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Cancer Science|March 29, 2016
Identification of anti-cancer chemical compounds using Xenopus embryosMasamitsu Tanaka, Sei Kuriyama, Go Itoh, et al.
Organic Letters|February 10, 2010
Syntheses and biological evaluation of irciniastatin A and the C1-C2 alkyne analogueTsubasa Watanabe, Takamichi Imaizumi, Takumi Chinen, et al.
Bioconjugate Chemistry|December 24, 2009
Cleavable linker for photo-cross-linked small-molecule affinity matrixNaoki Kanoh, Hiroshi Takayama, Kaori Honda, et al.
BMC Pharmacology|May 31, 2011
Synthesis of 86 species of 1,5-diaryl-3-oxo-1,4-pentadienes analogs of curcumin can yield a good lead in vivoChieko Kudo, Hiroyuki Yamakoshi, Atsuko Sato, et al.
Bioorganic & Medicinal Chemistry|January 12, 2010
Structure-activity relationship of C5-curcuminoids and synthesis of their molecular probes thereofHiroyuki Yamakoshi, Hisatsugu Ohori, Chieko Kudo, et al.
Angewandte Chemie (International Ed. in English)|May 22, 2023
Asymmetric Total Synthesis of Cytotrienin A: Late-Stage Installation of C11 Side Chain onto the Macrolactam ScaffoldYuki Tateishi, Ryo Sato, Shingo Komatsu, et al.
Cancer Science|January 29, 2011
Curcumin analog GO-Y030 is a novel inhibitor of IKKβ that suppresses NF-κB signaling and induces apoptosisAtsuko Sato, Chieko Kudo, Hiroyuki Yamakoshi, et al.
Nucleic Acids Symposium Series (2004)|November 22, 2007
Synthesis of an enantiomeric DNA oligomer and its T-HgII-T base-pair formationKaichiro Haruta, Yoshiyuki Tanaka, Takuya Kawamura, et al.
Chemistry, an Asian Journal|September 28, 2012
Synthesis and structure-activity relationship of vicenistatin, a cytotoxic 20-membered macrolactam glycosideHayato Fukuda, Yuko Nishiyama, Shiina Nakamura, et al.
Organic & Biomolecular Chemistry|November 2, 2016
Reversibility of the thia-Michael reaction of cytotoxic C5-curcuminoid and structure-activity relationship of bis-thiol-adducts thereofAki Kohyama, Michihiro Fukuda, Shunsuke Sugiyama, et al.
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