Kanoh N - Search Results

1

Syntheses of naturally occurring cytotoxic [7.7]paracyclophanes, (-)-cylindrocyclophane A and its enantiomer, and implications for biological activity.

Yamakoshi H, Ikarashi F, Minami M, Shibuya M, Sugahara T, Kanoh N, Ohori H, Shibata H, Iwabuchi Y. Yamakoshi H, et al. Among authors: kanoh n. Org Biomol Chem. 2009 Sep 21;7(18):3772-81. doi: 10.1039/b909646a. Epub 2009 Jul 14. Org Biomol Chem. 2009. PMID: 19707682

2

Synthesis of an enantiomeric DNA oligomer and its T-HgII-T base-pair formation.

Haruta K, Tanaka Y, Kawamura T, Kondo Y, Ono A, Yamakoshi H, Kanoh N, Iwabuchi Y. Haruta K, et al. Among authors: kanoh n. Nucleic Acids Symp Ser (Oxf). 2007;(51):187-8. doi: 10.1093/nass/nrm094. Nucleic Acids Symp Ser (Oxf). 2007. PMID: 18029649

3

Synthetic studies on daphnicyclidin A: enantiocontrolled construction of the BCD ring system.

Ikeda S, Shibuya M, Kanoh N, Iwabuchi Y. Ikeda S, et al. Among authors: kanoh n. Org Lett. 2009 Apr 16;11(8):1833-6. doi: 10.1021/ol9003405. Org Lett. 2009. PMID: 19320481

4

An expedient route to a potent gastrin/CCK-B receptor antagonist (+)-AG-041R.

Sato S, Shibuya M, Kanoh N, Iwabuchi Y. Sato S, et al. Among authors: kanoh n. J Org Chem. 2009 Oct 2;74(19):7522-4. doi: 10.1021/jo901352u. J Org Chem. 2009. PMID: 19719158

5

Highly enantioselective intramolecular aza-spiroannulation onto indoles using chiral rhodium catalysis: asymmetric entry to the spiro-beta-lactam core of chartellines.

Sato S, Shibuya M, Kanoh N, Iwabuchi Y. Sato S, et al. Among authors: kanoh n. Chem Commun (Camb). 2009 Nov 7;(41):6264-6. doi: 10.1039/b913770j. Epub 2009 Sep 2. Chem Commun (Camb). 2009. PMID: 19826689

6

Cleavable linker for photo-cross-linked small-molecule affinity matrix.

Kanoh N, Takayama H, Honda K, Moriya T, Teruya T, Simizu S, Osada H, Iwabuchi Y. Kanoh N, et al. Bioconjug Chem. 2010 Jan;21(1):182-6. doi: 10.1021/bc900316q. Bioconjug Chem. 2010. PMID: 20028022

7

Structure-activity relationship of C5-curcuminoids and synthesis of their molecular probes thereof.

Yamakoshi H, Ohori H, Kudo C, Sato A, Kanoh N, Ishioka C, Shibata H, Iwabuchi Y. Yamakoshi H, et al. Among authors: kanoh n. Bioorg Med Chem. 2010 Feb;18(3):1083-92. doi: 10.1016/j.bmc.2009.12.045. Epub 2009 Dec 23. Bioorg Med Chem. 2010. PMID: 20060305

8

Total synthesis and determination of the absolute configuration of (-)-idesolide.

Yamakoshi H, Shibuya M, Tomizawa M, Osada Y, Kanoh N, Iwabuchi Y. Yamakoshi H, et al. Among authors: kanoh n. Org Lett. 2010 Mar 5;12(5):980-3. doi: 10.1021/ol9029676. Org Lett. 2010. PMID: 20136117

9

Syntheses and biological evaluation of irciniastatin A and the C1-C2 alkyne analogue.

Watanabe T, Imaizumi T, Chinen T, Nagumo Y, Shibuya M, Usui T, Kanoh N, Iwabuchi Y. Watanabe T, et al. Among authors: kanoh n. Org Lett. 2010 Mar 5;12(5):1040-3. doi: 10.1021/ol1000389. Org Lett. 2010. PMID: 20141170

10

Irciniastatin A induces JNK activation that is involved in caspase-8-dependent apoptosis via the mitochondrial pathway.

Chinen T, Nagumo Y, Watanabe T, Imaizumi T, Shibuya M, Kataoka T, Kanoh N, Iwabuchi Y, Usui T. Chinen T, et al. Among authors: kanoh n. Toxicol Lett. 2010 Dec 15;199(3):341-6. doi: 10.1016/j.toxlet.2010.09.017. Toxicol Lett. 2010. PMID: 20920557

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