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Featured researches published by Toru Okayama.


Methods in Enzymology | 2002

Design of nonpeptides from peptide ligands for peptide receptors.

Victor J. Hruby; Wei Qiu; Toru Okayama; Vadim A. Soloshonok

Publisher Summary To develop nonpeptide ligands, efforts are in progress to develop templates and aspects of conformational design that permit assembling of all components necessary for molecular recognition and transduction. The proper choice of template that can place the key side chain residue in 3D space is still difficult, and thus only partial success has been achieved in terms of potent and selective ligands. Nonpeptide design is a highly multidisciplinary area that often relies on (1) new asymmetric synthesis and methodologies for the preparation of novel molecules, (2) high-throughput screening of ligands and libraries of ligands using multiple in vitro and in vivo biological assays, (3) computational methods, and (4) state-of-the-art biophysical methods for determining structural, conformational, topographical, and dynamic properties of designed ligands. Studies since the early 1980s have demonstrated that agonists and antagonists have different structure–activity relationships. There still is no universal approach to develop antagonists from agonists for peptide hormones and neurotransmitters, but once a lead has been obtained, there are general approaches that can be used to further develop antagonists.


Journal of Medicinal Chemistry | 2002

Synthesis and structure-activity relationships of an orally available and long-acting analgesic peptide, Nα-amidino-Tyr-D-Arg-Phe-Meβala-OH (ADAMB)

Tadashi Ogawa; Tetsuhisa Miyamae; Kimie Murayama; Kaori Okuyama; Toru Okayama; Masaki Hagiwara; Shinobu Sakurada; Tadanori Morikawa


Journal of Medicinal Chemistry | 1999

Exploring the structure-activity relationships of [1-(4-tert-butyl-3'-hydroxy)benzhydryl-4-benzylpiperazine] (SL-3111), a high-affinity and selective δ-opioid receptor nonpeptide agonist ligand

Josue Alfaro-Lopez; Toru Okayama; Keiko Hosohata; Peg Davis; Frank Porreca; Henry I. Yamamura; Victor J. Hruby


Archive | 1988

HYDROXAMIC ACID TETRAPEPTIDE DERIVATIVES

Shinjiro Odake; Toru Okayama; Masami Obata; Tadanori Morikawa; Yutaka Nagai


Chemical & Pharmaceutical Bulletin | 2003

Synthesis and antinociceptive activity of orally active opioid peptides: improvement of oral bioavailability by esterification.

Tadashi Ogawa; Mamoru Araki; Tetsuhisa Miyamae; Toru Okayama; Masaki Hagiwara; Shinobu Sakurada; Tadanori Morikawa


International Journal of Peptide and Protein Research | 2009

STRUCTURE-ACTIVITY STUDIES ON C-TERMINAL HIRUDIN PEPTIDES CONTAINING SULFATED TYROSINE RESIDUES

Ryo Muramatsu; Yasuhiko Komatsu; Eriko Nukui; Toru Okayama; Tadanori Morikawa; Kyoichi Kobashi; Hideya Hayashi


Organic Letters | 2000

4-Alkoxy-2-hydroxybenzaldehyde (AHB): a versatile aldehyde linker for solid-phase synthesis of C-terminal modified peptides and peptidomimetics.

Toru Okayama; and Andrew Burritt; Victor J. Hruby


Archive | 1988

Novel acylamino acid and acylpeptide compound

Masaki Hagiwara; Kazuya Hongo; Arinori Iwasaki; Shinjiro Kotake; Osamu Matsuo; Tetsuhisa Miyamae; Tadanori Morikawa; Masaharu Nakano; Toru Okayama; Eiko Ouchi; Keiji Takaoka-shi Sakamoto


Peptide science : proceedings of the ... Japanese Peptide Symposium | 2003

Exploration of Orally-Available and Long-Acting Opioid peptides

Toru Okayama; Tetsuhisa Miyamae; Hiroko Uchiyama; Tadashi Ogawa; Mamoru Araki; Masaki Hagiwara; Shinobu Sakurada; Tadanori Morikawa


Peptide science : proceedings of the ... Japanese Peptide Symposium | 2002

Synthesis and in vivo Structure-Activity Relationships (SAR) of Orally-Active Analgesic Peptide, N^α-Amidino-Tyr-D-Arg-Phe-MeβAla-OH (ADAMB)

Tadashi Ogawa; Mamoru Araki; Tetsuhisa Miyamae; Toru Okayama; Masaki Hagiwara; Shinobu Sakurada; Tadanori Morikawa

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Tadanori Morikawa

Tokyo Medical and Dental University

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Shinobu Sakurada

Tohoku Pharmaceutical University

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Mamoru Araki

Kyoto Pharmaceutical University

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Peg Davis

University of Arizona

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