Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Takashi, Kurohara"'
Autor:
Hanqiao Xu, Dr. Takashi Kurohara, Reina Takano, Dr. Hidetomo Yokoo, Dr. Norihito Shibata, Dr. Nobumichi Ohoka, Dr. Takao Inoue, Prof. Mikihiko Naito, Dr. Yosuke Demizu
Publikováno v:
ChemistryOpen, Vol 11, Iss 7, Pp n/a-n/a (2022)
Abstract Optimizing linker design is important for ensuring efficient degradation activity of proteolysis‐targeting chimeras (PROTACs). Therefore, developing a straightforward synthetic approach that combines the protein‐of‐interest ligand (POI
Externí odkaz:
https://doaj.org/article/2f0a8ecceb984a30b13e6945b3ae6014
Autor:
Hirokazu Mishima, Yukihiro Itoh, Takashi Kurohara, Takayoshi Suzuki, Naoya Asada, Ken‐ichi Kusakabe, Yuko Okamoto
Publikováno v:
Journal of Computational Chemistry. 44:1604-1609
Autor:
Mami Takyo, Yumi Sato, Naoya Hirata, Keisuke Tsuchiya, Hiroaki Ishida, Takashi Kurohara, Yuta Yanase, Takahito Ito, Yasunari Kanda, Keiko Yamamoto, Takashi Misawa, Yosuke Demizu
Publikováno v:
ACS Omega. 7(50):46573-46582
The vitamin D receptor (VDR) is a nuclear receptor, which is involved in several physiological processes, including differentiation and bone homeostasis. The VDR is a promising target for the development of drugs against cancer and bone-related disea
Autor:
Hidetomo Yokoo, Nobumichi Ohoka, Mami Takyo, Takahito Ito, Keisuke Tsuchiya, Takashi Kurohara, Kiyoshi Fukuhara, Takao Inoue, Mikihiko Naito, Yosuke Demizu
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8772 (2021)
Peptide-based target protein degradation inducers called PROTACs/SNIPERs have low cell penetrability and poor intracellular stability as drawbacks. These shortcomings can be overcome by easily modifying these peptides by conjugation with cell penetra
Externí odkaz:
https://doaj.org/article/bacf65a5757446ff8279bef36cf1143a
Autor:
Yuki Murakami, Hinata Osawa, Takashi Kurohara, Yuta Yanase, Takahito Ito, Hidetomo Yokoo, Norihito Shibata, Mikihiko Naito, Kosuke Aritake, Yosuke Demizu
Publikováno v:
RSC Medicinal Chemistry. 13:1495-1503
SAR studies of PROTACs that target H-PGDS, focusing on the E3 ligase ligand and the H-PGDS ligand, are described.
Autor:
Hirokazu Mishima, Takayoshi Suzuki, Yukihiro Itoh, Naoya Asada, Takashi Kurohara, Ken-ichi Kusakabe, Yuko Okamoto
Publikováno v:
Journal of Computational Chemistry; 7/5/2023, Vol. 44 Issue 18, p1604-1609, 6p
Autor:
Minami Fujita, Keisuke Tsuchiya, Takashi Kurohara, Kiyoshi Fukuhara, Takashi Misawa, Yosuke Demizu
Publikováno v:
Bioorganic & Medicinal Chemistry. 84:117264
Publikováno v:
Bioorganic & Medicinal Chemistry. 84:117259
Autor:
Yosuke Ota, Yukihiro Itoh, Takashi Kurohara, Ritesh Singh, Elghareeb E. Elboray, Chenliang Hu, Farzad Zamani, Anirban Mukherjee, Yuri Takada, Yasunobu Yamashita, Mie Morita, Mano Horinaka, Yoshihiro Sowa, Mitsuharu Masuda, Toshiyuki Sakai, Takayoshi Suzuki
Publikováno v:
ACS medicinal chemistry letters. 13(10)
Anticancer drug delivery by small molecules offers a number of advantages over conventional macromolecular drug delivery systems. We previously developed phenylcyclopropylamine (PCPA)-drug conjugates (PDCs) as small-molecule-based drug delivery vehic