Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Masaki Ishigai"'
Publikováno v:
IUCrData, Vol 2, Iss 9, p x171292 (2017)
In the title compound, C15H20N7O3S+·CH3O3S− (CH5132799 mesylate), two molecular entities form a salt with proton transfer from methanesulfonic acid to the aminopyrimidine moiety of CH5132799. In the crystal, methanesulfonate is retained by bifurca
Externí odkaz:
https://doaj.org/article/ca1c05c46ac14e978f3d5f6da182e843
Autor:
Akihisa Kaneko, Chihiro Endo-Tsukude, Motohiro Kato, Shino Kuramoto, Masaki Ishigai, Akinobu Hamada, Satofumi Iida
Publikováno v:
Drug Metabolism and Pharmacokinetics. 34:325-333
By using the Relative Factor (RF) method-a method that can simply assess cytochrome P450 (CYP) induction risk based on a maximum induction effect model-we evaluated the risk of CYP2C9 induction and examined its relationship with risk of CYP3A4 induct
Publikováno v:
Chemical and Pharmaceutical Bulletin. 66:1035-1040
We investigated the salt cocrystals formed by tofogliflozin with sodium acetate and potassium acetate by determining the crystal structures of the salt cocrystals and characterizing the solid states. The salt cocrystal screening using the slurry meth
Autor:
Noriyuki Takata, Koji Shiraki, Kazunori Kadota, Yuichi Tozuka, Takamitsu Ueto, Satoshi Tanida, Ryusuke Takano, Masaki Ishigai, Aya Sakon
Publikováno v:
CrystEngComm. 20:362-369
We succeeded in forming a benzoic acid cocrystal of CH5134731 by focusing on the isomorphism shown by its solvates. As a result of evaluation, the benzoic acid cocrystal showed good solubility. This crystal engineering approach made it possible to re
Publikováno v:
mAbs. 9:1210-1215
The pharmacokinetics (PK) of an antibody in the brain and the spinal cord is insufficiently understood, which is an obstacle to the discovery of antibody drugs that target diseases in the central nervous system. In this study, we focused on the elimi
Autor:
Hidetoshi Shindoh, Motohiro Kato, Nobuo Sekiguchi, Kenji Takanashi, Akihisa Kaneko, Keiichi Morita, Shunsuke Nagao, Masaki Ishigai
Publikováno v:
Xenobiotica. 47:1042-1051
1. A novel selective anaplastic lymphoma kinase (ALK) inhibitor, alectinib, has shown remarkable efficacy and safety in patients with ALK-positive non-small-cell lung cancer (NSCLC). The purpose of this study was to evaluate in vitro the potential to
Autor:
Yuki Iwayanagi, Tatsuhiko Tachibana, Atsuhiko Maeda, Tomoyuki Igawa, Kazuhisa Ozeki, Jun-ichi Nezu, Kenta Haraya, Masaki Ishigai
Publikováno v:
Drug Metabolism and Pharmacokinetics. 31:123-132
Previously, we have reported novel engineered antibody with pH-dependent antigen-binding (recycling antibody), and with both pH-dependent antigen-binding and increased FcRn-binding at neutral pH (sweeping antibody). The purpose of this study is to pe
Autor:
Chiyomi Kubo, Akira Takeiri, Futa Mimoto, Naoaki Murao, Shunsuke Ito, Shotaro Takata, Atsuhiko Maeda, Masaki Ishigai, Kumiko Muraoka, Yuki Iwayanagi, Ayako Takahashi, Nobuo Sekiguchi, Shuichi Chiba, Mariko Yano, Tetsuya Wakabayashi
Publikováno v:
mAbs. 10(8)
Immunogenicity is a key factor capable of influencing the efficacy and safety of therapeutic antibodies. A recently developed method called MHC-associated peptide proteomics (MAPPs) uses liquid chromatography/mass spectrometry to identify the peptide
Publikováno v:
Drug Metabolism and Pharmacokinetics. 34:S42-S43
Publikováno v:
IUCrData, Vol 2, Iss 9, p x171292 (2017)
In the title compound, C15H20N7O3S+·CH3O3S−(CH5132799 mesylate), two molecular entities form a salt with proton transfer from methanesulfonic acid to the aminopyrimidine moiety of CH5132799. In the crystal, methanesulfonate is retained by bifurcat