Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Tomokazu, Kusumoto"'
Autor:
Tomohiro Ohashi, Tomoteru Yamasaki, Yasuyuki Debori, Tatsuki Koike, Tomokazu Kusumoto, Ryouta Maeda, Masayuki Fujinaga, Akito Hata, Takeshi Wakabayashi, Yasushi Hattori, Ming-Rong Zhang, Miyanohana Yuhei, Ryo Yamashita, Maki Miyamoto, Yiding Zhang, Hidekatsu Wakizaka
Publikováno v:
Journal of Medicinal Chemistry. 64:11990-12002
Diacylglycerol kinase gamma (DGKγ) is a subtype of DGK enzyme, which catalyzes ATP-dependent conversion of diacylglycerol to phosphatidic acid. DGKγ, localized in the brain, plays an important role in the central nervous system. However, its functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fed7abf826a7d32a1858fd3c81b3bef
https://doi.org/10.1021/acs.jmedchem.1c00584
https://doi.org/10.1021/acs.jmedchem.1c00584
Autor:
Yasushi, Hattori, Tomoteru, Yamasaki, Tomohiro, Ohashi, Yuhei, Miyanohana, Tomokazu, Kusumoto, Ryouta, Maeda, Maki, Miyamoto, Yasuyuki, Debori, Akito, Hata, Yiding, Zhang, Hidekatsu, Wakizaka, Takeshi, Wakabayashi, Masayuki, Fujinaga, Ryo, Yamashita, Ming-Rong, Zhang, Tatsuki, Koike
Publikováno v:
Journal of medicinal chemistry. 64(16)
Diacylglycerol kinase gamma (DGKγ) is a subtype of DGK enzyme, which catalyzes ATP-dependent conversion of diacylglycerol to phosphatidic acid. DGKγ, localized in the brain, plays an important role in the central nervous system. However, its functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::637daea17022fe867db87f04fa2bb855
https://pubmed.ncbi.nlm.nih.gov/34347478
https://pubmed.ncbi.nlm.nih.gov/34347478
Autor:
Satoshi Sogabe, Shuhei Ikeda, Makoto Fushimi, Tomokazu Kusumoto, Naoto Arimura, Tatsuki Koike, Hideyuki Sugiyama, Jumpei Aida, Kazunobu Aoyama, Masako Sasaki
Publikováno v:
Journal of medicinal chemistry. 61(20)
Monoacylglycerol lipase (MAGL) is a major serine hydrolase that hydrolyzes 2-arachidonoylglycerol (2-AG) to arachidonic acid (AA) and glycerol in the brain. Because 2-AG and AA are endogenous biologically active ligands in the brain, inhibition of MA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bbac7b30fa3489c39d55272bb78fbdc
https://pubmed.ncbi.nlm.nih.gov/30251836
https://pubmed.ncbi.nlm.nih.gov/30251836
Autor:
Daisuke Tanima, Mohammad Nuruzzaman, Kazunori Tsubaki, Tomokazu Kusumoto, Takeo Kawabata, Kaoru Fuji
Publikováno v:
The Journal of Organic Chemistry. 70:4609-4616
Various types of chiral host molecules 2−7 based on a phenolphthalein skeleton and two crown ethers were prepared for use in visual enantiomeric recognition, and we examined their enantioselective coloration in complexation with chiral amino acid d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d647c1f04b2b1e724b152032d81ce38f
https://doi.org/10.1021/jo050387u
https://doi.org/10.1021/jo050387u
Autor:
Kaoru Fuji, Tomokazu Kusumoto, Daisuke Tanima, Kazunori Tsubaki, Noriyuki Hayashi, Takeo Kawabata
Publikováno v:
Tetrahedron: Asymmetry. 16:739-743
An efficient and convenient method for the synthesis of chiral triamines with two substituents at the α position to the terminal amino group (spermidine analogues) is described. These chiral N , N -bis(4-substituted-4-aminobutyl)amines may have anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd51defccbd0a6efe749c967f3d959cb
https://doi.org/10.1016/j.tetasy.2004.12.013
https://doi.org/10.1016/j.tetasy.2004.12.013
Publikováno v:
Organic Letters. 4:2313-2316
[structure: see text] A receptor 1 with phenolphthalein and two crown ethers in the molecule develops brilliant purple color in the presence of dipeptides with a specific amino acid-sequence containing a C-terminal lysine. This type of color developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad40d163fd07d5f2103c9c6fa0e1359
https://doi.org/10.1021/ol026191n
https://doi.org/10.1021/ol026191n
Publikováno v:
Organic Letters. 3:4067-4069
[structure: see text] A hybrid molecule 1 consisting of phenolphthalein and two crown ether moieties can be used to discriminate the length of linear triamines strictly by color development. The purple color is developed most deeply at -10 degrees C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b5146eb1e6ab3a83cdb32b21aab9f1
https://doi.org/10.1021/ol016823q
https://doi.org/10.1021/ol016823q
Publikováno v:
ChemInform. 32
Vinylselenonium ylide, which was generated from (Z)-vinylselenonium salt with a base such as sodium or potassium hydride, reacted with aromatic aldehydes to produce the α,β-unsaturated ketones, which were obtained in better yields from the aldehyde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a91ebbc22db955c1985207cfb265ccf
https://doi.org/10.1002/chin.200135099
https://doi.org/10.1002/chin.200135099
Autor:
Kazunori, Tsubaki, Daisuke, Tanima, Mohammad, Nuruzzaman, Tomokazu, Kusumoto, Kaoru, Fuji, Takeo, Kawabata
Publikováno v:
The Journal of organic chemistry. 70(12)
Various types of chiral host molecules 2-7 based on a phenolphthalein skeleton and two crown ethers were prepared for use in visual enantiomeric recognition, and we examined their enantioselective coloration in complexation with chiral amino acid der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b4b7019dbab2dc0e44a69a826d9dc82
https://pubmed.ncbi.nlm.nih.gov/15932296
https://pubmed.ncbi.nlm.nih.gov/15932296
Autor:
Kazunori Tsubaki, Wang Bin-Gui, Mohammad Nuruzzaman, Tomokazu Kusumoto, Kaoru Fuji, Noriyuki Hayashi
Publikováno v:
Organic letters. 3(25)
[structure: see text] Optically active artificial host molecules 2-5 based on a phenolphthalein skeleton have been prepared for visual enantiomeric recognition of alanine derivatives 8 and 9. The receptor 3 discriminates (R)-8 and (R)-9 from (S)-8 an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc41eaecaa772da3934969e10b9d8a43
https://pubmed.ncbi.nlm.nih.gov/11735587
https://pubmed.ncbi.nlm.nih.gov/11735587