Publication
Research Papers : 2012
- Aplication of SO3H-silica gel to deprotection of silyl ethers
Fujii, H.; Yamada, T.; Hayashida, K.; Kuwada, M.; Hamasaki, A.; Nobuhara, K.; Ozeki, S.; Nagase, H.
Heterocycles, 2012, 85, 2685-2691.
- Essential structure of opioid κ receptor agonist nalfurafine for binding to the κ receptor 3: Synthesis of decahydro(iminoethano)phenanthrene derivatives with an oxygen functionality at the 3-position and their pharmacologies
Fujii, H.; Imaide, S.; Hirayama, S.; Nemoto, T.; Gouda, H.: Hirono, S. Nagase, H.
Bioorg. Med. Chem. Lett., 2012, 22, 7711-7714.
- Synthesis of new opioid derivatives with a propellane skeleton and their pharmacologies: Part 3, novel propellane derivatives with pentacyclic skeletons
Fujii, H.; Nakajima, R.; Akiyama, J.; Yamamoto, N.; Hirayama, S.; Nemoto, T.; Gouda, H.: Hirono, S.; Nagase, H.
Bioorg. Med. Chem. Lett., 2012, 22, 7697-7701.
- Synthesis of novel triplet drugs with 1,3,5-trioxazatriquinane skeletons and their pharmacologies. 3: Synthesis of novel triplet drugs with the bis(epoxymethano) or bis(dimethylepoxymethano) structure (double-capped triplet)
Wada, N.; Fujii, H.; Koyano, K.; Hirayama, S.; Iwai, T.; Nemoto, T.; Nagase, H.
Bioorg. Med. Chem. Lett., 2012, 22, 7551-7554.
- Novel series of 3-amino-N-(4-aryl-1,1-dioxothian-4-yl)butanamides as potent and selective dipeptidyl peptidase IV inhibitors
Nitta, A.; Fujii, H.; Sakami, S.; Satoh, M.; Nakai, J.; Satoh, S.; Kumagai, H., Kawai, H.
Bioorg. Med. Chem. Lett., 2012, 22, 7036-7040.
- Synthesis of quinolinomorphinan derivatives as highly selective δ opioid receptor ligands
Ida, Y.; Matsubara, A.; Nemoto, T.; Saito, M.; Hirayama, S.: Fujii, H.; Nagase, H.
Bioorg. Med. Chem., 2012, 20, 5810-5831.
- Investigation of 7-benzylidenenaltrexone derivatives as resistance reverser for chloroquine-resistant Plasmodium chabaudi
Miyata, Y.; Fujii, H.; Uenohara, Y.; Kobayashi, S.; Takeuchi, T.; Nagase, H.
Bioorg. Med. Chem. Lett., 2012, 22, 5174-5176.
- Essential structure of opioid κ receptor agonist nalfurafine for binding to the κ receptor 2: Synthesis of decahydro(iminoethano)phenanthrene derivatives and their pharmacologies
Nagase, H.; Imaide, S.; Hirayama, S.; Nemoto, T.; Fujii, H.
Bioorg. Med. Chem. Lett., 2012, 22, 5071-5074.
- Essential structure of opioid κ receptor agonist nalfurafine for binding to κ receptor 1: Synthesis of decahydroisoquinoline derivatives and their pharmacologies
Nagase, H.; Imaide, S.; Yamada, T.; Hirayama, S.; Nemoto, T.; Yamaotsu, N.; Hirono, S.; Fujii, H.
Chem. Pharm. Bull., 2012, 60, 945-948.
- Synthesis of new opioid derivatives with a propellane skeleton and their pharmacology. Part 2: Propellane derivatives with an amide side chain
Nagase, H.; Akiyama, J.; Nakajima, R.; Hirayama, S.; Nemoto, T.; Gouda, H.; Hirono, S.; Fujii, H.
Bioorg. Med. Chem. Lett., 2012, 22, 2775-2779.
- Design and synthesis of novel opioid ligands with an azabicyclo[2.2.2]octane skeleton and their pharmacologies
Watanabe, Y.; Kitazawa, S.; Fujii, H.; Nemoto, T.; Hirayama, S.; Nagase, H.
Bioorg. Med. Chem. Lett., 2012, 22, 2689-2692.
- Effects of mirtazapine on sleep disturbance under neuropathic pain-like state
Enomoto, T.; Yamashita, A.; Torigoe, K.; Horiuchi, H.; Hirayama, S.; Nakahara, K.; Yanase, M.; Sakai, H.; Ikegami, D.; Nagase, H.; Suzuki, T.; Iseki, M.; Inada, E.; Narita, M.
Synapse, 2012, 66, 483-488.
- Synthesis of quinolinomorphinan-4-ol derivatives as δ opioid receptor agonists
Ida, Y.; Nemoto, T.; Hirayama, S.; Fujii, H.; Osa, Y.; Imai, M.; Nakamura, T.; Kanemasa, T.; Kato, A.; Nagase, H.
Bioorg. Med. Chem., 2012, 20, 949-961.
- Usefulness of Olanzapine as an Adjunct to Opioid Treatment and for the Treatment of Neuropathic Pain
Torigoe, K.; Nakahara, K.; Rahmadi, M.; Yoshizawa, K.; Horiuchi, H.; Hirayama, S.; Imai, S.; Kuzumaki, N.; Itoh, T.; Yamashita, A.; Shakunaga, K.; Yamasaki, M.; Nagase, H.; Matoba, M.; Suzuki, T.; Narita, M.
Anesthesiology, 2012, 116, 159-169.
Copyright (C) 2008 Laboratory of Medicinal Chemistry. All rights reserved.