Kato A - Search Results

1

Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues.

Wu QK, Kinami K, Kato A, Li YX, Fleet GWJ, Yu CY, Jia YM. Wu QK, et al. Among authors: kato a. Molecules. 2019 Oct 15;24(20):3712. doi: 10.3390/molecules24203712. Molecules. 2019. PMID: 31619020 Free PMC article.

2

Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis.

Asano N, Kato A, Miyauchi M, Kizu H, Kameda Y, Watson AA, Nash RJ, Fleet GW. Asano N, et al. Among authors: kato a. J Nat Prod. 1998 May;61(5):625-8. doi: 10.1021/np9705726. J Nat Prod. 1998. PMID: 9599261

3

Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.

Asano N, Nishida M, Kato A, Kizu H, Matsui K, Shimada Y, Itoh T, Baba M, Watson AA, Nash RJ, Lilley PM, Watkin DJ, Fleet GW. Asano N, et al. Among authors: kato a. J Med Chem. 1998 Jul 2;41(14):2565-71. doi: 10.1021/jm970836l. J Med Chem. 1998. PMID: 9651160

4

Polyhydroxylated pyrrolidine and pyrrolizidine alkaloids from Hyancinthoides non-scripta and Scilla campanulata.

Kato A, Adachi I, Miyauchi M, Ikeda K, Komae T, Kizu H, Kameda Y, Watson AA, Nash RJ, Wormald MR, Fleet GW, Asano N. Kato A, et al. Carbohydr Res. 1999 Mar 31;316(1-4):95-103. doi: 10.1016/s0008-6215(99)00043-9. Carbohydr Res. 1999. PMID: 10515698

5

Novel alpha-L-fucosidase inhibitors from the bark of Angylocalyx pynaertii (Leguminosae).

Asano N, Yasuda K, Kizu H, Kato A, Fan JQ, Nash RJ, Fleet GW, Molyneux RJ. Asano N, et al. Among authors: kato a. Eur J Biochem. 2001 Jan;268(1):35-41. doi: 10.1046/j.1432-1327.2001.01837.x. Eur J Biochem. 2001. PMID: 11121099 Free article.

6

New sugar-mimic alkaloids from the pods of Angylocalyx pynaertii.

Yasuda K, Kizu H, Yamashita T, Kameda Y, Kato A, Nash RJ, Fleet GW, Molyneux RJ, Asano N. Yasuda K, et al. Among authors: kato a. J Nat Prod. 2002 Feb;65(2):198-202. doi: 10.1021/np010360f. J Nat Prod. 2002. PMID: 11858756

7

Isolation of glycosidase-inhibiting hyacinthacines and related alkaloids from Scilla socialis.

Kato A, Kato N, Adachi I, Hollinshead J, Fleet GW, Kuriyama C, Ikeda K, Asano N, Nash RJ. Kato A, et al. Among authors: kato n. J Nat Prod. 2007 Jun;70(6):993-7. doi: 10.1021/np0700826. Epub 2007 May 31. J Nat Prod. 2007. PMID: 17536859

8

Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases.

Minami Y, Kuriyama C, Ikeda K, Kato A, Takebayashi K, Adachi I, Fleet GW, Kettawan A, Okamoto T, Asano N. Minami Y, et al. Among authors: kato a. Bioorg Med Chem. 2008 Mar 15;16(6):2734-40. doi: 10.1016/j.bmc.2008.01.032. Epub 2008 Jan 26. Bioorg Med Chem. 2008. PMID: 18258441

9

Synthesis and glycosidase inhibition of the enantiomer of (-)-steviamine, the first example of a new class of indolizidine alkaloid.

Hu XG, Bartholomew B, Nash RJ, Wilson FX, Fleet GW, Nakagawa S, Kato A, Jia YM, van Well R, Yu CY. Hu XG, et al. Among authors: kato a. Org Lett. 2010 Jun 4;12(11):2562-5. doi: 10.1021/ol1007718. Org Lett. 2010. PMID: 20438104

10

4-C-Me-DAB and 4-C-Me-LAB - enantiomeric alkyl-branched pyrrolidine iminosugars - are specific and potent α-glucosidase inhibitors; acetone as the sole protecting group.

da Cruz FP, Newberry S, Jenkinson SF, Wormald MR, Butters TD, Alonzi DS, Nakagawa S, Becq F, Norez C, Nash RJ, Kato A, Fleet GW. da Cruz FP, et al. Among authors: kato a. Tetrahedron Lett. 2011 Jan 12;52(2):219-223. doi: 10.1016/j.tetlet.2010.10.173. Tetrahedron Lett. 2011. PMID: 21157573 Free PMC article.

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