Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Akihito Ogasawara"'
Publikováno v:
Pharmacology Research & Perspectives, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Dersimelagon (formerly MT‐7117) is a novel, orally administered nonpeptide small molecule selective agonist for melanocortin 1 receptor currently being investigated for the treatment of erythropoietic protoporphyria, X‐linked protoporphy
Externí odkaz:
https://doaj.org/article/8c0fa5619e474aa9b0fcfcd6b9ae3e38
Autor:
Kei Ogawa, Ryosuke Ide, Kirstine Belongie, Minoru Tsuda, Hiroki Kawanishi, Renli Teng, Akihito Ogasawara
Publikováno v:
Clinical Pharmacology in Drug Development. 12:493-501
Publikováno v:
Pharmacology Research & Perspectives. 11
Autor:
Akihito Ogasawara, Kei Ogawa, Ryosuke Ide, Yuka Ikenaga, Chie Fukunaga, Satoshi Nakayama, Minoru Tsuda
Publikováno v:
European Journal of Clinical Pharmacology.
Purpose To describe outcomes from the first-in-human study of dersimelagon, an investigational oral selective MC1R agonist, under development for the treatment of erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP). Methods In this
Autor:
Yoshinobu Nakamaru, Akihito Ogasawara, Tomohisa Nakada, Koki Kojima, Hiroshi Yamazaki, Hidetoshi Shimizu, Kosuke Yoshida
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 47(2)
Predicting the pharmacokinetics of compounds in humans is an important part of the drug development process. In this study, the plasma concentration profiles of 10 marketed compounds exhibiting two-phase elimination after intravenous administration i
Publikováno v:
Drug Metabolism and Disposition. 37:2127-2136
Irreversible inhibition, characterized as mechanism-based inhibition (MBI), of cytochrome P450 in drugs has to be avoided for their safe use. A comprehensive assessment of drug-drug interaction (DDI) potential is important during the drug discovery p
Autor:
Ayumi Ueda, Kazuo Nii, Akihito Ogasawara, Takahiro Yoshikawa, Masahiro Utoh, Toshiyuki Kume, Koichiro Fukuzaki
Publikováno v:
Drug Metabolism and Disposition. 37:122-128
Drugs with potential drug-drug interactions (DDIs) may have a limited scope of use and, at worst, may have to be withdrawn from the market. Therefore, during the drug discovery process it is important to select drug candidates with reduced potential
Publikováno v:
Drug Metabolism and Disposition. 35:410-418
Because the expression of drug-metabolizing enzymes and drug efflux transporters has been shown in the intestine, the contribution of this tissue to the first-pass effect has become of significant interest. Consequently, a comprehensive understanding
Autor:
Akira Hara, Toshihiro Nakayama, Kumiko Sato, Masayuki Nakanishi, Akihito Ogasawara, Yoshihiro Deyashiki, Yoshiyuki Miyabe
Publikováno v:
The Biochemical journal. 299
Human liver contains two dihydrodiol dehydrogenases, DD2 and DD4, associated with 3 alpha-hydroxysteroid dehydrogenase activity. We have raised polyclonal antibodies that cross-reacted with the two enzymes and isolated two 1.2 kb cDNA clones (C9 and
Autor:
YOSHIHIRO, DEYASHIKI, AKIHITO, OGASAWARA, TOSHIHIRO, NAKAYAMA, MASAYUKI, NAKANISHI, YOSHIYUKI, MIYABE, KUMIKO, SATOH, AKIRA, HARA
Publikováno v:
岐阜藥科大學紀要 = The annual proceedings of Gifu College of Pharmacy. 44:83