Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Takanao Otsuka"'
Autor:
Shun Sato, Kana Yamamoto, Moeno Ito, Katsutoshi Nishino, Takanao Otsuka, Kazuhiro Irie, Masaya Nagao
Publikováno v:
Molecules, Vol 28, Iss 10, p 4197 (2023)
Background: Cathepsin K, which is involved in bone resorption, is a good target for treating osteoporosis, but no clinically approved medicine has been developed. Recently, allosteric inhibitors with high specificity and few side effects have been at
Externí odkaz:
https://doaj.org/article/c3309eb4348e4b84b3a4d29c2794a80d
Autor:
Takeshi Ishikawa, Kaori Ohta, Keinosuke Okamoto, Tomoe Negishi, Keiji Oguma, Takanao Otsuka, Yuta Yuhara, Sakae Arimoto-Kobayashi, Yoshihiro Nakajima, Yuka Ayabe
Publikováno v:
Mutagenesis. 30:537-544
Epidemiological studies have demonstrated a close association between infection with Helicobacter pylori (H.pylori) and the development of gastric carcinoma. Chronic H.pylori infection increases the frequency of mutation in gastric epithelial cells.
Autor:
Toshimasa, Yamamoto, Takanao, Otsuka
Publikováno v:
Naturalistae. 17:63-65
Autor:
Hiroshi Hatanaka, Seiji Hashimoto, Masanori Okamoto, Yuko Muramatsu, Tomoko Nakanishi, Motohiro Hino, Takanao Otsuka
Publikováno v:
The Journal of Antibiotics. 53:449-458
WF14865A and B, novel cathepsins B and L inhibitors, were produced and isolated separately from the culture mycelium of a fungal strain Aphanoascus fulvescens No. 14865. Spectroscopic analysis revealed that both WF14865A and B were composed of trans-
Autor:
Tomoko Nakanishi, Masanori Okamoto, Shigehiro Takase, Seiji Hashimoto, Takanao Otsuka, Yuko Muramatsu, Hiroshi Hatanaka, Motohiro Hino, Tomoji Fujisawa Pharmaceutical Co. Ltd. Higaki
Publikováno v:
The Journal of Antibiotics. 52:536-541
WF14861, a novel cathepsins B and L inhibitor, was obtained from the culture mycelium of a fungus strain Colletotrichum sp. No. 14861. Spectroscopic analysis showed that WF14861 consisted of trans-epoxysuccinic acid, L-tyrosine and spermidine, WF1486
Autor:
Keiji Hemmi, Seiji Yoshimura, Takanao Otsuka, Shigehiro Takase, Masanori Okamoto, Okada Satoshi
Publikováno v:
The Journal of Antibiotics. 51:655-664
The structure of WA8242B, a potent novel inhibitor against phospholipase A2, was fully characterized by spectroscopic methods and chemical degradation. The success of total synthesis of WA8242B confirmed the structure and allowed the pharmacological
Autor:
Masanori Okamoto, Yasuhisa Tsurumi, Masakuni Okuhara, Seiji Yoshimura, Yuko Muramatsu, Takanao Otsuka, Hiroshi Hatanaka, Seiji Hashimoto
Publikováno v:
The Journal of Antibiotics. 51:1-7
WA8242A1, A2 and B, novel inhibitors of secretory phospholipase A2, were obtained from the cultured mycelium of Streptomyces violaceusniger No. 8242. WA8242A1, A2 and B are structurally related compounds with α-aminoadipic acid and with various leng
Autor:
Takanao Otsuka, Masanori Okamoto, Yasuhisa Tsurumi, Hiroshi Hatanaka, Seiji Hashimoto, S. Yoshimura, Masakuni Okuhara, Y. Muramatsu
Publikováno v:
ChemInform. 29
Publikováno v:
ChemInform. 29
Autor:
Motohiro Hino, Masanori Okamoto, Seiji Hashimoto, Tomoko Nakanishi, Takanao Otsuka, Yuko Muramatsu, Tomoji Fujisawa Pharmaceutical Co. Ltd. Higaki, Hiroshi Hatanaka, Shigehiro Takase
Publikováno v:
ChemInform. 30