Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Aarti L. Joshi"'
Autor:
Meenakshi Upreti, Timothy C. Chambers, Kwangyul Moon, Aarti L. Joshi, Elena N. Galitovskaya, Matthias C. McIntosh, T. David Bateman
Publikováno v:
ChemInform. 41
Three structurally related sets of hydroisobenzofuran analogs of sclerophytin A were prepared in three or four steps from ( S )-(+)-carvone via an aldol-cycloaldol sequence. The most potent members of each set of analogs exhibited IC 50 ’s of 1–3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b80e37a43e4c68673936c4a6a6f28b1
https://doi.org/10.1002/chin.201016092
https://doi.org/10.1002/chin.201016092
Publikováno v:
Journal of inorganic biochemistry. 104(8)
Simple and novel nuclease models have been synthesized. These involve metal-binding ligand 1,4,7,10-tetraazlcyclododecane (cyclen) tethered to an acridine ring (a DNA-binding group) by amide linkers of various lengths. Binding of these probes to DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bfd59fb3840f8afc92ae621b11361fb
https://pubmed.ncbi.nlm.nih.gov/20483162
https://pubmed.ncbi.nlm.nih.gov/20483162
Autor:
Kwangyul Moon, Aarti L. Joshi, T. David Bateman, Timothy C. Chambers, Matthias C. McIntosh, Elena N. Galitovskaya, Meenakshi Upreti
Publikováno v:
Bioorganicmedicinal chemistry letters. 19(24)
Three structurally related sets of hydroisobenzofuran analogs of sclerophytin A were prepared in three or four steps from ( S )-(+)-carvone via an aldol-cycloaldol sequence. The most potent members of each set of analogs exhibited IC 50 ’s of 1–3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1720d00818b9ca25b766df904f9d210d
https://pubmed.ncbi.nlm.nih.gov/19896844
https://pubmed.ncbi.nlm.nih.gov/19896844