Terashima S - Search Results

1

Synthesis and biological activity of enantiomeric pairs of 5-(Alk-2-enyl)thiolactomycin and 5-[(E)-Cycloalk-2-enylidenemethyl]thiolactomycin congeners.

Ohata K, Terashima S. Ohata K, et al. Among authors: terashima s. Chem Pharm Bull (Tokyo). 2009 Sep;57(9):920-36. doi: 10.1248/cpb.57.920. Chem Pharm Bull (Tokyo). 2009. PMID: 19721252 Free article.

2

Synthesis and biological activity of enantiomeric pairs of 5-vinylthiolactomycin congeners.

Ohata K, Terashima S. Ohata K, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2007 Jul 15;17(14):4070-4. doi: 10.1016/j.bmcl.2007.04.067. Epub 2007 Apr 25. Bioorg Med Chem Lett. 2007. PMID: 17507223

3

Synthesis and biological activity of enantiomeric pairs of 5-[(E)-cycloalk-2-enylidenemethyl]thiolactomycin congeners.

Ohata K, Terashima S. Ohata K, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2008 Oct 15;18(20):5598-600. doi: 10.1016/j.bmcl.2008.08.103. Epub 2008 Aug 31. Bioorg Med Chem Lett. 2008. PMID: 18805004

4

Synthesis and matrix metalloproteinase-12 inhibitory activity of ageladine A analogs.

Ando N, Terashima S. Ando N, et al. Among authors: terashima s. Chem Pharm Bull (Tokyo). 2011;59(5):579-96. doi: 10.1248/cpb.59.579. Chem Pharm Bull (Tokyo). 2011. PMID: 21532196 Free article.

5

Synthesis and muscarinic M(2) subtype antagonistic activity of enantiomeric pairs of 3-demethylhimbacine (3-norhimbacine) and its C(4)-epimer.

Takadoi M, Yamaguchi K, Terashima S. Takadoi M, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2002 Nov 18;12(22):3271-3. doi: 10.1016/s0960-894x(02)00695-9. Bioorg Med Chem Lett. 2002. PMID: 12392730

6

Synthesis and muscarinic M2 subtype antagonistic activity of unnatural ent-himbacine and an enantiomeric pair of (2'S,6'R)-diepihimbacine.

Takadoi M, Terashima S. Takadoi M, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2002 Oct 21;12(20):2871-3. doi: 10.1016/s0960-894x(02)00566-8. Bioorg Med Chem Lett. 2002. PMID: 12270166

7

Synthesis of novel ageladine A analogs showing more potent matrix metalloproteinase (MMP)-12 inhibitory activity than the natural product.

Ando N, Terashima S. Ando N, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2009 Sep 15;19(18):5461-3. doi: 10.1016/j.bmcl.2009.07.099. Epub 2009 Jul 23. Bioorg Med Chem Lett. 2009. PMID: 19665375

8

Palbinone, a novel terpenoid from Paeonia albiflora; potent inhibitory activity on 3 alpha-hydroxysteroid dehydrogenase.

Kadota S, Terashima S, Basnet P, Kikuchi T, Namba T. Kadota S, et al. Among authors: terashima s. Chem Pharm Bull (Tokyo). 1993 Mar;41(3):487-90. doi: 10.1248/cpb.41.487. Chem Pharm Bull (Tokyo). 1993. PMID: 8477499

9

Synthetic studies on himbacine, a potent antagonist of the muscarinic M2 subtype receptor. Part 2: synthesis and muscarinic M2 subtype antagonistic activity of the novel himbacine congeners modified at the C-3 position of lactone moiety.

Takadoi M, Yamaguchi K, Terashima S. Takadoi M, et al. Among authors: terashima s. Bioorg Med Chem. 2003 Apr 3;11(7):1169-86. doi: 10.1016/s0968-0896(02)00665-x. Bioorg Med Chem. 2003. PMID: 12628644

10

Synthesis and matrix metalloproteinase (MMP)-12 inhibitory activity of ageladine A and its analogs.

Ando N, Terashima S. Ando N, et al. Among authors: terashima s. Bioorg Med Chem Lett. 2007 Aug 15;17(16):4495-9. doi: 10.1016/j.bmcl.2007.06.005. Epub 2007 Jun 6. Bioorg Med Chem Lett. 2007. PMID: 17574851

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