Kittipan Siwawannapong

College of Sciences

Works (3)

Updated: May 25th, 2024 05:00

2024 article

Extension of nature's NIR-I chromophore into the NIR-II region

Siwawannapong, K., Diers, J. R., Magdaong, N. C. M., Nalaoh, P., Kirmaier, C., Lindsey, J. S., … Bocian, D. F. (2024, May 1). PHYSICAL CHEMISTRY CHEMICAL PHYSICS, Vol. 5.

By: K. Siwawannapong n, J. Diers *, N. Magdaong *, P. Nalaoh *, C. Kirmaier *, J. Lindsey n , D. Holten *, D. Bocian *

UN Sustainable Development Goal Categories
Sources: Web Of Science, NC State University Libraries
Added: May 20, 2024

2022 article

Simple Dipyrrin Analogues of Prodigiosin for Use as Colistin Adjuvants

Siwawannapong, K., Nemeth, A. M., Melander, R. J., Rong, J., Davis, J. R., Taniguchi, M., … Melander, C. (2022, July 8). CHEMMEDCHEM, Vol. 7.

By: K. Siwawannapong n, A. Nemeth*, R. Melander *, J. Rong  n, J. Davis  n, M. Taniguchi n , M. Carpenter*, J. Lindsey n , C. Melander*

Contributors: K. Siwawannapong n, A. Nemeth*, R. Melander *, J. Rong  n, J. Davis  n, M. Taniguchi n , M. Carpenter*, J. Lindsey n , C. Melander*

author keywords: dipyrrin; colistin; adjuvant; antibiotic resistance; gram negative
MeSH headings : Acinetobacter baumannii; Adjuvants, Pharmaceutic / pharmacology; Anti-Bacterial Agents / pharmacology; Anti-Bacterial Agents / therapeutic use; Colistin / pharmacology; Drug Resistance, Multiple, Bacterial; Microbial Sensitivity Tests; Prodigiosin / pharmacology; Pseudomonas aeruginosa
TL;DR: A series of dipyrrins and pyrrole derivatives designed as analogues of prodigiosin and obatoclax potentiate the activity of colistin against Klebsiella pneumoniae, with lead compounds also potentiating colist in against Acinetobacter baumannii and Pseudomonas aeruginosa. (via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being (Web of Science; OpenAlex)
Sources: Web Of Science, NC State University Libraries, ORCID
Added: July 18, 2022

2022 journal article

Tailoring the AIE Chromogen 2-(2-Hydroxyphenyl)benzothiazole for Use in Enzyme-Triggered Molecular Brachytherapy

MOLECULES, 27(24).

By: Z. Wu n, J. Dou n, K. Nguyen n, J. Eppley  n, K. Siwawannapong n, Y. Zhang n, J. Lindsey n 

author keywords: aggregation; cancer; insolubilization; molecular design; phosphodiester; precipitation; radiotherapy
MeSH headings : Prodrugs; Brachytherapy; Benzothiazoles; Polyethylene Glycols
TL;DR: Several 2-(2-hydroxyphenyl)benzothiazole substrates that readily aggregate in aqueous solution (and afford AIE) were elaborated, taking a step forward on the long road toward molecular brachytherapy. (via Semantic Scholar)
UN Sustainable Development Goal Categories
Sources: Web Of Science, NC State University Libraries
Added: January 17, 2023

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