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Organic & Biomolecular Chemistry|March 25, 2006
Synthesis of beta-analogues of C-mannosyltryptophan, a novel C-glycosylamino acid found in proteinsToshio Nishikawa, Yuya Koide, Akira Kanakubo, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2007
Geldanamycin derivatives and neuroprotective effect on cultured P19-derived neuronsSarin Tadtong, Duangdeun Meksuriyen, Somboon Tanasupawat, et al.
Proceedings of the Japan Academy. Series B, Physical and Biological Sciences|November 11, 2008
Cysteine-390 is the binding site of luminous substance with symplectin, a photoprotein from Okinawan squid, Symplectoteuthis oualaniensisMinoru Isobe, Masaki Kuse, Naoki Tani, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 6, 2022
A hybrid of 1-deoxynojirimycin and benzotriazole induces preferential inhibition of butyrylcholinesterase (BuChE) over acetylcholinesterase (AChE)Tereza Cristina Santos Evangelista, Óscar López, Adrián Puerta, et al.
Toxicon : Official Journal of the International Society on Toxinology|October 8, 2003
Biological activity of 8,11-dideoxytetrodotoxin: lethality to mice and the inhibitory activity to cytotoxicity of ouabain and veratridine in mouse neuroblastoma cells, Neuro-2aMari Yotsu-Yamashita, Daisuke Urabe, Masanori Asai, et al.
Royal Society Open Science|February 20, 2025
An isofagomine analogue with an amidine group in the 1,6-positionI Caroline Vaaland Holmgard, Idd Andrea Christensen, Ljupcho Pejov, et al.
Chemistry, an Asian Journal|April 19, 2007
Synthesis of urea-tethered disaccharides in waterYoshiyasu Ichikawa, Yohei Matsukawa, Mari Tamura, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 25, 2014
Total synthesis of chiriquitoxin, an analogue of tetrodotoxin isolated from the skin of a dart frogMasaatsu Adachi, Takuya Imazu, Ryo Sakakibara, et al.
Organic Letters|July 14, 2006
One-pot transformation of trichloroacetamide into readily deprotectable carbamatesToshio Nishikawa, Daisuke Urabe, Miho Tomita, et al.
Organic Letters|December 1, 2006
Stereocontrolled route to vicinal diamines by [3.3] sigmatropic rearrangement of allyl cyanate: asymmetric synthesis of anti-(2R,3R)- and syn-(2R,3S)-2,3-diaminobutanoic acidsYoshiyasu Ichikawa, Haruka Egawa, Takashi Ito, et al.
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