Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Manabu Nakazono"'
Autor:
Manabu Nakazono, Kenji Hamase
Publikováno v:
Dyes and Pigments. 213:111175
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03b5048222d248db247481654129059e
https://doi.org/10.1016/j.dyepig.2023.111175
https://doi.org/10.1016/j.dyepig.2023.111175
Publikováno v:
Journal of Oleo Science. 70:1677-1684
Methyl groups were introduced on the acridine moiety in chemiluminescent acridinium esters that have electron-withdrawing groups (trifluoromethyl, cyano, nitro, ethoxycarbonyl) at the 4-position on the phenyl ester. The introduction of methyl groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f56fcea2f707f76149d5b40da13fa85d
https://doi.org/10.5650/jos.ess21186
https://doi.org/10.5650/jos.ess21186
Publikováno v:
Tokai Journal of Experimental & Clinical Medicine; Apr2023, Vol. 48 Issue 1, p10-12, 3p
Autor:
Norihito Fukada1, Hisashi Kobayashi2, Manabu Nakazono1, Keita Ohyachi1, Akinori Takeda1, Takashi Yaguchi3, Miyuki Okada4, Tomotaka Sato1 satotomo@med.teikyo-u.ac.jp
Publikováno v:
Medical Mycology Journal. 2024, Vol. 65 Issue 1, p23-26. 4p.
Publikováno v:
The Journal of Organic Chemistry. 82:2450-2461
Various novel acridinium ester derivatives having phenyl and biphenyl moieties were synthesized, and their optimal chemiluminescence conditions were investigated. Several strongly chemiluminescent acridinium esters under neutral conditions were found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac5d336b2aa5a7e5d9c8e4df2adb317
https://doi.org/10.1021/acs.joc.6b02748
https://doi.org/10.1021/acs.joc.6b02748
Publikováno v:
Journal of Oleo Science; 2021, Vol. 70 Issue 11, p1677-1684, 8p
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 403:112851
Methoxycarbonylphenyl 10-methyl-10λ4-2,7-disubstituted acridine-9-carboxylate derivatives were synthesized, and both their chemiluminescence intensities at pH 7−10 and their chemical stabilities were clarified. The products and generation efficien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f753a1eb54c83363165e7dce6ad55622
https://doi.org/10.1016/j.jphotochem.2020.112851
https://doi.org/10.1016/j.jphotochem.2020.112851
Autor:
Nao Kusano, Akio Ojida, Yurika Miyoshi, Masashi Mita, Wolfgang Lindner, Sumio Ohtsuki, Tsubasa Oyama, Eiichi Negishi, Manabu Nakazono, Kenji Hamase, Hirohisa Onigahara
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 116:71-79
A new pre-column derivatization reagent with a 6-methoxy-4-quinolone (6-MOQ) moiety for amino acid analysis, 2,5-dioxopyrrolidin-1-yl(2-(6-methoxy-4-oxoquinolin-1(4H)-yl)ethyl) carbonate (6-MOQ-EtOCOOSu), was designed and synthesized. 6-MOQ is a ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9846a8ff550ce16d96ae7a95eac94d7b
https://doi.org/10.1016/j.jpba.2015.05.039
https://doi.org/10.1016/j.jpba.2015.05.039
Autor:
Manabu Nakazono, Shinkoh Nanbu
Publikováno v:
Luminescence : the journal of biological and chemical luminescence. 33(2)
Enhancement effect on the chemiluminescence of acridinium ester derivatives under neutral conditions was investigated. Additions of phenols did not enhance the chemiluminescence intensities of acridinium ester derivatives in the presence of horseradi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723c54a780758ca627e82db446231909
https://pubmed.ncbi.nlm.nih.gov/29115007
https://pubmed.ncbi.nlm.nih.gov/29115007
Autor:
Yukio Ando, Katsumi Tomiyoshi, Kazumi Sasamoto, Manabu Nakazono, Genki Suenaga, Konen Obayashi
Publikováno v:
Clinica Chimica Acta. 436:27-34
Background Various styrylbenzene compounds were synthesized and evaluated as mainly Aβ amyloid sensors. These compounds, however, cannot be used for detecting amyloid deposition in peripheral nerves because of the inherent sensitivity of the compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec052b274cec63ba7f720954f9b7765
https://doi.org/10.1016/j.cca.2014.04.028
https://doi.org/10.1016/j.cca.2014.04.028