Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kriangsak Khownium"'
Autor:
Chatchai Muanprasat, Kriangsak Khownium, Suparerk Borwornpinyo, Jariya Romsaiyud, Tirayut Vilaivan, Somsak Ruchirawat, Pawin Pongkorpsakol, Bundet Boekfa, Preedajit Wongkrasant, Jumras Limtrakul
Publikováno v:
New Journal of Chemistry. 43:7051-7056
A novel bispyrene compound (BPTG) was developed as a selective lipopolysaccharide (LPS) sensor. The BPTG probe exhibited high selectivity and sensitivity toward LPS with a fluorescence ‘off–on’ behavior in HEPES-buffered DMSO–H2O (1 : 6 (v/v)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1017c65b010d0ae60732ba33950de040
https://doi.org/10.1039/c9nj00323a
https://doi.org/10.1039/c9nj00323a
Publikováno v:
ChemMedChem. 11:1600-1616
Analogues of the anticancer natural product oximidine II were prepared and evaluated for cytotoxicity. One analogue of oximidine II that carries a C15 allylic amide side chain as well as two analogues with C15 vinyl sulfone side chains were found to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbcda8344830ef881886fbe2b6b9f7c1
https://doi.org/10.1002/cmdc.201600024
https://doi.org/10.1002/cmdc.201600024
Publikováno v:
Organometallics. 23:5268-5274
Epoxides and episulfides react stereospecifically with Tp‘ReO2, generated in situ from Tp‘ReO3 and PPh3 (Tp‘ = hydrido-tris(3,5-dimethylpyrazolyl)borate). A combination of direct atom transfer, res...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31f93db949ead78f03a258f3e8654408
https://doi.org/10.1021/om049534p
https://doi.org/10.1021/om049534p
Autor:
Wei Li, Jared T. Spletstoser, Gunda I. Georg, Christopher M. Schneider, Kriangsak Khownium, Torsten Haack
Publikováno v:
Angewandte Chemie International Edition. 50:7855-7857
An intramolecular copper-mediated reductive Castro-Stephens reaction furnished a key macrocyclic triene intermediate for the total synthesis of oximidine II. Herein we describe the total synthesis of the natural product as well as studies to deduce t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adfd1f3e818cfb30fa62d6dfb0e2df1
https://doi.org/10.1002/anie.201103081
https://doi.org/10.1002/anie.201103081
Publikováno v:
ChemMedChem. 11:1578-1578
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26e3d4d6fc4b0e12ed92edc65e51e342
https://doi.org/10.1002/cmdc.201600376
https://doi.org/10.1002/cmdc.201600376
Autor:
Stewart J. Wood, Sunil A. David, Kriangsak Khownium, Thuan B. Nguyen, Matthew R. Kimbrell, Rajalakshmi Balakrishna, Kelly A. Miller, Gunda I. Georg
Publikováno v:
Bioorganicmedicinal chemistry letters. 16(5)
We have shown that lipopolyamines bind to the lipid A moiety of lipopolysaccharide, a constituent of Gram-negative bacterial membranes, and neutralize its toxicity in animal models of endotoxic shock. In an effort to identify non-polyamine scaffolds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cccb17cb9bfa246325281809e6c9689
https://pubmed.ncbi.nlm.nih.gov/16377188
https://pubmed.ncbi.nlm.nih.gov/16377188