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An ultra-low detection limit gold(III) probe based on rhodamine-covalent hydrogel sensor.

Environmental technology

Kaewtong C, Wanich S, Wanno B, Tuntulani T, Pulpoka B.
PMID: 33280570
Environ Technol. 2020 Dec 07;1-9. doi: 10.1080/09593330.2020.1850873. Epub 2020 Dec 07.

A highly sensitive and selective optical chemosensor (

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Kaewtong C, Wanich S, Wanno B, et al. An ultra-low detection limit gold(III) probe based on rhodamine-covalent hydrogel sensor. Environ Technol. 2020;1-9doi: 10.1080/09593330.2020.1850873.
Kaewtong, C., Wanich, S., Wanno, B., Tuntulani, T., & Pulpoka, B. (2020). An ultra-low detection limit gold(III) probe based on rhodamine-covalent hydrogel sensor. Environmental technology, 1-9. https://doi.org/10.1080/09593330.2020.1850873
Kaewtong, Chatthai, et al. "An ultra-low detection limit gold(III) probe based on rhodamine-covalent hydrogel sensor." Environmental technology vol. (2020): 1-9. doi: https://doi.org/10.1080/09593330.2020.1850873
Kaewtong C, Wanich S, Wanno B, Tuntulani T, Pulpoka B. An ultra-low detection limit gold(III) probe based on rhodamine-covalent hydrogel sensor. Environ Technol. 2020 Dec 07;1-9. doi: 10.1080/09593330.2020.1850873. Epub 2020 Dec 07. PMID: 33280570.
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Chemoinformatic Characterization of Synthetic Screening Libraries Focused on Epigenetic Targets.

Molecular informatics

Flores-Padilla EA, Juárez-Mercado KE, Naveja JJ, Kim TD, Alain Miranda-Quintana R, Medina-Franco JL.
PMID: 34931466
Mol Inform. 2021 Dec 20;e2100285. doi: 10.1002/minf.202100285. Epub 2021 Dec 20.

The importance of epigenetic drug and probe discovery is on the rise. This is not only paramount to identify and develop therapeutic treatments associated with epigenetic processes but also to understand the underlying epigenetic mechanisms involved in biological processes....

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Flores-Padilla EA, Juárez-Mercado KE, Naveja JJ, et al. Chemoinformatic Characterization of Synthetic Screening Libraries Focused on Epigenetic Targets. Mol Inform. 2021;e2100285doi: 10.1002/minf.202100285.
Flores-Padilla, E. A., Juárez-Mercado, K. E., Naveja, J. J., Kim, T. D., Alain Miranda-Quintana, R., & Medina-Franco, J. L. (2021). Chemoinformatic Characterization of Synthetic Screening Libraries Focused on Epigenetic Targets. Molecular informatics, e2100285. https://doi.org/10.1002/minf.202100285
Flores-Padilla, E Alexis, et al. "Chemoinformatic Characterization of Synthetic Screening Libraries Focused on Epigenetic Targets." Molecular informatics vol. (2021): e2100285. doi: https://doi.org/10.1002/minf.202100285
Flores-Padilla EA, Juárez-Mercado KE, Naveja JJ, Kim TD, Alain Miranda-Quintana R, Medina-Franco JL. Chemoinformatic Characterization of Synthetic Screening Libraries Focused on Epigenetic Targets. Mol Inform. 2021 Dec 20;e2100285. doi: 10.1002/minf.202100285. Epub 2021 Dec 20. PMID: 34931466.
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Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide.

The Journal of organic chemistry

Kaewtong C, Muangsin N, Chaichit N, Pulpoka B.
PMID: 18576605
J Org Chem. 2008 Jul 18;73(14):5574-7. doi: 10.1021/jo800461r. Epub 2008 Jun 25.

N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide in partial cone conformation was selectively synthesized by appropriately controlling the steric effect during the amidation reactions of N-benzylhexahomotriaza-p-chlorocalix[3]tri(ethyl acetate) in cone or partial cone conformations with use of 1-aminomethylnaphthalene. The conformation was confirmed by (1)H, (13)C, and...

