152.5/6618

Chain of custody

source
Harvested from
University of Texas Southwestern Medical Center
Base URL
utswmed-ir.tdl.org/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Brumley, David Anderson. Precursor-Directed Identification of Natural Product Scaffolds. 2019. https://hdl.handle.net/2152.5/6618