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Richard Cox

Publications and source records attributed to Richard Cox.

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Canalesolide A, a Structurally Unique Polyhydroxy Macrolide from the Marine Cyanobacterium Okeania sp. with Potent Antitrypanosomal Activity.

The discovery of structurally novel natural products remains central to expanding biologically relevant chemical space, particularly within underexplored marine metabolite classes. Herein, we report the discovery and complete structural elucidation of canalesolide A, a new polyhydroxylated macrolide isolated from the marine cyanobacterium Okeania sp. The compound was identified through an integrated workflow combining phenotypic screening against Trypanosoma brucei and LC-MS/MS-based molecular networking, enabling rapid prioritization of bioactive fractions and dereplication of known metabolite families. Spectroscopic analysis revealed that canalesolide A belongs to the bastimolide-related class of macrolides but exhibits a distinct structural architecture. Its structure was established by integrating ultrahigh-resolution NMR spectroscopy, empirical configurational analysis of polyol systems, targeted model compound synthesis, and controlled chemical degradation and derivatization. This combined strategy resolved stereochemical motifs that were inaccessible by direct analysis of the intact macrolide alone, providing a transferable approach for assigning densely oxygenated marine macrolides. Genome mining identified the putative biosynthetic gene cluster and proposed biosynthetic pathway for a bastimolide-related macrolide. Canalesolide A displays potent, low nanomolar antitrypanosomal activity against human-infective subspecies of T. brucei with rapid elimination of parasites within 1 h at 1 μM. Although moderate mammalian cytotoxicity was observed, preliminary in vivo efficacy/toxicity studies in infected mice suggest a narrow therapeutic window highlighting the need for improved selectivity. This study expands the structural and biosynthetic diversity of polyhydroxylated macrolides and establishes a generalizable framework for resolving stereochemically complex natural products.

Macrolides↗

Reconnecting interpretation to reasoning through individual differences.

Computational theories of mind assume that participants interpret information and then reason from those interpretations. Research on interpretation in deductive reasoning has claimed to show that subjects' interpretation of single syllogistic premises in an "immediate inference" task is radically different from their interpretation of pairs of the same premises in syllogistic reasoning tasks (Newstead, 1989, 1995; Roberts, Newstead, & Griggs, 2001). Narrow appeal to particular Gricean implicatures in this work fails to bridge the gap. Grice's theory taken as a broad framework for credulous discourse processing in which participants construct speakers' "intended models" of discourses can reconcile these results, purchasing continuity of interpretation through variety of logical treatments. We present exploratory experimental data on immediate inference and subsequent syllogistic reasoning. Systematic patterns of interpretation driven by two factors (whether the subject's model of the discourse is credulous, and their degree of reliance on information packaging) are shown to transcend particular quantifier inferences and to drive systematic differences in subjects' subsequent syllogistic reasoning. We conclude that most participants do not understand deductive tasks as experimenters intend, and just as there is no single logical model of reasoning, so there is no reason to expect a single "fundamental human reasoning mechanism".

Cognition↗

New drugs.

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Journal Article↗