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Kaewtong C, Muangsin N, Chaichit N, et al. Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide. J Org Chem. 2008;73(14):5574-7doi: 10.1021/jo800461r.
Kaewtong, C., Muangsin, N., Chaichit, N., & Pulpoka, B. (2008). Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide. The Journal of organic chemistry, 73(14), 5574-7. https://doi.org/10.1021/jo800461r
Kaewtong, Chatthai, et al. "Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide." The Journal of organic chemistry vol. 73,14 (2008): 5574-7. doi: https://doi.org/10.1021/jo800461r
Kaewtong C, Muangsin N, Chaichit N, Pulpoka B. Conformation-selective synthesis and binding properties of N-benzylhexahomotriaza-p-chlorocalix[3]trinaphthylamide. J Org Chem. 2008 Jul 18;73(14):5574-7. doi: 10.1021/jo800461r. Epub 2008 Jun 25. PMID: 18576605.
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Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor.

Dalton transactions (Cambridge, England : 2003)

Kaewtong C, Wanno B, Uppa Y, Morakot N, Pulpoka B, Tuntulani T.
PMID: 22027958
Dalton Trans. 2011 Dec 14;40(46):12578-83. doi: 10.1039/c1dt11307k. Epub 2011 Oct 26.

Fluorescence-active chemosensors (L1-L4), comprising a rhodamine scaffold and a pseudo azacrown cation-binding subunit, have been proposed and characterized as a fluorescent chemosensor for Hg(2+). An on-off type fluorescent enhancement was observed by the formation of the ring-opened amide form...

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Kaewtong C, Wanno B, Uppa Y, et al. Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor. Dalton Trans. 2011;40(46):12578-83doi: 10.1039/c1dt11307k.
Kaewtong, C., Wanno, B., Uppa, Y., Morakot, N., Pulpoka, B., & Tuntulani, T. (2011). Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor. Dalton transactions (Cambridge, England : 2003), 40(46), 12578-83. https://doi.org/10.1039/c1dt11307k
Kaewtong, Chatthai, et al. "Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor." Dalton transactions (Cambridge, England : 2003) vol. 40,46 (2011): 12578-83. doi: https://doi.org/10.1039/c1dt11307k
Kaewtong C, Wanno B, Uppa Y, Morakot N, Pulpoka B, Tuntulani T. Facile synthesis of rhodamine-based highly sensitive and fast responsive colorimetric and off-on fluorescent reversible chemosensors for Hg2+: preparation of a fluorescent thin film sensor. Dalton Trans. 2011 Dec 14;40(46):12578-83. doi: 10.1039/c1dt11307k. Epub 2011 Oct 26. PMID: 22027958.
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Novel C3v-symmetrical N7-Hexahomotriazacalix[3]cryptand: a highly efficient receptor for halide anions.

Organic letters

Kaewtong C, Fuangswasdi S, Muangsin N, Chaichit N, Vicens J, Pulpoka B.
PMID: 16597110
Org Lett. 2006 Apr 13;8(8):1561-4. doi: 10.1021/ol060052e.

[structure: see text] We report the synthesis of a novel C(3)(v)()-symmetrical N(7)-hexahomotriazacalix[3]cryptand (1). Compound 1 was shown to be in a fixed cone conformation by (1)H NMR spectroscopy and X-ray single-crystal structure determination. Complexation studies showed that 1 is...

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Kaewtong C, Fuangswasdi S, Muangsin N, et al. Novel C3v-symmetrical N7-Hexahomotriazacalix[3]cryptand: a highly efficient receptor for halide anions. Org Lett. 2006;8(8):1561-4doi: 10.1021/ol060052e.
Kaewtong, C., Fuangswasdi, S., Muangsin, N., Chaichit, N., Vicens, J., & Pulpoka, B. (2006). Novel C3v-symmetrical N7-Hexahomotriazacalix[3]cryptand: a highly efficient receptor for halide anions. Organic letters, 8(8), 1561-4. https://doi.org/10.1021/ol060052e
Kaewtong, Chatthai, et al. "Novel C3v-symmetrical N7-Hexahomotriazacalix[3]cryptand: a highly efficient receptor for halide anions." Organic letters vol. 8,8 (2006): 1561-4. doi: https://doi.org/10.1021/ol060052e
Kaewtong C, Fuangswasdi S, Muangsin N, Chaichit N, Vicens J, Pulpoka B. Novel C3v-symmetrical N7-Hexahomotriazacalix[3]cryptand: a highly efficient receptor for halide anions. Org Lett. 2006 Apr 13;8(8):1561-4. doi: 10.1021/ol060052e. PMID: 16597110.
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Showing 1 to 5 of 5 entries