Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hideaki Funami"'
Autor:
Ryutaro Kanada, Yoshiko Kagoshima, Takashi Suzuki, Akifumi Nakamura, Hideaki Funami, Jun Watanabe, Masayoshi Asano, Mizuki Takahashi, Osamu Ubukata, Kanae Suzuki, Tomoya Aikawa, Kazumi Sato, Megumi Goto, Genzui Setsu, Kentaro Ito, Kawori Kihara, Mutsumi Kuroha, Takashi Kohno, Hideaki Ogiwara, Takeshi Isoyama, Yuichi Tominaga, Saito Higuchi, Hiroyuki Naito
Publikováno v:
Journal of medicinal chemistry.
Histone acetylation is a post-translational modification of histones that is catalyzed by histone acetyltransferases (HATs) and plays an essential role in cellular processes. The HAT domain of EP300/CBP has recently emerged as a potential drug target
Autor:
Hideaki Funami, Makoto Shibata, Makoto Koyama, Tsuyoshi Muto, Bitoku Takahashi, Hiroshi Maruoka, Satomi Kanki
Publikováno v:
Chemicalpharmaceutical bulletin. 63(10)
Structural optimization of 2-aminonicotinamide derivatives as ghrelin receptor inverse agonists is reported. So as to avoid mechanism-based inactivation (MBI) of CYP3A4, 1,3-benzodioxol ring of the lead compound was modified. Improvement of the main
Autor:
Makoto Koyama, Tsuyoshi Muto, Hideaki Funami, Bitoku Takahashi, Satomi Kanki, Hiroshi Maruoka, Makoto Shibata, Asako Nagahira, Takehiko Iwaki, Yoshiyuki Igawa, Yoshiyuki Kamiide
Publikováno v:
Bioorganicmedicinal chemistry. 23(15)
A series of 2-alkylamino nicotinamide analogs was prepared as orally active ghrelin receptor (ghrelinR) inverse agonists. Starting from compound 1, oral bioavailability was improved by modifying metabolically unstable sites and reducing molecular wei
Autor:
Asako Nagahira, Tsuyoshi Matsuo, Makoto Koyama, Yoshiyuki Kamiide, Hirokazu Annoura, Takehiko Iwaki, Hideaki Funami, Tsuyoshi Muto, Bitoku Takahashi, Hiroshi Maruoka
Publikováno v:
Bioorganicmedicinal chemistry letters. 25(13)
New inverse agonists of the ghrelin receptor (ghrelinR) were obtained through high-throughput screening and subsequent structural modification of 2-aminoalkyl nicotinamide derivatives. The key structural feature to improve in vitro activity was the i
Autor:
Jun Takaya, Masahide Shido, Yoshihiro Hara, Hiroyuki Kusama, Hideaki Funami, Nobuharu Iwasawa
Publikováno v:
Journal of the American Chemical Society. 127:2709-2716
Novel tungsten-containing carbonyl ylides 7, generated by the reaction of the o-alkynylphenyl carbonyl derivatives 1 with a catalytic amount of W(CO)(5)(thf), reacted with alkenes to give polycyclic compounds 5 through [3 + 2]-cycloaddition reaction
Publikováno v:
ChemInform. 41
A Pt(II)-catalyzed [3 + 2] cycloaddition reaction of silyl propadienyl ethers and alkenyl ethers has been developed as the first example of the utilization of allenes as a three-carbon unit in a transition-metal-catalyzed intermolecular cycloaddition
Publikováno v:
ChemInform. 39
Publikováno v:
Angewandte Chemie (International ed. in English). 47(26)
Publikováno v:
ChemInform. 38
A concise method for the preparation of 1-acyl-4-alkoxy- or 1-acyl-4-alkylsulfanylnaphthalenes has been developed by the PtCl 2 -catalyzed reaction of O-ethynylbenzoates or benzothioates with vinyl ethers. Treatment of O-alkynylbenzoate derivatives w
Publikováno v:
ChemInform. 38