Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tetsuro Ohgami"'
Autor:
Kenji Sudo, Masao Matsuoka, Hiroshi Inoue, Shunji Kageyama, Toshifumi Hatta, Hiroshi Suzuki, Yasuaki Shimizu, Osamu Yamamoto, Mitsuaki Ohta, Masaya Orita, Naoyuki Masuda, Tetsuro Ohgami, Masahiro Fujii, Eiichi Kodama
Publikováno v:
Scopus-Elsevier
Background: YM-215389 and YM-228855 are thiazolidenebenzenesulfonamide (TBS) derivatives and novel non-nucleoside reverse transcriptase inhibitors (NNRTIs) that inhibit not only wild-type, but also the K103N- and Y181C-substituted reverse transcripta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48283c0b194ca4ac1bb99505bea3c508
https://doi.org/10.1177/095632020801900304
https://doi.org/10.1177/095632020801900304
Autor:
Ayako Moritomo, Mitsuaki Ohta, Shunji Kageyama, Toru Kontani, Osamu Yamamoto, Naoyuki Masuda, Tetsuro Ohgami, Masahiro Fujii
Publikováno v:
Synthetic Communications. 35:2305-2316
Various N‐3‐alkylated thiazolidenesulfonamide derivatives were efficiently prepared by the direct endo‐selective alkylation of thiazolylsulfonamides. The effects of different bases and solvents were investigated, and the NaH–THF combination w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb157e6356debf4a1bd34704cd1d7a2
https://doi.org/10.1080/00397910500186730
https://doi.org/10.1080/00397910500186730
Autor:
Masatoshi Fujiwara, Tetsuro Ohgami, Shiro Shigeta, Jiro Fujiyasu, Yasuaki Shimizu, Osamu Yamamoto, Ayako Moritomo, Toshifumi Hatta, Naoyuki Masuda, Masanori Baba, Toru Kontani, Masahiro Fujii, Hiroyuki Kurihara, Kenji Sudo, Mitsuaki Ohta, Eiichi Kodama, Masao Matsuoka, Shunji Kageyama, Hironobu Koga, Masaya Orita, Hiroshi Inoue, Masafumi Shintani, Tomoyuki Yokota, Hiroshi Suzuki
Publikováno v:
Bioorganicmedicinal chemistry. 13(4)
In a previous study, we described the structure–activity relationships (SARs) for a series of thiazolidenebenzenesulfonamide derivatives. These compounds were found to be highly potent inhibitors of the wild type (WT) and Y181C mutant reverse trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e91f81e71c7f5b15107d903d8e862cbc
https://pubmed.ncbi.nlm.nih.gov/15670903
https://pubmed.ncbi.nlm.nih.gov/15670903
Autor:
Masaya Orita, Tomoyuki Yokota, Hiroshi Suzuki, Toru Kontani, Hironobu Koga, Masao Matsuoka, Ayako Moritomo, Kenji Sudo, Tetsuro Ohgami, Hideaki Nakahara, Masahiro Fujii, Shunji Kageyama, Osamu Yamamoto, Masanori Baba, Yasuaki Shimizu, Naoyuki Masuda, Hiroyuki Kurihara, Hiroshi Inoue, Jiro Fujiyasu, Toshifumi Hatta, Eiichi Kodama, Masatoshi Fujiwara, Mitsuaki Ohta, Shiro Shigeta
Publikováno v:
Bioorganicmedicinal chemistry. 12(23)
A random high-throughput screening (HTS) program to discover novel nonnucleoside reverse transcriptase inhibitors (NNRTIs) has been carried out with MT-4 cells against a nevirapine-resistant virus, HIV-1 IIIB-R . The primary hit, a thiazolidenebenzen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f5a3e3e21460517253c918a4ab93d07
https://pubmed.ncbi.nlm.nih.gov/15519161
https://pubmed.ncbi.nlm.nih.gov/15519161
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82a60a07ca2d3c22a742a521347e906d
https://doi.org/10.1002/chin.200108196
https://doi.org/10.1002/chin.200108196
Publikováno v:
Carbohydrate research. 329(2)
Three kanamycin A analogs containing 6-amino-6-deoxyglycofuranoses have been prepared as candidates for potential activity against resistant bacteria producing 6′- N -acetyltransferase. They are 4- O -(6-amino-3,5,6-trideoxy-α- d -, -β- d -, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2528a7b11ea0131eac58d7147a9e02e
https://pubmed.ncbi.nlm.nih.gov/11117316
https://pubmed.ncbi.nlm.nih.gov/11117316